催化作用
电化学
选择性
材料科学
铋
无机化学
碳纳米管
可逆氢电极
过氧化氢
化学工程
阴极
电极
电催化剂
氧气
纳米管
碳纤维
密度泛函理论
法拉第效率
单斜晶系
热液循环
水热合成
氧化还原
产量(工程)
化学
选择性还原
析氧
纳米技术
氢
过氧化物
作者
Jinfeng Chen,Wu Wang,Yuxuan Ding,Zhangfeng Shen,Lijuan Yu,Songhui Wan,Qinshuang Ma,Lingchang Jiang,Jing Zhang,Haiying Yu,Qineng Xia,Yongyong Cao
出处
期刊:Chemsuschem
[Wiley]
日期:2026-03-05
卷期号:19 (5): e202502310-e202502310
标识
DOI:10.1002/cssc.202502310
摘要
The electrochemical two‐electron oxygen reduction reaction (2e − ORR) represents a promising on‐site approach for the decentralized and green production of hydrogen peroxide (H 2 O 2 ). Nevertheless, the development of efficient catalysts that exhibit high activity and selectivity remains a significant challenge. Herein, bismuth phosphate/oxidized carbon nanotube composites (BPO/CNTs‐O) constructed via a simple hydrothermal method were used to generate H 2 O 2 in an alkaline environment through electrocatalytic 2e − ORR. With an appropriate BPO content, the BPO/CNT‐O‐3 catalyst demonstrated a high H 2 O 2 selectivity of 91.32% at 0.40 V RHE during the rotating ring‐disk electrode test. Density functional theory calculations indicate that the interaction between monoclinic BPO and CNTs‐O could regulate the interfacial electronic structure and provide a suitable binding strength of oxygen (O 2 ) for subsequent hydrogenation to H 2 O 2 . In a flow‐cell setup, the BPO/CNT‐O‐3‐based cathode could provide a H 2 O 2 yield of 4.0 mol g − 1 cat h −1 with Faraday efficiency around 60%, and the on‐site accumulated H 2 O 2 could rapidly achieve organic dye degradation. This work provides a new perspective on the design and construction of electrocatalytic systems for H 2 O 2 production.
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