Kathleen Lonsdale Materials Chemistry, Department of Chemistry, University College London, 20 Gordon Street, London, WC1H 0AJ, UK.
Department of Chemistry, Quaid-i-Azam University, Islamabad, 45320, Pakistan.
Adv Mater. 2021 Dec;33(52):e2105195. doi: 10.1002/adma.202105195. Epub 2021 Oct 7.
Photocatalytic water splitting is considered one of the most important and appealing approaches for the production of green H to address the global energy demand. The utmost possible form of artificial photosynthesis is a two-step photoexcitation known as "Z-scheme", which mimics the natural photosystem. This process solely relies on the effective coupling and suitable band positions of semiconductors (SCs) and redox mediators for the purpose to catalyze the surface chemical reactions and significantly deter the backward reaction. In recent years, the Z-scheme strategies and their key role have been studied progressively through experimental approaches. In addition, theoretical studies based on density functional theory have provided detailed insight into the mechanistic aspects of some breathtakingly complex problems associated with hydrogen evolution reaction and oxygen evolution reaction. In this context, this critical review gives an overview of the fundamentals of Z-scheme photocatalysis, including both theoretical and experimental advancements in the field of photocatalytic water splitting, and suggests future perspectives.
光催化水分解被认为是生产绿色氢气以满足全球能源需求的最重要和最有吸引力的方法之一。最理想的人工光合作用形式是两步光激发,称为“Z 型方案”,它模拟了自然光合作用系统。该过程仅依赖于半导体 (SCs) 和氧化还原介质的有效耦合和适当的能带位置,以催化表面化学反应,并显著抑制逆反应。近年来,通过实验方法逐步研究了 Z 型方案策略及其关键作用。此外,基于密度泛函理论的理论研究为与析氢反应和析氧反应相关的一些复杂问题的机械方面提供了详细的见解。在这方面,本评论批判性地概述了 Z 型光催化的基本原理,包括光催化水分解领域的理论和实验进展,并提出了未来的展望。