Production of green hydrogen through water electrolysis powered by renewable energy sources has garnered increasing attention as an attractive strategy for the storage of clean and sustainable energy.Among various ele...Production of green hydrogen through water electrolysis powered by renewable energy sources has garnered increasing attention as an attractive strategy for the storage of clean and sustainable energy.Among various electrolysis technologies,the emerging anion exchange membrane water electrolyser(AEMWE)exhibits the most potential for green hydrogen production,offering a potentially costeffective and sustainable approach that combines the advantages of high current density and fast start from proton exchange membrane water electrolyser(PEMWE)and low-cost catalyst from traditional alkaline water electrolyser(AWE)systems.Due to its relatively recent emergence over the past decade,a series of efforts are dedicated to improving the electrochemical reaction performance to accelerate the development and commercialization of AEMWE technology.A catalytic electrode comprising a gas diffusion layer(GDL)and a catalyst layer(CL)is usually called a gas diffusion electrode(GDE)that serves as a fundamental component within AEMWE,and also plays a core role in enhancing mass transfer during the electrolysis process.Inside the GDEs,bubbles nucleate and grow within the CL and then are transported through the GDL before eventually detaching to enter the electrolyte in the flow field.The transfer processes of water,gas bubbles,charges,and ions are intricately influenced by bubbles.This phenomenon is referred to as bubble-associated mass transfer.Like water management in fuel cells,effective bubble management is crucial in electrolysers,as its failure can result in various overpotential losses,such as activation losses,ohmic losses,and mass transfer losses,ultimately degrading the AEMWE performance.Despite significant advancements in the development of new materials and techniques in AEMWE,there is an urgent need for a comprehensive discussion focused on GDEs,with a particular emphasis on bubbleassociated mass transfer phenomena.This review aims to highlight recent findings regarding mass transfer in GDEs,particularly the impacts of bubble accumulation;and presents the latest advancements in designing CLs and GDLs to mitigate bubble-related issues.It is worth noting that a series of innovative bubble-free-GDE designs for water electrolysis are also emphasized in this review.This review is expected to be a valuable reference for gaining a deeper understanding of bubble-related mass transfer,especially the complex bubble behavior associated with GDEs,and for developing innovative practical strategies to advance AEMWE for green hydrogen production.展开更多
Ti/SnO2–Sb electrode has a good effect on the removal of organic pollutants. But its short service life limits its large-scale application in industry. Electro-catalytic degradation performances and service life of t...Ti/SnO2–Sb electrode has a good effect on the removal of organic pollutants. But its short service life limits its large-scale application in industry. Electro-catalytic degradation performances and service life of the electrode can be significantly improved by doping rare earth（RE） ions into the oxide coating of Ti/SnO2–Sb electrode. Ti/SnO2–Sb electrodes doped with different RE elements（Ce, Dy, La, and Eu） were prepared by the thermal decomposition method at 550 ℃. Electro-catalytic degradation performances of electrodes doped with different RE elements were evaluated by linear sweep voltammetry（LSV） and Tafel curves. During the electrolysis,the conversion of p-nitrophenol was performed with these electrodes as anodes under galvanostatic control. The structures and morphologies of the surface coating of the electrodes were characterized by scanning electron microscope（SEM）. The results demonstrate that the electro-catalytic degradation performances of Ti/SnO2–Sb electrodes are improved to different levels by doping different RE ions. Improved Ti/SnO2–Sb electrodes by the introduction of different RE have higher oxygen evolution potential, better electro-catalysis ability, better coverage,and longer electrode life.展开更多
The preparation method of H_4MoO_(26)-polyaniline film modified electrode and its voltammetric behaviour are described. The modified electrode has high electrocatalytic activity on chlorate ions.
Phenothiazine-coated silver electrode prepared by a simple reaction of phenothiazine with the metal is very stable and can make the reduction of hemoglobin possible.
