杂原子
催化作用
材料科学
硫化物
热液循环
过渡金属
电催化剂
选择性
硫化铜
化学工程
水热合成
无机化学
纳米技术
化学
电化学
铜
冶金
物理化学
电极
有机化学
工程类
戒指(化学)
作者
Ao Zhang,Zhongqing Jiang,Shaoda Zhang,Penghua Lan,Naihua Miao,Weiheng Chen,Ning Huang,Xiaoning Tian,Yangjié Liu,Zhongyu Cai
标识
DOI:10.1016/j.apcatb.2023.122721
摘要
We report the development of non-noble transition metal sulfide catalysts Mn-CuS-x for high-efficiency and selective H2O2 production. In this study, we synthesized Mn-CuS-x with coral-shaped hierarchical porous structure through one-pot hydrothermal reaction. The Mn-CuS-x possesses large specific surface area with plenty of crystalline defects via heteroatom doping of Mn. The Mn-CuS-x kinetically favored 2e− pathway over 4e− pathway, resulting in high selectivity (>92%) to H2O2 production and high H2O2 concentration (∼24.5 mM at 0.6 V vs. RHE) within 3 h for the optimized Mn-CuS-2 catalysts (synthesized with a molar ratio of 1:3:8 (MnCl2·4 H2O: CuCl2·2 H2O: C2H5NS)). The Mn-CuS-2 showed excellent stability, indicating that the Mn-CuS electrocatalysts can simultaneously achieve both high stability and enhanced H2O2 production. Our first-principles calculations further confirmed that the heteroatom Mn doping to CuS thermodynamically makes the 2e–-ORR pathway more favorable. This study provides a green, low-cost, and efficient route to produce H2O2, which is very promising for generating chemicals and liquid fuels.
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