材料科学
析氧
过电位
分解水
纳米线
催化作用
纳米结构
化学工程
纳米技术
兴奋剂
电化学
光催化
光电子学
物理化学
电极
化学
生物化学
工程类
作者
Jiayao Fan,Mingyu Chen,Bingxue Liu,Dongdong Xu,Yue Lin,Naien Shi,Ying Liu,Zhihui Dai,Jianchun Bao,Min Han,Wei Huang
标识
DOI:10.1002/admi.202200098
摘要
Abstract Metal phosphosulfides (layered MPS 3 or pyrite‐type MPS) nanostructures have emerged as promising active materials for optoelectronics, magnetism, energy storage, and catalysis. Despite great progress that has been achieved, controllable synthesis of cationic‐doped CoPS nanostructures or related superstructures arrays remains challenging, and their electrocatalytic applications toward oxygen evolution reaction (OER) are not explored. Herein, the self‐supported Mn‐doped CoPS nanowire‐based gold‐silk‐chrysanthemum‐like superstructures arrays on carbon cloth (CC) with variable Mn‐content (Mn‐CoPS‐ x %/CC) are fabricated by thermal conversion of MnCo‐layered‐double‐hydroxides‐x%/CC precursors under P x S y vapor/Ar atmosphere. Compared with pure CoPS/CC, all the Mn‐CoPS‐ x %/CC show greatly enhanced electrocatalytic OER activity. Due to the suited Mn‐doping content and unique microstructure‐induced superhydrophilic and superaerophobic surface that can optimize electronic structure, offer more available active sites, and foster desorption of O 2 product, the Mn‐CoPS‐5%/CC manifests the best OER activity with a low overpotential (270 mV) to reach 20 mA cm −2 current density and high turnover frequency (0.13 s −1 ), outperforming its counterparts, IrO 2 /CC and most of recently reported OER catalysts. Moreover, such Mn‐CoPS‐5%/CC exhibits good catalytic stability. This work offers an efficient avenue for optimizing MPS nanostructures toward OER by combining doping and structure engineering strategies, and may promote their applications in water‐splitting or other clean energy options.
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