纳米片
钴
析氧
氢氧化钴
钼
氢氧化物
材料科学
过电位
催化作用
无机化学
电催化剂
化学工程
化学
纳米技术
电化学
电极
有机化学
物理化学
工程类
作者
Chao Wang,Wen Li,Andrey A. Kistanov,Harishchandra Singh,Yves Kayser,Wei Cao,Baoyou Geng
标识
DOI:10.1016/j.jcis.2022.08.069
摘要
Cobalt-based hydroxide are ideal candidates for the oxygen evolution reaction. Herein, we use molybdenum oxide nanorods as sacrificial templates to construct a self-supporting molybdenum-doped cobalt hydroxide nanosheet hierarchical microtubule structure based on a structural engineering strategy to improve the active area of the catalyst. X-ray-based spectroscopic tests revealed that Mo (VI) with tetrahedral coordination intercalated into the interlayer of cobalt hydroxide, promoting interlayer separation. At the same time, Mo is connected with Co through oxygen bonds, which promotes the transfer of Co charges to Mo and reduces the electron cloud density of Co ions. In 1 M KOH, optimized molybdenum-doped cobalt hydroxide nanosheet microtubules only needs an overpotential of 288 mV to drive a current density of 10 mA cm-2, which is significantly better than that of pure Co(OH)2 nanosheets and RuO2. Structural engineering and electronic state regulation can effectively improve the oxygen evolution activity of cobalt-based hydroxide, which provides a design idea for the development of efficient oxygen evolution catalysts.
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