The review is a comprehensive discussion of current research advances,commercial scale developments,challenges,and techno-eco nomics for the entire H_(2) value chain,including production,mainly focusing on sustainable...The review is a comprehensive discussion of current research advances,commercial scale developments,challenges,and techno-eco nomics for the entire H_(2) value chain,including production,mainly focusing on sustainable sources,storage,and transport.The challenges,advantages,and uses of H_(2) energy are included at length.Moreover,apart from the sustainable production approaches,the approaches and current developments for combating the carbon dioxide(CO_(2))emissions from existing H_(2) production facilities are highlighted in terms of ca rbon capture,utilization,and storage(CCUS).Concisely,the review discusses current material and recent technological adva ncements in developing pilot projects and large-scale establishments for viable and rapidly emerging sou rce-ba sed H_(2) productio n.Moreover,the review also aims to provide an in-depthdiscussion and explore current developments based on the advantages of H_(2) energy in terms of its utilization,based on its high energy density,and its ability to be used as a feedstock and fuel.On the other hand,the challenges of H_(2) are also elabo rated.Next,the role of CCUS in a carbon-neutral economy and value chain for minimization of emissions from existing facilities is thoroughly deliberated,and the recent commercial-scale implementation of CCUS technologies is highlighted.Extending the utilization and recycling of captured CO_(2) emissions along with H_(2) to produce e-fuels in terms of current advances is detailed in this review.Fu rthermore,the most applicable,efficient,a nd develo ping approaches are discussed for physical and chemical H_(2) storage,considering recent la rge-scale implementations of liquid carriers and liquid organic hydrogen carriers as storage options.Lastly,the review elaborates on recent insights into advances in H_(2) transport infrastructure,including compressed and liquid H_(2) delivery via roads,ships,pipelines,and flight cargo.The review gives precise insights into the recent scenario through an elaborated conclusion of each discussion topic separately and a discussion of future perspectives.The current review will help researchers to fully understand the ongoing research advancements and challenges in the H_(2) value chain for formulating new solutions for sustainable H_(2) production,alo ng with focusing on suitable approaches for its storage and tra nsport to make the production and utilization of H_(2) applicable on a large scale.展开更多
MgH_(2) is a promising high-capacity solid-state hydrogen storage material,while its application is greatly hindered by the high desorption temperature and sluggish kinetics.Herein,intertwined 2D oxygen vacancy-rich V...MgH_(2) is a promising high-capacity solid-state hydrogen storage material,while its application is greatly hindered by the high desorption temperature and sluggish kinetics.Herein,intertwined 2D oxygen vacancy-rich V_(2)O_(5) nanosheets(H-V_(2)O_(5))are specifically designed and used as catalysts to improve the hydrogen storage properties of MgH_(2).The as-prepared MgH_(2)-H-V_(2)O_(5) composites exhibit low desorption temperatures(Tonset=185℃)with a hydrogen capacity of 6.54 wt%,fast kinetics(Ea=84.55±1.37 kJ mol^(-1) H_(2) for desorption),and long cycling stability.Impressively,hydrogen absorption can be achieved at a temperature as low as 30℃ with a capacity of 2.38 wt%within 60 min.Moreover,the composites maintain a capacity retention rate of~99%after 100 cycles at 275℃.Experimental studies and theoretical calculations demonstrate that the in-situ formed VH_(2)/V catalysts,unique 2D structure of H-V_(2)O_(5) nanosheets,and abundant oxygen vacancies positively contribute to the improved hydrogen sorption properties.Notably,the existence of oxygen vacancies plays a double role,which could not only directly accelerate the hydrogen ab/de-sorption rate of MgH_(2),but also indirectly affect the activity of the catalytic phase VH_(2)/V,thereby further boosting the hydrogen storage performance of MgH_(2).This work highlights an oxygen vacancy excited“hydrogen pump”effect of VH_(2)/V on the hydrogen sorption of Mg/MgH_(2).The strategy developed here may pave a new way toward the development of oxygen vacancy-rich transition metal oxides catalyzed hydride systems.展开更多
Zero-carbon parks have broad prospects in carbon neutralization.As an energy hub,hydrogen energy storage plays an important role in zero-carbon parks.However,the nonlinear characteristics of hydrogen energy storage sy...Zero-carbon parks have broad prospects in carbon neutralization.As an energy hub,hydrogen energy storage plays an important role in zero-carbon parks.However,the nonlinear characteristics of hydrogen energy storage systems(HESSs)have a significant impact on the system economy.Therefore,considering the variable working condition characteristics of HESSs,a hybrid operation method is proposed for HESS,to support the efficient and economic operation of zero-carbon parks,By analyzing the operating principle of a zero-carbon park with HESS,the system structure framework and variable condition linearization model of the equipment in HESS are established.Moreover,considering the energy output characteristics of hydrogen energy storage equipment under variable working conditions,a multimodule hybrid operation strategy is proposed for electrolytic and fuel cells,effectively meeting the thermoelectric load demand of zero-carbon parks in different scenarios.Finally,the economy of the proposed hybrid operation strategy was verified in typical scenarios,using a zero-carbon park embedded with a HESS.展开更多
Underground hydrogen storage(UHS)and compressed air energy storage(CAES)are two viable largescale energy storage technologies for mitigating the intermittency of wind and solar power.Therefore,it is meaningful to comp...Underground hydrogen storage(UHS)and compressed air energy storage(CAES)are two viable largescale energy storage technologies for mitigating the intermittency of wind and solar power.Therefore,it is meaningful to compare the properties of hydrogen and air with typical thermodynamic storage processes.This study employs a multi-physical coupling model to compare the operations of CAES and UHS,integrating gas thermodynamics within caverns,thermal conduction,and mechanical deformation around rock caverns.Gas thermodynamic responses are validated using additional simulations and the field test data.Temperature and pressure variations of air and hydrogen within rock caverns exhibit similarities under both adiabatic and diabatic simulation modes.Hydrogen reaches higher temperature and pressure following gas charging stage compared to air,and the ideal gas assumption may lead to overestimation of gas temperature and pressure.Unlike steel lining of CAES,the sealing layer(fibre-reinforced plastic FRP)in UHS is prone to deformation but can effectively mitigates stress in the sealing layer.In CAES,the first principal stress on the surface of the sealing layer and concrete lining is tensile stress,whereas UHS exhibits compressive stress in the same areas.Our present research can provide references for the selection of energy storage methods.展开更多
