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Photocatalytic and Photocurrent Responses to Visible Light of the Lone-Pair-Based Oxysulfide Sr6Cd2Sb6S10O7

Al Bacha, Sandy; Saitzek, Sébastien; McCabe, Emma E.; Kabbour, Houria

Photocatalytic and Photocurrent Responses to Visible Light of the Lone-Pair-Based Oxysulfide Sr6Cd2Sb6S10O7 Thumbnail


Authors

Sandy Al Bacha

Sébastien Saitzek

Houria Kabbour



Abstract

We present a combined experimental and computational study on the recently reported oxysulfide Sr6Cd2Sb6S10O7. Our spectroscopy and photoelectrochemical measurements and tests for photocatalytic activity indicate the potential of Sr6Cd2Sb6S10O7 for photocatalytic applications. In particular, the transient photocurrent response shows a reproducible photo-generated current which depends on light intensity and which indicates an efficient electron−hole separation upon visible light illumination. Density functional theory calculations, combined with crystal orbital Hamiltonian population analysis, give insights into the electronic structure of Sr6Cd2Sb6S10O7 and the origin of its physical properties. Our comprehensive investigation into Sr6Cd2Sb6S10O7 reveals the roles of its polar structure, polar Sb3+ coordination environments, and the 5s2 lone pair in making this compound a potential candidate for solar water splitting photocatalysis.

Citation

Al Bacha, S., Saitzek, S., McCabe, E. E., & Kabbour, H. (2022). Photocatalytic and Photocurrent Responses to Visible Light of the Lone-Pair-Based Oxysulfide Sr6Cd2Sb6S10O7. Inorganic Chemistry, 61(46), 18611-18621. https://doi.org/10.1021/acs.inorgchem.2c03040

Journal Article Type Article
Acceptance Date Oct 18, 2022
Online Publication Date Nov 7, 2022
Publication Date Nov 21, 2022
Deposit Date Nov 7, 2022
Publicly Available Date Nov 8, 2023
Journal Inorganic Chemistry
Print ISSN 0020-1669
Electronic ISSN 1520-510X
Publisher American Chemical Society
Peer Reviewed Peer Reviewed
Volume 61
Issue 46
Pages 18611-18621
DOI https://doi.org/10.1021/acs.inorgchem.2c03040
Public URL https://durham-repository.worktribe.com/output/1186604

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Copyright Statement
This document is the Accepted Manuscript version of a Published Work that appeared in final form in Inorganic Chemistry, copyright © American Chemical Society after peer review and technical editing by the publisher. To access the final edited and published work see https://doi.org/10.1021/acs.inorgchem.2c03040.


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