Inspired by the Chinese Knotting weave structure,an electromagnetic interference(EMI)nanofiber composite membrane with a twill surface was prepared.Poly(vinyl alcohol-co-ethylene)(Pva-co-PE)nanofibers and twill nylon ...Inspired by the Chinese Knotting weave structure,an electromagnetic interference(EMI)nanofiber composite membrane with a twill surface was prepared.Poly(vinyl alcohol-co-ethylene)(Pva-co-PE)nanofibers and twill nylon fabric were used as the matrix and filter templates,respectively.A Pva-co-PEMXene/silver nanowire(Pva-co-PE-MXene/AgNW,PM_(x)Ag)membrane was successfully prepared using a template method.When the MXene/AgNW content was only 7.4 wt%(PM_(7.4)Ag),the EMI shielding efficiency(SE)of the composite membrane with the oblique twill structure on the surface was 103.9 dB and the surface twill structure improved the EMI by 38.5%.This result was attributed to the pre-interference of the oblique twill structure in the direction of the incident EM wave,which enhanced the probability of the electromagnetic waves randomly colliding with the MXene nanosheets.Simultaneously,the internal reflection and ohmic and resonance losses were enhanced.The PM_(7.4)Ag membrane with the twill structure exhibited both an outstanding tensile strength of 22.8 MPa and EMI SE/t of 3925.2 dB cm^(-1).Moreover,the PM_(x)Ag nanocomposite membranes demonstrated an excellent thermal management performance,hydrophobicity,non-flammability,and performance stability,which was demonstrated by an EMI SE of 97.3%in a high-temperature environment of 140℃.The successful preparation of surface-twill composite membranes makes it difficult to achieve both a low filler content and a high EMI SE in electromagnetic shielding materials.This strategy provides a new approach for preparing thin membranes with excellent EMI properties.展开更多
A membrane with high stability and ion conductivity in wide pH range is essential for energy storage devices.Here,we report a novel membrane with hierarchical core-shell structure,which demonstrates high stability and...A membrane with high stability and ion conductivity in wide pH range is essential for energy storage devices.Here,we report a novel membrane with hierarchical core-shell structure,which demonstrates high stability and ion conductivity,simultaneously under a wide pH range applications.Spectral characterizations and theoretical calculation indicate that the non-solvent induces the chain segment configuration and eventually leads to polymer-polymer phase separation,thus forming hierarchical porous core-shell structure.Benefiting from this structure,an acidic vanadium flow battery(VFB)with such a membrane shows excellent performance over 400 cycles with an energy efficiency(EE)of above 81%at current density of 120 mA cm^(-2) and an alkaline zinc-iron flow battery(AZIFB)delivers a cycling stability for more than 200 cycles at 160 mA cm^(-2),along with an EE of above 82%.This paper provides a cost-effective and simple way to fabricate membranes with high performance for variety of energyrelated devices.展开更多
Building well-developed ion-conductive highways is highly desirable for anion exchange membranes(AEMs).Grafting side chain is a highly effective approach for constructing a well-defined phaseseparated morphological st...Building well-developed ion-conductive highways is highly desirable for anion exchange membranes(AEMs).Grafting side chain is a highly effective approach for constructing a well-defined phaseseparated morphological structure and forming unblocked ion pathways in AEMs for fast ion transport.Fluorination of side chains can further enhance phase separation due to the superhydrophobic nature of fluorine groups.However,their electronic effect on the alkaline stability of side chains and membranes is rarely reported.Here,fluorine-containing and fluorine-free side chains are introduced into the polyaromatic backbone in proper configuration to investigate the impact of the fluorine terminal group on the stability of the side chains and membrane properties.The poly(binaphthyl-co-p-terphenyl piperidinium)AEM(QBNp TP)has the highest molecular weight and most dimensional stability due to its favorable backbone arrangement among ortho-and meta-terphenyl