Metal–organic frameworks(MOFs)are highly promising porous materials known for their exceptional porosity,extensive surface area,and customizable pore structures,making them an ideal solution for hydrogen storage.Howe...Metal–organic frameworks(MOFs)are highly promising porous materials known for their exceptional porosity,extensive surface area,and customizable pore structures,making them an ideal solution for hydrogen storage.However,most MOFs research remains confined to the laboratory,lacking practical applications.To address this,the author proposes a shift towards practical applications,the creation of a comprehensive MOFs database,alignment of synthesis with practical considerations,and diversification of MOFs applications.These steps are crucial for harnessing the full potential of MOFs in real-world energy challenges.展开更多
Amidst the rapid development of renewable energy,the intermittency and instability of energy supply pose severe challenges and impose higher requirements on energy storage systems.Among the various energy storage tech...Amidst the rapid development of renewable energy,the intermittency and instability of energy supply pose severe challenges and impose higher requirements on energy storage systems.Among the various energy storage technologies,the coupled approach of power-to-hydrogen(H2)and underground H2storage(UHS)offers advantages such as extended storage duration and large-scale capacity,making it highly promising for future development.However,during UHS,particularly in porous media,microbial metabolic processes such as methanogenesis,acetogenesis,and sulfate reduction may lead to H2consumption and the production of byproducts.These microbial activities can impact the efficiency and safety of UHS both positively and negatively.Therefore,this paper provides a comprehensive review of experimental,numerical,and field studies on microbial interactions in UHS within porous media,aiming to capture research progress and elucidate microbial effects.It begins by outlining the primary types of UHS and the key microbial metabolic processes involved.Subsequently,the paper introduces the experimental approaches for investigating gas-water-rock-microbe interactions and interfacial properties,the models and simulators used in numerical studies,and the procedures implemented in field trials.Furthermore,it analyzes and discusses microbial interactions and their positive and negative impacts on UHS in porous media,focusing on aspects such as H2consumption,H2flow,and storage safety.Based on these insights,recommendations for site selection,engineering operations,and on-site monitoring of UHS,as well as potential future research directions,are provided.展开更多
Hydrogen is a generally abundant, safe, clean and environmentally apt alternative fuel, which replenishes the void generated by depleting fossil fuel reserves. The adoption of hydrogen as an energy source has been res...Hydrogen is a generally abundant, safe, clean and environmentally apt alternative fuel, which replenishes the void generated by depleting fossil fuel reserves. The adoption of hydrogen as an energy source has been restricted to low levels due to the complications associated with its viable storage and usage. Existing technologies, such as storage of hydrogen in compressed and liquefied forms are not adequate to meet the broad on-board applications. The gravimetric energy density(120 MJ/kg) of hydrogen is three times higher than that of gasoline products, so solid-state hydrogen storage is advantageous.Metal-organic frameworks(MOFs), multi-walled carbon nanotubes(MWCNTs) and graphene are solid adsorbents majorly employed for efficient H_2 storage. The prominent features of MOFs such as permanent porosity, structural rigidity, and surface area are attractive and ideal for hydrogen storage. In addition,nanostructured carbon materials(MWCNTs and graphene) and their composites have demonstrated significant hydrogen storage capacities. Some important parameters for the success of the hydrogen economy include high storage density, adsorption/desorption temperature and cycling time. Cryo-hydrogen storage was achieved in MOFs and their composites with carbon structures, but storage at ambient temperature and acceptable pressures is a major hurdle. This review discusses various strategies and mechanisms in the design of adsorbents explored to improve H_2 storage capacities and afford opportunities to develop new sustainable hydrogen technologies to meet energy targets.展开更多
The effects of Sr TiO_3 on the hydrogen storage properties of MgH_2 have been studied for the first time.The onset dehydrogenation temperature of the MgH_2-10 wt% SrTiO_3 is found to be 275 ℃, which is 55 ℃ lower as...The effects of Sr TiO_3 on the hydrogen storage properties of MgH_2 have been studied for the first time.The onset dehydrogenation temperature of the MgH_2-10 wt% SrTiO_3 is found to be 275 ℃, which is 55 ℃ lower as compared to the as-milled MgH_2. The composite is able to absorb 4.3 wt% of hydrogen in 60 min instead of 1.1 wt% for the as-milled Mg H_2. Meanwhile, the composite is able to release 5.3 wt% of hydrogen in 17 min compared to 1.9 wt% by the as-milled Mg H_2 at 320 ℃. The calculated Eaof the Mg H_2-10 wt% SrTiO_3 is 109 k J/mol, which is 26.3 kJ/mol lower than the calculated Eaof the as-milled MgH_2. The Sr TiO_3 is not decomposed during the ball milling and the re/dehydrogenation processes. The catalytic effect shown by the SrTiO_3 is owing to its ability to change the physical structure of the MgH_2 particles during the ball milling process.展开更多
In this study, the hydrogen storage properties of MgH-X wt% KNiF（X = 5, 10, 15, 20, and 50） were investigated for the first time. From the analysis of the onset desorption temperature and isothermal de/absorption ki...In this study, the hydrogen storage properties of MgH-X wt% KNiF（X = 5, 10, 15, 20, and 50） were investigated for the first time. From the analysis of the onset desorption temperature and isothermal de/absorption kinetics, it was shown that MgH+ 5 wt% KNiFsample has the best performance. The 5wt% doped sample started to release hydrogen at about 260 °C, which was a reduction of about 95 °C and 157 oC compared with the as-milled and as-received MgH. In addition, the de/absorption kinetics of the MgH+ 5 wt% KNiFwere also improved significantly compared to the un-doped MgH. The apparent activation energy for hydrogen desorption exhibited the decrement from 167.0 k J/mol for as-milled MgHto 111.0 k J/mol with the addition of 5 wt% KNiF. Moreover, the X-ray diffraction spectra displayed the formation of new phases of KF, KH, MgNi and MgNiHby doping the KNiFwith MgHafter the dehydrogenation and rehydrogenation processes. The scanning electron microscope results revealed that MgHdoped with 5 wt% KNiFdemonstrated the smallest particle size compared to the as-received and as-milled MgH. It is believed that the formation of in situ active species of KF, KH, and MgNi could provide a synergetic catalytic effect in enhancing the hydrogen sorption properties of MgH.展开更多
