Low-concentration coal mine methane(LC-CMM),which is predominantly composed of methane,serves as a clean and low-carbon energy resource with significant potential for utilization.Utilizing LC-CMM as fuel for solid oxi...Low-concentration coal mine methane(LC-CMM),which is predominantly composed of methane,serves as a clean and low-carbon energy resource with significant potential for utilization.Utilizing LC-CMM as fuel for solid oxide fuel cells(SOFCs)represents an efficient and promising strategy for its effective utilization.However,direct application in Ni-based anodes induces carbon deposition,which severely degrades cell performance.Herein,a medium-entropy oxide Sr_(2)FeNi_(0.1)Cr_(0.3)Mn_(0.3)Mo_(0.3)O_(6−δ)(SFNCMM)was developed as an anode internal reforming catalyst.Following reduction treatment,FeNi_(3) nano-alloy particles precipitate on the surface of the material,thereby significantly enhancing its catalytic activity for LC-CMM reforming process.The catalyst achieved a methane conversion rate of 53.3%,demonstrating excellent catalytic performance.Electrochemical evaluations revealed that SFNCMM-Gd_(0.1)Ce_(0.9)O_(2−δ)(GDC)with a weight ratio of 7:3 exhibited superior electrochemical performance when employed as the anodic catalytic layer.With H_(2) and LC-CMM as fuels,the single cell achieved maximum power densities of 1467.32 and 1116.97 mW·cm^(−2) at 800℃,respectively,with corresponding polarization impedances of 0.17 and 1.35Ω·cm^(2).Furthermore,the single cell maintained stable operation for over 100 h under LC-CMM fueling without significant carbon deposition,confirming its robust resistance to carbon formation.These results underscore the potential of medium-entropy oxides as highly effective catalytic layers for mitigating carbon deposition in SOFCs.展开更多
Direct ethanol fuel cells(DEFCs)are a promising alternative to conventional energy sources,offering high energy density,environmental sustainability,and operational safety.Compared to methanol fuel cells,DEFCs exhibit...Direct ethanol fuel cells(DEFCs)are a promising alternative to conventional energy sources,offering high energy density,environmental sustainability,and operational safety.Compared to methanol fuel cells,DEFCs exhibit lower toxicity and a more mature preparation process.Unlike hydrogen fuel cells,DEFCs provide superior storage and transport feasibility,as well as cost-effectiveness,significantly enhancing their commercial viability.However,the stable C-C bond in ethanol creates a high activation energy barrier,often resulting in incomplete electrooxidation.Current commercial platinum(Pt)-and palladium(Pd)-based catalysts demonstrate low C-C bond cleavage efficiency(<7.5%),severely limiting DEFC energy output and power density.Furthermore,high catalyst costs and insufficient activity impede large-scale commercialization.Recent advances in DEFC anode catalyst design have focused on optimizing material composition and elucidating catalytic mechanisms.This review systematically examines developments in ethanol electrooxidation catalysts over the past five years,highlighting strategies to improve C1 pathway selectivity and C-C bond activation.Key approaches,such as alloying,nanostructure engineering,and interfacial synergy effects,are discussed alongside their mechanistic implications.Finally,we outline current challenges and future prospects for DEFC commercialization.展开更多
Bismuth(Bi)anodes have been widely investigated for potential application in sodium-ion batteries(SIBs)due to their ultrahigh theoretical volumetric capacity(3800 mAh cm^(-3))and suitable sodiation potential(0.5-0.7 V...Bismuth(Bi)anodes have been widely investigated for potential application in sodium-ion batteries(SIBs)due to their ultrahigh theoretical volumetric capacity(3800 mAh cm^(-3))and suitable sodiation potential(0.5-0.7 V).Unfortunately,either Bi or Bi-based compounds still face tricky challenges of unsatisfying reversible capacity(<350 mAh g^(-1))and inferior initial Coulombic efficiency(ICE,<70%).Herein,a controllable trace-sulfurization strategy is proposed to address these challenges by developing a yolkshell Bi/Bi_(2)S_(3)heterostructure encapsulated within S-doped carbon shells(TS-Bi/C).This approach strategically incorporates a trace amount of high-capacity Bi_(2)S_(3)phase with metallic Bi,consequently building regional Bi/Bi_(2)S_(3)heterointerfaces for enhancing interfacial charge transfer and sodium storage reversibility.Moreover,a thin and homogeneous solid electrolyte film(~5 nm)was formed on the surface of TS-Bi/C during the initial discharge-charge process.These merits result in an approximate 30%increase in ICE of TS-Bi/C(87.4%)compared to pure Bi/C(57,6%)when employed as anodes in SIBs,together with boosted discharge capacity of 462.3 mAh g^(-1)at 0.1 A g^(-1)and high rate capability of 382.4 mAh g^(-1)at 10 A g^(-1).Importantly,as compared to both Bi/C and Bi_(2)S_(3)/C counterparts,TS-Bi/C can deliver superior volumetric capacity as high as 1553 mAh cm^(-3)owing to its considerable tap density of 3.43 g cm^(-3).展开更多
This work is devoted to the development of a low cost dimensionally stable anode with high oxygen evolution catalytic activity for practical applications.For this purpose,a Ti/SnO_(x)/MnO_(2) anode was fabricated thro...This work is devoted to the development of a low cost dimensionally stable anode with high oxygen evolution catalytic activity for practical applications.For this purpose,a Ti/SnO_(x)/MnO_(2) anode was fabricated through an innovative strategy involving Sn electrodeposition,oxidation,and MnO_(2)-layer preparation.The structure of the anode was characterized,and the oxygen evolution performance was evaluated in a H_(2)SO_(4) solution.The results show that compared with the Ti/SnO_(2)/MnO_(2) anode prepared by the conventional brushing-annealing process,the Ti/SnO_(x)/MnO_(2) anode fabricated through the innovative procedure exhibits a lower oxygen evolution potential and a nearly 40%longer accelerated lifespan.The superior oxygen evolution performance of the Ti/SnO_(x)/MnO_(2) anode is attributed to the distinctive SnO_(x) intermediate layer fabricated through Sn electrodeposition followed by oxidation,which indicates the great potential of the anode as a dimensionally stable anode for metal electrowinning and hydrogen production by electrolysis,etc.展开更多
