Journal article
Metal-centred states control carrier lifetimes in transition metal oxide photocatalysts
- Abstract:
- Efficient sunlight-to-energy conversion requires materials that can generate long-lived charge carriers upon illumination. However, the targeted design of semiconductors possessing intrinsically long lifetimes remains a key challenge. Here using a series of transition metal oxides, we establish a link between carrier lifetime and electronic configuration in transition metal-based semiconductors. We identify a subpicosecond relaxation mechanism via metal-centred ligand field states that compromise quantum yields in open d-shell transition metal oxides (for example, Fe2O3, Co3O4, Cr2O3 and NiO), which is more reminiscent of molecular complexes than crystalline semiconductors. We found that materials with spin-forbidden ligand field transitions could partially mitigate this relaxation pathway, explaining why Fe2O3 achieves higher photoelectrochemical activity than other visible light-absorbing transition metal oxides. However, achieving high yields of long-lived charges requires transition metal oxides with d0 or d10 electronic configurations (for example, TiO2 and BiVO4), where ligand field states are absent. These trends translate to transition metal-containing semiconductors beyond oxides, enabling the design of photoabsorbers with better-controlled recombination channels in photovoltaics, photocatalysis and communication devices
- Publication status:
- Published
- Peer review status:
- Peer reviewed
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(Preview, Version of record, pdf, 1.8MB, Terms of use)
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- Publisher copy:
- 10.1038/s41557-025-01868-y
Authors
- Publisher:
- Nature Research
- Journal:
- Nature Chemistry More from this journal
- Volume:
- 17
- Issue:
- 9
- Pages:
- 1348-1355
- Publication date:
- 2025-07-02
- DOI:
- EISSN:
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1755-4349
- ISSN:
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1755-4330
- Language:
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English
- Keywords:
- Pubs id:
-
2343801
- Local pid:
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pubs:2343801
- Source identifiers:
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W4411924579
- Deposit date:
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2025-12-04
- ARK identifier:
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Terms of use
- Copyright date:
- 2025
- Licence:
- CC Attribution (CC BY)
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