With the depletion of fossil fuels and global warming,there is an urgent demand to seek green,low-cost,and high-efficiency energy resources.Hydrogen has been considered as a potential candidate to replace fossil fuels...With the depletion of fossil fuels and global warming,there is an urgent demand to seek green,low-cost,and high-efficiency energy resources.Hydrogen has been considered as a potential candidate to replace fossil fuels,due to its high gravimetric energy density(142 MJ kg^(-1)),high abundance(H_(2)O),and environmentalfriendliness.However,due to its low volume density,effective and safe hydrogen storage techniques are now becoming the bottleneck for the"hydrogen economy".Under such a circumstance,Mg-based hydrogen storage materials garnered tremendous interests due to their high hydrogen storage capacity(~7.6 wt%for MgH_(2)),low cost,and excellent reversibility.However,the high thermodynamic stability(ΔH=-74.7 kJ mol^(-1)H_(2))and sluggish kinetics result in a relatively high desorption temperature(>300℃),which severely restricts widespread applications of MgH_(2).Nano-structuring has been proven to be an effective strategy that can simultaneously enhance the ab/de-sorption thermodynamic and kinetic properties of MgH_(2),possibly meeting the demand for rapid hydrogen desorption,economic viability,and effective thermal management in practical applications.Herein,the fundamental theories,recent advances,and practical applications of the nanostructured Mg-based hydrogen storage materials are discussed.The synthetic strategies are classified into four categories:free-standing nano-sized Mg/MgH_(2)through electrochemical/vapor-transport/ultrasonic methods,nanostructured Mg-based composites via mechanical milling methods,construction of core-shell nano-structured Mg-based composites by chemical reduction approaches,and multi-dimensional nano-sized Mg-based heterostructure by nanoconfinement strategy.Through applying these strategies,near room temperature ab/de-sorption(<100℃)with considerable high capacity(>6 wt%)has been achieved in nano Mg/MgH_(2)systems.Some perspectives on the future research and development of nanostructured hydrogen storage materials are also provided.展开更多
Activated carbons derived from corncob （CACs） were prepared by pyrolysis carbonization and KOH activation. Through modifying activation conditions, samples with large pore volume and ultrahigh BET specific surface a...Activated carbons derived from corncob （CACs） were prepared by pyrolysis carbonization and KOH activation. Through modifying activation conditions, samples with large pore volume and ultrahigh BET specific surface area could be obtained. The sample achieved the highest hydrogen uptake capacity of 5.80 wt% at 40 bar and -196℃ The as-obtained samples were characterized by N2-sorption, transmission electron microscopy （TEM） and scanning electron microscopy （SEM）. Besides, thermogravimetric analysis was also employed to investigate the activation behavior of CACs. Detailed investigation on the activation parameters reveals that moderate activation temperature and heating rate are favorable for preparing CACs with high surface area, large pore volume and optimal pore size distribution. Meanwhile, the micropore volume between 0.65 nm and 0.85 nm along with BET surface area and total pore volume has great effects on hydrogen uptake capacities. The present results indicate that CACs are the most promising materials for hydrogen storage application.展开更多
Zr1-xTixCo(x = 0, 0.1, 0.2, 0.3) alloys were prepared by arc-melting method and the effect of Ti substitution on hydrogen storage properties was studied systematically. Hydrogen desorption pressure-composition-tempera...Zr1-xTixCo(x = 0, 0.1, 0.2, 0.3) alloys were prepared by arc-melting method and the effect of Ti substitution on hydrogen storage properties was studied systematically. Hydrogen desorption pressure-composition-temperature(PCT) measurements were carried out using Sievert’s type volumetric apparatus for ZrCo(at 473 K, 573 K and 673 K) and Zr1-xTixCo alloys(at 673 K), respectively. Products after dehydrogenation were characterized by X-ray diffraction(XRD). In addition, the kinetics of Zr1-xTixCo hydride was investigated at 473 K and 673 K,respectively, under hydrogen pressure of 5 MPa. Results showed that Ti substitution for Zr did not change the crystal structure of ZrCo phase.With the increase of temperature from 473 K to 673 K, the extent of disproportionation for ZrCo alloy increased. With Ti content increasing at 673 K, the desorption equilibrium pressure of Zr1-xTixCo-H2 systems elevated and the disproportionation reaction of Zr1-xTixCo alloys was inhibited effectively. Ti substitution decreased the kinetics rate and the effective hydrogen storage capacity of Zr1-xTixCo alloys slightly.Generally speaking, it was found that Zr0.8Ti0.2Co alloy had better anti-disproportionation property with less decrease of effective hydrogen storage capacity which was beneficial to tritium application in the International Thermonuclear Experimental Reactor(ITER).展开更多
Gas hydrate is a new technology for energy gas（methane/hydrogen）storage due to its large capacity of gas storage and safe.But industrial application of hydrate storage process was hindered by someproblems.For methan...Gas hydrate is a new technology for energy gas（methane/hydrogen）storage due to its large capacity of gas storage and safe.But industrial application of hydrate storage process was hindered by someproblems.For methane,the main problems are low formation rateand storage capacity,which can be solved by strengthening mass andheat transfer,such as adding additives,stirring,bubbling,etc.Onekind of additives can change the equilibrium curve to reduce the formation pressure of methane hydrate,and the other kind of additivesis surfactant,which can form micelle with water and increase the interface of water-gas.Dry water has the similar effects on the methanehydrate as surfactant.Additionally,stirring,bubbling,and sprayingcan increase formation rate and storage capacity due to mass transferstrengthened.Inserting internal or external heat exchange also canimprove formation rate because of good heat transfer.For hydrogen,the main difficulties are very high pressure for hydrate formed.Tetrahydrofuran（THF）,tetrabutylammonium bromide（TBAB） andtetrabutylammonium fluoride（TBAF） have been proved to be able todecrease the hydrogen hydrate formation pressure significantly.展开更多
Three types of carbon nano-onions（CNOs） including Ni@CNOs.Fe3C@CNOs and Fe0.64Ni0.36@CNOs nanoparticles have been synthesized by catalytic decomposition of methane at 850 ℃ using nickel,iron and iron-nickel alloy c...Three types of carbon nano-onions（CNOs） including Ni@CNOs.Fe3C@CNOs and Fe0.64Ni0.36@CNOs nanoparticles have been synthesized by catalytic decomposition of methane at 850 ℃ using nickel,iron and iron-nickel alloy catalysts.Comparative and systematic studies have been carried out on the morphology,structural characteristics and graphitic crystallinity of these CNOs products.Furthermore,the electrochemical hydrogen storage properties of three types of CNOs have been investigated.Measurements show that the Ni@CNOs have the highest discharge capacity of 387.2 mAh/g,coiTesponding to a hydrogen storage of 1.42%.This comparison study shows the advantages of each catalyst in the growth of CNOs.enabling the controllable synthesis and tuning the properties of CNOs by mediating different metals and their alloy for using in the fuel cell system.展开更多