Since the commercialization of the fuel cell electric vehicles (FCEVs), the polymer electrolyte membrane fuel cell system has been actively improved as a powertrain for ultimate environment-friendly vehicle. During th...Since the commercialization of the fuel cell electric vehicles (FCEVs), the polymer electrolyte membrane fuel cell system has been actively improved as a powertrain for ultimate environment-friendly vehicle. During the FCEV operation, various transient conditions such as start-up/shut-down and fuel starvation occur irregularly, which deteriorates the durability of the membrane electrode assembly. In particular, when fuel starvation occurs, the carbon support in the anode is oxidized within few minutes, thus the mitigation of this phenomenon is essential for securing the durability. This short review introduces the concept of reversal tolerant anode (RTA), which is a mitigation method using an oxygen evolution catalyst and reviews some previous reports. In addition, new approach for RTA suggested by authors recently, which is the replacement of Pt anode catalyst by multifunctional IrRu alloy catalyst that simultaneously exhibits the activities for the hydrogen oxidation reaction and the oxygen evolution reaction is introduced.展开更多
Metallic-monolith catalyst support with self-growing porous anodic alumina(PAA)film was prepared by anodizing Al plate.The effect of hydrothermal treatment(HTT)on the crystalline state and textural properties of PAA f...Metallic-monolith catalyst support with self-growing porous anodic alumina(PAA)film was prepared by anodizing Al plate.The effect of hydrothermal treatment(HTT)on the crystalline state and textural properties of PAA film was investigated by XRD,BET,SEM and TG.The HTT treatment above 50°C and the subsequent calcination above 300°C could convert the amorphous skeleton alumina intoγ-alumina and increase the specific surface area(SBET).However,SEM images showed the HTT modification was a non-uniform process along the thickness of PAA film.The promotion effect of HTT on SBETwas non-linear,and the slope of SBETgradually decreased with the HTT temperature or time increased.The limited HTT effect should be attributed to a changed pore structure caused by an unfavorable pore sealing limitation.Pore widening treatment(PWT)before HTT could break the pore sealing limitation,because of the reduced internal diffusion resistance of hydrothermal reaction.The synergistic combination of PWT and HTT developed a PAA support with a large SBETcomparable to commercialγ-alumina.In the catalytic combustion of toluene,the Pt-based catalyst prepared by using the PWT and HTT comodified PAA support gave higher Pt dispersion and more favorable catalytic activity than that treated by HTT alone.The presence of a bimodal pore structure was suggested to be a decisive reason.展开更多
The actual performance of vanadium redox flow batteries (VRFBs) is still significantly constrained by the slow kinetics and major parasitic reactivity of anode issues. Herein, a B-site management strategy of SrBO3 (B ...The actual performance of vanadium redox flow batteries (VRFBs) is still significantly constrained by the slow kinetics and major parasitic reactivity of anode issues. Herein, a B-site management strategy of SrBO3 (B = Ti, Zr, Hf) perovskites was proposed to promote the anode reaction jointly explored by experiments and first-principle calculations. As the atomic number of B increases, the enhanced polarity of the B-O bond and the increased oxygen defect can boost the adsorption of vanadium ions, while the weakened orbital hybridization of the B-O bond facilitates the charge transfer of anode reaction. Compared with SrTiO3 and SrZrO3, oversized particles and deformed crystals of SrHfO3 reduce its catalysis. Of SrBO3 perovskites, SrZrO3 stands out in catalysis, owing to its outstanding combination of high hydrophilicity, large surface area, and desired crystal structure. Further, the VRFB using SrZrO3 presents a superior energy efficiency (EE) of 63.2% at 300 mA cm-2 and an increase of 15% in EE compared with the pristine cell at 200 mA cm-2. This work lays the foundation for building the connections between the structural and compositional flexibility and the tunable perovskite properties desirable for vanadium redox reactions.展开更多
Ni-based anodes of SOFCs are susceptible to coking, which greatly limits practical application of direct methane-based fuels. An indirect internal reformer is an effective way to convert methane-based fuels into synga...Ni-based anodes of SOFCs are susceptible to coking, which greatly limits practical application of direct methane-based fuels. An indirect internal reformer is an effective way to convert methane-based fuels into syngas before they reach anode. In this work, catalytic activity of a redox-stable perovskite La0.7Sr0.3Cr0.8Fe0.2O3-δ(LSCrFO) for methane conversion was evaluated. The catalyst was fabricated as an anodic protective layer to improve coking resistance of a Ni cermet anode. Using wet CH4 as a fuel, the LSCrFO-modified cell showed excellent power output and good coking resistance with peak power density of 1.59 W cm-2 at 800℃. The cell demonstrated good durability lasting for at least 100 h. While the bare cell without the protective layer showed poor durability with the cell voltage fast dropped from 0.75 V to 0.4 V within 30 min. Under wet coal bed methane (CBM) operation, obvious performance degradation within 35 h (1.7 mV h^-1) was observed due to the influence of heavy carbon compounds in CBM. The pre-and post-mortem microstructures and carbon analysis of the anode surface and catalyst surface were further conducted.展开更多
Well aligned quasi-straight single-walled carbon nanotubes (SWCNTs) and straight SWCNTs bundle have been prepared in large scale by anode-arc vaporization of gr aphite with metallic catalysts. Various parameters such ...Well aligned quasi-straight single-walled carbon nanotubes (SWCNTs) and straight SWCNTs bundle have been prepared in large scale by anode-arc vaporization of gr aphite with metallic catalysts. Various parameters such as the catalyst preparat ion, the kinds and pressure of the buffer gases, the quantity of anode-arc curre nt intensity, and the method of purification have been examined. The influence o f these parameters on the deposited carbon yield is reported, together with obse rvations of the produced material. Improvement in synthetic techniques has resul ted in the optimal conditions for the production of large quantities of high qua lity SWCNTs in our semi-continuous synthesis method. The formation of carbon nan otubes (CNTs) was studied briefly in this paper. Owing to the magnetic pinching effect of arc current, the CNTs arrange in parallel lines along the arc current direction.展开更多