Hydrogen evolution reaction(HER)catalytic electrodes under actual working conditions show interesting mass transfer behaviors at solid(electrode)/liquid(electrolyte)/gas(hydrogen)three-phase interfaces.These behaviors...Hydrogen evolution reaction(HER)catalytic electrodes under actual working conditions show interesting mass transfer behaviors at solid(electrode)/liquid(electrolyte)/gas(hydrogen)three-phase interfaces.These behaviors are essential for forming a continuous and effective physical contact region between the electrolyte and the electrode and require further detailed understanding.Here,a case study on 1 T-2 H phase molybdenum disulfide(Mo S_(2))/carbon fiber paper(CFP)catalytic electrodes is performed.Rapid gas-liquid mass transfer at the interface for enhancing the working area stability and capillarity for increasing the electrode working area is found.The real scenario,wherein the energy utilization efficiency of the as-prepared non-noble metal catalytic electrode exceeds that of the noble metal catalytic electrode,is disclosed.Specifically,a fluid dynamics model is developed to investigate the behavior mechanism of hydrogen bubbles from generation to desorption on the catalytic electrode surface with different hydrophilic and hydrophobic properties.These new insights and theoretical evidence on the non-negligible three-phase interface behaviors will identify opportunities and motivate future research in high-efficiency,stability,and low-cost HER catalytic electrode development.展开更多
Development of noble-metal-free materials with remarkable electrocatalytic water-splitting performance in acidic or neutral media has sparked considerable attention in recent years.Herein,we review the latest research...Development of noble-metal-free materials with remarkable electrocatalytic water-splitting performance in acidic or neutral media has sparked considerable attention in recent years.Herein,we review the latest research on design and fabrication of precious-metal-free catalytic materials for overall water electrolysis in non-alkaline environment,especially highlighting several optimizing approaches to enhance the catalytic behavior and to realize effective bifunctional electrocatalysts.All these involved noble-metal-free electrocatalysts are classified into transition-metal oxides(TMOs),transition-metal nitrides(TMNs),transition-metal carbides(TMCs),transition-metal phosphides(TMPs),transition-metal chalcogenides,metal complexes,and metal-free carbons,as shown in the main part.Besides,the paper also offers an introduction of the fundamental electrochemistry of water splitting before entering the subject,as well as a prospective discussion on mechanism understanding,novel catalysts fabrication,and standardized performance measurements/evaluation in the last section.展开更多
Rechargeable Zn-air batteries(ZABs)have received extensive attention,while their real applications are highly restricted by the slow kinetics of the oxygen reduction and oxygen evolution reactions(ORR/OER).Herein,we r...Rechargeable Zn-air batteries(ZABs)have received extensive attention,while their real applications are highly restricted by the slow kinetics of the oxygen reduction and oxygen evolution reactions(ORR/OER).Herein,we report a“bridge”structured flexible self-supporting bifunctional oxygen electrode(CNT@Co-CNFF50-900)with strong active and stable Co-N/C@pyridine N/C@CNTs reaction centers.Benefiting from the electron distribution optimization and the advantages of hierarchical catalytic design,the CNT@Co-CNF_(F50-900)electrode had superior ORR/OER activity with a small potential gap(ΔE)of 0.74 V.Reinforced by highly graphitized carbon and the“π-π”bond,the free-standing CNT@Co-CNFF50-900 electrode exhibited outstanding catalytic stability with only 36 mV attenuation.Impressively,the CNT@Co-CNFF50-900-based liquid ZAB showed a high power density of 371 mW cm^(−2),a high energy density of 894 Wh kg^(−1),and a long cycling life of over 130 h.The assembled quasi-solid-state ZAB also demonstrated a high power density,attaining 81 mW cm^(−2),with excellent charge-discharge durability beyond 100 h and extremely high flexibility under the multi-angle application.This study provides an effective electrospinning solution for integrating high-efficiency electrocatalysts and electrodes for energy storage and conversion devices.展开更多
基金support from the National Natural Science Foundation of China(Grant No.52006029)the Promotion Foundation for Young Science and Technology Talents in Jilin Province(Grant No.QT202113)+2 种基金the Special Foundation of Industrial Innovation in Jilin Province(Grant No.2019C056-2)the Special Foundation for Outstanding Young Talents Training in Jilin(Grant No.20200104107)the UK EPSRC(EP/W03784X/1)。