Stability of borohydrides is determined by the localization of the negative charge on the boron atom.Ionic liquids(ILs) allow to modify the stability of the borohydrides and promote new dehydrogenation pathways with a...Stability of borohydrides is determined by the localization of the negative charge on the boron atom.Ionic liquids(ILs) allow to modify the stability of the borohydrides and promote new dehydrogenation pathways with a lower activation energy. The combination of borohydride and IL is very easy to realize and no expensive rare earth metals are required. The composite of the ILs with complex hydrides decreases the enthalpy and activation energy for the hydrogen desorption. The Coulomb interaction between borohydride and IL leads to a destabilization of the materials with a significantly lower enthalpy for hydrogen desorption. Here, we report a simple ion exchange reaction using various ILs, such as vinylbenzyltrimethylammonium chloride([VBTMA][Cl]), 1-butyl-3-methylimidazolium chloride([bmim][Cl]), and 1-ethyl-1-methylpyrrolidinium bromide([EMPY][Br]) with NaBH4 to decrease the hydrogen desorption temperature. Dehydrogenation of 1-butyl-3-methylimidazolium borohydride([bmim][BH4]) starts below 100℃. The quantity of desorbed hydrogen ranges between 2.4 wt% and 2.9 wt%, which is close to the theoretical content of hydrogen. The improvement in dehydrogenation is due to the strong amine cation that destabilizes borohydride by charge transfer.展开更多
Mg-based hydrogen storage materials are considered to be one of the most promising solid-state hydrogen storage materials due to their large hydrogen storage capacity and low cost. However, slow hydrogen absorption/de...Mg-based hydrogen storage materials are considered to be one of the most promising solid-state hydrogen storage materials due to their large hydrogen storage capacity and low cost. However, slow hydrogen absorption/desorption rate and excessive hydrogen absorption/desorption temperature limit the application of Mg-based hydrogen storage materials.The present paper reviews the advances in the research of Mg-based hydrogen storage film in recent years, including the advantage of the film, the function theory of fabricating method and its functional theory, and the influencing factors in the technological process. The research status worldwide is introduced in detail. By comparing pure Mg, Pd-caped Mg, nonpalladium capped Mg, and Mg alloy hydrogen storage films, an ideal tendency for producing Mg-based film is pointed out,for example, looking for a cheap metal element to replace the high-priced Pd, compositing Mg film with other hydrogen storage alloy of catalytic elements, and so on.展开更多
(La;Mg;);(Ni;Co;);（x = 0.125, 0.25, 0.5） alloys were synthesized from the sintered mixture of La;O;+ Ni O + Co O + Mg O in the molten CaCl;electrolyte at 750 °C and the electrochemical hydrogen storage capaciti...(La;Mg;);(Ni;Co;);（x = 0.125, 0.25, 0.5） alloys were synthesized from the sintered mixture of La;O;+ Ni O + Co O + Mg O in the molten CaCl;electrolyte at 750 °C and the electrochemical hydrogen storage capacities of the synthesized alloys were measured. Non-hygroscopic LaNiO;phase formed during sintering（at 1200 °C for 2 h） as a result of the reaction of hygroscopic La;O;with NiO. Another sinter product was Mg;Ni;O phase. Both mixed oxide sinter products facilitated the La-Ni and Mg-Ni phase formations. X-ray diffraction peaks indicated that the first stable phase appeared in the alloy structure was LaNi;which formed upon reduction of La;NiO;phase. Increase in Mg content caused formation of La;Mg;Ni;phase in the alloy structure and the presence of this phase improved the hydrogen storage performance of the electrodes. It was observed that(La;Mg;);(Ni;Co;);（x = 0.125, 0.25, 0.5） alloys have promising discharge capacities change between 319 m Ah/g and 379 m Ah/g depending on the alloy Mg content.展开更多
With reduced dehydrogenation enthalpy change and reduced dehydrogenation temperature compared with its phenol-cyclohexanol pair,sodium phenoxide-cyclohexanolate pair developed recently is promising for large-scale ene...With reduced dehydrogenation enthalpy change and reduced dehydrogenation temperature compared with its phenol-cyclohexanol pair,sodium phenoxide-cyclohexanolate pair developed recently is promising for large-scale energy storage and long-distance hydrogen transportation.In the present work,we investigate the kinetic behavior of the pair in the hydrogenation and dehydrogenation in water over three commercial catalysts.It is shown that 5%Ru/Al2O3 and 5%Pt/C perform well in the hydrogenation and dehydrogenation,respectively.Kinetic analyses show that the hydrogenation of sodium phenoxide is of first-order with respect to H2 pressure and zero-order to the concentration of sodium phenoxide in the presence of Ru/Al2O3 catalyst.>99%conversion of cyclohexanol and>99%selectivity to phenoxide can be achieved in the dehydrogenation catalyzed by Pt/C catalyst and in the presence of Na OH at 100℃,where cyclohexanone was observed as an intermediate.According to the kinetic analysis,the hydrogenation of sodium phenoxide may undergo the hydrolysis and hydrogenation pathway.For the dehydrogenation,an intermediate,i.e.,cyclohexanone,was detected and two possible pathways are proposed accordingly.展开更多
MgH_(2) has attracted intensive interests as one of the most promising hydrogen storage materials.Nevertheless,the high desorption temperature,sluggish kinetics,and rapid capacity decay hamper its commercial applicati...MgH_(2) has attracted intensive interests as one of the most promising hydrogen storage materials.Nevertheless,the high desorption temperature,sluggish kinetics,and rapid capacity decay hamper its commercial application.Herein,2D TiO_(2) nanosheets with abundant oxygen vacancies are used to fabricate a flower-like MgH_(2)/TiO_(2) heterostructure with enhanced hydrogen storage performances.Particularly,the onset hydrogen desorption temperature of the MgH_(2)/TiO_(2) heterostructure is lowered down to 180℃(295℃ for blank MgH_(2)).The initial desorption rate of MgH_(2)/TiO_(2) reaches 2.116 wt% min^(-1) at 300℃,35 times of the blank MgH_(2) under the same conditions.Moreover,the capacity retention is as high as 98.5% after 100 cycles at 300℃,remarkably higher than those of the previously reported MgH_(2)-TiO_(2) composites.Both in situ HRTEM observations and ex situ XPS analyses confirm that the synergistic effects from multi-valance of Ti species,accelerated electron transportation caused by oxygen vacancies,formation of catalytic Mg-Ti oxides,and stabilized MgH_(2) NPs confined by TiO_(2) nanosheets contribute to the high stability and kinetically accelerated hydrogen storage performances of the composite.The strategy of using 2D substrates with abundant defects to support nano-sized energy storage materials to build heterostructure is therefore promising for the design of high-performance energy materials.展开更多
Aluminum hydride(AlH3) is a binary metal hydride that contains more than 10.1 wt% of hydrogen and possesses a high volumetric hydrogen density of 148 kg H2 m^(-3).Pristine AlH3 can readily release hydrogen at a modera...Aluminum hydride(AlH3) is a binary metal hydride that contains more than 10.1 wt% of hydrogen and possesses a high volumetric hydrogen density of 148 kg H2 m^(-3).Pristine AlH3 can readily release hydrogen at a moderate temperature below 200℃.Such high hydrogen density and low desorption temperature make AlH3 one of most promising hydrogen storage media for mobile application.This review covers the research activity on the structures,synthesis,decomposition thermodynamics and kinetics,regeneration and application validation of AlH3 over the past decades.Finally,the future research directions of AlH3 as a hydrogen storage material will be revealed.展开更多
基金part of a research project PIF Alfa HI initiative 726174Alfaisal University and its Office of Research&Innovation for their continuous support throughout this study。