Microbial fuel cell(MFC) is an advanced bioelectrochemical technique that can utilize biomass materials in the process of simultaneously generating electricity and biodegrading or bio transforming toxic pollutants fro...Microbial fuel cell(MFC) is an advanced bioelectrochemical technique that can utilize biomass materials in the process of simultaneously generating electricity and biodegrading or bio transforming toxic pollutants from wastewater. The overall performance of the system is largely dependent on the efficiency of the anode electrode to enhance electron transportation. Furthermore, the anode electrode has a significant impact on the overall cost of MFC setup. Hence, the need to explore research focused towards developing cost-effective material as anode in MFC. This material must also have favourable properties for electron transportation. Graphene oxide(GO) derivatives and its modification with nanomaterials have been identified as a viable anode material. Herein, we discussed an economically effective strategy for the synthesis of graphene derivatives from waste biomass materials and its subsequent fabrication into anode electrode for MFC applications. This review article offers a promising approach towards replacing commercial graphene materials with biomass-derived graphene derivatives in a view to achieve a sustainable and commercialized MFC.展开更多
The aim of this work was to investigate the effects of calcination/acid-activation on the composition, structure, and photocatalytic （PC） reduction property of an anodic oxidation TiO2/Ti film catalyst. The surface ...The aim of this work was to investigate the effects of calcination/acid-activation on the composition, structure, and photocatalytic （PC） reduction property of an anodic oxidation TiO2/Ti film catalyst. The surface morphology and phase composition were examined by scanning electron microscopy and X-ray diffraction. The catalytic property of the film catalysts was evaluated through the removal rate of potassium chromate during the PC reduction process. The results showed that the film catalysts were composed of anatase and rutile TiO2 with a micro-porous surface structure. The calcination treatment increased the content of TiO2 in the film, changed the relative ratio of anatase and rutile TiO2, and decreased the size of the micro pores of the film catalysts. The removal rate of potassium chromate was related to the technique parameters of calcination/acid-activation treatment. When the anodic oxidation TiO2/Ti film catalyst was calcined at 873 K for 30 min and then acid-activated in the concentrated H2SO4 for 60 min, it presented the highest catalytic property, with the removal rate of potassium chromate of 96.3% during the PC reduction process under the experimental conditions.展开更多
Fuel cells using borohydride as the fuel have received much attention because of high energy density and theoretical working potential.In this work,LaNi4.5Al0.5 hydrogen storage alloy used as the anodic material has b...Fuel cells using borohydride as the fuel have received much attention because of high energy density and theoretical working potential.In this work,LaNi4.5Al0.5 hydrogen storage alloy used as the anodic material has been investigated.It was found that the increasing operation temperature was helpful to the open-circuit potential,the discharge potential and the power density,but showed a negative effect on the utilization of the fuel due to the accelerated hydrogen evolution.The high KOH concentration was favorable for high-rate discharge capability.The adsorption and transformation of hydrogen on LaNi4.5Al0.5 alloy electrode has been observed,but its contribution to the discharge capability during a high-rate discharge was small.展开更多
Electrochemical CO_(2)reduction reaction(CO_(2)RR)to formate presents a technoeconomic route for CO_(2)utilization under mild conditions,yet practical implementation is constrained by the high energy consumption(>9...Electrochemical CO_(2)reduction reaction(CO_(2)RR)to formate presents a technoeconomic route for CO_(2)utilization under mild conditions,yet practical implementation is constrained by the high energy consumption(>90%of total input)of the anodic oxygen evolution reaction(OER).Replacement of OER by partial methanol oxidation reaction(MOR)could lead to simultaneous formate production at both electrodes and remarkably reduce the overall energy consumption.Herein,we designed a two-electrode system featuring a nickel foam-supported crystalline/amorphous bismuth-bismuth nickel oxide composite cathode(Bi-BiNiO_(x)/NF)and aβ-Ni(OH)_(2)anode,achieving excellent formate production behavior.The crystalline/amorphous Bi-BiNiO_(x)/NF cathode delivers exceptional CO_(2)RR performance,achieving 98.9%formate Faradaic efficiency(FEformate)at−0.90 V vs.reversible hydrogen electrode(RHE)and maintaining>90.7%FEformate over 72 h continuous operation-attributed to its Bi-Ni bimetallic synergy and crystalline/amorphous heterostructure that enhance active site exposure and reaction kinetics.The integrated CO_(2)RR||MOR system operates stably for 90 h at 2.2 V and 10 mA·cm^(−2),sustaining>90%FE_(formate)at both electrodes with a cell voltage(1.760 V)significantly lower than conventional CO_(2)RR||OER systems(1.953 V).This work demonstrates efficient concurrent formate electrosynthesis and establishes an energy-efficient paradigm for electrocatalytic CO_(2)valorization through synergistic catalyst design and reaction pathway integration.展开更多
