Oxygen evolution reaction （OER） electrolysis, as an important reaction involved in water splitting and rechargeable metal-air batteries, has attracted increasing attention for clean energy generation and efficient e...Oxygen evolution reaction （OER） electrolysis, as an important reaction involved in water splitting and rechargeable metal-air batteries, has attracted increasing attention for clean energy generation and efficient energy storage. Nickel/iron （NiFe）-based compounds have been known as active OER catalysts since the last century, and renewed interest has been witnessed in recent years on developing advanced NiFe-based materials for better activity and stability. In this review, we present the early discovery and recent progress on NiFe-based OER electrocatalysts in terms of chemical properties, synthetic methodologies and catalytic performances. The advantages and disadvantages of each class of NiFe-based compounds are summarized, including NiFe alloys, electrodeposited films and layered double hydroxide nanoplates. Some mechanistic studies of the active phase of NiFe-based compounds are introduced and discussed to give insight into the nature of active catalytic sites, which could facilitate further improving NiFe based OER electrocatalysts. Finally, some applications of NiFe- based compounds for OER are described, including the development of an electrolyzer operating with a single AAA battery with voltage below 1.5 V and high performance rechargeable Zn-air batteries.展开更多
比较了甲醇对 Pt/C和炭载四羧基酞菁钴 (Co Pc Tc/C)催化氧还原性能的影响 .结果表明 ,甲醇使Pt/C催化氧还原的性能严重降低 ,而对经 80 0℃热处理的 Co Pc Tc/C(Co Pc Tc/C-80 0 )基本没有影响 ;并且Co Pc Tc/C-80 0催化氧还原的性能...比较了甲醇对 Pt/C和炭载四羧基酞菁钴 (Co Pc Tc/C)催化氧还原性能的影响 .结果表明 ,甲醇使Pt/C催化氧还原的性能严重降低 ,而对经 80 0℃热处理的 Co Pc Tc/C(Co Pc Tc/C-80 0 )基本没有影响 ;并且Co Pc Tc/C-80 0催化氧还原的性能优于经其它温度热处理的 Co Pc Tc/C,Co Pc Tc/C-80 0是一种较好的直接甲醇燃料电池的耐甲醇阴极电催化剂 .XPS结果表明 ,Co Pc Tc/C-80 0的活性位可能是含 Co N4结构的物质和零价 Co的混合物 .展开更多
A novel compound formulated [NH2(CH2)4CHNH2COOH]H6P2Mo18O62 has been synthesized and its structure has been characterized, which is the first example of aminoacid-heteropolyacid species. Crystal system is orthorhombic...A novel compound formulated [NH2(CH2)4CHNH2COOH]H6P2Mo18O62 has been synthesized and its structure has been characterized, which is the first example of aminoacid-heteropolyacid species. Crystal system is orthorhombic, space group P21212, unit cell dimensions: α=1. 572 2(3) nm, b=2.118 1 (4) nm, c=1.238 3(3) nm, α=90.04(3)°, β=90.00 (2)°, γ= 89. 99 (3)°, V = 4.123 6(14) nm3, Z=2, D0=2.437×103 kg/m3, R=0.038 7. Experimental result shows that the title compound has electrocatalysis reactivity.展开更多
Oxygen evolution reaction(OER),as an important half‐reaction involved in water splitting,has been intensely studied since the last century.Transition metal phosphide and sulfide‐based compounds have attracted increa...Oxygen evolution reaction(OER),as an important half‐reaction involved in water splitting,has been intensely studied since the last century.Transition metal phosphide and sulfide‐based compounds have attracted increasing attention as active OER catalysts due to their excellent physical and chemical characters,and massive efforts have been devoted to improving the phosphide and sulfide‐based materials with better activity and stability in recent years.In this review,the recent progress on phosphide and sulfide‐based OER electrocatalysts in terms of chemical properties,synthetic methodologies,catalytic performances evaluation and improvement strategy is reviewed.The most accepted reaction pathways as well as the thermodynamics and electrochemistry of the OER are firstly introduced in brief,followed by a summary of the recent research and optimization strategy of phosphide and sulfide‐based OER electrocatalysts.Finally,some mechanistic studies of the active phase of phosphide and sulfide‐based compounds are discussed to give insight into the nature of active catalytic sites.It is expected to indicate guidance for further improving the performances of phosphide and sulfide‐based OER electrocatalysts.展开更多
N-doped porous carbon materials have been prepared by a simple one-step pyrolysis of ethylenediaminetetraacetic acid （EDTA） and melamine in the presence of KOH and Co（NO3）2·6H20. The combination of the high s...N-doped porous carbon materials have been prepared by a simple one-step pyrolysis of ethylenediaminetetraacetic acid （EDTA） and melamine in the presence of KOH and Co（NO3）2·6H20. The combination of the high specific area （1,485 m2.g-l）, high nitrogen content （10.8%） and suitable graphitic degree results in catalysts exhibiting high activity （with onset and half-wave potentials of 0.88 and 0.79 V vs the reversible hydrogen electrode （RHE）, respectively） and four-electron selectivity for the oxygen reduction reaction （ORR） in alkaline medium---comparable to a commercial Pt/C catalyst, but far exceeding Pt/C in stability and durability. Owing to their superb ORR performance, low cost and facile preparation, the catalysts have great potential applications in fuel cells, metal-air batteries, and ORR-related electrochemical industries.展开更多
