Importance of surface oxygen vacancies for ultrafast hot carrier relaxation and transport in Cu_{2}O

Cu_{2}O has appealing properties as an electrode for photoelectrochemical water splitting, yet its practical performance is severely limited by inefficient charge extraction at the interface. Using hybrid DFT calculations, we investigate carrier capture processes by oxygen vacancies (V_{O}) in the e...

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Main Authors: Chiara Ricca, Lisa Grad, Matthias Hengsberger, Jürg Osterwalder, Ulrich Aschauer
Format: Article
Language:English
Published: American Physical Society 2021-12-01
Series:Physical Review Research
Online Access:http://doi.org/10.1103/PhysRevResearch.3.043219
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author Chiara Ricca
Lisa Grad
Matthias Hengsberger
Jürg Osterwalder
Ulrich Aschauer
author_facet Chiara Ricca
Lisa Grad
Matthias Hengsberger
Jürg Osterwalder
Ulrich Aschauer
author_sort Chiara Ricca
collection DOAJ
description Cu_{2}O has appealing properties as an electrode for photoelectrochemical water splitting, yet its practical performance is severely limited by inefficient charge extraction at the interface. Using hybrid DFT calculations, we investigate carrier capture processes by oxygen vacancies (V_{O}) in the experimentally observed (sqrt[3]×sqrt[3])R30^{∘} reconstruction of the dominant (111) surface. Our results show that these V_{O} are doubly ionized and that associated defects states strongly suppress electron transport. In particular, the excited electronic state of a singly charged V_{O} plays a crucial role in the nonradiative electron capture process with a capture coefficient of about 10^{−9}cm^{3}/s and a lifetime of 0.04 ps, explaining the experimentally observed ultrafast carrier relaxation. These results highlight that engineering the surface V_{O} chemistry will be a crucial step in optimizing Cu_{2}O for photoelectrode applications.
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spelling doaj.art-487767ed39504f329dacad81148299922024-04-12T17:16:44ZengAmerican Physical SocietyPhysical Review Research2643-15642021-12-013404321910.1103/PhysRevResearch.3.043219Importance of surface oxygen vacancies for ultrafast hot carrier relaxation and transport in Cu_{2}OChiara RiccaLisa GradMatthias HengsbergerJürg OsterwalderUlrich AschauerCu_{2}O has appealing properties as an electrode for photoelectrochemical water splitting, yet its practical performance is severely limited by inefficient charge extraction at the interface. Using hybrid DFT calculations, we investigate carrier capture processes by oxygen vacancies (V_{O}) in the experimentally observed (sqrt[3]×sqrt[3])R30^{∘} reconstruction of the dominant (111) surface. Our results show that these V_{O} are doubly ionized and that associated defects states strongly suppress electron transport. In particular, the excited electronic state of a singly charged V_{O} plays a crucial role in the nonradiative electron capture process with a capture coefficient of about 10^{−9}cm^{3}/s and a lifetime of 0.04 ps, explaining the experimentally observed ultrafast carrier relaxation. These results highlight that engineering the surface V_{O} chemistry will be a crucial step in optimizing Cu_{2}O for photoelectrode applications.http://doi.org/10.1103/PhysRevResearch.3.043219
spellingShingle Chiara Ricca
Lisa Grad
Matthias Hengsberger
Jürg Osterwalder
Ulrich Aschauer
Importance of surface oxygen vacancies for ultrafast hot carrier relaxation and transport in Cu_{2}O
Physical Review Research
title Importance of surface oxygen vacancies for ultrafast hot carrier relaxation and transport in Cu_{2}O
title_full Importance of surface oxygen vacancies for ultrafast hot carrier relaxation and transport in Cu_{2}O
title_fullStr Importance of surface oxygen vacancies for ultrafast hot carrier relaxation and transport in Cu_{2}O
title_full_unstemmed Importance of surface oxygen vacancies for ultrafast hot carrier relaxation and transport in Cu_{2}O
title_short Importance of surface oxygen vacancies for ultrafast hot carrier relaxation and transport in Cu_{2}O
title_sort importance of surface oxygen vacancies for ultrafast hot carrier relaxation and transport in cu 2 o
url http://doi.org/10.1103/PhysRevResearch.3.043219
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