High-performance and low-cost anode materials are critical for superior sodium-ion batteries(SIBs).Herein,high-yield porous carbon nanofiber(CNF)anode materials(named CNFs@Cu–Ni)are prepared by chemical vapor deposit...High-performance and low-cost anode materials are critical for superior sodium-ion batteries(SIBs).Herein,high-yield porous carbon nanofiber(CNF)anode materials(named CNFs@Cu–Ni)are prepared by chemical vapor deposition using a specialized nanoporous Cu–Ni alloy catalyst.Density functional theory calculations indicate that Ni incorporation results in a shift of the d-band center of the catalyst from−2.34157 to−1.93682 eV.This phenomenon elucidates the remarkable adsorption capacity of the Cu–Ni catalyst toward C2H2,thereby facilitating the catalytic growth of high-performance CNFs.With this approach,a superior yield of 258.6%for deposited carbon is reached after growth for 1 h.The CNFs@Cu–Ni anode presents an outstanding discharge capacity of 193.6 mAh·g^(−1) at 1.0 A·g^(−1)over 1000 cycles and an exceptional rate capability by maintaining a capacity of 158.9 mAh·g^(−1)even at 5.0 A·g^(−1)in an ether-based electrolyte.It also exhibits excellent performance in the CNFs@Cu–Ni//NVP full battery attributed to the presence of abundant Na+adsorption sites on its surface.This study presents a new concept for the advancement of high-performance carbonaceous electrodes for SIBs.展开更多
Nickel nanowire and nanotube arrays as supports for Pt-Pd catalyst were prepared by elec- troless deposition with anodic aluminum oxide template. Pt-Pd composite catalyst was de- posited on the arrays by displacement ...Nickel nanowire and nanotube arrays as supports for Pt-Pd catalyst were prepared by elec- troless deposition with anodic aluminum oxide template. Pt-Pd composite catalyst was de- posited on the arrays by displacement reaction. SEM images show that the nickel nanowires have an average diameter of I00 nm and the nickel nanotubes have an average inner diameter of 200 nm. EDS scanning reveals that elemental Pt and Pd disperse uniformly on the arrays. Cyclic voltammetry study indicates that the nickel nanotube array loaded with Pt-Pd pos- sesses a higher electrochemical activity for ethanol oxidation than the nickel nanowire array with Pt-Pd.展开更多
Direct methanol fuel cells （DMFCs） are very promising power source for stationary and portable miniatureelectric appliances due to its high efficiency and low emissions of pollutants. As the key material, cata-lysts...Direct methanol fuel cells （DMFCs） are very promising power source for stationary and portable miniatureelectric appliances due to its high efficiency and low emissions of pollutants. As the key material, cata-lysts for both cathode and anode face several problems which hinder the commercialization of DMFCs.In this review, we mainly focus on anode catalysts of DMFCs. The process and mechanism of methanolelectrooxidation on Pt and Pt-based catalysts in acidic medium have been introduced. The influences ofsize effect and morphology on electrocatalytic activity are discussed though whether there is a size effectin MOP, catalyst is under debate. Besides, the non Pt catalysts are also listed to emphasize though Pt isstill deemed as the indispensable element in anode catalyst of DMFCs in acidic medium. Different cata-lyst systems are compared to illustrate the level of research at present. ome debates need to be verifiedwith experimental evidences.展开更多
Sustainable conversion of carbon dioxide(CO_(2))to high value-added chemicals and fuels is a promising solution to solve the problem of excessive CO_(2) emissions and alleviate the shortage of fossil fuels,maintaining...Sustainable conversion of carbon dioxide(CO_(2))to high value-added chemicals and fuels is a promising solution to solve the problem of excessive CO_(2) emissions and alleviate the shortage of fossil fuels,maintaining the balance of the carbon cycle in nature.The development of catalytic system is of great significance to improve the efficiency and selectivity for electrochemical CO_(2) conversion.In particular,bismuth(Bi)based catalysts are the most promising candidates,while confronting challenges.This review aims to elucidate the fundamental issues of efficient and stable Bi-based catalysts,constructing a bridge between the category,synthesis approach and electrochemical performance.In this review,the categories of Bi-based catalysts are firstly introduced,such as metals,alloys,single atoms,compounds and composites.Followed by the statement of the reliable and versatile synthetic approaches,the representative optimization strategies,such as morphology manipulation,defect engineering,component and heterostructure regulation,have been highlighted in the discussion,paving in-depth insight upon the design principles,reaction activity,selectivity and stability.Afterward,in situ characterization techniques will be discussed to illustrate the mechanisms of electrochemical CO_(2) conversion.In the end,the challenges and perspectives are also provided,promoting a systematic understanding in terms of the bottleneck and opportunities in the field of electrochemical CO_(2) conversion.展开更多
The development of cost-effective and energy-efficient anode materials is essential for the advancement of industrial water electrolysis.Herein,we report a rapid,ambient-temperature method to prepare largearea nickel ...The development of cost-effective and energy-efficient anode materials is essential for the advancement of industrial water electrolysis.Herein,we report a rapid,ambient-temperature method to prepare largearea nickel mesh electrodes(SFN/NM)via surface functionalization completed within 3 min,without relying on thermal treatments or noble metals.The as-prepared electrodes achieve a high current density of 100 m A/cm^(2)at an overpotential of just 300 m V in 6 mol/L KOH,and exhibit remarkable stability over1600 h of continuous operation.With comparable activity to commercial Raney nickel yet significantly lower processing and material costs(reduced by 50%-70%),this approach provides a practical solution for low-energy water splitting.Beyond its industrial relevance,the strategy offers a scalable model for engineering high-performance OER electrodes,inspiring future directions in electrocatalyst design.展开更多
基金supported by the National Key R&D Program of China(No.2024YFB4007501)the Natural Science Foundation of Jiangsu Province(No.BK20240109)the project of Jiangsu Key Laboratory for Clean Utilization of Carbon Resources(No.BM2024007).
