Transition-Metal-Doped Perovskite Oxide Materials: A Key Pathway for Photocatalytic Water Splitting Under Visible-Light Irradiation

The global transition from fossil fuels to renewable energy demands innovative hydrogen production technologies, with photocatalytic water splitting emerging as a sustainable and eco-friendly solution. In this process, photocatalysts harness sunlight and split water into hydrogen and oxygen, offering a clean and efficient means of solar energy conversion. Among different photocatalyst materials, transition-metal-doped perovskite oxides (TMPOs) have attracted attention for their visible-light activity, structural flexibility, and stability. Compared with other oxide semiconductors, TMPOs can host a wide variety of dopants at both the A- and B-sites, which makes it possible to tune the band structure while still keeping the perovskite lattice intact. This combination of resilience and tunability has led to benchmark results in one-step and Z-scheme water splitting, making TMPO a key material platform in photocatalysis research. They are also useful as model systems for studying defect chemistry, carrier dynamics, and dopant interactions, knowledge that can be applied to other oxide photocatalysts. In this review, we highlight the evolution of TMPOs from bandgap-tuned materials to nanostructured platforms. We propose that their future lies in precise defect control, scalable synthesis, and performance validation under real-world conditions. By positioning transition-metal doping as a core design principle, this work outlines a roadmap toward practical applications of TMPO-based systems in catalytic energy technologies.

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Publication Details

Journal
ACS Catalysis
Published
2025-12-19
DOI
https://doi.org/10.1021/acscatal.5c05792
Citations
2
Primary Topic
Advanced Photocatalysis Techniques
Type
article
Field-Weighted Citation Impact
0.73
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article

Transition-Metal-Doped Perovskite Oxide Materials: A Key Pathway for Photocatalytic Water Splitting Under Visible-Light Irradiation

Zhenhua Pan, Han Fu, Daisuke Ioka
2 citations
ACS Catalysis
Advanced Photocatalysis Techniques
0.73
article

Transition-Metal-Doped Perovskite Oxide Materials: A Key Pathway for Photocatalytic Water Splitting Under Visible-Light Irradiation

Zhenhua Pan, Han Fu, Daisuke Ioka
article en
2 citations

Abstract

The global transition from fossil fuels to renewable energy demands innovative hydrogen production technologies, with photocatalytic water splitting emerging as a sustainable and eco-friendly solution. In this process, photocatalysts harness sunlight and split water into hydrogen and oxygen, offering a clean and efficient means of solar energy conversion. Among different photocatalyst materials, transition-metal-doped perovskite oxides (TMPOs) have attracted attention for their visible-light activity, structural flexibility, and stability. Compared with other oxide semiconductors, TMPOs can host a wide variety of dopants at both the A- and B-sites, which makes it possible to tune the band structure while still keeping the perovskite lattice intact. This combination of resilience and tunability has led to benchmark results in one-step and Z-scheme water splitting, making TMPO a key material platform in photocatalysis research. They are also useful as model systems for studying defect chemistry, carrier dynamics, and dopant interactions, knowledge that can be applied to other oxide photocatalysts. In this review, we highlight the evolution of TMPOs from bandgap-tuned materials to nanostructured platforms. We propose that their future lies in precise defect control, scalable synthesis, and performance validation under real-world conditions. By positioning transition-metal doping as a core design principle, this work outlines a roadmap toward practical applications of TMPO-based systems in catalytic energy technologies.

ACS CatalysisVol. 16(1)
University of Hyogo (JP), State Key Laboratory of Building Safety and Built Environment (CN), Arizona State University (US), Graduate School USA (US)
Openalex Percentile: Top 26%
Advanced Photocatalysis Techniques
0.73
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