过电位
催化作用
电催化剂
钴
锌
化学
无机化学
阴极
材料科学
电化学
电极
物理化学
有机化学
冶金
作者
Ziyang Lu,Bo Wang,Yongfeng Hu,Wei Liu,Yufeng Zhao,Ruoou Yang,Zhiping Li,Jun Luo,Bin Chi,Zheng Jiang,Minsi Li,Shichun Mu,Shijun Liao,Jiujun Zhang,Xueliang Sun
标识
DOI:10.1002/anie.201810175
摘要
Abstract A competitive complexation strategy has been developed to construct a novel electrocatalyst with Zn‐Co atomic pairs coordinated on N doped carbon support (Zn/CoN‐C). Such architecture offers enhanced binding ability of O 2 , significantly elongates the O−O length (from 1.23 Å to 1.42 Å), and thus facilitates the cleavage of O−O bond, showing a theoretical overpotential of 0.335 V during ORR process. As a result, the Zn/CoN‐C catalyst exhibits outstanding ORR performance in both alkaline and acid conditions with a half‐wave potential of 0.861 and 0.796 V respectively. The in situ XANES analysis suggests Co as the active center during the ORR. The assembled zinc–air battery with Zn/CoN‐C as cathode catalyst presents a maximum power density of 230 mW cm −2 along with excellent operation durability. The excellent catalytic activity in acid is also verified by H 2 /O 2 fuel cell tests (peak power density of 705 mW cm −2 ).
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