Development of computational agent organizations or “societies” has become the domiant computing paradigm in the arena of Distributed Artificial Intelligence, and many foreseeable future applications need agent orga...Development of computational agent organizations or “societies” has become the domiant computing paradigm in the arena of Distributed Artificial Intelligence, and many foreseeable future applications need agent organizations, in which diversified agents cooperate in a distributed manner, forming teams. In such scenarios, the agents would need to know each other in order to facilitate the interactions. Moreover, agents in such an environment are not statically defined in advance but they can adaptively enter and leave an organization. This begs the question of how agents locate each other in order to cooperate in achieving organizational goals. Locating agents is a quite challenging task, especially in organizations that involve a large number of agents and where the resource avaiability is intermittent. The authors explore here an approach based on self organization map (SOM) which will serve as a clustering method in the light of the knowledge gathered about various agents. The approach begins by categorizing agents using a selected set of agent properties. These categories are used to derive various ranks and a distance matrix. The SOM algorithm uses this matrix as input to obtain clusters of agents. These clusters reduce the search space, resulting in a relatively short agent search time.展开更多
AgVO_(3)/ZIF-8 composites with enhanced photocatalytic effect were prepared by the combination of AgVO_(3)and ZIF-8.X-ray diffraction(XRD),scanning electron microscopy(SEM),high-power transmission electron microscopy(...AgVO_(3)/ZIF-8 composites with enhanced photocatalytic effect were prepared by the combination of AgVO_(3)and ZIF-8.X-ray diffraction(XRD),scanning electron microscopy(SEM),high-power transmission electron microscopy(HRTEM),X-ray photoelectron spectroscopy(XPS),ultraviolet-visible diffuse reflectance spectroscopy(UV-Vis DRS),photoluminescence(PL)spectroscopy,electron spin resonance(ESR)spectroscopy,transient photocurrent and electrochemical impedance spectroscopy(EIS)were used to characterize binary composites.Tetracycline(TC)was used as a substrate to study the performance efficiency of the degradation of photocatalysts under light conditions,and the degradation effect of TC was also evaluated under different mass concentrations and ionic contents.In addition,we further investigated the photocatalytic mechanism of the binary composite material AgVO_(3)/ZIF-8 and identified the key active components responsible for the catalytic degradation of this new photocatalyst.The experimental results show that the degradation efficiency of 10%-AZ,prepared with a molar ratio of 10%AgVO_(3)and ZIF-8 to TC,was 75.0%.This indicates that the photocatalytic activity can be maintained even under a certain ionic content,making it a suitable photocatalyst for optimal use.In addition,the photocatalytic mechanism of binary composites was further studied by the active species trapping experiment.展开更多
Sulfur-doped iron-cobalt tannate nanorods(S-FeCoTA)derived from metal-organic frameworks(MOFs)as electrocatalysts were synthesized via a one-step hydrothermal method.The optimized S-FeCoTA was interlaced by loose nano...Sulfur-doped iron-cobalt tannate nanorods(S-FeCoTA)derived from metal-organic frameworks(MOFs)as electrocatalysts were synthesized via a one-step hydrothermal method.The optimized S-FeCoTA was interlaced by loose nanorods,which had many voids.The S-FeCoTA catalysts exhibited excellent electrochemical oxygen evolution reaction(OER)performance with a low overpotential of 273 mV at 10 mA·cm^(-2)and a small Tafel slope of 36 mV·dec^(-1)in 1 mol·L^(-1)KOH.The potential remained at 1.48 V(vs RHE)at 10 mA·cm^(-2)under continuous testing for 15 h,implying that S-FeCoTA had good stability.The Faraday efficiency of S-FeCoTA was 94%.The outstanding OER activity of S-FeCoTA is attributed to the synergistic effects among S,Fe,and Co,thus promoting electron transfer,reducing the reaction kinetic barrier,and enhancing the OER performance.展开更多
(2E,6E)-4-methyl-2,6-bis(pyridin-3-ylmethylene)cyclohexan-1-one(L_(1))and 4-methyl-2,6-bis[(E)-4-(pyridin-4-yl)benzylidene]cyclohexan-1-one(L_(2))were synthesized and combined with isophthalic acid(H_(2)IP),then under...(2E,6E)-4-methyl-2,6-bis(pyridin-3-ylmethylene)cyclohexan-1-one(L_(1))and 4-methyl-2,6-bis[(E)-4-(pyridin-4-yl)benzylidene]cyclohexan-1-one(L_(2))were synthesized and combined with isophthalic acid(H_(2)IP),then under solvothermal conditions,to react with transition metals achieving four novel metal-organic frameworks(MOFs):[Zn(IP)(L_(1))]_(n)(1),{[Cd(IP)(L_(1))]·H_(2)O}_(n)(2),{[Co(IP)(L_(1))]·H_(2)O}_(n)(3),and[Zn(IP)(L_(2))(H_(2)O)]_(n)(4).MOFs 1-4 have been characterized by single-crystal X-ray diffraction,powder X-ray diffraction,thermogravimetry,and elemental analysis.Single-crystal X-ray diffraction shows that MOF 1 crystallizes in the monoclinic crystal system with space group P2_(1)/n,and MOFs 2-4 belong to the triclinic system with the P1 space group.1-3 are 2D sheet structures,2 and 3 have similar structural characters,whereas 4 is a 1D chain structure.Furthermore,1-3 exhibited certain photocatalytic capability in the degradation of rhodamine B(Rh B)and pararosaniline hydrochloride(PH).4could be used as a heterogeneous catalyst for the Knoevenagel reaction starting with benzaldehyde derivative and malononitrile.4 could promote the reaction to achieve corresponding products in moderate yields within 3 h.Moreover,the catalyst exhibited recyclability for up to three cycles without significantly dropping its activity.A mechanism for MOF 4 catalyzed Knoevenagel condensation reaction of aromatic aldehyde and malononitrile has been initially proposed.CCDC:2356488,1;2356497,2;2356499,3;2356498,4.展开更多
