过电位
催化作用
材料科学
氧烷
带隙
纳米技术
过渡金属
兴奋剂
分解水
氢
氢燃料
解吸
化学工程
光催化
物理化学
化学
光电子学
光谱学
物理
有机化学
吸附
工程类
量子力学
电化学
电极
作者
Zhiyan Chen,Yao Song,Jinyan Cai,Xusheng Zheng,Dongdong Han,Jinyan Cai,Yipeng Zang,Shuwen Niu,Yun Liu,Junfa Zhu,Xiaojing Liu,Gongming Wang
标识
DOI:10.1002/anie.201801834
摘要
Abstract Endowing materials with specific functions that are not readily available is always of great importance, but extremely challenging. Co 4 N, with its beneficial metallic characteristics, has been proved to be highly active for the oxidation of water, while it is notoriously poor for catalyzing the hydrogen evolution reaction (HER), because of its unfavorable d‐band energy level. Herein, we successfully endow Co 4 N with prominent HER catalytic capability by tailoring the positions of the d‐band center through transition‐metal doping. The V‐doped Co 4 N nanosheets display an overpotential of 37 mV at 10 mA cm −2 , which is substantially better than Co 4 N and even close to the benchmark Pt/C catalysts. XANES, UPS, and DFT calculations consistently reveal the enhanced performance is attributed to the downshift of the d‐band center, which helps facilitate the H desorption. This concept could provide valuable insights into the design of other catalysts for HER and beyond.
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