Defect Properties, Anion Ordering, and Photochromic Mechanism in Yttrium Oxyhydride

Yttrium oxyhydride (YHO) undergoes a reversible photochromic transition when exposed to ultraviolet light. However, the mechanism for this transformation is not fully understood, and the structure and precise chemical composition of YHO remain under debate. Here, we use first-principles density functional theory calculations with a hybrid functional to study the structure, chemical stability, and point defect properties of YHO. As experiments have shown, we find that YHO prefers a cubic structure, with H and O anions present in equal concentrations and located on tetrahedral sites. Stoichiometric and ordered YHO is chemically stable, but it has a wide band gap of 5.01 eV, considerably larger than that measured in experiments (2.4–3.8 eV). On the other hand, Y4H10O has a smaller band gap of 2.97 eV and also has a region of chemical stability; thus, the actual material may include some fraction of this H-rich structure. The defect chemistry of YHO is dominated by anionic antisite species (HO and OH), with hydrogen interstitials (Hi) and vacancies (VH) also present in reasonably high concentrations. We show that antisite disorder lowers the band gap relative to the perfectly ordered structure, bringing the magnitude of the gap into closer agreement with experiment. Based on our calculations of defect migration and the positions of defect states relative to the band edges, we link the onset of photochromic behavior to the reaction HO– → VO0 + Hi–, which follows photoexcitation of a HO+ defect. Hi– can subsequently migrate away and be trapped by additional HO+ defects, contributing to the persistence of the reaction, while the resultant oxygen vacancy, VO0, introduces an occupied defect state that leads to optical absorption at visible wavelengths. Our results can explain reported discrepancies between experimental and computational results for YHO, and they allow us to propose specific atomic-scale processes that can lead to photochromism. Understanding these mechanisms is key for unlocking YHO’s application in devices ranging from smart windows and optoelectronics to electrochemical synapses for neural networks.

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Publication Details

Journal
The Journal of Physical Chemistry C
Published
2024-11-18
DOI
https://doi.org/10.1021/acs.jpcc.4c04988
Citations
3
Primary Topic
Advanced Photocatalysis Techniques
Type
article
Field-Weighted Citation Impact
0.31

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article

Defect Properties, Anion Ordering, and Photochromic Mechanism in Yttrium Oxyhydride

Chris G. Van de Walle, Andrew J. E. Rowberg
3 citations
The Journal of Physical Chemistry C
Advanced Photocatalysis Techniques
0.31
article

Defect Properties, Anion Ordering, and Photochromic Mechanism in Yttrium Oxyhydride

Chris G. Van de Walle, Andrew J. E. Rowberg
article en
3 citations

Abstract

Yttrium oxyhydride (YHO) undergoes a reversible photochromic transition when exposed to ultraviolet light. However, the mechanism for this transformation is not fully understood, and the structure and precise chemical composition of YHO remain under debate. Here, we use first-principles density functional theory calculations with a hybrid functional to study the structure, chemical stability, and point defect properties of YHO. As experiments have shown, we find that YHO prefers a cubic structure, with H and O anions present in equal concentrations and located on tetrahedral sites. Stoichiometric and ordered YHO is chemically stable, but it has a wide band gap of 5.01 eV, considerably larger than that measured in experiments (2.4–3.8 eV). On the other hand, Y4H10O has a smaller band gap of 2.97 eV and also has a region of chemical stability; thus, the actual material may include some fraction of this H-rich structure. The defect chemistry of YHO is dominated by anionic antisite species (HO and OH), with hydrogen interstitials (Hi) and vacancies (VH) also present in reasonably high concentrations. We show that antisite disorder lowers the band gap relative to the perfectly ordered structure, bringing the magnitude of the gap into closer agreement with experiment. Based on our calculations of defect migration and the positions of defect states relative to the band edges, we link the onset of photochromic behavior to the reaction HO– → VO0 + Hi–, which follows photoexcitation of a HO+ defect. Hi– can subsequently migrate away and be trapped by additional HO+ defects, contributing to the persistence of the reaction, while the resultant oxygen vacancy, VO0, introduces an occupied defect state that leads to optical absorption at visible wavelengths. Our results can explain reported discrepancies between experimental and computational results for YHO, and they allow us to propose specific atomic-scale processes that can lead to photochromism. Understanding these mechanisms is key for unlocking YHO’s application in devices ranging from smart windows and optoelectronics to electrochemical synapses for neural networks.

The Journal of Physical Chemistry CVol. 128(47)
Lawrence Livermore National Laboratory (US), University of California, Santa Barbara (US), Quantum Simulations (United States) (US)
National Science Foundation, U.S. Department of Energy, Semiconductor Research Corporation, China Scholarship Council, Defense Advanced Research Projects Agency, University of California, Santa Barbara, Advanced Research Projects Agency, Materials Research Science and Engineering Center, Harvard University, Division of Materials Research, California NanoSystems Institute, Lawrence Livermore National Laboratory
Openalex Percentile: Top 51%
Advanced Photocatalysis Techniques
0.31
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