Shining a Light on Some Fundamental Research Opportunities in Semiconductor Photoelectrochemistry

光电化学 纳米技术 半导体 材料科学 光电子学 半导体材料 工程物理 物理 光电探测器 发光二极管 半导体器件
作者
Paul J. L. Bean,Dominic J. Covelli,Xinyi Elaine Shen,Nathan S. Lewis
出处
期刊:ACS central science [American Chemical Society]
卷期号:12 (4): 428-445
标识
DOI:10.1021/acscentsci.5c02044
摘要

Decades of research in semiconductor photoelectrochemistry have yielded a deep understanding of charge transfer, energetics, and stability at solid-liquid interfaces. Theoretical frameworks developed by Gerischer and contemporaries, together with extensive experimental validation, have clarified the key principles affecting the interfacial kinetics and energetics of semiconductor photoelectrodes. Nevertheless, significant opportunities remain for advances in fundamental understanding of semiconductor photoelectrochemistry. Exciting opportunities include exploiting advances in theory, synthesis, and instrumentation to determine the chemical identity and reactivity of surface states; exerting control of band-edge energetics through molecular-level surface modification processes; and systematically improving emerging photoelectrode protection strategies to enable long-term photoelectrode operation under both oxidative and reductive conditions. Advanced morphologies, such as nanowire and microwire arrays, present new pathways to combine efficient light absorption with effective charge collection and catalyst integration. Unique light-matter interactions during photoelectrochemical deposition of p-type semiconductors readily allow preparation at scale of complex 3D morphologies that are difficult, if not impossible, to access by other methods. Continued exploration of these avenues will expand the fundamental understanding of semiconductor-liquid interfaces and could additionally advance the realization of efficient, stable, and scalable systems for solar fuel generation and other emerging photoelectrochemical applications.
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