based AEMs.Importantly,by introducing both a fluorinated piperidinium side chain and a hexane chain into the p-terphenyl-based backbone,the prepared AEM(QBNp TP-QFC)presents an enhanced conductivity(150.6 m S cm^(-1))and a constrained swelling at 80℃.The electronic effect of fluorinated side chains is contemplated by experiments and simulations.The results demonstrate that the presence of strong electro-withdrawing fluorine groups weakens the electronic cloud of adjacent C atoms,increasing OH^(-)attack on the C atom and improving the stability of piperidinium cations.Hence QBNp TP-QFC possesses a robust alkaline stability at 80℃(95.3%conductivity retention after testing in 2 M Na OH for 2160 h).An excellent peak power density of 1.44 W cm^(-2)and a remarkable durability at 80℃(4.5%voltage loss after 100 h)can be observed.展开更多
The utilization of all-solid-state electrolytes is considered to be an effective way to enhance the safety performance of lithium metal batteries.However,the low ionic conductivity and poor interface compatibility gre...The utilization of all-solid-state electrolytes is considered to be an effective way to enhance the safety performance of lithium metal batteries.However,the low ionic conductivity and poor interface compatibility greatly restrict the development of all-solid-state battery.In this study,a composite electrolyte combining the electrospun polyamide 6(PA6)nanofiber membrane with hierarchical structure and the polyethylene oxide(PEO)polymer is investigated.The introduction of PA6 nanofiber membrane can effectively reduce the crystallinity of the polymer,so that the ionic conductivity of the electrolyte can be enhanced.Moreover,it is found that the presence of finely branched fibers in the hierarchical structure PA6 membrane allows the polar functional groups(C=O and N-H bonds)to be fully exposed,which provides sufficient functional sites for lithium ion transport and helps to regulate the uniform deposition of lithium metal.Moreover,the hierarchical structure can enhance the mechanical strength(9.2 MPa)of the electrolyte,thereby effectively improving the safety and cycle stability of the battery.The prepared Li/Li symmetric battery can be stably cycled for 1500 h under 0.3 mA cm^(-2) and 60℃.This study demonstrates that the prepared electrolyte has excellent application prospects in the next generation all-solid-state lithium metal batteries.展开更多
The semi-interpenetrating network anion exchange membranes(AEMs)based on quaternized polyvinyl alcohol(QPVA)and poly(-diallyldimethylammonium chloride)(PDDA)are synthesized.The chemical cross-linking structure is form...The semi-interpenetrating network anion exchange membranes(AEMs)based on quaternized polyvinyl alcohol(QPVA)and poly(-diallyldimethylammonium chloride)(PDDA)are synthesized.The chemical cross-linking structure is formed between hydroxyl groups of QPVA and aldehyde groups of glutaraldehyde(GA),which makes PDDA more stable embed in the QPVA matrix and also improves the mechanical properties and dimensional stability of AEMs.Due to the phase separation phenomenon of AEMs swelling in water,a microporous structure may be formed in the membrane,which reduces the transmission resistance of hydroxide ions and provides a larger space for the transfer of hydroxide ions,thus improving the conductivity.The ring structure of PDDA is introduced as a cationic group to transfer hydroxide ions,and shields the nucleophilic attack of the hydroxide ions through the steric hindrance effect,which improves alkaline stability.The hydroxide conductivity of semi-interpenetrating network membrane(QPVA/PDDA0.5-GA)is 36.5 mS cm^(-1) at 60℃.And the membrane of QPVA/PDDA0.5-GA exhibits excellent mechanical property with maximum tensile strength of 19.6 MPa.After immersing into hot 3 mol L^(-1) NaOH solutions at 60℃ for 300 h,the OHconductivity remains 78%of its initial value.The semi-interpenetrating network AEMs with microporous structure exhibit good ionic conductivity,mechanical strength and alkaline durability.展开更多