In recent years,numer-ous single-atom catalysts(SACs)have been synthesized to activate persulfate(PS)by a non-radical pathway because of its high se-lectivity,and activity for the cata-lyst.Metal-nitrogen-carbon(M-N_(...In recent years,numer-ous single-atom catalysts(SACs)have been synthesized to activate persulfate(PS)by a non-radical pathway because of its high se-lectivity,and activity for the cata-lyst.Metal-nitrogen-carbon(M-N_(x)-C)has been identified as the key active site in SACs.Although methods for preparing SACs have been extensively reported,a systematic summary of the direct construction of M-N_(x)-C,espe-cially unconventional metal-nitrogen-carbon(UM-N_(x)-C,x≠4),on SACs for PS non-radical activation has still not been reported.The role of the M-N_(x)-C active sites on PS non-radical activation is discussed and methods for the formation of M-N_(x)-C and UM-N_(x)-C active sites in SACs and the effect of catalyst carriers such as carbon nitride(g-C_(3)N_(4)),MOFs,COFs,and other car-bon materials are reviewed.Direct and indirect methods,especially for UM-N_(x)-C active site formation,are also elaborated.Factors affecting the formation of a M-N_(x)-C active site on SACs are also discussed.Prospects for the use of M-N_(x)-C active sites for the non-radical activation of PS by SACs to remove organic contaminants from wastewater are evaluated.展开更多
Traditional polymeric photocatalysts are typically constructed using aromatic building blocks to enhanceπ-conjugation.However,their inherent hydrophobicity and rigid structure lead to poor dispersibility in aqueous s...Traditional polymeric photocatalysts are typically constructed using aromatic building blocks to enhanceπ-conjugation.However,their inherent hydrophobicity and rigid structure lead to poor dispersibility in aqueous solutions,resulting in significant optical losses and exciton recombination.In this study,two series of six novel polymer photocatalysts(FLUSO,FLUSO-PEG10,FLUSO-PEG30;CPDTSO,CPDTSO-PEG10,CPDTSO-PEG30)are designed and synthesized by incorporating the hydrophilic,non-conjugated polyethylene glycol(PEG)chain,into both the main and side chains of polymers.By precisely optimizing the ratio of hydrophilic PEG segments,the water dispersibility is significantly improved while the light absorption capability of the polymer photocatalysts is well maintained.The experimental results confirm that the optimized FLUSO-PEG10 exhibits excellent photocatalytic hydrogen evolution rate,reaching up to 33.9 mmol/(g·h),which is nearly three times higher than that of fullyπ-conjugated counterparts.Water contact angles and particle size analyses reveal that incorporating non-conjugated segments into the main chains enhances the capacitance of the polymer/water interface and reduces particle aggregation,leading to improved photocatalyst dispersion and enhanced charge generation.展开更多
Aim Journal of Shenzhen University Science and Engineering,a bimonthly journal with its first issuing in 1984,is now administered and sponsored by Shenzhen University and published by the Science Press.It is a peer-re...Aim Journal of Shenzhen University Science and Engineering,a bimonthly journal with its first issuing in 1984,is now administered and sponsored by Shenzhen University and published by the Science Press.It is a peer-reviewed journal that publishes original papers of high scientific value.Innovation is always the starting point for the progress of our journal.We pay more attention to funded projects and major topics during manuscript organization to present the latest scientific and engineering achievements in China,as well as innovations in Shenzhen and Shenzhen University.展开更多
The poor electronic conductivity of metal-organic framework(MOF)materials hinders their direct application in the field of electrocatalysis in fuel cells.Herein,we proposed a strategy of embedding carbon nanotubes(CNT...The poor electronic conductivity of metal-organic framework(MOF)materials hinders their direct application in the field of electrocatalysis in fuel cells.Herein,we proposed a strategy of embedding carbon nanotubes(CNTs)during the growth process of MOF crystals,synthesizing a metalloporphyrin-based MOF catalyst TCPPCo-MOF-CNT with a unique CNT-intercalated MOF structure.Physical characterization revealed that the CNTs enhance the overall conductivity while retaining the original characteristics of the MOF and metalloporphyrin.Simultaneously,the insertion of CNTs generated adequate mesopores and created a hierarchical porous structure that enhances mass transfer efficiency.X-ray photoelectron spectroscopic analysis confirmed that the C atom in CNT changed the electron cloud density on the catalytic active center Co,optimizing the electronic structure.Consequently,the E_(1/2) of the TCPPCo-MOF-CNT catalyst under neutral conditions reached 0.77 V(vs.RHE),outperforming the catalyst without CNTs.When the TCPPCo-MOF-CNT was employed as the cathode catalyst in assembling microbial fuel cells(MFCs)with Nafion-117 as the proton exchange membrane,the maxi-mum power density of MFCs reached approximately 500 mW·m^(-2).展开更多
