Interface engineering of Co nanoparticles decorated by Ir confined in N-doped carbon nanotubes for flexible Zn-air batteries and pH-universal overall water splitting

被引:0
|
作者
YingGang Sun [1 ]
Xin Du [2 ]
JiGang Wang [1 ]
Qiang Liu [1 ]
JingLin Mu [1 ]
ZhongFang Li [1 ]
HeQing Jiang [3 ]
LiKai Wang [1 ,3 ,4 ]
机构
[1] School of Chemistry and Chemical Engineering,Shandong University of Technology
[2] School of Chemistry,Zhengzhou University
[3] Qingdao Key Laboratory of Functional Membrane Material and Membrane Technology,Qingdao Institute of Bioenergy and Bioprocess Technology,Chinese Academy of Sciences
[4] School of Chemical and Biological Engineering,and Institute of Chemical Process,Seoul National
关键词
D O I
暂无
中图分类号
TM912 [蓄电池]; TQ116.21 []; TQ426 [催化剂(触媒)];
学科分类号
080502 ; 081705 ;
摘要
To alleviate the crisis of energy shortages,the scalable fabrication of highly efficient electrocatalysts is highly sought after for metal-air batteries and pH-universal overall water splitting.Hereby,an in situ construction to achieve Co@Ir nanoparticles in N-doped carbon nanotubes has been explored,which were directly fabricated by the pyrolysis and galvanic replacement.The interface engineering of Co@Ir core-shell structures could enhance interfacial and synergistic effects,achieving the tailorable electrocatalytic activities for oxygen reduction reaction,oxygen evolution reaction and hydrogen evolution reaction.Co@Ir-NT demonstrates the outstanding stability for overall water splitting under pH-universal conditions.Co@Ir-NT-based r-ZABs display a high power density of295.1 mW·cm-2 and a ultralong cycle stability over 2000continuous charge-discharge cycles,and Co@Ir-NT-based F-ZABs maintain the similar performance at different bending angles,suggesting its promising potential in the application of wearable electronics.The corresponding theoretical calculations also indicate that Co@Ir core-shell structure could improve the adsorption capacity and facilitate the breakage of O-O band.Hence,this work might be helpful for developing multifunctional catalysts for metalair batteries and water splitting under pH-universal conditions.
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收藏
页码:6447 / 6459
页数:13
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