期刊文献+
共找到1篇文章
< 1 >
每页显示 20 50 100
The Enhancement of Selectivity and Activity for Two-Electron Oxygen Reduction Reaction by Tuned Oxygen Defects on Amorphous Hydroxide Catalysts 被引量:1
1
作者 Junheng Huang Changle Fu +3 位作者 Junxiang Chen Nangan Senthilkumar Xinxin Peng Zhenhai Wen 《CCS Chemistry》 CAS 2022年第2期566-583,共18页
Amorphous catalysts,thanks to their uniquely coordinated unsaturated properties and abundance of defect sites,tend to possess higher activity and selectivity than their crystalline counterparts.In this work,we report ... Amorphous catalysts,thanks to their uniquely coordinated unsaturated properties and abundance of defect sites,tend to possess higher activity and selectivity than their crystalline counterparts.In this work,we report a facile and general solventcontrolled precipitation method to prepare hybrids of graphene oxide(GO)supporting amorphous metal hydroxide[A-M(OH)_(x)/GO,M=Cu,Co,and Mn],which provides us with tangible materials to study the structure–performance relationship of various amorphous oxides.The systematic investigation of A-Cu(OH)_(2)/GO by coupling ex situ/in situ characteristic techniques with electrochemical studies reveals that electrocatalytic activity and selectivity toward a two-electron oxygen reduction reaction(ORR)is highly dependent on the coordinated Cu catalytic sites and the disordered structure of A-Cu(OH)_(2).In situ X-ray absorption near-edge structure(XANES)and density functional theory(DFT)calculation verify that the degree of OH*poisoning(ΔG0 OH*)tuned by three-OH-coordinated Cu sites in amorphous structures plays a crucial role in selective catalysis of ORR for H_(2)O_(2) production.The optimized A-Cu(OH)_(2)/GO shows superior activity and high selectivity(~95%)toward H_(2)O_(2),as demonstrated by a zinc–air battery capable of on-site H_(2)O_(2) production with a rate as high as 3401.5 mmol h^(−1) g^(−1). 展开更多
关键词 amorphous hydroxide general preparation two-electron ORR on-site H_(2)O_(2)production three-oh-coordinated Cu sites
原文传递
上一页 1 下一页 到第
使用帮助 返回顶部