欢迎访问《电化学(中英文)》期刊官方网站,今天是

电化学(中英文)

• 研究论文 •    

氮掺杂分级多孔碳锚定钴原子高效酸性电合成过氧化氢

黄晓a,c, 战梓昊a, 牛浩旭a, 罗官宇b, 黄劲陶b, 靳博暄b, 王得丽b,*   

  1. a. 武汉工程大学, 磷矿及其共伴生资源绿色高效开发利用全国重点实验室, 化学与环境工程学院, 湖北 武汉 430205; b. 华中科技大学, 能量转换与存储材料化学教育部重点实验室, 材料化学与服役失效湖北省重点实验室, 化学与化工学院, 湖北 武汉 430074; c. 黄冈师范学院, 催化材料制备及应用湖北省重点实验室, 化学化工学院, 湖北 黄冈438000.
  • 发布日期:2026-06-11
  • 通讯作者: 王得丽 E-mail:wangdl81125@hust.edu.cn

Efficient Acidic H2O2 Electrosynthesis over Co Atoms Anchored on Nitrogen–doped Hierarchical Porous Carbon

Xiao Huanga,c, Zihao Zhana, Haoxu Niua, Guanyu Luob, Jintao Huangb, Boxuan Jinb, Deli Wangb,*   

  1. a. State Key Laboratory of Green and Efficient Development of Phosphorus Resources, School of Chemistry and Environmental Engineering, Wuhan Institute of Technology, Wuhan 430205, China; b. Key Laboratory of Material Chemistry for Energy Conversion and Storage, Ministry of Education, Hubei Key Laboratory of Material Chemistry and Service Failure, School of Chemistry and Chemical Engineering, Huazhong University of Science and Technology, Wuhan 430074, China; c. Hubei Key Laboratory of Processing and Application of Catalytic Materials, College of Chemistry and Chemical Engineering, Huanggang Normal University, Huanggang 438000, China.
  • Online:2026-06-11
  • Contact: Deli Wang E-mail:wangdl81125@hust.edu.cn

摘要: 双电子氧还原反应(2e⁻ ORR)为过氧化氢(H2O2)的现场制备提供了一条有前景的途径,可作为高能耗蒽醌工艺的绿色替代方案。然而,在目标2e⁻路径上,竞争性的4e⁻ ORR具有较高选择性,导致H2O2的法拉第效率偏低,这成为催化剂设计中的一个关键挑战。本文构建了一种锚定有Co原子的氮掺杂中空分级多孔碳材料(Co−N/HPC),用于高性能H2O2电合成。该Co−N/HPC催化剂展现出优异的2e⁻ ORR性能,在0.4 V(vs. RHE)的施加电位下,H2O2选择性接近100%。此外,原位生成的H2O2在降解有机污染物方面表现出高效性,展示了该材料在环境修复中的双功能特性。物理表征与模拟计算证实,性能的提升归因于独特的分级结构,该结构促进了电解质的快速扩散并提高了H2O2选择性。本研究为设计集高效H2O2生产与直接应用为一体的先进电催化剂开辟了新途径。

关键词: 氧化还原, H2O2, 电合成, 氮掺杂碳, 分级结构

Abstract: The two–electron oxygen reduction reaction (2e ORR) presents a promising route for the on-site production of hydrogen peroxide (H2O2), offering a green alternative to energy–consuming anthraquinone process. However, the high selectivity toward the competing 4e ORR over the desired 2e pathway leads to low Faradaic efficiency for H2O2, posing a critical challenge in catalyst design. In this work, a nitrogen–doped hollow hierarchical porous carbon with anchored Co atoms (Co−N/HPC) is constructed for high-performance H2O2 production. The Co−N/HPC catalyst shows excellent 2e ORR performance, achieving an H2O2 selectivity approaching 100% at an applied potential of 0.4 V (vs. RHE). Moreover, the in situ generated H2O2 proves highly effective in degrading organic pollutants, showcasing a dual-functionality for environmental remediation. Physical characterization and simulations confirm that the enhanced performance is attributed to the unique hierarchical structure, which facilitates fast electrolyte diffusion and boosts H2O2 selectivity. This work opens a new avenue for the design of advanced electrocatalysts that integrate efficient H2O2 production with direct application.

Key words: Oxygen reduction reaction, H2O2, Electrosynthesis, Nitrogen–doped carbon, Hierarchical structure