Bu Yunfei, Wang Yaobin, Han Gao-Feng, Zhao Yunxia, Ge Xinlei, Li Feng, Zhang Zhihui, Zhong Qin, Baek Jong-Beom
Jiangsu Collaborative Innovation Center of Atmospheric Environment and Equipment Technology (CICAEET), Jiangsu Key Laboratory of Atmospheric Environment Monitoring and Pollution Control (AEMPC), UNIST-NUIST Research Center of Environment and Energy, (UNNU), School of Environmental Science and Technology, Nanjing University of Information Science and Technology (NUIST), Nanjing, 210044, P. R. China.
School of Energy and Chemical Engineering/Center for Dimension Controllable Organic Frameworks, Ulsan National Institute of Science and Technology (UNIST), 50 UNIST, Ulsan, 44919, South Korea.
Adv Mater. 2021 Dec;33(49):e2103266. doi: 10.1002/adma.202103266. Epub 2021 Sep 24.
Hydrogen peroxide (H O ) is an environment-friendly and efficient oxidant with a wide range of applications in different industries. Recently, the production of hydrogen peroxide through direct electrosynthesis has attracted widespread research attention, and has emerged as the most promising method to replace the traditional energy-intensive multi-step anthraquinone process. In ongoing efforts to achieve highly efficient large-scale electrosynthesis of H O , carbon-based materials have been developed as 2e oxygen reduction reaction catalysts, with the benefits of low cost, abundant availability, and optimal performance. This review comprehensively introduces the strategies for optimizing carbon-based materials toward H O production, and the latest advances in carbon-based hybrid catalysts. The active sites of the carbon-based materials and the influence of coordination heteroatom doping on the selectivity of H O are extensively analyzed. In particular, the appropriate design of functional groups and understanding the effect of the electrolyte pH are expected to further improve the selective efficiency of producing H O via the oxygen reduction reaction. Methods for improving catalytic activity by interface engineering and reaction kinetics are summarized. Finally, the challenges carbon-based catalysts face before they can be employed for commercial-scale H O production are identified, and prospects for designing novel electrochemical reactors are proposed.
过氧化氢(H₂O₂)是一种环境友好且高效的氧化剂,在不同行业有着广泛应用。近年来,通过直接电合成生产过氧化氢引起了广泛的研究关注,并已成为取代传统能源密集型多步蒽醌法最具前景的方法。在实现高效大规模电合成H₂O₂的持续努力中,碳基材料已被开发为2e氧还原反应催化剂,具有成本低、可用性丰富和性能优化等优点。本文综述全面介绍了优化碳基材料用于H₂O₂生产的策略以及碳基混合催化剂的最新进展。广泛分析了碳基材料的活性位点以及配位杂原子掺杂对H₂O₂选择性的影响。特别是,官能团的合理设计以及对电解质pH效应的理解有望进一步提高通过氧还原反应生产H₂O₂的选择性效率。总结了通过界面工程和反应动力学提高催化活性的方法。最后,确定了碳基催化剂在用于商业规模H₂O₂生产之前面临的挑战,并提出了设计新型电化学反应器的前景。