Development of high-performance hydroxide-conductive membranes is a focus research subject owing to promising applications in electrochemical reduction of CO_(2)(eCO_(2)RR).However,few satisfactory membranes have been...Development of high-performance hydroxide-conductive membranes is a focus research subject owing to promising applications in electrochemical reduction of CO_(2)(eCO_(2)RR).However,few satisfactory membranes have been developed to maximize the performance of CO_(2) electrolyzers,despite its role as the core in regulating ion transport and preventing product crossover or fuel loss.Herein,we report the synthesis of alkaline anion-exchange membranes fabricated by poly(vinyl-alcohol)(PVA)and poly[(3-methyl-1-vinylimidazoliummethylsulfate)-co-(1-vinylpyrrolidone)](PQ44)for use in CO_(2) electrolysis.Owing to the unique imidazolium ring structure coupled with a three-dimensional semiinterpenetrating porous internal architecture,the PVA/PQ44-OH-membranes provide a high hydroxide conductivity(21.47 mS cm^(-1)),preferable mechanical property and thermal stability.In particular,the eCO_(2)RR used PVA/PQ44-OH^(-) as electrolyte membrane realized a charming Faradaic efficiency(88%)and partial current density(29 mA cm^(-2))at0.96 VRHE and,delivered the excellent durability over 20 h electrolysis in 0.5 mol L^(-1) KHCO_(3) electrolyte.Notably,it can even enable an ultrahigh current density beyond 100 mA cm^(-2) at^(-1).11 VRHE when the electrolyte was KOH instead,and produced the FEHCOOof 85%at a low potential of0.81 VRHE,superior to both commercial alkaline A201 and acidic Nafion117 membrane.展开更多
Porous biomass electrodes have emerged as a critical material for electrocatalytic hydrogen evolution reaction(HER).However,most approaches for synthesizing porous electrodes from biomass require high energy consumpti...Porous biomass electrodes have emerged as a critical material for electrocatalytic hydrogen evolution reaction(HER).However,most approaches for synthesizing porous electrodes from biomass require high energy consumption,which is resulted from the smash of biomass and the undergoing of serial assembly.Herein,a self-supported wood-derived"breathable"membrane is utilized directly as electrodes for highefficient HER via an assembly of Fe-doped NiP alloys.The well-designed hierarchical porous structures in natural wood membrane(NWM)are unusually beneficial for electrolytes accessibility and hydrogen gas removal.The obtained wood-derived membrane exhibits a high electrocatalytic activity and good cycling durability in acidic and alkaline electrolytes.Remarkably,the Fe_(0.074) NiP alloys/NWM electrode affords a large current density of 100 m A cm^(-2) at extremely low overpotentials of 168 mV in acidic electrolyte and174 m V in alkaline electrolyte.Density functional theory calculations unveil that the Fe atom doped in NiP alloys can create much more charge accumulation around Fe and Ni active sites,which helps decrease the △GH_(*)and △G_(H2O)and significantly promote the HER process.This new insight will promote further explorations of economic,high-efficient,and biodegradable wood-derived electrocatalysts for HER.展开更多
The phospholipid membrane plays a key role in myriad biological processes and phenomena, and the arrangement structure of membrane determines its function. However, the molecular arrangement structure of phospholipids...The phospholipid membrane plays a key role in myriad biological processes and phenomena, and the arrangement structure of membrane determines its function. However, the molecular arrangement structure of phospholipids in cell membranes is difficult to detect experimentally. On the basis of molecular dynamic simulations both in a non-destructive way and at native environment, we observed and confirmed that the phospholipids self-assemble to a hexagonal arrangement structure under physiological conditions. The underlying mechanism was revealed to be that there are hexagonal arrangement regions with a lower free energy around each lipid molecule. The findings potentially advance the understanding of biological functions of phospholipid bilayers.展开更多