Organic semiconductor materials have shown unique advantages in the development of optoelectronic devices due to their ease of preparation,low cost,lightweight,and flexibility.In this work,we explored the application ...Organic semiconductor materials have shown unique advantages in the development of optoelectronic devices due to their ease of preparation,low cost,lightweight,and flexibility.In this work,we explored the application of the organic semiconductor Y6-1O single crystal in photodetection devices.Firstly,Y6-1O single crystal material was prepared on a silicon substrate using solution droplet casting method.The optical properties of Y6-1O material were characterized by polarized optical microscopy,fluorescence spectroscopy,etc.,confirming its highly single crystalline performance and emission properties in the near-infrared region.Phototransistors based on Y6-1O materials with different thicknesses were then fabricated and tested.It was found that the devices exhibited good visible to near-infrared photoresponse,with the maximum photoresponse in the near-infrared region at 785 nm.The photocurrent on/off ratio reaches 10^(2),and photoresponsivity reaches 16 mA/W.It was also found that the spectral response of the device could be regulated by gate voltage as well as the material thickness,providing important conditions for optimizing the performance of near-infrared photodetectors.This study not only demonstrates the excellent performance of organic phototransistors based on Y6-1O single crystal material in near-infrared detection but also provides new ideas and directions for the future development of infrared detectors.展开更多
Two tetrasubstituted carbazole derivatives TBICz and TOXDCz have been designed and synthesized,which possess the twist skeletons and exhibit excellent thermal and morphological stabilities.Utilizing these novel compou...Two tetrasubstituted carbazole derivatives TBICz and TOXDCz have been designed and synthesized,which possess the twist skeletons and exhibit excellent thermal and morphological stabilities.Utilizing these novel compounds as host material,high efficiency solution-processed green phosphorescent organic light-emitting diodes(PhOLEDs)have been achieved.The high triplet energies of TBICz and TOXDCz ensure efficient energy transfer from the host to the phosphor and triplet exciton confinement on the phosphor.Solution-processable green phospho⁃rescent devices employing Ir(ppy)3 as guest and the two tetrasubstituted carbazole derivatives as hosts exhibit high ef⁃ficiencies.The best EL performance is achieved for the TBICz-based device,with a maximum current efficiency of 27.3 cd/A,a maximum power efficiency of 15.9 lm/W,and a maximum external quantum efficiency of 7.8%,which provides more host material options for solution-processed OLEDs.展开更多
We have examined the theoretical implications of combining two main and three auxiliary ligands to form several Ir(Ⅲ)complexes featuring a transition metal as their core atom to identify some appropriate organic ligh...We have examined the theoretical implications of combining two main and three auxiliary ligands to form several Ir(Ⅲ)complexes featuring a transition metal as their core atom to identify some appropriate organic lightemitting diode(OLED)materials.By utilizing electronic structure,frontier molecular orbitals,minimum single-line absorption,triplet excited states,and emission spectral data derived from the density functional theory,the usefulness of these Ir(Ⅲ)complexes,including(piq)_(2)Ir(acac),(piq)_(2)Ir(tmd),(piq)_(2)Ir(tpip),(fpiq)_(2)Ir(acac),(fpiq)_(2)Ir(tmd),and(fpiq)_(2)Ir(tpip),in OLEDs was examined,where piq=1-phenylisoquinoline,fpiq=1-(4-fluorophenyl)isoquinoline,acac=(3Z)-4-hydroxypent-3-en-2-one,tmd=(4Z)-5-hydroxy-2,2,6,6-tetramethylhept-4-en-3-one,and tpip=tetraphenylimido-diphosphonate.These complexes all have low-efficiency roll-off properties,especially(fpiq)_(2)Ir(tpip).Some researchers have successfully synthesized complexes extremely similar to(piq)_(2)Ir(acac)through the Suzuki-Miyaura coupling reaction.展开更多
Biochar-derived dissolved organic matter(BCDOM),an essential component of biochar,plays a vital role in regulating the physicochemical and biological properties of soils during biochar application.However,the influenc...Biochar-derived dissolved organic matter(BCDOM),an essential component of biochar,plays a vital role in regulating the physicochemical and biological properties of soils during biochar application.However,the influence of BCDOM on soil organisms has not been clearly explained.Hence,this review aims to discuss the factors affecting BCDOM and its interaction with soil substances including organic pollutants,heavy metals,and microorganisms.Results displayed that the quantity of BCDOM ranges from 0.17 to 37.03 mg/g,which was influenced by feedstock,preparation methods of biochar,and extraction methods.With the decrease in lignin content of feedstocks,carbonization temperature,and acidity of extraction solution,the content of BCDOM increased.Through complexation and adsorption,protein-like components in BCDOM interact with heavy metals,promoting the adsorption and immobilization of heavy metals onto biochar.Furthermore,BCDOM enhances the adsorption of organic pollutants by biochar throughπ−πinteractions,hydrogen bonding,and redox processes.More importantly,BCDOM promotes plant growth by enhancing microbial activities,providing nutrients,and improving soil properties.However,the transport and fate of BCDOM in soil have not been well studied,and more researches are needed to explore the interaction mechanisms between BCDOM and soil organisms.展开更多
