Cao Shuang, Sun Tong, Peng Yong, Yu Xianghui, Li Qinzhu, Meng Fan Lu, Yang Fan, Wang Han, Xie Yunhui, Hou Chun-Chao, Xu Qiang
College of Chemistry and Chemical Engineering, Institute for Sustainable Energy and Resources, Qingdao University, Qingdao, Shandong, 266071, China.
Leibniz Institute for Catalysis e.V., Albert-Einstein-Strasse 29a, 18059, Rostock, Germany.
Small. 2024 Nov;20(45):e2404285. doi: 10.1002/smll.202404285. Epub 2024 Jul 27.
The solar-driven overall water splitting (2HO→2H + O) is considered as one of the most promising strategies for reducing carbon emissions and meeting energy demands. However, due to the sluggish performance and high H cost, there is still a big gap for the current photocatalytic systems to meet the requirements for practical sustainable H production. Economic feasibility can be attained through simultaneously generating products of greater value than O, such as hydrogen peroxide (HO, 2HO→H + HO). Compared with overall water splitting, this approach is more kinetically feasible and generates more high-value products of H and HO. In several years, there has been an increasing surge in exploring the possibility and substantial progress has been achieved. In this review, a concise overview of the importance and underlying principles of PIWS is first provided. Next, the reported typical photocatalysts for PIWS are discussed, including commonly used semiconductors and cocatalysts, essential design features of these photocatalysts, and connections between their structures and activities, as well as the selected approaches for enhancing their stability. Then, the techniques used to quantify HO and the operando characterization techniques that can be employed to gain a thorough understanding of the reaction mechanisms are summarized. Finally, the current existing challenges and the direction needing improvement are presented. This review aims to provide a thorough summary of the most recent research developments in PIWS and sets the stage for future advancements and discoveries in this emerging area.
太阳能驱动的全水分解(2H₂O→2H₂ + O₂)被认为是减少碳排放和满足能源需求最有前景的策略之一。然而,由于性能迟缓以及高制氢成本,当前的光催化系统在满足实际可持续制氢要求方面仍存在很大差距。通过同时生成比O₂更具价值的产物,如过氧化氢(H₂O₂,2H₂O→H₂ + H₂O₂),可以实现经济可行性。与全水分解相比,这种方法在动力学上更可行,并且能生成更多高价值的H₂和H₂O₂产物。近年来,探索这种可能性的研究激增,并取得了实质性进展。在这篇综述中,首先简要概述了光催化制过氧化氢(PIWS)的重要性和基本原理。接下来,讨论了报道的用于PIWS的典型光催化剂,包括常用的半导体和助催化剂、这些光催化剂的基本设计特点、它们的结构与活性之间的联系,以及提高其稳定性的选定方法。然后,总结了用于量化H₂O₂的技术以及可用于深入了解反应机理的原位表征技术。最后,介绍了当前存在的挑战和需要改进的方向。这篇综述旨在全面总结PIWS的最新研究进展,并为这一新兴领域的未来发展和发现奠定基础。