The design of the catalyst layer(CL)offers a feasible way to realize the commercialization of proton exchange membrane fuel cells(PEMFCs).An in-depth understanding of catalyst inks is critical to achieving the optimal...The design of the catalyst layer(CL)offers a feasible way to realize the commercialization of proton exchange membrane fuel cells(PEMFCs).An in-depth understanding of catalyst inks is critical to achieving the optimal CL structure and cell performance.In this work,the effects of the solvent evaporation process during ink drying on the formation of the CL microstructure are particularly considered to reveal the structure-property correlations among the catalyst ink,drying process,CL microstructure and fuel cell performance.An increase in the alcohol content of the catalyst ink increases the amount of free ionomers while allowing the ionomer backbone to be more stretched in the dispersion medium.The higher alcohol content contributes to rapid solvent evaporation and thus inhibits the formation of coffee rings;as a result,a more developed ionomer network with a denser pore structure is obtained.Therefore,the alcohol-rich electrode exhibits better proton conduction capability,but higher oxygen transport resistance.For complex fuel cell operating conditions,a catalyst ink formulation with 50 wt%alcohol content is preferred due to its proper ionomer and pore size distribution,providing satisfactory fuel cell performance.展开更多
Engineering failure of membrane electrode assembly caused by increasingly fuel poisoning in the high temperature polymer electrolyte membrane fuel cells fed with humidified reformate gases is firstly demonstrated here...Engineering failure of membrane electrode assembly caused by increasingly fuel poisoning in the high temperature polymer electrolyte membrane fuel cells fed with humidified reformate gases is firstly demonstrated herein this work. Based on the results of the in-situ environmental scanning electron microscope, electrochemical analyses, and limiting current method, a water-induced phosphoric acid invasion model is constructed in the porous electrode to elucidate the failure causations of the hindered hydrogen mass transport and the enhanced carbon monoxide poisoning. To optimize the phosphoric acid distribution under the inevitably humidified circumstance, a facile and effective strategy of constructing acid-proofed electrode is proposed and demonstrates outstanding stability with highly humidified reformate gases as anode fuel. This work discusses a potential defect that was rarely studied previously under practical working circumstance for high temperature polymer electrolyte membrane fuel cells, providing an alternative opinion of electrode design based on the fundamental aspects towards the engineering problems.展开更多
基金supported by the National Natural Science Foundation of China(12205225,52373063,and 51873166)。
文摘Inspired by the Chinese Knotting weave structure,an electromagnetic interference(EMI)nanofiber composite membrane with a twill surface was prepared.Poly(vinyl alcohol-co-ethylene)(Pva-co-PE)nanofibers and twill nylon fabric were used as the matrix and filter templates,respectively.A Pva-co-PEMXene/silver nanowire(Pva-co-PE-MXene/AgNW,PM_(x)Ag)membrane was successfully prepared using a template method.When the MXene/AgNW content was only 7.4 wt%(PM_(7.4)Ag),the EMI shielding efficiency(SE)of the composite membrane with the oblique twill structure on the surface was 103.9 dB and the surface twill structure improved the EMI by 38.5%.This result was attributed to the pre-interference of the oblique twill structure in the direction of the incident EM wave,which enhanced the probability of the electromagnetic waves randomly colliding with the MXene nanosheets.Simultaneously,the internal reflection and ohmic and resonance losses were enhanced.The PM_(7.4)Ag membrane with the twill structure exhibited both an outstanding tensile strength of 22.8 MPa and EMI SE/t of 3925.2 dB cm^(-1).Moreover,the PM_(x)Ag nanocomposite membranes demonstrated an excellent thermal management performance,hydrophobicity,non-flammability,and performance stability,which was demonstrated by an EMI SE of 97.3%in a high-temperature environment of 140℃.The successful preparation of surface-twill composite membranes makes it difficult to achieve both a low filler content and a high EMI SE in electromagnetic shielding materials.This strategy provides a new approach for preparing thin membranes with excellent EMI properties.