文摘The review is a comprehensive discussion of current research advances,commercial scale developments,challenges,and techno-eco nomics for the entire H_(2) value chain,including production,mainly focusing on sustainable sources,storage,and transport.The challenges,advantages,and uses of H_(2) energy are included at length.Moreover,apart from the sustainable production approaches,the approaches and current developments for combating the carbon dioxide(CO_(2))emissions from existing H_(2) production facilities are highlighted in terms of ca rbon capture,utilization,and storage(CCUS).Concisely,the review discusses current material and recent technological adva ncements in developing pilot projects and large-scale establishments for viable and rapidly emerging sou rce-ba sed H_(2) productio n.Moreover,the review also aims to provide an in-depthdiscussion and explore current developments based on the advantages of H_(2) energy in terms of its utilization,based on its high energy density,and its ability to be used as a feedstock and fuel.On the other hand,the challenges of H_(2) are also elabo rated.Next,the role of CCUS in a carbon-neutral economy and value chain for minimization of emissions from existing facilities is thoroughly deliberated,and the recent commercial-scale implementation of CCUS technologies is highlighted.Extending the utilization and recycling of captured CO_(2) emissions along with H_(2) to produce e-fuels in terms of current advances is detailed in this review.Fu rthermore,the most applicable,efficient,a nd develo ping approaches are discussed for physical and chemical H_(2) storage,considering recent la rge-scale implementations of liquid carriers and liquid organic hydrogen carriers as storage options.Lastly,the review elaborates on recent insights into advances in H_(2) transport infrastructure,including compressed and liquid H_(2) delivery via roads,ships,pipelines,and flight cargo.The review gives precise insights into the recent scenario through an elaborated conclusion of each discussion topic separately and a discussion of future perspectives.The current review will help researchers to fully understand the ongoing research advancements and challenges in the H_(2) value chain for formulating new solutions for sustainable H_(2) production,alo ng with focusing on suitable approaches for its storage and tra nsport to make the production and utilization of H_(2) applicable on a large scale.
基金the support from the National Key Research&Development Program(2022YFB3803700)of ChinaNational Natural Science Foundation(No.52171186)the financial support from the Center of Hydrogen Science,Shanghai Jiao Tong University。
文摘MgH_(2) is a promising high-capacity solid-state hydrogen storage material,while its application is greatly hindered by the high desorption temperature and sluggish kinetics.Herein,intertwined 2D oxygen vacancy-rich V_(2)O_(5) nanosheets(H-V_(2)O_(5))are specifically designed and used as catalysts to improve the hydrogen storage properties of MgH_(2).The as-prepared MgH_(2)-H-V_(2)O_(5) composites exhibit low desorption temperatures(Tonset=185℃)with a hydrogen capacity of 6.54 wt%,fast kinetics(Ea=84.55±1.37 kJ mol^(-1) H_(2) for desorption),and long cycling stability.Impressively,hydrogen absorption can be achieved at a temperature as low as 30℃ with a capacity of 2.38 wt%within 60 min.Moreover,the composites maintain a capacity retention rate of~99%after 100 cycles at 275℃.Experimental studies and theoretical calculations demonstrate that the in-situ formed VH_(2)/V catalysts,unique 2D structure of H-V_(2)O_(5) nanosheets,and abundant oxygen vacancies positively contribute to the improved hydrogen sorption properties.Notably,the existence of oxygen vacancies plays a double role,which could not only directly accelerate the hydrogen ab/de-sorption rate of MgH_(2),but also indirectly affect the activity of the catalytic phase VH_(2)/V,thereby further boosting the hydrogen storage performance of MgH_(2).This work highlights an oxygen vacancy excited“hydrogen pump”effect of VH_(2)/V on the hydrogen sorption of Mg/MgH_(2).The strategy developed here may pave a new way toward the development of oxygen vacancy-rich transition metal oxides catalyzed hydride systems.
基金supported by Natural Science Foundation of China(no.72471087)Natural Science Foundation of Beijing Municipality(no.9242015).
文摘Zero-carbon parks have broad prospects in carbon neutralization.As an energy hub,hydrogen energy storage plays an important role in zero-carbon parks.However,the nonlinear characteristics of hydrogen energy storage systems(HESSs)have a significant impact on the system economy.Therefore,considering the variable working condition characteristics of HESSs,a hybrid operation method is proposed for HESS,to support the efficient and economic operation of zero-carbon parks,By analyzing the operating principle of a zero-carbon park with HESS,the system structure framework and variable condition linearization model of the equipment in HESS are established.Moreover,considering the energy output characteristics of hydrogen energy storage equipment under variable working conditions,a multimodule hybrid operation strategy is proposed for electrolytic and fuel cells,effectively meeting the thermoelectric load demand of zero-carbon parks in different scenarios.Finally,the economy of the proposed hybrid operation strategy was verified in typical scenarios,using a zero-carbon park embedded with a HESS.
基金the financial support from the Natural Science Foundation of China (Nos.52179118,52209151 and 42307238)the Science and Technology Project of Jiangsu Provincial Department of Science and Technology-Carbon Emissions Peak and Carbon Neutrality Science and Technology Innovation Specia Fund Project (No.BK20220025)+3 种基金the Excellent Postdoctoral Program of Jiangsu Province (No.2023ZB602)the China Postdoctora Science Foundation (Nos.2023M733773 and 2023M733772)Xuzhou City Science and Technology Innovation Special Basic Research Plan (KC23045)State Key Laboratory of Intelligent Construction and Healthy Operation and Maintenance of Deep Underground Engineering,China University of Mining&Technology (No SKLGDUEK1916)。
文摘Underground hydrogen storage(UHS)and compressed air energy storage(CAES)are two viable largescale energy storage technologies for mitigating the intermittency of wind and solar power.Therefore,it is meaningful to compare the properties of hydrogen and air with typical thermodynamic storage processes.This study employs a multi-physical coupling model to compare the operations of CAES and UHS,integrating gas thermodynamics within caverns,thermal conduction,and mechanical deformation around rock caverns.Gas thermodynamic responses are validated using additional simulations and the field test data.Temperature and pressure variations of air and hydrogen within rock caverns exhibit similarities under both adiabatic and diabatic simulation modes.Hydrogen reaches higher temperature and pressure following gas charging stage compared to air,and the ideal gas assumption may lead to overestimation of gas temperature and pressure.Unlike steel lining of CAES,the sealing layer(fibre-reinforced plastic FRP)in UHS is prone to deformation but can effectively mitigates stress in the sealing layer.In CAES,the first principal stress on the surface of the sealing layer and concrete lining is tensile stress,whereas UHS exhibits compressive stress in the same areas.Our present research can provide references for the selection of energy storage methods.
