Fu Hui, Wu Yaqiang, Guo Yuhao, Sakurai Takuya, Zhang Qianqian, Liu Yuanyuan, Zheng Zhaoke, Cheng Hefeng, Wang Zeyan, Huang Baibiao, Wang Qian, Domen Kazunari, Wang Peng
State Key Laboratory of Crystal Materials, Institute of Crystal Materials, Shandong University, Jinan, China.
Graduate School of Engineering, Nagoya University, Nagoya, Japan.
Nat Commun. 2025 Jan 24;16(1):990. doi: 10.1038/s41467-025-56314-x.
Solar-driven photocatalytic water splitting offers a sustainable pathway to produce green hydrogen, yet its practical application encounters several challenges including inefficient photocatalysts, sluggish water oxidation, severe reverse reactions and the necessity of separating produced hydrogen and oxygen gases. Herein, we design and develop a photocatalytic system composed of two separate reaction parts: a hydrogen evolution cell containing halide perovskite photocatalysts (MoSe-loaded CH(NH)PbBrI) and an oxygen evolution cell containing NiFe-layered double hydroxide modified BiVO photocatalysts. These components are bridged by a I/I redox couple to facilitate electron transfer, realizing efficient overall water splitting with a solar-to-hydrogen conversion efficiency of 2.47 ± 0.03%. Additionally, an outdoor scaled-up setup of 692.5 cm achieves an average solar-to-hydrogen conversion efficiency of 1.21% during a week-long test under natural sunlight. By addressing major limitations inherent in conventional photocatalytic systems, such as the cooccurrence of hydrogen and oxygen in a single cell and the resultant severe reverse reactions from hydrogen and oxygen recombination, this work introduces an alternative concept for photocatalytic system design, which enhances both efficiency and practicality.
太阳能驱动的光催化水分解为绿色氢气的生产提供了一条可持续的途径,但其实际应用面临着几个挑战,包括光催化剂效率低下、水氧化反应缓慢、严重的逆反应以及分离产生的氢气和氧气的必要性。在此,我们设计并开发了一种由两个独立反应部分组成的光催化系统:一个包含卤化物钙钛矿光催化剂(负载MoSe的CH(NH)PbBrI)的析氢电池和一个包含镍铁层状双氢氧化物修饰的BiVO光催化剂的析氧电池。这些组件通过I/I氧化还原对桥接以促进电子转移,实现了高效的全水分解,太阳能到氢气的转换效率为2.47±0.03%。此外,一个692.5平方厘米的户外放大装置在自然阳光下进行的为期一周的测试中,平均太阳能到氢气的转换效率达到了1.21%。通过解决传统光催化系统固有的主要限制,如在单个电池中氢气和氧气同时出现以及氢气和氧气重组导致的严重逆反应,这项工作引入了一种光催化系统设计的替代概念,提高了效率和实用性。