基金the financial support from NSFC(21925804,U1808209 and 21908214)CAS Engineering Laboratory for Electrochemical Energy Storage,CAS,STS program.Major scientific and technological innovation project of Shandong(2018YFJH0106)+1 种基金the CAS(DNL201910)Youth Innovation Promotion Association CAS。
文摘A membrane with high stability and ion conductivity in wide pH range is essential for energy storage devices.Here,we report a novel membrane with hierarchical core-shell structure,which demonstrates high stability and ion conductivity,simultaneously under a wide pH range applications.Spectral characterizations and theoretical calculation indicate that the non-solvent induces the chain segment configuration and eventually leads to polymer-polymer phase separation,thus forming hierarchical porous core-shell structure.Benefiting from this structure,an acidic vanadium flow battery(VFB)with such a membrane shows excellent performance over 400 cycles with an energy efficiency(EE)of above 81%at current density of 120 mA cm^(-2) and an alkaline zinc-iron flow battery(AZIFB)delivers a cycling stability for more than 200 cycles at 160 mA cm^(-2),along with an EE of above 82%.This paper provides a cost-effective and simple way to fabricate membranes with high performance for variety of energyrelated devices.
基金the financial support from the National Natural Science Foundation of China(22078272&22278340)。
文摘Building well-developed ion-conductive highways is highly desirable for anion exchange membranes(AEMs).Grafting side chain is a highly effective approach for constructing a well-defined phaseseparated morphological structure and forming unblocked ion pathways in AEMs for fast ion transport.Fluorination of side chains can further enhance phase separation due to the superhydrophobic nature of fluorine groups.However,their electronic effect on the alkaline stability of side chains and membranes is rarely reported.Here,fluorine-containing and fluorine-free side chains are introduced into the polyaromatic backbone in proper configuration to investigate the impact of the fluorine terminal group on the stability of the side chains and membrane properties.The poly(binaphthyl-co-p-terphenyl piperidinium)AEM(QBNp TP)has the highest molecular weight and most dimensional stability due to its favorable backbone arrangement among ortho-and meta-terphenyl based AEMs.Importantly,by introducing both a fluorinated piperidinium side chain and a hexane chain into the p-terphenyl-based backbone,the prepared AEM(QBNp TP-QFC)presents an enhanced conductivity(150.6 m S cm^(-1))and a constrained swelling at 80℃.The electronic effect of fluorinated side chains is contemplated by experiments and simulations.The results demonstrate that the presence of strong electro-withdrawing fluorine groups weakens the electronic cloud of adjacent C atoms,increasing OH^(-)attack on the C atom and improving the stability of piperidinium cations.Hence QBNp TP-QFC possesses a robust alkaline stability at 80℃(95.3%conductivity retention after testing in 2 M Na OH for 2160 h).An excellent peak power density of 1.44 W cm^(-2)and a remarkable durability at 80℃(4.5%voltage loss after 100 h)can be observed.
基金the National Natural Science Foundation of China(51973157,51673148 and 51678411),Chinathe China Postdoctoral Science Foundation Grant(2019 M651047),Chinathe Science and Technology Plans of Tianjin(No.17PTSYJC00040 and 18PTSYJC00180),China for the financial support。
文摘The utilization of all-solid-state electrolytes is considered to be an effective way to enhance the safety performance of lithium metal batteries.However,the low ionic conductivity and poor interface compatibility greatly restrict the development of all-solid-state battery.In this study,a composite electrolyte combining the electrospun polyamide 6(PA6)nanofiber membrane with hierarchical structure and the polyethylene oxide(PEO)polymer is investigated.The introduction of PA6 nanofiber membrane can effectively reduce the crystallinity of the polymer,so that the ionic conductivity of the electrolyte can be enhanced.Moreover,it is found that the presence of finely branched fibers in the hierarchical structure PA6 membrane allows the polar functional groups(C=O and N-H bonds)to be fully exposed,which provides sufficient functional sites for lithium ion transport and helps to regulate the uniform deposition of lithium metal.Moreover,the hierarchical structure can enhance the mechanical strength(9.2 MPa)of the electrolyte,thereby effectively improving the safety and cycle stability of the battery.The prepared Li/Li symmetric battery can be stably cycled for 1500 h under 0.3 mA cm^(-2) and 60℃.This study demonstrates that the prepared electrolyte has excellent application prospects in the next generation all-solid-state lithium metal batteries.