The objective of this incubation study was to comprehensively evaluate the effects of organic fertilizer and biochar,both individually and in combination,on soil respiration dynamics,key enzyme activities and the conc...The objective of this incubation study was to comprehensively evaluate the effects of organic fertilizer and biochar,both individually and in combination,on soil respiration dynamics,key enzyme activities and the concentrations of various organic carbon components in degraded mollisol.This study used a completely randomized factorial design with three application rates of organic fertilizer(M0:0,M1:13.64 g·kg^(-1),M2:27.27 g·kg^(-1))and biochar(C0:0,C1:1.36 g·kg^(-1),C2:2.73 g·kg^(-1)),resulting in nine treatments with four replicates each.Soil CO_(2) flux,organic carbon fractions including the total,active and microbial biomass carbon,and enzyme activities(sucrase,catalase and polyphenol oxidase)were measured over 120 days.Results indicated that the factors and their interactions significantly influenced all measured parameters.Soil respiration peaked at day 15,with M1C2 treatment exhibiting a rate of 10.90-fold higher than the control.The concentrations of the total,active and microbial biomass organic carbon reached maximum values on days 60,30 and 80,respectively.Notably,M2C1 treatment yielded the highest total organic carbon(86.35%increase)and microbial biomass carbon(17.84%increase).Enzyme activities were significantly enhanced,with the highest catalase activity observed for M0C2 treatment(10.14%increase).These results demonstrated that the co-application of organic fertilizer and biochar was a effective strategy for improving soil biological health and promoting carbon sequestration in degraded mollisol.The treatment combining a high rate of organic fertilizer with a low rate of biochar(M2C1)was identified as the most promising amendment strategy for fertility restoration.展开更多
In order to explore the remediation effects of lignite and biochar on Zn-contaminated soil,this experiment studied the impacts of adding lignite and biochar on soil respiration,soil enzyme activity,and organic carbon ...In order to explore the remediation effects of lignite and biochar on Zn-contaminated soil,this experiment studied the impacts of adding lignite and biochar on soil respiration,soil enzyme activity,and organic carbon in Zn-contaminated soil through soil culture experiments,which provided a theoretical basis for the remediation and improvement as well as for the development and utilization of Zn-contaminated soil.The study was an L8(4×2^(2))orthogonal experimental design with eight treatments,in which there were four levels of Zn contamination concentration(Z0:0;Z1:125 mg•kg^(-1);Z2:250 mg•kg^(-1);Z3:500 mg•kg^(-1)),low-Zn(125-250 mg•kg^(-1))and high-Zn(500 mg•kg^(-1)),two levels of lignite(H0:0;H1:13.33 g•kg^(-1)),two levels of biochar(C0:0;C1:3.33 g•kg^(-1)),with four replicates per treatment.The results showed that lignite or biochar and their interaction had extremely significant effects on both respiration rate and accumulation in Zn-contaminated soil.Among the high Zn-contaminated treatments,the mixed application of lignite and biochar(Z3H1C1 treatment)had the fastest soil respiration rate and the highest soil respiration accumulation.Lignite,biochar and their interaction had significant or extremely significant effects on sucrase,catalase and polyphenol oxidase activities in Zn-contaminated soil.Among the high Zn-contaminated treatments(Z3),the addition of biochar alone had the most significant effects on the increase of soil sucrase and catalase enzyme activities,while the mixed application of lignite and biochar had the most significant effects on the increase of soil polyphenol oxidase activity.Lignite,biochar and their interaction had significant or extremely significant effects on the total organic carbon,active organic carbon and microbial carbon content of Zn-contaminated soils.Soil total organic carbon content in general peaked at day 80.Among the high Zn-contaminated treatments,the addition of biochar alone had the most significant effects on the total organic carbon content of the soil,while the mixed application of lignite and biochar had the most significant effect on the microbiomass carbon content.展开更多
The desensitization of nitramine explosives while maintaining energetic performance is challenging.A highly efficient desensitizer is the key to solving the antinomy.This study focuses on using porous organic cages(PO...The desensitization of nitramine explosives while maintaining energetic performance is challenging.A highly efficient desensitizer is the key to solving the antinomy.This study focuses on using porous organic cages(POCs),specifically CC3 and RCC3,to desensitize RDX.By coating 0.1 wt%–5 wt%of POCs on RDX particles,a series of composite energetic materials were prepared.Characterization results show that POCs change the surface morphology of RDX,and there are interfacial interactions between them.The RDX@POCs composites exhibit enhanced stabilities in terms of heat,impact,friction,and electrostatic spark.For the RDX@RCC3-5%composite,the impact sensitivity(E_(IS)),friction sensitivity(E_(FS)),and electrostatic sensitivity(EES)were significantly reduced by 66.7%,68.8%,and 56.5%,respectively,while the detonation velocity decreased by merely 3.1%.These findings indicate that POCs,especially RCC3,are promising desensitizers for nitramine explosives,and their desensitization mechanisms likely involve barrier and buffering effects.The distinct desensitization behavior of RDX@RCC3 highlights the effectiveness of POCs in reducing the sensitivity of RDX without significantly compromising its energetic properties.展开更多