文摘Production of green hydrogen through water electrolysis powered by renewable energy sources has garnered increasing attention as an attractive strategy for the storage of clean and sustainable energy.Among various electrolysis technologies,the emerging anion exchange membrane water electrolyser(AEMWE)exhibits the most potential for green hydrogen production,offering a potentially costeffective and sustainable approach that combines the advantages of high current density and fast start from proton exchange membrane water electrolyser(PEMWE)and low-cost catalyst from traditional alkaline water electrolyser(AWE)systems.Due to its relatively recent emergence over the past decade,a series of efforts are dedicated to improving the electrochemical reaction performance to accelerate the development and commercialization of AEMWE technology.A catalytic electrode comprising a gas diffusion layer(GDL)and a catalyst layer(CL)is usually called a gas diffusion electrode(GDE)that serves as a fundamental component within AEMWE,and also plays a core role in enhancing mass transfer during the electrolysis process.Inside the GDEs,bubbles nucleate and grow within the CL and then are transported through the GDL before eventually detaching to enter the electrolyte in the flow field.The transfer processes of water,gas bubbles,charges,and ions are intricately influenced by bubbles.This phenomenon is referred to as bubble-associated mass transfer.Like water management in fuel cells,effective bubble management is crucial in electrolysers,as its failure can result in various overpotential losses,such as activation losses,ohmic losses,and mass transfer losses,ultimately degrading the AEMWE performance.Despite significant advancements in the development of new materials and techniques in AEMWE,there is an urgent need for a comprehensive discussion focused on GDEs,with a particular emphasis on bubbleassociated mass transfer phenomena.This review aims to highlight recent findings regarding mass transfer in GDEs,particularly the impacts of bubble accumulation;and presents the latest advancements in designing CLs and GDLs to mitigate bubble-related issues.It is worth noting that a series of innovative bubble-free-GDE designs for water electrolysis are also emphasized in this review.This review is expected to be a valuable reference for gaining a deeper understanding of bubble-related mass transfer,especially the complex bubble behavior associated with GDEs,and for developing innovative practical strategies to advance AEMWE for green hydrogen production.
基金financially supported by the National Natural Science Foundation of China (No. 51364024 and 51404124)Gansu Province Department of Education Fund (No. 2013A-029)the Foundation of State Key Laboratory of Gansu Advanced Nonferrous Metal Materials (Nos. SKL 1316 and SKL 1314)
文摘Ti/SnO2–Sb electrode has a good effect on the removal of organic pollutants. But its short service life limits its large-scale application in industry. Electro-catalytic degradation performances and service life of the electrode can be significantly improved by doping rare earth（RE） ions into the oxide coating of Ti/SnO2–Sb electrode. Ti/SnO2–Sb electrodes doped with different RE elements（Ce, Dy, La, and Eu） were prepared by the thermal decomposition method at 550 ℃. Electro-catalytic degradation performances of electrodes doped with different RE elements were evaluated by linear sweep voltammetry（LSV） and Tafel curves. During the electrolysis,the conversion of p-nitrophenol was performed with these electrodes as anodes under galvanostatic control. The structures and morphologies of the surface coating of the electrodes were characterized by scanning electron microscope（SEM）. The results demonstrate that the electro-catalytic degradation performances of Ti/SnO2–Sb electrodes are improved to different levels by doping different RE ions. Improved Ti/SnO2–Sb electrodes by the introduction of different RE have higher oxygen evolution potential, better electro-catalysis ability, better coverage,and longer electrode life.
文摘The preparation method of H_4MoO_(26)-polyaniline film modified electrode and its voltammetric behaviour are described. The modified electrode has high electrocatalytic activity on chlorate ions.
文摘Phenothiazine-coated silver electrode prepared by a simple reaction of phenothiazine with the metal is very stable and can make the reduction of hemoglobin possible.