文摘Low-concentration coal mine methane(LC-CMM),which is predominantly composed of methane,serves as a clean and low-carbon energy resource with significant potential for utilization.Utilizing LC-CMM as fuel for solid oxide fuel cells(SOFCs)represents an efficient and promising strategy for its effective utilization.However,direct application in Ni-based anodes induces carbon deposition,which severely degrades cell performance.Herein,a medium-entropy oxide Sr_(2)FeNi_(0.1)Cr_(0.3)Mn_(0.3)Mo_(0.3)O_(6−δ)(SFNCMM)was developed as an anode internal reforming catalyst.Following reduction treatment,FeNi_(3) nano-alloy particles precipitate on the surface of the material,thereby significantly enhancing its catalytic activity for LC-CMM reforming process.The catalyst achieved a methane conversion rate of 53.3%,demonstrating excellent catalytic performance.Electrochemical evaluations revealed that SFNCMM-Gd_(0.1)Ce_(0.9)O_(2−δ)(GDC)with a weight ratio of 7:3 exhibited superior electrochemical performance when employed as the anodic catalytic layer.With H_(2) and LC-CMM as fuels,the single cell achieved maximum power densities of 1467.32 and 1116.97 mW·cm^(−2) at 800℃,respectively,with corresponding polarization impedances of 0.17 and 1.35Ω·cm^(2).Furthermore,the single cell maintained stable operation for over 100 h under LC-CMM fueling without significant carbon deposition,confirming its robust resistance to carbon formation.These results underscore the potential of medium-entropy oxides as highly effective catalytic layers for mitigating carbon deposition in SOFCs.
基金supported by the National Natural Science Foundation of China(22472023,22202037)the Jilin Province Science and Technology Development Program(20250102077JC)the Fundamental Research Funds for the Central Universities(2412024QD014,2412023QD019).
文摘Direct ethanol fuel cells(DEFCs)are a promising alternative to conventional energy sources,offering high energy density,environmental sustainability,and operational safety.Compared to methanol fuel cells,DEFCs exhibit lower toxicity and a more mature preparation process.Unlike hydrogen fuel cells,DEFCs provide superior storage and transport feasibility,as well as cost-effectiveness,significantly enhancing their commercial viability.However,the stable C-C bond in ethanol creates a high activation energy barrier,often resulting in incomplete electrooxidation.Current commercial platinum(Pt)-and palladium(Pd)-based catalysts demonstrate low C-C bond cleavage efficiency(<7.5%),severely limiting DEFC energy output and power density.Furthermore,high catalyst costs and insufficient activity impede large-scale commercialization.Recent advances in DEFC anode catalyst design have focused on optimizing material composition and elucidating catalytic mechanisms.This review systematically examines developments in ethanol electrooxidation catalysts over the past five years,highlighting strategies to improve C1 pathway selectivity and C-C bond activation.Key approaches,such as alloying,nanostructure engineering,and interfacial synergy effects,are discussed alongside their mechanistic implications.Finally,we outline current challenges and future prospects for DEFC commercialization.
基金financial support from the National Natural Science Foundation of China(21878192 and 51904193)the Science and Technology Cooperation Special Fund of Sichuan University and Zigong City(2022CDZG-9 and 2023CDZG-5)。
文摘Bismuth(Bi)anodes have been widely investigated for potential application in sodium-ion batteries(SIBs)due to their ultrahigh theoretical volumetric capacity(3800 mAh cm^(-3))and suitable sodiation potential(0.5-0.7 V).Unfortunately,either Bi or Bi-based compounds still face tricky challenges of unsatisfying reversible capacity(<350 mAh g^(-1))and inferior initial Coulombic efficiency(ICE,<70%).Herein,a controllable trace-sulfurization strategy is proposed to address these challenges by developing a yolkshell Bi/Bi_(2)S_(3)heterostructure encapsulated within S-doped carbon shells(TS-Bi/C).This approach strategically incorporates a trace amount of high-capacity Bi_(2)S_(3)phase with metallic Bi,consequently building regional Bi/Bi_(2)S_(3)heterointerfaces for enhancing interfacial charge transfer and sodium storage reversibility.Moreover,a thin and homogeneous solid electrolyte film(~5 nm)was formed on the surface of TS-Bi/C during the initial discharge-charge process.These merits result in an approximate 30%increase in ICE of TS-Bi/C(87.4%)compared to pure Bi/C(57,6%)when employed as anodes in SIBs,together with boosted discharge capacity of 462.3 mAh g^(-1)at 0.1 A g^(-1)and high rate capability of 382.4 mAh g^(-1)at 10 A g^(-1).Importantly,as compared to both Bi/C and Bi_(2)S_(3)/C counterparts,TS-Bi/C can deliver superior volumetric capacity as high as 1553 mAh cm^(-3)owing to its considerable tap density of 3.43 g cm^(-3).