This study focuses on using a green reagent scheme of methanesulfonic acid (MSA) and citric acid (CA) to extract valuable metals from the cathodes, aiming to minimize environmental impact during the recycling process....This study focuses on using a green reagent scheme of methanesulfonic acid (MSA) and citric acid (CA) to extract valuable metals from the cathodes, aiming to minimize environmental impact during the recycling process. Leaching studies on LiCoO_(2) identified optimal conditions as follows: 2.4 mol/L MSA, 1.6 mol/L CA, S/L ratio of 80 g/L, leaching temperature of 90oC and leaching time of 6 h. The maximum Co and Li extraction achieved was 92% and 85%, respectively. LiCoO_(2) dissolution in MSA-CA leaching solution is highly impacted by temperature;Avrami equation showed a good fitting for the leaching data. The experimental activation energy of Co and Li was 50.98 kJ/mol and 50.55 kJ/mol, respectively, indicating that it is a chemical reaction-controlled process. Furthermore, cobalt was efficiently recovered from the leachate using oxalic acid, achieving a precipitation efficiency of 99.91% and a high-purity cobalt oxalate product (99.85 wt.%). In the MSA-CA leaching solution, MSA served as a lixiviant, while CA played a key role in reducing Co in LiCoO_(2). The overall organic acid leaching methodology presents an attractive option due to its reduced environmental impact.展开更多
文摘Development of computational agent organizations or “societies” has become the domiant computing paradigm in the arena of Distributed Artificial Intelligence, and many foreseeable future applications need agent organizations, in which diversified agents cooperate in a distributed manner, forming teams. In such scenarios, the agents would need to know each other in order to facilitate the interactions. Moreover, agents in such an environment are not statically defined in advance but they can adaptively enter and leave an organization. This begs the question of how agents locate each other in order to cooperate in achieving organizational goals. Locating agents is a quite challenging task, especially in organizations that involve a large number of agents and where the resource avaiability is intermittent. The authors explore here an approach based on self organization map (SOM) which will serve as a clustering method in the light of the knowledge gathered about various agents. The approach begins by categorizing agents using a selected set of agent properties. These categories are used to derive various ranks and a distance matrix. The SOM algorithm uses this matrix as input to obtain clusters of agents. These clusters reduce the search space, resulting in a relatively short agent search time.
文摘AgVO_(3)/ZIF-8 composites with enhanced photocatalytic effect were prepared by the combination of AgVO_(3)and ZIF-8.X-ray diffraction(XRD),scanning electron microscopy(SEM),high-power transmission electron microscopy(HRTEM),X-ray photoelectron spectroscopy(XPS),ultraviolet-visible diffuse reflectance spectroscopy(UV-Vis DRS),photoluminescence(PL)spectroscopy,electron spin resonance(ESR)spectroscopy,transient photocurrent and electrochemical impedance spectroscopy(EIS)were used to characterize binary composites.Tetracycline(TC)was used as a substrate to study the performance efficiency of the degradation of photocatalysts under light conditions,and the degradation effect of TC was also evaluated under different mass concentrations and ionic contents.In addition,we further investigated the photocatalytic mechanism of the binary composite material AgVO_(3)/ZIF-8 and identified the key active components responsible for the catalytic degradation of this new photocatalyst.The experimental results show that the degradation efficiency of 10%-AZ,prepared with a molar ratio of 10%AgVO_(3)and ZIF-8 to TC,was 75.0%.This indicates that the photocatalytic activity can be maintained even under a certain ionic content,making it a suitable photocatalyst for optimal use.In addition,the photocatalytic mechanism of binary composites was further studied by the active species trapping experiment.
文摘Sulfur-doped iron-cobalt tannate nanorods(S-FeCoTA)derived from metal-organic frameworks(MOFs)as electrocatalysts were synthesized via a one-step hydrothermal method.The optimized S-FeCoTA was interlaced by loose nanorods,which had many voids.The S-FeCoTA catalysts exhibited excellent electrochemical oxygen evolution reaction(OER)performance with a low overpotential of 273 mV at 10 mA·cm^(-2)and a small Tafel slope of 36 mV·dec^(-1)in 1 mol·L^(-1)KOH.The potential remained at 1.48 V(vs RHE)at 10 mA·cm^(-2)under continuous testing for 15 h,implying that S-FeCoTA had good stability.The Faraday efficiency of S-FeCoTA was 94%.The outstanding OER activity of S-FeCoTA is attributed to the synergistic effects among S,Fe,and Co,thus promoting electron transfer,reducing the reaction kinetic barrier,and enhancing the OER performance.