基金supported by the National Natural Science Foundation of China(No.62004051)the Natural Science Foundation of Heilongjiang province(No.LH2020F013)+1 种基金the China Postdoctoral Science Fund(No.2020M670909)the Heilongjiang Postdoctoral Science Fund(No.LBH-Z19017)。
文摘Hydrogen evolution reaction(HER)catalytic electrodes under actual working conditions show interesting mass transfer behaviors at solid(electrode)/liquid(electrolyte)/gas(hydrogen)three-phase interfaces.These behaviors are essential for forming a continuous and effective physical contact region between the electrolyte and the electrode and require further detailed understanding.Here,a case study on 1 T-2 H phase molybdenum disulfide(Mo S_(2))/carbon fiber paper(CFP)catalytic electrodes is performed.Rapid gas-liquid mass transfer at the interface for enhancing the working area stability and capillarity for increasing the electrode working area is found.The real scenario,wherein the energy utilization efficiency of the as-prepared non-noble metal catalytic electrode exceeds that of the noble metal catalytic electrode,is disclosed.Specifically,a fluid dynamics model is developed to investigate the behavior mechanism of hydrogen bubbles from generation to desorption on the catalytic electrode surface with different hydrophilic and hydrophobic properties.These new insights and theoretical evidence on the non-negligible three-phase interface behaviors will identify opportunities and motivate future research in high-efficiency,stability,and low-cost HER catalytic electrode development.
基金M.Ni thanks the funding support(Project Number:PolyU 152214/17E and PolyU 152064/18E)from Research Grant Council,University Grants Committee,Hong Kong SAR。
文摘Development of noble-metal-free materials with remarkable electrocatalytic water-splitting performance in acidic or neutral media has sparked considerable attention in recent years.Herein,we review the latest research on design and fabrication of precious-metal-free catalytic materials for overall water electrolysis in non-alkaline environment,especially highlighting several optimizing approaches to enhance the catalytic behavior and to realize effective bifunctional electrocatalysts.All these involved noble-metal-free electrocatalysts are classified into transition-metal oxides(TMOs),transition-metal nitrides(TMNs),transition-metal carbides(TMCs),transition-metal phosphides(TMPs),transition-metal chalcogenides,metal complexes,and metal-free carbons,as shown in the main part.Besides,the paper also offers an introduction of the fundamental electrochemistry of water splitting before entering the subject,as well as a prospective discussion on mechanism understanding,novel catalysts fabrication,and standardized performance measurements/evaluation in the last section.
基金supported by the National Key Research and Development Program of China(2022YFE0138900)National Natural Science Foundation of China(21972017)+2 种基金the Fundamental Research Funds for the Central Universities(2232022D-18,CUSF-DH-T-2023061)Shanghai Sailing Program(22YF1400700)the Chenguang Program of Shanghai Education Development Foundation and Shanghai Municipal Education Commission(22CGA37).
文摘Rechargeable Zn-air batteries(ZABs)have received extensive attention,while their real applications are highly restricted by the slow kinetics of the oxygen reduction and oxygen evolution reactions(ORR/OER).Herein,we report a“bridge”structured flexible self-supporting bifunctional oxygen electrode(CNT@Co-CNFF50-900)with strong active and stable Co-N/C@pyridine N/C@CNTs reaction centers.Benefiting from the electron distribution optimization and the advantages of hierarchical catalytic design,the CNT@Co-CNF_(F50-900)electrode had superior ORR/OER activity with a small potential gap(ΔE)of 0.74 V.Reinforced by highly graphitized carbon and the“π-π”bond,the free-standing CNT@Co-CNFF50-900 electrode exhibited outstanding catalytic stability with only 36 mV attenuation.Impressively,the CNT@Co-CNFF50-900-based liquid ZAB showed a high power density of 371 mW cm^(−2),a high energy density of 894 Wh kg^(−1),and a long cycling life of over 130 h.The assembled quasi-solid-state ZAB also demonstrated a high power density,attaining 81 mW cm^(−2),with excellent charge-discharge durability beyond 100 h and extremely high flexibility under the multi-angle application.This study provides an effective electrospinning solution for integrating high-efficiency electrocatalysts and electrodes for energy storage and conversion devices.