文摘This work is devoted to the development of a low cost dimensionally stable anode with high oxygen evolution catalytic activity for practical applications.For this purpose,a Ti/SnO_(x)/MnO_(2) anode was fabricated through an innovative strategy involving Sn electrodeposition,oxidation,and MnO_(2)-layer preparation.The structure of the anode was characterized,and the oxygen evolution performance was evaluated in a H_(2)SO_(4) solution.The results show that compared with the Ti/SnO_(2)/MnO_(2) anode prepared by the conventional brushing-annealing process,the Ti/SnO_(x)/MnO_(2) anode fabricated through the innovative procedure exhibits a lower oxygen evolution potential and a nearly 40%longer accelerated lifespan.The superior oxygen evolution performance of the Ti/SnO_(x)/MnO_(2) anode is attributed to the distinctive SnO_(x) intermediate layer fabricated through Sn electrodeposition followed by oxidation,which indicates the great potential of the anode as a dimensionally stable anode for metal electrowinning and hydrogen production by electrolysis,etc.
基金supported by Hyundai Mobis(No. G106280)the Gwangju Institute of Science and Technology in 2019
文摘Since the commercialization of the fuel cell electric vehicles (FCEVs), the polymer electrolyte membrane fuel cell system has been actively improved as a powertrain for ultimate environment-friendly vehicle. During the FCEV operation, various transient conditions such as start-up/shut-down and fuel starvation occur irregularly, which deteriorates the durability of the membrane electrode assembly. In particular, when fuel starvation occurs, the carbon support in the anode is oxidized within few minutes, thus the mitigation of this phenomenon is essential for securing the durability. This short review introduces the concept of reversal tolerant anode (RTA), which is a mitigation method using an oxygen evolution catalyst and reviews some previous reports. In addition, new approach for RTA suggested by authors recently, which is the replacement of Pt anode catalyst by multifunctional IrRu alloy catalyst that simultaneously exhibits the activities for the hydrogen oxidation reaction and the oxygen evolution reaction is introduced.
文摘Metallic-monolith catalyst support with self-growing porous anodic alumina(PAA)film was prepared by anodizing Al plate.The effect of hydrothermal treatment(HTT)on the crystalline state and textural properties of PAA film was investigated by XRD,BET,SEM and TG.The HTT treatment above 50°C and the subsequent calcination above 300°C could convert the amorphous skeleton alumina intoγ-alumina and increase the specific surface area(SBET).However,SEM images showed the HTT modification was a non-uniform process along the thickness of PAA film.The promotion effect of HTT on SBETwas non-linear,and the slope of SBETgradually decreased with the HTT temperature or time increased.The limited HTT effect should be attributed to a changed pore structure caused by an unfavorable pore sealing limitation.Pore widening treatment(PWT)before HTT could break the pore sealing limitation,because of the reduced internal diffusion resistance of hydrothermal reaction.The synergistic combination of PWT and HTT developed a PAA support with a large SBETcomparable to commercialγ-alumina.In the catalytic combustion of toluene,the Pt-based catalyst prepared by using the PWT and HTT comodified PAA support gave higher Pt dispersion and more favorable catalytic activity than that treated by HTT alone.The presence of a bimodal pore structure was suggested to be a decisive reason.
基金financially supported by the National Natural Science Foundation of China(Grant Nos.51872090 and 51772097)the Hebei Natural Science Fund for Distinguished Young Scholar(Grant No.E2019209433)+2 种基金the Youth Talent Program of Hebei Provincial Education Department(Grant No.BJ2018020)the Natural Science Foundation of Hebei Province(Grant No.E2020209151)the Natural Science Foundation of Liaoning Province(Grant No.2020-MS-012).
文摘The actual performance of vanadium redox flow batteries (VRFBs) is still significantly constrained by the slow kinetics and major parasitic reactivity of anode issues. Herein, a B-site management strategy of SrBO3 (B = Ti, Zr, Hf) perovskites was proposed to promote the anode reaction jointly explored by experiments and first-principle calculations. As the atomic number of B increases, the enhanced polarity of the B-O bond and the increased oxygen defect can boost the adsorption of vanadium ions, while the weakened orbital hybridization of the B-O bond facilitates the charge transfer of anode reaction. Compared with SrTiO3 and SrZrO3, oversized particles and deformed crystals of SrHfO3 reduce its catalysis. Of SrBO3 perovskites, SrZrO3 stands out in catalysis, owing to its outstanding combination of high hydrophilicity, large surface area, and desired crystal structure. Further, the VRFB using SrZrO3 presents a superior energy efficiency (EE) of 63.2% at 300 mA cm-2 and an increase of 15% in EE compared with the pristine cell at 200 mA cm-2. This work lays the foundation for building the connections between the structural and compositional flexibility and the tunable perovskite properties desirable for vanadium redox reactions.
基金supported by the Coal Seam Gas Joint Foundation of Shanxi(2015012016)Shanxi Province Science Foundation(2016011025)+2 种基金Shanxi Scholarship Council of China(2016-010)Shanxi “1331 Project” Key Innovative Research Team(“1331KIRT”)the Open Funding from State Key Laboratory of Materialoriented Chemical Engineering(No.KL16-03)
文摘Ni-based anodes of SOFCs are susceptible to coking, which greatly limits practical application of direct methane-based fuels. An indirect internal reformer is an effective way to convert methane-based fuels into syngas before they reach anode. In this work, catalytic activity of a redox-stable perovskite La0.7Sr0.3Cr0.8Fe0.2O3-δ(LSCrFO) for methane conversion was evaluated. The catalyst was fabricated as an anodic protective layer to improve coking resistance of a Ni cermet anode. Using wet CH4 as a fuel, the LSCrFO-modified cell showed excellent power output and good coking resistance with peak power density of 1.59 W cm-2 at 800℃. The cell demonstrated good durability lasting for at least 100 h. While the bare cell without the protective layer showed poor durability with the cell voltage fast dropped from 0.75 V to 0.4 V within 30 min. Under wet coal bed methane (CBM) operation, obvious performance degradation within 35 h (1.7 mV h^-1) was observed due to the influence of heavy carbon compounds in CBM. The pre-and post-mortem microstructures and carbon analysis of the anode surface and catalyst surface were further conducted.