文摘(2E,6E)-4-methyl-2,6-bis(pyridin-3-ylmethylene)cyclohexan-1-one(L_(1))and 4-methyl-2,6-bis[(E)-4-(pyridin-4-yl)benzylidene]cyclohexan-1-one(L_(2))were synthesized and combined with isophthalic acid(H_(2)IP),then under solvothermal conditions,to react with transition metals achieving four novel metal-organic frameworks(MOFs):[Zn(IP)(L_(1))]_(n)(1),{[Cd(IP)(L_(1))]·H_(2)O}_(n)(2),{[Co(IP)(L_(1))]·H_(2)O}_(n)(3),and[Zn(IP)(L_(2))(H_(2)O)]_(n)(4).MOFs 1-4 have been characterized by single-crystal X-ray diffraction,powder X-ray diffraction,thermogravimetry,and elemental analysis.Single-crystal X-ray diffraction shows that MOF 1 crystallizes in the monoclinic crystal system with space group P2_(1)/n,and MOFs 2-4 belong to the triclinic system with the P1 space group.1-3 are 2D sheet structures,2 and 3 have similar structural characters,whereas 4 is a 1D chain structure.Furthermore,1-3 exhibited certain photocatalytic capability in the degradation of rhodamine B(Rh B)and pararosaniline hydrochloride(PH).4could be used as a heterogeneous catalyst for the Knoevenagel reaction starting with benzaldehyde derivative and malononitrile.4 could promote the reaction to achieve corresponding products in moderate yields within 3 h.Moreover,the catalyst exhibited recyclability for up to three cycles without significantly dropping its activity.A mechanism for MOF 4 catalyzed Knoevenagel condensation reaction of aromatic aldehyde and malononitrile has been initially proposed.CCDC:2356488,1;2356497,2;2356499,3;2356498,4.
文摘In recent years,numer-ous single-atom catalysts(SACs)have been synthesized to activate persulfate(PS)by a non-radical pathway because of its high se-lectivity,and activity for the cata-lyst.Metal-nitrogen-carbon(M-N_(x)-C)has been identified as the key active site in SACs.Although methods for preparing SACs have been extensively reported,a systematic summary of the direct construction of M-N_(x)-C,espe-cially unconventional metal-nitrogen-carbon(UM-N_(x)-C,x≠4),on SACs for PS non-radical activation has still not been reported.The role of the M-N_(x)-C active sites on PS non-radical activation is discussed and methods for the formation of M-N_(x)-C and UM-N_(x)-C active sites in SACs and the effect of catalyst carriers such as carbon nitride(g-C_(3)N_(4)),MOFs,COFs,and other car-bon materials are reviewed.Direct and indirect methods,especially for UM-N_(x)-C active site formation,are also elaborated.Factors affecting the formation of a M-N_(x)-C active site on SACs are also discussed.Prospects for the use of M-N_(x)-C active sites for the non-radical activation of PS by SACs to remove organic contaminants from wastewater are evaluated.
文摘Traditional polymeric photocatalysts are typically constructed using aromatic building blocks to enhanceπ-conjugation.However,their inherent hydrophobicity and rigid structure lead to poor dispersibility in aqueous solutions,resulting in significant optical losses and exciton recombination.In this study,two series of six novel polymer photocatalysts(FLUSO,FLUSO-PEG10,FLUSO-PEG30;CPDTSO,CPDTSO-PEG10,CPDTSO-PEG30)are designed and synthesized by incorporating the hydrophilic,non-conjugated polyethylene glycol(PEG)chain,into both the main and side chains of polymers.By precisely optimizing the ratio of hydrophilic PEG segments,the water dispersibility is significantly improved while the light absorption capability of the polymer photocatalysts is well maintained.The experimental results confirm that the optimized FLUSO-PEG10 exhibits excellent photocatalytic hydrogen evolution rate,reaching up to 33.9 mmol/(g·h),which is nearly three times higher than that of fullyπ-conjugated counterparts.Water contact angles and particle size analyses reveal that incorporating non-conjugated segments into the main chains enhances the capacitance of the polymer/water interface and reduces particle aggregation,leading to improved photocatalyst dispersion and enhanced charge generation.
文摘Aim Journal of Shenzhen University Science and Engineering,a bimonthly journal with its first issuing in 1984,is now administered and sponsored by Shenzhen University and published by the Science Press.It is a peer-reviewed journal that publishes original papers of high scientific value.Innovation is always the starting point for the progress of our journal.We pay more attention to funded projects and major topics during manuscript organization to present the latest scientific and engineering achievements in China,as well as innovations in Shenzhen and Shenzhen University.
基金the financial support from the National Natural Science Foundation of China(No.22178307)China Southern Power Grid(Grant Nos.0470002022030103HX00002-01).
文摘The poor electronic conductivity of metal-organic framework(MOF)materials hinders their direct application in the field of electrocatalysis in fuel cells.Herein,we proposed a strategy of embedding carbon nanotubes(CNTs)during the growth process of MOF crystals,synthesizing a metalloporphyrin-based MOF catalyst TCPPCo-MOF-CNT with a unique CNT-intercalated MOF structure.Physical characterization revealed that the CNTs enhance the overall conductivity while retaining the original characteristics of the MOF and metalloporphyrin.Simultaneously,the insertion of CNTs generated adequate mesopores and created a hierarchical porous structure that enhances mass transfer efficiency.X-ray photoelectron spectroscopic analysis confirmed that the C atom in CNT changed the electron cloud density on the catalytic active center Co,optimizing the electronic structure.Consequently,the E_(1/2) of the TCPPCo-MOF-CNT catalyst under neutral conditions reached 0.77 V(vs.RHE),outperforming the catalyst without CNTs.When the TCPPCo-MOF-CNT was employed as the cathode catalyst in assembling microbial fuel cells(MFCs)with Nafion-117 as the proton exchange membrane,the maxi-mum power density of MFCs reached approximately 500 mW·m^(-2).
