Citation

BibTex format

@article{Sachs:2025,
author = {Sachs, M and Harnett-Caulfield, L and Davies, B and Sowood, DJC and Moss, B and Kafizas, A and Nelson, J and Walsh, A and Durrant, J},
journal = {Nature Chemistry},
title = {Metal-centred states control carrier lifetimes in transition metal oxide photocatalysts},
year = {2025}
}

RIS format (EndNote, RefMan)

TY  - JOUR
AB - 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.
AU - Sachs,M
AU - Harnett-Caulfield,L
AU - Davies,B
AU - Sowood,DJC
AU - Moss,B
AU - Kafizas,A
AU - Nelson,J
AU - Walsh,A
AU - Durrant,J
PY - 2025///
SN - 1755-4330
TI - Metal-centred states control carrier lifetimes in transition metal oxide photocatalysts
T2 - Nature Chemistry
ER -

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