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Photo-induced self-catalysis of nano-Bi(2)MoO(6) for solar energy harvesting and charge storage

Efficient, sustainable, and integrated energy systems require the development of novel multifunctional materials to simultaneously achieve solar energy harvesting and charge storage. Bi-based oxysalt aurivillius phase materials are potential candidates due to their typical photovoltaic effect and th...

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Detalles Bibliográficos
Autores principales: Si, Jiangju, Guo, Changmeng, Liu, Haojie, Li, Weiwei, Guo, Xiaowei, Bai, Peidong, Liu, Yanghong, Chen, Gairong, Sun, Ningbo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9057184/
https://www.ncbi.nlm.nih.gov/pubmed/35515186
http://dx.doi.org/10.1039/d0ra07020c
Descripción
Sumario:Efficient, sustainable, and integrated energy systems require the development of novel multifunctional materials to simultaneously achieve solar energy harvesting and charge storage. Bi-based oxysalt aurivillius phase materials are potential candidates due to their typical photovoltaic effect and their pseudo-capacitance charge storage behavior. Herein, we synthesized nano-Bi(2)MoO(6) as a material for both solar energy harvesting and charge storage due to its suitable band gap for absorption of visible light and its well-defined faradaic redox reaction from Bi metal to Bi(3+). The irradiation of visible light significantly affected the electrochemical processes and the dynamics of the Bi(2)MoO(6) electrode. The photo-induced self-catalytic redox mechanism was carefully explored by adding sacrificial agents in photocatalysis reaction. In accordance with the rule of energy matching, the photo-generated holes oxidized the Bi metal to Bi(3+), and the corresponding peak current increased by 79.5% at a scanning rate of 50 mV s(−1). More importantly, the peak current retention rate remained higher than 92.5% during the entire 200 cycles. The photo-generated electrons facilitated a decrease of 184 mV in the overpotential of the reduction process. Furthermore, the irradiation of visible light also accelerated the ionic diffusion of the electrolyte. These investigations provide a unique perspective for the design and development of new multifunctional materials to synergistically realize solar energy harvesting and charge storage.