基金This work was supported by Natural Science Foundation of Gansu provincethe Tackle Key Problems Foundation of Gansu pronince,China.
文摘Well aligned quasi-straight single-walled carbon nanotubes (SWCNTs) and straight SWCNTs bundle have been prepared in large scale by anode-arc vaporization of gr aphite with metallic catalysts. Various parameters such as the catalyst preparat ion, the kinds and pressure of the buffer gases, the quantity of anode-arc curre nt intensity, and the method of purification have been examined. The influence o f these parameters on the deposited carbon yield is reported, together with obse rvations of the produced material. Improvement in synthetic techniques has resul ted in the optimal conditions for the production of large quantities of high qua lity SWCNTs in our semi-continuous synthesis method. The formation of carbon nan otubes (CNTs) was studied briefly in this paper. Owing to the magnetic pinching effect of arc current, the CNTs arrange in parallel lines along the arc current direction.
基金supported by the National Research Foundation of Korea (NRF) grant funded by the Korea government (MSIT) (2021R1A2B5B01002656)。
文摘Microbial fuel cell(MFC) is an advanced bioelectrochemical technique that can utilize biomass materials in the process of simultaneously generating electricity and biodegrading or bio transforming toxic pollutants from wastewater. The overall performance of the system is largely dependent on the efficiency of the anode electrode to enhance electron transportation. Furthermore, the anode electrode has a significant impact on the overall cost of MFC setup. Hence, the need to explore research focused towards developing cost-effective material as anode in MFC. This material must also have favourable properties for electron transportation. Graphene oxide(GO) derivatives and its modification with nanomaterials have been identified as a viable anode material. Herein, we discussed an economically effective strategy for the synthesis of graphene derivatives from waste biomass materials and its subsequent fabrication into anode electrode for MFC applications. This review article offers a promising approach towards replacing commercial graphene materials with biomass-derived graphene derivatives in a view to achieve a sustainable and commercialized MFC.
基金supported by the National High Technology Research and Development Program of China (No. 2007AA03Z337)the Harbin Special Creation Foundation for Science and Technology of Fellow in China (No. 2006RFQXG032)
文摘The aim of this work was to investigate the effects of calcination/acid-activation on the composition, structure, and photocatalytic （PC） reduction property of an anodic oxidation TiO2/Ti film catalyst. The surface morphology and phase composition were examined by scanning electron microscopy and X-ray diffraction. The catalytic property of the film catalysts was evaluated through the removal rate of potassium chromate during the PC reduction process. The results showed that the film catalysts were composed of anatase and rutile TiO2 with a micro-porous surface structure. The calcination treatment increased the content of TiO2 in the film, changed the relative ratio of anatase and rutile TiO2, and decreased the size of the micro pores of the film catalysts. The removal rate of potassium chromate was related to the technique parameters of calcination/acid-activation treatment. When the anodic oxidation TiO2/Ti film catalyst was calcined at 873 K for 30 min and then acid-activated in the concentrated H2SO4 for 60 min, it presented the highest catalytic property, with the removal rate of potassium chromate of 96.3% during the PC reduction process under the experimental conditions.
基金supported by the Zhejiang Natural Science Foundation (Nos. Y405496 and 2008C14040)the National Fundamental Research "973" Prophase Project (2007CB216409)
文摘Fuel cells using borohydride as the fuel have received much attention because of high energy density and theoretical working potential.In this work,LaNi4.5Al0.5 hydrogen storage alloy used as the anodic material has been investigated.It was found that the increasing operation temperature was helpful to the open-circuit potential,the discharge potential and the power density,but showed a negative effect on the utilization of the fuel due to the accelerated hydrogen evolution.The high KOH concentration was favorable for high-rate discharge capability.The adsorption and transformation of hydrogen on LaNi4.5Al0.5 alloy electrode has been observed,but its contribution to the discharge capability during a high-rate discharge was small.
基金supported by the National Natural Science Foundation of China(No.22171167)the Talent Introduction and Training Program for Youth Innovation Teams in Colleges and Universities of Shandong Province。
文摘Electrochemical CO_(2)reduction reaction(CO_(2)RR)to formate presents a technoeconomic route for CO_(2)utilization under mild conditions,yet practical implementation is constrained by the high energy consumption(>90%of total input)of the anodic oxygen evolution reaction(OER).Replacement of OER by partial methanol oxidation reaction(MOR)could lead to simultaneous formate production at both electrodes and remarkably reduce the overall energy consumption.Herein,we designed a two-electrode system featuring a nickel foam-supported crystalline/amorphous bismuth-bismuth nickel oxide composite cathode(Bi-BiNiO_(x)/NF)and aβ-Ni(OH)_(2)anode,achieving excellent formate production behavior.The crystalline/amorphous Bi-BiNiO_(x)/NF cathode delivers exceptional CO_(2)RR performance,achieving 98.9%formate Faradaic efficiency(FEformate)at−0.90 V vs.reversible hydrogen electrode(RHE)and maintaining>90.7%FEformate over 72 h continuous operation-attributed to its Bi-Ni bimetallic synergy and crystalline/amorphous heterostructure that enhance active site exposure and reaction kinetics.The integrated CO_(2)RR||MOR system operates stably for 90 h at 2.2 V and 10 mA·cm^(−2),sustaining>90%FE_(formate)at both electrodes with a cell voltage(1.760 V)significantly lower than conventional CO_(2)RR||OER systems(1.953 V).This work demonstrates efficient concurrent formate electrosynthesis and establishes an energy-efficient paradigm for electrocatalytic CO_(2)valorization through synergistic catalyst design and reaction pathway integration.
