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Photocatalytic Z‐Scheme Overall Water Splitting: Recent Advances in Theory and Experiments

Jamal Abdul NasirDepartment of Chemistry Quaid‐i‐Azam University Islamabad 45320 PakistanAkhtar MunirDepartment of Chemistry & Chemical Engineering SBA School of Science & Engineering Lahore University of Management Sciences (LUMS) DHA Lahore 54792 PakistanNaveed AhmadInstitute of Pharmaceutical Science Faculty of Life Science and Medicine King's College London 150 Stamford Street London SE1 9NH UKTanveer ul HaqSustainable Energy Engineering Frank H. Dotterweich College of Engineering Texas A&M University Kingsville TX 78363‐8202 USAZaibunisa KhanKathleen Lonsdale Materials Chemistry Department of Chemistry University College London 20 Gordon Street London WC1H 0AJ UKZiaur RehmanDepartment of Chemistry Quaid‐i‐Azam University Islamabad 45320 Pakistan
2021en
ABI

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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.

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