Zhang De-Shan, Wang Lei, Zhang Xiaodong, Li Xu-Bing, Xu Hangxun, Tung Chen-Ho, Wu Li-Zhu
New Cornerstone Science Laboratory, Technical Institute of Physics and Chemistry, Chinese Academy of Science, Beijing 100190, P. R. China.
School of Future Technology, University of Chinese Academy of Science, Beijing 100049, P. R. China.
Chem Soc Rev. 2025 Sep 24. doi: 10.1039/d5cs00378d.
The pursuit of sustainable energy technologies has long inspired the development of efficient photocatalysts capable of converting solar energy into hydrogen (H) overall water (HO) splitting. While inorganic semiconductors, such as metal oxides, oxynitrides, and oxysulfides, have demonstrated reasonable activity and robustness, their intrinsic limitations in light harvesting and charge separation continue to hinder their photocatalytic performance. Conversely, organic semiconductors offer compelling advantages, including tunable electronic structures, visible-light absorption, and synthetic versatility. However, their application in overall HO splitting remains constrained by short exciton diffusion lengths, low carrier mobility, and poor activity in multi-electron processes. Recently, integrating organic and inorganic materials into hybrid photocatalysts has emerged as a powerful strategy to overcome these bottlenecks. By synergistically combining the efficient charge transport of inorganic frameworks with the structural adaptability and optoelectronic tunability of organic materials, rationally designed hybrid systems have shown remarkable potential in enhancing light utilization, facilitating exciton dissociation, and suppressing recombination. These advances not only improve overall HO splitting efficiency but also open new avenues for photocatalyst design. This review critically examines the fundamental principles, interfacial interactions, and photophysical mechanisms underpinning inorganic-organic hybrid photocatalysts for solar-driven overall HO splitting. We highlight recent breakthroughs, analyse the remaining scientific and engineering challenges, and propose strategic directions for next-generation hybrid systems with improved scalability, efficiency, and durability. Our goal is to establish a forward-looking roadmap that defines the role of hybrid photocatalysts as a transformative platform in achieving a sustainable, carbon-neutral society.
长期以来,对可持续能源技术的追求推动了高效光催化剂的发展,这种光催化剂能够将太阳能转化为氢气(H),实现整体水(H₂O)分解。虽然无机半导体,如金属氧化物、氮氧化物和氧硫化物,已展现出合理的活性和稳定性,但其在光捕获和电荷分离方面的固有局限性仍在阻碍其光催化性能。相反,有机半导体具有显著优势,包括可调节的电子结构、可见光吸收能力以及合成多样性。然而,它们在整体水分解中的应用仍受到激子扩散长度短、载流子迁移率低以及多电子过程中活性差的限制。最近,将有机和无机材料整合到混合光催化剂中已成为克服这些瓶颈的有力策略。通过将无机框架的高效电荷传输与有机材料的结构适应性和光电可调性协同结合,合理设计的混合体系在提高光利用率、促进激子解离和抑制复合方面展现出显著潜力。这些进展不仅提高了整体水分解效率,还为光催化剂设计开辟了新途径。本综述批判性地审视了用于太阳能驱动整体水分解的无机 - 有机混合光催化剂的基本原理、界面相互作用和光物理机制。我们强调了最近的突破,分析了剩余的科学和工程挑战,并为具有更高可扩展性、效率和耐久性的下一代混合体系提出了战略方向。我们的目标是建立一个前瞻性路线图,将混合光催化剂定义为实现可持续、碳中和社会的变革性平台。