基金The authors gratefully acknowledge the financial support of this work by Natural Science Foundation of China(grant no.s 51673030,51603017 and 51803011)Jilin Provincial Science&Technology Department(grant no.s 20200801011GH,20180101209JC,20160520138JH,20160519020JH)+1 种基金Jilin Province Development and Reform Commission(Grant nos:2019C042-5)ChangBai Mountain Scholars Program of Jilin Province.
文摘The semi-interpenetrating network anion exchange membranes(AEMs)based on quaternized polyvinyl alcohol(QPVA)and poly(-diallyldimethylammonium chloride)(PDDA)are synthesized.The chemical cross-linking structure is formed between hydroxyl groups of QPVA and aldehyde groups of glutaraldehyde(GA),which makes PDDA more stable embed in the QPVA matrix and also improves the mechanical properties and dimensional stability of AEMs.Due to the phase separation phenomenon of AEMs swelling in water,a microporous structure may be formed in the membrane,which reduces the transmission resistance of hydroxide ions and provides a larger space for the transfer of hydroxide ions,thus improving the conductivity.The ring structure of PDDA is introduced as a cationic group to transfer hydroxide ions,and shields the nucleophilic attack of the hydroxide ions through the steric hindrance effect,which improves alkaline stability.The hydroxide conductivity of semi-interpenetrating network membrane(QPVA/PDDA0.5-GA)is 36.5 mS cm^(-1) at 60℃.And the membrane of QPVA/PDDA0.5-GA exhibits excellent mechanical property with maximum tensile strength of 19.6 MPa.After immersing into hot 3 mol L^(-1) NaOH solutions at 60℃ for 300 h,the OHconductivity remains 78%of its initial value.The semi-interpenetrating network AEMs with microporous structure exhibit good ionic conductivity,mechanical strength and alkaline durability.
基金support from the“Scientific and Technical Innovation Action Plan”Basic Research Field of Shanghai Science and Technology Committee (19JC1410500)the National Natural Science Foundation of China (21972017).
文摘Development of high-performance hydroxide-conductive membranes is a focus research subject owing to promising applications in electrochemical reduction of CO_(2)(eCO_(2)RR).However,few satisfactory membranes have been developed to maximize the performance of CO_(2) electrolyzers,despite its role as the core in regulating ion transport and preventing product crossover or fuel loss.Herein,we report the synthesis of alkaline anion-exchange membranes fabricated by poly(vinyl-alcohol)(PVA)and poly[(3-methyl-1-vinylimidazoliummethylsulfate)-co-(1-vinylpyrrolidone)](PQ44)for use in CO_(2) electrolysis.Owing to the unique imidazolium ring structure coupled with a three-dimensional semiinterpenetrating porous internal architecture,the PVA/PQ44-OH-membranes provide a high hydroxide conductivity(21.47 mS cm^(-1)),preferable mechanical property and thermal stability.In particular,the eCO_(2)RR used PVA/PQ44-OH^(-) as electrolyte membrane realized a charming Faradaic efficiency(88%)and partial current density(29 mA cm^(-2))at0.96 VRHE and,delivered the excellent durability over 20 h electrolysis in 0.5 mol L^(-1) KHCO_(3) electrolyte.Notably,it can even enable an ultrahigh current density beyond 100 mA cm^(-2) at^(-1).11 VRHE when the electrolyte was KOH instead,and produced the FEHCOOof 85%at a low potential of0.81 VRHE,superior to both commercial alkaline A201 and acidic Nafion117 membrane.