基金financially supported by the National Natural Science Foundation of China(Nos.52271011 and 52102291)the Structure Design and Mass Preparation of High Stability and Low Cost PEM Hydroelectrolysis Non-Iridium Catalyst,China(No.KC22453)
文摘High-performance and low-cost anode materials are critical for superior sodium-ion batteries(SIBs).Herein,high-yield porous carbon nanofiber(CNF)anode materials(named CNFs@Cu–Ni)are prepared by chemical vapor deposition using a specialized nanoporous Cu–Ni alloy catalyst.Density functional theory calculations indicate that Ni incorporation results in a shift of the d-band center of the catalyst from−2.34157 to−1.93682 eV.This phenomenon elucidates the remarkable adsorption capacity of the Cu–Ni catalyst toward C2H2,thereby facilitating the catalytic growth of high-performance CNFs.With this approach,a superior yield of 258.6%for deposited carbon is reached after growth for 1 h.The CNFs@Cu–Ni anode presents an outstanding discharge capacity of 193.6 mAh·g^(−1) at 1.0 A·g^(−1)over 1000 cycles and an exceptional rate capability by maintaining a capacity of 158.9 mAh·g^(−1)even at 5.0 A·g^(−1)in an ether-based electrolyte.It also exhibits excellent performance in the CNFs@Cu–Ni//NVP full battery attributed to the presence of abundant Na+adsorption sites on its surface.This study presents a new concept for the advancement of high-performance carbonaceous electrodes for SIBs.
文摘Nickel nanowire and nanotube arrays as supports for Pt-Pd catalyst were prepared by elec- troless deposition with anodic aluminum oxide template. Pt-Pd composite catalyst was de- posited on the arrays by displacement reaction. SEM images show that the nickel nanowires have an average diameter of I00 nm and the nickel nanotubes have an average inner diameter of 200 nm. EDS scanning reveals that elemental Pt and Pd disperse uniformly on the arrays. Cyclic voltammetry study indicates that the nickel nanotube array loaded with Pt-Pd pos- sesses a higher electrochemical activity for ethanol oxidation than the nickel nanowire array with Pt-Pd.
基金supported by the National Natural Science Foundation of China (21633008,21673221)the Jilin Province Science and Technology Development Program (20160622037JC,20170203003SF,and 20170520150JH)+1 种基金the Hundred Talents Program of the Chinese Academy of Sciencesthe Recruitment Program of Foreign Experts (WQ20122200077)
文摘Direct methanol fuel cells （DMFCs） are very promising power source for stationary and portable miniatureelectric appliances due to its high efficiency and low emissions of pollutants. As the key material, cata-lysts for both cathode and anode face several problems which hinder the commercialization of DMFCs.In this review, we mainly focus on anode catalysts of DMFCs. The process and mechanism of methanolelectrooxidation on Pt and Pt-based catalysts in acidic medium have been introduced. The influences ofsize effect and morphology on electrocatalytic activity are discussed though whether there is a size effectin MOP, catalyst is under debate. Besides, the non Pt catalysts are also listed to emphasize though Pt isstill deemed as the indispensable element in anode catalyst of DMFCs in acidic medium. Different cata-lyst systems are compared to illustrate the level of research at present. ome debates need to be verifiedwith experimental evidences.
文摘Sustainable conversion of carbon dioxide(CO_(2))to high value-added chemicals and fuels is a promising solution to solve the problem of excessive CO_(2) emissions and alleviate the shortage of fossil fuels,maintaining the balance of the carbon cycle in nature.The development of catalytic system is of great significance to improve the efficiency and selectivity for electrochemical CO_(2) conversion.In particular,bismuth(Bi)based catalysts are the most promising candidates,while confronting challenges.This review aims to elucidate the fundamental issues of efficient and stable Bi-based catalysts,constructing a bridge between the category,synthesis approach and electrochemical performance.In this review,the categories of Bi-based catalysts are firstly introduced,such as metals,alloys,single atoms,compounds and composites.Followed by the statement of the reliable and versatile synthetic approaches,the representative optimization strategies,such as morphology manipulation,defect engineering,component and heterostructure regulation,have been highlighted in the discussion,paving in-depth insight upon the design principles,reaction activity,selectivity and stability.Afterward,in situ characterization techniques will be discussed to illustrate the mechanisms of electrochemical CO_(2) conversion.In the end,the challenges and perspectives are also provided,promoting a systematic understanding in terms of the bottleneck and opportunities in the field of electrochemical CO_(2) conversion.
基金supported by the National Natural Science Foundation of China(Nos.52473299,52201009,52301013 and52231008)the Key Research and Development Program of Hainan Province(No.ZDYF2024GXJS006)+1 种基金International Science&Technology Cooperation Program of Hainan Province(No.GHYF2023007)the Education Department of Hainan Province(No.Hnky2024ZD-2)。
文摘The development of cost-effective and energy-efficient anode materials is essential for the advancement of industrial water electrolysis.Herein,we report a rapid,ambient-temperature method to prepare largearea nickel mesh electrodes(SFN/NM)via surface functionalization completed within 3 min,without relying on thermal treatments or noble metals.The as-prepared electrodes achieve a high current density of 100 m A/cm^(2)at an overpotential of just 300 m V in 6 mol/L KOH,and exhibit remarkable stability over1600 h of continuous operation.With comparable activity to commercial Raney nickel yet significantly lower processing and material costs(reduced by 50%-70%),this approach provides a practical solution for low-energy water splitting.Beyond its industrial relevance,the strategy offers a scalable model for engineering high-performance OER electrodes,inspiring future directions in electrocatalyst design.
