材料科学
兴奋剂
选择性
氟
电子转移
硫黄
纳米技术
化学工程
光化学
光电子学
有机化学
冶金
催化作用
工程类
化学
作者
Fei Xiang,Xuhong Zhao,Jian Yang,Ning Li,Wenxiao Gong,Yizhen Liu,Arturo Burguete‐Lopez,Yulan Li,Xiaobin Niu,Andrea Fratalocchi
标识
DOI:10.1002/adma.202208533
摘要
Abstract Electrocatalytic two‐electron oxygen reduction (2e − ORR) to hydrogen peroxide (H 2 O 2 ) is attracting broad interest in diversified areas including paper manufacturing, wastewater treatment, production of liquid fuels, and public sanitation. Current efforts focus on researching low‐cost, large‐scale, and sustainable electrocatalysts with high activity and selectivity. Here a large‐scale H 2 O 2 electrocatalysts based on metal‐free carbon fibers with a fluorine and sulfur dual‐doping strategy is engineered. Optimized samples yield with a high onset potential of 0.814 V versus reversible hydrogen electrode (RHE), an almost ideal 2e − pathway selectivity of 99.1%, outperforming most of the recently reported carbon‐based or metal‐based electrocatalysts. First principle theoretical computations and experiments demonstrate that the intermolecular charge transfer coupled with electron spin redistribution from fluorine and sulfur dual‐doping is the crucial factor contributing to the enhanced performances in 2e − ORR. This work opens the door to the design and implementation of scalable, earth‐abundant, highly selective electrocatalysts for H 2 O 2 production and other catalytic fields of industrial interest.
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