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Boosting photoelectrochemical efficiency by near-infrared-active lattice-matched morphological heterojunctions

Photoelectrochemical catalysis is an attractive way to provide direct hydrogen production from solar energy. However, solar conversion efficiencies are hindered by the fact that light harvesting has so far been of limited efficiency in the near-infrared region as compared to that in the visible and...

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Detalles Bibliográficos
Autores principales: Liu, Guo-Qiang, Yang, Yuan, Li, Yi, Zhuang, Taotao, Li, Xu-Feng, Wicks, Joshua, Tian, Jie, Gao, Min-Rui, Peng, Jin-Lan, Ju, Huan-Xin, Wu, Liang, Pan, Yun-Xiang, Shi, Lu-An, Zhu, Haiming, Zhu, Junfa, Yu, Shu-Hong, Sargent, Edward H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8280183/
https://www.ncbi.nlm.nih.gov/pubmed/34262051
http://dx.doi.org/10.1038/s41467-021-24569-9
Descripción
Sumario:Photoelectrochemical catalysis is an attractive way to provide direct hydrogen production from solar energy. However, solar conversion efficiencies are hindered by the fact that light harvesting has so far been of limited efficiency in the near-infrared region as compared to that in the visible and ultraviolet regions. Here we introduce near-infrared-active photoanodes that feature lattice-matched morphological hetero-nanostructures, a strategy that improves energy conversion efficiency by increasing light-harvesting spectral range and charge separation efficiency simultaneously. Specifically, we demonstrate a near-infrared-active morphological heterojunction comprised of BiSeTe ternary alloy nanotubes and ultrathin nanosheets. The heterojunction’s hierarchical nanostructure separates charges at the lattice-matched interface of the two morphological components, preventing further carrier recombination. As a result, the photoanodes achieve an incident photon-to-current conversion efficiency of 36% at 800 nm in an electrolyte solution containing hole scavengers without a co-catalyst.