文摘Oxygen evolution reaction （OER） electrolysis, as an important reaction involved in water splitting and rechargeable metal-air batteries, has attracted increasing attention for clean energy generation and efficient energy storage. Nickel/iron （NiFe）-based compounds have been known as active OER catalysts since the last century, and renewed interest has been witnessed in recent years on developing advanced NiFe-based materials for better activity and stability. In this review, we present the early discovery and recent progress on NiFe-based OER electrocatalysts in terms of chemical properties, synthetic methodologies and catalytic performances. The advantages and disadvantages of each class of NiFe-based compounds are summarized, including NiFe alloys, electrodeposited films and layered double hydroxide nanoplates. Some mechanistic studies of the active phase of NiFe-based compounds are introduced and discussed to give insight into the nature of active catalytic sites, which could facilitate further improving NiFe based OER electrocatalysts. Finally, some applications of NiFe- based compounds for OER are described, including the development of an electrolyzer operating with a single AAA battery with voltage below 1.5 V and high performance rechargeable Zn-air batteries.
文摘比较了甲醇对 Pt/C和炭载四羧基酞菁钴 (Co Pc Tc/C)催化氧还原性能的影响 .结果表明 ,甲醇使Pt/C催化氧还原的性能严重降低 ,而对经 80 0℃热处理的 Co Pc Tc/C(Co Pc Tc/C-80 0 )基本没有影响 ;并且Co Pc Tc/C-80 0催化氧还原的性能优于经其它温度热处理的 Co Pc Tc/C,Co Pc Tc/C-80 0是一种较好的直接甲醇燃料电池的耐甲醇阴极电催化剂 .XPS结果表明 ,Co Pc Tc/C-80 0的活性位可能是含 Co N4结构的物质和零价 Co的混合物 .
文摘A novel compound formulated [NH2(CH2)4CHNH2COOH]H6P2Mo18O62 has been synthesized and its structure has been characterized, which is the first example of aminoacid-heteropolyacid species. Crystal system is orthorhombic, space group P21212, unit cell dimensions: α=1. 572 2(3) nm, b=2.118 1 (4) nm, c=1.238 3(3) nm, α=90.04(3)°, β=90.00 (2)°, γ= 89. 99 (3)°, V = 4.123 6(14) nm3, Z=2, D0=2.437×103 kg/m3, R=0.038 7. Experimental result shows that the title compound has electrocatalysis reactivity.
文摘Oxygen evolution reaction(OER),as an important half‐reaction involved in water splitting,has been intensely studied since the last century.Transition metal phosphide and sulfide‐based compounds have attracted increasing attention as active OER catalysts due to their excellent physical and chemical characters,and massive efforts have been devoted to improving the phosphide and sulfide‐based materials with better activity and stability in recent years.In this review,the recent progress on phosphide and sulfide‐based OER electrocatalysts in terms of chemical properties,synthetic methodologies,catalytic performances evaluation and improvement strategy is reviewed.The most accepted reaction pathways as well as the thermodynamics and electrochemistry of the OER are firstly introduced in brief,followed by a summary of the recent research and optimization strategy of phosphide and sulfide‐based OER electrocatalysts.Finally,some mechanistic studies of the active phase of phosphide and sulfide‐based compounds are discussed to give insight into the nature of active catalytic sites.It is expected to indicate guidance for further improving the performances of phosphide and sulfide‐based OER electrocatalysts.
文摘N-doped porous carbon materials have been prepared by a simple one-step pyrolysis of ethylenediaminetetraacetic acid （EDTA） and melamine in the presence of KOH and Co（NO3）2·6H20. The combination of the high specific area （1,485 m2.g-l）, high nitrogen content （10.8%） and suitable graphitic degree results in catalysts exhibiting high activity （with onset and half-wave potentials of 0.88 and 0.79 V vs the reversible hydrogen electrode （RHE）, respectively） and four-electron selectivity for the oxygen reduction reaction （ORR） in alkaline medium---comparable to a commercial Pt/C catalyst, but far exceeding Pt/C in stability and durability. Owing to their superb ORR performance, low cost and facile preparation, the catalysts have great potential applications in fuel cells, metal-air batteries, and ORR-related electrochemical industries.
