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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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Publisher copy:
10.1038/s41557-025-01868-y

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Role:
Author
ORCID:
0000-0001-9775-9336
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Role:
Author
ORCID:
0000-0002-6945-0945
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Role:
Author
ORCID:
0000-0001-5334-6855
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Role:
Author
ORCID:
0000-0001-7122-2231


Publisher:
Nature Research
Journal:
Nature Chemistry More from this journal
Volume:
17
Issue:
9
Pages:
1348-1355
Publication date:
2025-07-02
DOI:
EISSN:
1755-4349
ISSN:
1755-4330


Language:
English
Keywords:
Pubs id:
2343801
Local pid:
pubs:2343801
Source identifiers:
W4411924579
Deposit date:
2025-12-04
ARK identifier:
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