基金Supported by the National Key Research and Development Program of China(2021YFB2012601)National Natural Science Foundation of China(12204109)+1 种基金Science and Technology Innovation Plan of Shanghai Science and Technology Commission(21JC1400200)Higher Education Indus⁃try Support Program of Gansu Province(2022CYZC-06)。
文摘Organic semiconductor materials have shown unique advantages in the development of optoelectronic devices due to their ease of preparation,low cost,lightweight,and flexibility.In this work,we explored the application of the organic semiconductor Y6-1O single crystal in photodetection devices.Firstly,Y6-1O single crystal material was prepared on a silicon substrate using solution droplet casting method.The optical properties of Y6-1O material were characterized by polarized optical microscopy,fluorescence spectroscopy,etc.,confirming its highly single crystalline performance and emission properties in the near-infrared region.Phototransistors based on Y6-1O materials with different thicknesses were then fabricated and tested.It was found that the devices exhibited good visible to near-infrared photoresponse,with the maximum photoresponse in the near-infrared region at 785 nm.The photocurrent on/off ratio reaches 10^(2),and photoresponsivity reaches 16 mA/W.It was also found that the spectral response of the device could be regulated by gate voltage as well as the material thickness,providing important conditions for optimizing the performance of near-infrared photodetectors.This study not only demonstrates the excellent performance of organic phototransistors based on Y6-1O single crystal material in near-infrared detection but also provides new ideas and directions for the future development of infrared detectors.
文摘Two tetrasubstituted carbazole derivatives TBICz and TOXDCz have been designed and synthesized,which possess the twist skeletons and exhibit excellent thermal and morphological stabilities.Utilizing these novel compounds as host material,high efficiency solution-processed green phosphorescent organic light-emitting diodes(PhOLEDs)have been achieved.The high triplet energies of TBICz and TOXDCz ensure efficient energy transfer from the host to the phosphor and triplet exciton confinement on the phosphor.Solution-processable green phospho⁃rescent devices employing Ir(ppy)3 as guest and the two tetrasubstituted carbazole derivatives as hosts exhibit high ef⁃ficiencies.The best EL performance is achieved for the TBICz-based device,with a maximum current efficiency of 27.3 cd/A,a maximum power efficiency of 15.9 lm/W,and a maximum external quantum efficiency of 7.8%,which provides more host material options for solution-processed OLEDs.
文摘We have examined the theoretical implications of combining two main and three auxiliary ligands to form several Ir(Ⅲ)complexes featuring a transition metal as their core atom to identify some appropriate organic lightemitting diode(OLED)materials.By utilizing electronic structure,frontier molecular orbitals,minimum single-line absorption,triplet excited states,and emission spectral data derived from the density functional theory,the usefulness of these Ir(Ⅲ)complexes,including(piq)_(2)Ir(acac),(piq)_(2)Ir(tmd),(piq)_(2)Ir(tpip),(fpiq)_(2)Ir(acac),(fpiq)_(2)Ir(tmd),and(fpiq)_(2)Ir(tpip),in OLEDs was examined,where piq=1-phenylisoquinoline,fpiq=1-(4-fluorophenyl)isoquinoline,acac=(3Z)-4-hydroxypent-3-en-2-one,tmd=(4Z)-5-hydroxy-2,2,6,6-tetramethylhept-4-en-3-one,and tpip=tetraphenylimido-diphosphonate.These complexes all have low-efficiency roll-off properties,especially(fpiq)_(2)Ir(tpip).Some researchers have successfully synthesized complexes extremely similar to(piq)_(2)Ir(acac)through the Suzuki-Miyaura coupling reaction.
基金Project(2020YFC1908802)supported by the National Key Research and Development Project of China。
文摘Biochar-derived dissolved organic matter(BCDOM),an essential component of biochar,plays a vital role in regulating the physicochemical and biological properties of soils during biochar application.However,the influence of BCDOM on soil organisms has not been clearly explained.Hence,this review aims to discuss the factors affecting BCDOM and its interaction with soil substances including organic pollutants,heavy metals,and microorganisms.Results displayed that the quantity of BCDOM ranges from 0.17 to 37.03 mg/g,which was influenced by feedstock,preparation methods of biochar,and extraction methods.With the decrease in lignin content of feedstocks,carbonization temperature,and acidity of extraction solution,the content of BCDOM increased.Through complexation and adsorption,protein-like components in BCDOM interact with heavy metals,promoting the adsorption and immobilization of heavy metals onto biochar.Furthermore,BCDOM enhances the adsorption of organic pollutants by biochar throughπ−πinteractions,hydrogen bonding,and redox processes.More importantly,BCDOM promotes plant growth by enhancing microbial activities,providing nutrients,and improving soil properties.However,the transport and fate of BCDOM in soil have not been well studied,and more researches are needed to explore the interaction mechanisms between BCDOM and soil organisms.