基金supported by the National Natural Science Foundation of China(52270027,52170037,and U20A20322)the Science and Technology Program of Jilin Province(20210201066GX)+1 种基金Scientific research project of Ecological Environment Department of Jilin Province(2023-05)Jilin Provincial Science and Technology Department Science and Technology Innovation and Entrepreneurship outstanding talent program for young and middle-aged(20230508051RC).
文摘Metal–organic frameworks(MOFs)are highly promising porous materials known for their exceptional porosity,extensive surface area,and customizable pore structures,making them an ideal solution for hydrogen storage.However,most MOFs research remains confined to the laboratory,lacking practical applications.To address this,the author proposes a shift towards practical applications,the creation of a comprehensive MOFs database,alignment of synthesis with practical considerations,and diversification of MOFs applications.These steps are crucial for harnessing the full potential of MOFs in real-world energy challenges.
基金supported by the European Union's“Horizon Europe programme”—LOC3G(Grant No.101129729)the Henan Center for Outstanding Overseas Scientists(Grant No.GZS2024001)。
文摘Amidst the rapid development of renewable energy,the intermittency and instability of energy supply pose severe challenges and impose higher requirements on energy storage systems.Among the various energy storage technologies,the coupled approach of power-to-hydrogen(H2)and underground H2storage(UHS)offers advantages such as extended storage duration and large-scale capacity,making it highly promising for future development.However,during UHS,particularly in porous media,microbial metabolic processes such as methanogenesis,acetogenesis,and sulfate reduction may lead to H2consumption and the production of byproducts.These microbial activities can impact the efficiency and safety of UHS both positively and negatively.Therefore,this paper provides a comprehensive review of experimental,numerical,and field studies on microbial interactions in UHS within porous media,aiming to capture research progress and elucidate microbial effects.It begins by outlining the primary types of UHS and the key microbial metabolic processes involved.Subsequently,the paper introduces the experimental approaches for investigating gas-water-rock-microbe interactions and interfacial properties,the models and simulators used in numerical studies,and the procedures implemented in field trials.Furthermore,it analyzes and discusses microbial interactions and their positive and negative impacts on UHS in porous media,focusing on aspects such as H2consumption,H2flow,and storage safety.Based on these insights,recommendations for site selection,engineering operations,and on-site monitoring of UHS,as well as potential future research directions,are provided.
基金the National Research Foundation of South Africa and the University of KwaZulu-Natal,South Africa for financial assistance and research facilities
文摘Hydrogen is a generally abundant, safe, clean and environmentally apt alternative fuel, which replenishes the void generated by depleting fossil fuel reserves. The adoption of hydrogen as an energy source has been restricted to low levels due to the complications associated with its viable storage and usage. Existing technologies, such as storage of hydrogen in compressed and liquefied forms are not adequate to meet the broad on-board applications. The gravimetric energy density(120 MJ/kg) of hydrogen is three times higher than that of gasoline products, so solid-state hydrogen storage is advantageous.Metal-organic frameworks(MOFs), multi-walled carbon nanotubes(MWCNTs) and graphene are solid adsorbents majorly employed for efficient H_2 storage. The prominent features of MOFs such as permanent porosity, structural rigidity, and surface area are attractive and ideal for hydrogen storage. In addition,nanostructured carbon materials(MWCNTs and graphene) and their composites have demonstrated significant hydrogen storage capacities. Some important parameters for the success of the hydrogen economy include high storage density, adsorption/desorption temperature and cycling time. Cryo-hydrogen storage was achieved in MOFs and their composites with carbon structures, but storage at ambient temperature and acceptable pressures is a major hurdle. This review discusses various strategies and mechanisms in the design of adsorbents explored to improve H_2 storage capacities and afford opportunities to develop new sustainable hydrogen technologies to meet energy targets.
基金financially supported by the Ministry of Higher Education Malaysia under the Fundamental Research Grant Scheme (FRGS 59362)
文摘The effects of Sr TiO_3 on the hydrogen storage properties of MgH_2 have been studied for the first time.The onset dehydrogenation temperature of the MgH_2-10 wt% SrTiO_3 is found to be 275 ℃, which is 55 ℃ lower as compared to the as-milled MgH_2. The composite is able to absorb 4.3 wt% of hydrogen in 60 min instead of 1.1 wt% for the as-milled Mg H_2. Meanwhile, the composite is able to release 5.3 wt% of hydrogen in 17 min compared to 1.9 wt% by the as-milled Mg H_2 at 320 ℃. The calculated Eaof the Mg H_2-10 wt% SrTiO_3 is 109 k J/mol, which is 26.3 kJ/mol lower than the calculated Eaof the as-milled MgH_2. The Sr TiO_3 is not decomposed during the ball milling and the re/dehydrogenation processes. The catalytic effect shown by the SrTiO_3 is owing to its ability to change the physical structure of the MgH_2 particles during the ball milling process.
基金supported by Ministry of Higher Education Malaysia Fundamental Research Grant Scheme(FRGS 59362)
文摘In this study, the hydrogen storage properties of MgH-X wt% KNiF（X = 5, 10, 15, 20, and 50） were investigated for the first time. From the analysis of the onset desorption temperature and isothermal de/absorption kinetics, it was shown that MgH+ 5 wt% KNiFsample has the best performance. The 5wt% doped sample started to release hydrogen at about 260 °C, which was a reduction of about 95 °C and 157 oC compared with the as-milled and as-received MgH. In addition, the de/absorption kinetics of the MgH+ 5 wt% KNiFwere also improved significantly compared to the un-doped MgH. The apparent activation energy for hydrogen desorption exhibited the decrement from 167.0 k J/mol for as-milled MgHto 111.0 k J/mol with the addition of 5 wt% KNiF. Moreover, the X-ray diffraction spectra displayed the formation of new phases of KF, KH, MgNi and MgNiHby doping the KNiFwith MgHafter the dehydrogenation and rehydrogenation processes. The scanning electron microscope results revealed that MgHdoped with 5 wt% KNiFdemonstrated the smallest particle size compared to the as-received and as-milled MgH. It is believed that the formation of in situ active species of KF, KH, and MgNi could provide a synergetic catalytic effect in enhancing the hydrogen sorption properties of MgH.