基金supported by the Shandong Provincial Natural Science Foundation(ZR2019BC007)the Postdoctoral Science Foundation of China(No.2018M632626)+2 种基金the National Natural Science Foundation of China(No.31870535 and No.51973099)the Outstanding Youth of Natural Science in Shandong Province(JQ201713)the Taishan Scholar Program of Shandong Province,and the ARC Discovery Project(No.170103317)。
文摘Porous biomass electrodes have emerged as a critical material for electrocatalytic hydrogen evolution reaction(HER).However,most approaches for synthesizing porous electrodes from biomass require high energy consumption,which is resulted from the smash of biomass and the undergoing of serial assembly.Herein,a self-supported wood-derived"breathable"membrane is utilized directly as electrodes for highefficient HER via an assembly of Fe-doped NiP alloys.The well-designed hierarchical porous structures in natural wood membrane(NWM)are unusually beneficial for electrolytes accessibility and hydrogen gas removal.The obtained wood-derived membrane exhibits a high electrocatalytic activity and good cycling durability in acidic and alkaline electrolytes.Remarkably,the Fe_(0.074) NiP alloys/NWM electrode affords a large current density of 100 m A cm^(-2) at extremely low overpotentials of 168 mV in acidic electrolyte and174 m V in alkaline electrolyte.Density functional theory calculations unveil that the Fe atom doped in NiP alloys can create much more charge accumulation around Fe and Ni active sites,which helps decrease the △GH_(*)and △G_(H2O)and significantly promote the HER process.This new insight will promote further explorations of economic,high-efficient,and biodegradable wood-derived electrocatalysts for HER.
基金Project supported by the National Natural Science Foundation of China(Grant No.11904231)the National Key R&D Program of China(Grant Nos.2018YFE0205501 and 2018YFB1801500)Shanghai Sailing Program,China(Grant No.19YF1434100)。
文摘The phospholipid membrane plays a key role in myriad biological processes and phenomena, and the arrangement structure of membrane determines its function. However, the molecular arrangement structure of phospholipids in cell membranes is difficult to detect experimentally. On the basis of molecular dynamic simulations both in a non-destructive way and at native environment, we observed and confirmed that the phospholipids self-assemble to a hexagonal arrangement structure under physiological conditions. The underlying mechanism was revealed to be that there are hexagonal arrangement regions with a lower free energy around each lipid molecule. The findings potentially advance the understanding of biological functions of phospholipid bilayers.
基金financially supported by the National Key Research and Development Program of China(2018YFB1502503)the Strategic Priority Research Program of the Chinese Academy of Sciences(XDA21090101)。
文摘The design of the catalyst layer(CL)offers a feasible way to realize the commercialization of proton exchange membrane fuel cells(PEMFCs).An in-depth understanding of catalyst inks is critical to achieving the optimal CL structure and cell performance.In this work,the effects of the solvent evaporation process during ink drying on the formation of the CL microstructure are particularly considered to reveal the structure-property correlations among the catalyst ink,drying process,CL microstructure and fuel cell performance.An increase in the alcohol content of the catalyst ink increases the amount of free ionomers while allowing the ionomer backbone to be more stretched in the dispersion medium.The higher alcohol content contributes to rapid solvent evaporation and thus inhibits the formation of coffee rings;as a result,a more developed ionomer network with a denser pore structure is obtained.Therefore,the alcohol-rich electrode exhibits better proton conduction capability,but higher oxygen transport resistance.For complex fuel cell operating conditions,a catalyst ink formulation with 50 wt%alcohol content is preferred due to its proper ionomer and pore size distribution,providing satisfactory fuel cell performance.
基金financially supported by the National Science Foundation of China, China (22179130, 91834301)the Foundation of the Key Laboratory of Chinese Academy of Sciences (CXJJ21S024)Dalian Institute of Chemical Physics, China (DICPI202023)。
文摘Engineering failure of membrane electrode assembly caused by increasingly fuel poisoning in the high temperature polymer electrolyte membrane fuel cells fed with humidified reformate gases is firstly demonstrated herein this work. Based on the results of the in-situ environmental scanning electron microscope, electrochemical analyses, and limiting current method, a water-induced phosphoric acid invasion model is constructed in the porous electrode to elucidate the failure causations of the hindered hydrogen mass transport and the enhanced carbon monoxide poisoning. To optimize the phosphoric acid distribution under the inevitably humidified circumstance, a facile and effective strategy of constructing acid-proofed electrode is proposed and demonstrates outstanding stability with highly humidified reformate gases as anode fuel. This work discusses a potential defect that was rarely studied previously under practical working circumstance for high temperature polymer electrolyte membrane fuel cells, providing an alternative opinion of electrode design based on the fundamental aspects towards the engineering problems.