基金Supported by the Special Fund for Agro-scientific Research in Public Interest in China(201503119-06-01)。
文摘The objective of this incubation study was to comprehensively evaluate the effects of organic fertilizer and biochar,both individually and in combination,on soil respiration dynamics,key enzyme activities and the concentrations of various organic carbon components in degraded mollisol.This study used a completely randomized factorial design with three application rates of organic fertilizer(M0:0,M1:13.64 g·kg^(-1),M2:27.27 g·kg^(-1))and biochar(C0:0,C1:1.36 g·kg^(-1),C2:2.73 g·kg^(-1)),resulting in nine treatments with four replicates each.Soil CO_(2) flux,organic carbon fractions including the total,active and microbial biomass carbon,and enzyme activities(sucrase,catalase and polyphenol oxidase)were measured over 120 days.Results indicated that the factors and their interactions significantly influenced all measured parameters.Soil respiration peaked at day 15,with M1C2 treatment exhibiting a rate of 10.90-fold higher than the control.The concentrations of the total,active and microbial biomass organic carbon reached maximum values on days 60,30 and 80,respectively.Notably,M2C1 treatment yielded the highest total organic carbon(86.35%increase)and microbial biomass carbon(17.84%increase).Enzyme activities were significantly enhanced,with the highest catalase activity observed for M0C2 treatment(10.14%increase).These results demonstrated that the co-application of organic fertilizer and biochar was a effective strategy for improving soil biological health and promoting carbon sequestration in degraded mollisol.The treatment combining a high rate of organic fertilizer with a low rate of biochar(M2C1)was identified as the most promising amendment strategy for fertility restoration.
基金Supported by the Special Fund for Agro-scientific Research in Public Interest in China(201503119-06-01)。
文摘In order to explore the remediation effects of lignite and biochar on Zn-contaminated soil,this experiment studied the impacts of adding lignite and biochar on soil respiration,soil enzyme activity,and organic carbon in Zn-contaminated soil through soil culture experiments,which provided a theoretical basis for the remediation and improvement as well as for the development and utilization of Zn-contaminated soil.The study was an L8(4×2^(2))orthogonal experimental design with eight treatments,in which there were four levels of Zn contamination concentration(Z0:0;Z1:125 mg•kg^(-1);Z2:250 mg•kg^(-1);Z3:500 mg•kg^(-1)),low-Zn(125-250 mg•kg^(-1))and high-Zn(500 mg•kg^(-1)),two levels of lignite(H0:0;H1:13.33 g•kg^(-1)),two levels of biochar(C0:0;C1:3.33 g•kg^(-1)),with four replicates per treatment.The results showed that lignite or biochar and their interaction had extremely significant effects on both respiration rate and accumulation in Zn-contaminated soil.Among the high Zn-contaminated treatments,the mixed application of lignite and biochar(Z3H1C1 treatment)had the fastest soil respiration rate and the highest soil respiration accumulation.Lignite,biochar and their interaction had significant or extremely significant effects on sucrase,catalase and polyphenol oxidase activities in Zn-contaminated soil.Among the high Zn-contaminated treatments(Z3),the addition of biochar alone had the most significant effects on the increase of soil sucrase and catalase enzyme activities,while the mixed application of lignite and biochar had the most significant effects on the increase of soil polyphenol oxidase activity.Lignite,biochar and their interaction had significant or extremely significant effects on the total organic carbon,active organic carbon and microbial carbon content of Zn-contaminated soils.Soil total organic carbon content in general peaked at day 80.Among the high Zn-contaminated treatments,the addition of biochar alone had the most significant effects on the total organic carbon content of the soil,while the mixed application of lignite and biochar had the most significant effect on the microbiomass carbon content.
文摘The desensitization of nitramine explosives while maintaining energetic performance is challenging.A highly efficient desensitizer is the key to solving the antinomy.This study focuses on using porous organic cages(POCs),specifically CC3 and RCC3,to desensitize RDX.By coating 0.1 wt%–5 wt%of POCs on RDX particles,a series of composite energetic materials were prepared.Characterization results show that POCs change the surface morphology of RDX,and there are interfacial interactions between them.The RDX@POCs composites exhibit enhanced stabilities in terms of heat,impact,friction,and electrostatic spark.For the RDX@RCC3-5%composite,the impact sensitivity(E_(IS)),friction sensitivity(E_(FS)),and electrostatic sensitivity(EES)were significantly reduced by 66.7%,68.8%,and 56.5%,respectively,while the detonation velocity decreased by merely 3.1%.These findings indicate that POCs,especially RCC3,are promising desensitizers for nitramine explosives,and their desensitization mechanisms likely involve barrier and buffering effects.The distinct desensitization behavior of RDX@RCC3 highlights the effectiveness of POCs in reducing the sensitivity of RDX without significantly compromising its energetic properties.
文摘This study focuses on using a green reagent scheme of methanesulfonic acid (MSA) and citric acid (CA) to extract valuable metals from the cathodes, aiming to minimize environmental impact during the recycling process. Leaching studies on LiCoO_(2) identified optimal conditions as follows: 2.4 mol/L MSA, 1.6 mol/L CA, S/L ratio of 80 g/L, leaching temperature of 90oC and leaching time of 6 h. The maximum Co and Li extraction achieved was 92% and 85%, respectively. LiCoO_(2) dissolution in MSA-CA leaching solution is highly impacted by temperature;Avrami equation showed a good fitting for the leaching data. The experimental activation energy of Co and Li was 50.98 kJ/mol and 50.55 kJ/mol, respectively, indicating that it is a chemical reaction-controlled process. Furthermore, cobalt was efficiently recovered from the leachate using oxalic acid, achieving a precipitation efficiency of 99.91% and a high-purity cobalt oxalate product (99.85 wt.%). In the MSA-CA leaching solution, MSA served as a lixiviant, while CA played a key role in reducing Co in LiCoO_(2). The overall organic acid leaching methodology presents an attractive option due to its reduced environmental impact.