基金support from the National Key Research&Development Program(2022YFB3803700)of ChinaNational Natural Science Foundation(No.52171186)financial support from the Center of Hydrogen Science,Shanghai Jiao Tong University。
文摘With the depletion of fossil fuels and global warming,there is an urgent demand to seek green,low-cost,and high-efficiency energy resources.Hydrogen has been considered as a potential candidate to replace fossil fuels,due to its high gravimetric energy density(142 MJ kg^(-1)),high abundance(H_(2)O),and environmentalfriendliness.However,due to its low volume density,effective and safe hydrogen storage techniques are now becoming the bottleneck for the"hydrogen economy".Under such a circumstance,Mg-based hydrogen storage materials garnered tremendous interests due to their high hydrogen storage capacity(~7.6 wt%for MgH_(2)),low cost,and excellent reversibility.However,the high thermodynamic stability(ΔH=-74.7 kJ mol^(-1)H_(2))and sluggish kinetics result in a relatively high desorption temperature(>300℃),which severely restricts widespread applications of MgH_(2).Nano-structuring has been proven to be an effective strategy that can simultaneously enhance the ab/de-sorption thermodynamic and kinetic properties of MgH_(2),possibly meeting the demand for rapid hydrogen desorption,economic viability,and effective thermal management in practical applications.Herein,the fundamental theories,recent advances,and practical applications of the nanostructured Mg-based hydrogen storage materials are discussed.The synthetic strategies are classified into four categories:free-standing nano-sized Mg/MgH_(2)through electrochemical/vapor-transport/ultrasonic methods,nanostructured Mg-based composites via mechanical milling methods,construction of core-shell nano-structured Mg-based composites by chemical reduction approaches,and multi-dimensional nano-sized Mg-based heterostructure by nanoconfinement strategy.Through applying these strategies,near room temperature ab/de-sorption(<100℃)with considerable high capacity(>6 wt%)has been achieved in nano Mg/MgH_(2)systems.Some perspectives on the future research and development of nanostructured hydrogen storage materials are also provided.
基金supported by the National High Technology Research and Development Program of China(863 Program)(2012AA053305)the International Cooperation Project from Ministry of Science and Technology of China(2010DFA64080)
文摘Activated carbons derived from corncob （CACs） were prepared by pyrolysis carbonization and KOH activation. Through modifying activation conditions, samples with large pore volume and ultrahigh BET specific surface area could be obtained. The sample achieved the highest hydrogen uptake capacity of 5.80 wt% at 40 bar and -196℃ The as-obtained samples were characterized by N2-sorption, transmission electron microscopy （TEM） and scanning electron microscopy （SEM）. Besides, thermogravimetric analysis was also employed to investigate the activation behavior of CACs. Detailed investigation on the activation parameters reveals that moderate activation temperature and heating rate are favorable for preparing CACs with high surface area, large pore volume and optimal pore size distribution. Meanwhile, the micropore volume between 0.65 nm and 0.85 nm along with BET surface area and total pore volume has great effects on hydrogen uptake capacities. The present results indicate that CACs are the most promising materials for hydrogen storage application.
基金supported by the National Magnetic Confinement Fusion Science Program of China(Grant No.2011GB111003)the National HighTech Research and Development Program of China(Grant No.2011AA03A408)
文摘Zr1-xTixCo(x = 0, 0.1, 0.2, 0.3) alloys were prepared by arc-melting method and the effect of Ti substitution on hydrogen storage properties was studied systematically. Hydrogen desorption pressure-composition-temperature(PCT) measurements were carried out using Sievert’s type volumetric apparatus for ZrCo(at 473 K, 573 K and 673 K) and Zr1-xTixCo alloys(at 673 K), respectively. Products after dehydrogenation were characterized by X-ray diffraction(XRD). In addition, the kinetics of Zr1-xTixCo hydride was investigated at 473 K and 673 K,respectively, under hydrogen pressure of 5 MPa. Results showed that Ti substitution for Zr did not change the crystal structure of ZrCo phase.With the increase of temperature from 473 K to 673 K, the extent of disproportionation for ZrCo alloy increased. With Ti content increasing at 673 K, the desorption equilibrium pressure of Zr1-xTixCo-H2 systems elevated and the disproportionation reaction of Zr1-xTixCo alloys was inhibited effectively. Ti substitution decreased the kinetics rate and the effective hydrogen storage capacity of Zr1-xTixCo alloys slightly.Generally speaking, it was found that Zr0.8Ti0.2Co alloy had better anti-disproportionation property with less decrease of effective hydrogen storage capacity which was beneficial to tritium application in the International Thermonuclear Experimental Reactor(ITER).
基金supported by the National 863 Program (2007AA03Z229)the Fundamental Research Funds for the Central Universities (2009ZM0185)
文摘Gas hydrate is a new technology for energy gas（methane/hydrogen）storage due to its large capacity of gas storage and safe.But industrial application of hydrate storage process was hindered by someproblems.For methane,the main problems are low formation rateand storage capacity,which can be solved by strengthening mass andheat transfer,such as adding additives,stirring,bubbling,etc.Onekind of additives can change the equilibrium curve to reduce the formation pressure of methane hydrate,and the other kind of additivesis surfactant,which can form micelle with water and increase the interface of water-gas.Dry water has the similar effects on the methanehydrate as surfactant.Additionally,stirring,bubbling,and sprayingcan increase formation rate and storage capacity due to mass transferstrengthened.Inserting internal or external heat exchange also canimprove formation rate because of good heat transfer.For hydrogen,the main difficulties are very high pressure for hydrate formed.Tetrahydrofuran（THF）,tetrabutylammonium bromide（TBAB） andtetrabutylammonium fluoride（TBAF） have been proved to be able todecrease the hydrogen hydrate formation pressure significantly.
基金supported by the National Natural Science Foundation of China(51272173,51002188)the National Basic Research Program of China(2010CB934703)Tianjin Municipal Science and Technology Commission(12ZCZDGX00800)
文摘Three types of carbon nano-onions（CNOs） including Ni@CNOs.Fe3C@CNOs and Fe0.64Ni0.36@CNOs nanoparticles have been synthesized by catalytic decomposition of methane at 850 ℃ using nickel,iron and iron-nickel alloy catalysts.Comparative and systematic studies have been carried out on the morphology,structural characteristics and graphitic crystallinity of these CNOs products.Furthermore,the electrochemical hydrogen storage properties of three types of CNOs have been investigated.Measurements show that the Ni@CNOs have the highest discharge capacity of 387.2 mAh/g,coiTesponding to a hydrogen storage of 1.42%.This comparison study shows the advantages of each catalyst in the growth of CNOs.enabling the controllable synthesis and tuning the properties of CNOs by mediating different metals and their alloy for using in the fuel cell system.
基金part of the activities of SCCER HeE, which is financially supported by Innosuisse – Swiss Innovation Agency
文摘Stability of borohydrides is determined by the localization of the negative charge on the boron atom.Ionic liquids(ILs) allow to modify the stability of the borohydrides and promote new dehydrogenation pathways with a lower activation energy. The combination of borohydride and IL is very easy to realize and no expensive rare earth metals are required. The composite of the ILs with complex hydrides decreases the enthalpy and activation energy for the hydrogen desorption. The Coulomb interaction between borohydride and IL leads to a destabilization of the materials with a significantly lower enthalpy for hydrogen desorption. Here, we report a simple ion exchange reaction using various ILs, such as vinylbenzyltrimethylammonium chloride([VBTMA][Cl]), 1-butyl-3-methylimidazolium chloride([bmim][Cl]), and 1-ethyl-1-methylpyrrolidinium bromide([EMPY][Br]) with NaBH4 to decrease the hydrogen desorption temperature. Dehydrogenation of 1-butyl-3-methylimidazolium borohydride([bmim][BH4]) starts below 100℃. The quantity of desorbed hydrogen ranges between 2.4 wt% and 2.9 wt%, which is close to the theoretical content of hydrogen. The improvement in dehydrogenation is due to the strong amine cation that destabilizes borohydride by charge transfer.
