材料科学
分解水
钴
析氧
催化作用
双功能
纳米线
钼
化学工程
兴奋剂
纳米技术
氢
单层
电化学
光电子学
电极
冶金
物理化学
有机化学
化学
工程类
光催化
作者
Van Hien Hoa,Duy Thanh Tran,Dinh Chuong Nguyen,Do Hwan Kim,Nam Hoon Kim,Joong Hee Lee
标识
DOI:10.1002/adfm.202002533
摘要
Abstract The necessity for better water splitting requires speedy development of efficient catalysts with high activity, long‐term stability, and cost effectiveness. In this work, a bifunctional catalyst originating from the interfacial assembly of a thin Mo,P‐codoped Co layer (≈50 nm) shelled Co nanowire (Co‐Mo‐P/CoNWs) network is fabricated via a facile approach. The catalyst exhibits low overpotentials of 0.08 and 0.27 V to reach a current response of 20 mA cm −2 for the hydrogen evolution reaction and oxygen evolution reaction, respectively, together with long‐term stability in 1.0 m KOH medium. The outstanding performance is further demonstrated by a Co‐Mo‐P/CoNWs‐based electrolyzer, which enables a cell voltage of only 1.495 V to reach 10 mA cm −2 , superior to one derived from commercial (Pt/C + RuO 2 /C) as well as to various reports recently published elsewhere. It is recognized that the formation of multiactive centers together with the increased active site number caused by Mo and P dual doping synergistically promote both hydrogen and oxygen evolution performance. Such a hybrid material opens a new approach for developing efficient and cost‐effective catalysts for water splitting application.
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