基金Project supported by the Competitiveness Enhancement Program of National Research Tomsk Polytechnic University(Grant No.VIU-OEF-66/2019)
文摘Mg-based hydrogen storage materials are considered to be one of the most promising solid-state hydrogen storage materials due to their large hydrogen storage capacity and low cost. However, slow hydrogen absorption/desorption rate and excessive hydrogen absorption/desorption temperature limit the application of Mg-based hydrogen storage materials.The present paper reviews the advances in the research of Mg-based hydrogen storage film in recent years, including the advantage of the film, the function theory of fabricating method and its functional theory, and the influencing factors in the technological process. The research status worldwide is introduced in detail. By comparing pure Mg, Pd-caped Mg, nonpalladium capped Mg, and Mg alloy hydrogen storage films, an ideal tendency for producing Mg-based film is pointed out,for example, looking for a cheap metal element to replace the high-priced Pd, compositing Mg film with other hydrogen storage alloy of catalytic elements, and so on.
基金Financial assistance from The Scientific and Technological Research Council of Turkey is gratefully acknowledged(Project No:MAG 113M139)
文摘(La;Mg;);(Ni;Co;);（x = 0.125, 0.25, 0.5） alloys were synthesized from the sintered mixture of La;O;+ Ni O + Co O + Mg O in the molten CaCl;electrolyte at 750 °C and the electrochemical hydrogen storage capacities of the synthesized alloys were measured. Non-hygroscopic LaNiO;phase formed during sintering（at 1200 °C for 2 h） as a result of the reaction of hygroscopic La;O;with NiO. Another sinter product was Mg;Ni;O phase. Both mixed oxide sinter products facilitated the La-Ni and Mg-Ni phase formations. X-ray diffraction peaks indicated that the first stable phase appeared in the alloy structure was LaNi;which formed upon reduction of La;NiO;phase. Increase in Mg content caused formation of La;Mg;Ni;phase in the alloy structure and the presence of this phase improved the hydrogen storage performance of the electrodes. It was observed that(La;Mg;);(Ni;Co;);（x = 0.125, 0.25, 0.5） alloys have promising discharge capacities change between 319 m Ah/g and 379 m Ah/g depending on the alloy Mg content.
基金financial support from the project of the National Natural Science Foundation of China(51671178,21875246)the project from DICP(DICP ZZBS201616)the support from Sino-Japanese Research Cooperative Program of Ministry of Science and Technology(2016YFE0118300) and iChEM·2011
文摘With reduced dehydrogenation enthalpy change and reduced dehydrogenation temperature compared with its phenol-cyclohexanol pair,sodium phenoxide-cyclohexanolate pair developed recently is promising for large-scale energy storage and long-distance hydrogen transportation.In the present work,we investigate the kinetic behavior of the pair in the hydrogenation and dehydrogenation in water over three commercial catalysts.It is shown that 5%Ru/Al2O3 and 5%Pt/C perform well in the hydrogenation and dehydrogenation,respectively.Kinetic analyses show that the hydrogenation of sodium phenoxide is of first-order with respect to H2 pressure and zero-order to the concentration of sodium phenoxide in the presence of Ru/Al2O3 catalyst.>99%conversion of cyclohexanol and>99%selectivity to phenoxide can be achieved in the dehydrogenation catalyzed by Pt/C catalyst and in the presence of Na OH at 100℃,where cyclohexanone was observed as an intermediate.According to the kinetic analysis,the hydrogenation of sodium phenoxide may undergo the hydrolysis and hydrogenation pathway.For the dehydrogenation,an intermediate,i.e.,cyclohexanone,was detected and two possible pathways are proposed accordingly.
基金the support from the National Natural Science Foundation (No. 52171186)the Science and Technology Commission of Shanghai Municipality under No. 19511108100+1 种基金Shanghai Education Commission “Shuguang” scholar Project (16SG08)the financial support from the Center of Hydrogen Science, Shanghai Jiao Tong University
文摘MgH_(2) has attracted intensive interests as one of the most promising hydrogen storage materials.Nevertheless,the high desorption temperature,sluggish kinetics,and rapid capacity decay hamper its commercial application.Herein,2D TiO_(2) nanosheets with abundant oxygen vacancies are used to fabricate a flower-like MgH_(2)/TiO_(2) heterostructure with enhanced hydrogen storage performances.Particularly,the onset hydrogen desorption temperature of the MgH_(2)/TiO_(2) heterostructure is lowered down to 180℃(295℃ for blank MgH_(2)).The initial desorption rate of MgH_(2)/TiO_(2) reaches 2.116 wt% min^(-1) at 300℃,35 times of the blank MgH_(2) under the same conditions.Moreover,the capacity retention is as high as 98.5% after 100 cycles at 300℃,remarkably higher than those of the previously reported MgH_(2)-TiO_(2) composites.Both in situ HRTEM observations and ex situ XPS analyses confirm that the synergistic effects from multi-valance of Ti species,accelerated electron transportation caused by oxygen vacancies,formation of catalytic Mg-Ti oxides,and stabilized MgH_(2) NPs confined by TiO_(2) nanosheets contribute to the high stability and kinetically accelerated hydrogen storage performances of the composite.The strategy of using 2D substrates with abundant defects to support nano-sized energy storage materials to build heterostructure is therefore promising for the design of high-performance energy materials.
基金financially supported by the National Natural Science Foundation of China (No. 51771171, and 51971199)Education Department of Guangxi Zhuang Autonomous Region (No. 2019KY0021)the Natural Science Foundation of Guangxi Province (2019GXNSFBA185004, and 2018GXNSFAA281308)。
文摘Aluminum hydride(AlH3) is a binary metal hydride that contains more than 10.1 wt% of hydrogen and possesses a high volumetric hydrogen density of 148 kg H2 m^(-3).Pristine AlH3 can readily release hydrogen at a moderate temperature below 200℃.Such high hydrogen density and low desorption temperature make AlH3 one of most promising hydrogen storage media for mobile application.This review covers the research activity on the structures,synthesis,decomposition thermodynamics and kinetics,regeneration and application validation of AlH3 over the past decades.Finally,the future research directions of AlH3 as a hydrogen storage material will be revealed.
