Round-the-Clock Photocatalysts in the Post-Irradiation Dark Period: From Light Charging to “Memory” Dark Discharging Toward Hydrogen Production

Abstract The intermittent nature of solar irradiance is a critical constraint for the realization of continuous photocatalytic hydrogen evolution, thus urging the development of more powerful systems persistently active after illumination. This limitation is bypassed in round-the-clock photocatalytic architectures, which incorporate advanced charge storage to de-correlate photon absorption and catalytic turnover time scales. The strategies involve defect-mediated trap states, multi-electron redox processes, radical-dependent stabilization, and an interfacial charge pool in Faradaic junctions to work together, leading to extended hydrogen evolution reaction (HER) in the dark. Long afterglow phosphorescent materials (e.g., Sr 2 MgSi 2 O 7 :Eu 2+ , Dy 3+ ) incorporated in heterojunction architectures with type II or Z-scheme band alignments can also promote fast charge separation for energy storage and subsequently enable controlled release after light quenching by the phosphorescent emission. Advances in band-structure engineering, plasmonic coupling, and redox-active interfacial design result in systems with extraordinary stability and catalytic activity under natural day–night cycles. These stable photocatalytic systems offer a fundamentally new strategy for efficient and environmentally benign sunlight-driven fuel production, meeting both performance and sustainability challenges to renewable energy technologies. Graphical Abstract This work presents an emerging strategy for round-the-clock hydrogen evolution by integrating long afterglow phosphorescent materials into heterojunction photocatalysts. The system enables sustained HER even in darkness by utilizing defect engineering, Faradaic charge storage, and phosphorescence-driven delayed charge release. This approach offers a breakthrough in decoupling light absorption from catalytic activity, addressing solar intermittency, and paving the way for stable, efficient, and sustainable solar-to-hydrogen energy conversion.

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Publication Details

Journal
Transactions of Tianjin University
Published
2025-11-05
DOI
https://doi.org/10.1007/s12209-025-00448-y
Citations
2
Primary Topic
Advanced Photocatalysis Techniques
Type
article
Field-Weighted Citation Impact
0.73
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article

Round-the-Clock Photocatalysts in the Post-Irradiation Dark Period: From Light Charging to “Memory” Dark Discharging Toward Hydrogen Production

Pankaj Raizada, Archana Singh, Krishna Kumar Yadav, Duc Anh Dinh et al.
2 citations
Transactions of Tianjin University
Advanced Photocatalysis Techniques
0.73
article

Round-the-Clock Photocatalysts in the Post-Irradiation Dark Period: From Light Charging to “Memory” Dark Discharging Toward Hydrogen Production

Pankaj Raizada, Archana Singh, Krishna Kumar Yadav, Duc Anh Dinh, Van‐Huy Nguyen, Xuan‐Cuong Luu, Maha Awjan Alreshidi, Balvinder Kaur
article en
2 citations

Abstract

Abstract The intermittent nature of solar irradiance is a critical constraint for the realization of continuous photocatalytic hydrogen evolution, thus urging the development of more powerful systems persistently active after illumination. This limitation is bypassed in round-the-clock photocatalytic architectures, which incorporate advanced charge storage to de-correlate photon absorption and catalytic turnover time scales. The strategies involve defect-mediated trap states, multi-electron redox processes, radical-dependent stabilization, and an interfacial charge pool in Faradaic junctions to work together, leading to extended hydrogen evolution reaction (HER) in the dark. Long afterglow phosphorescent materials (e.g., Sr 2 MgSi 2 O 7 :Eu 2+ , Dy 3+ ) incorporated in heterojunction architectures with type II or Z-scheme band alignments can also promote fast charge separation for energy storage and subsequently enable controlled release after light quenching by the phosphorescent emission. Advances in band-structure engineering, plasmonic coupling, and redox-active interfacial design result in systems with extraordinary stability and catalytic activity under natural day–night cycles. These stable photocatalytic systems offer a fundamentally new strategy for efficient and environmentally benign sunlight-driven fuel production, meeting both performance and sustainability challenges to renewable energy technologies. Graphical Abstract This work presents an emerging strategy for round-the-clock hydrogen evolution by integrating long afterglow phosphorescent materials into heterojunction photocatalysts. The system enables sustained HER even in darkness by utilizing defect engineering, Faradaic charge storage, and phosphorescence-driven delayed charge release. This approach offers a breakthrough in decoupling light absorption from catalytic activity, addressing solar intermittency, and paving the way for stable, efficient, and sustainable solar-to-hydrogen energy conversion.

Transactions of Tianjin UniversityVol. 31(6)
Ton Duc Thang University (VN), Thi Qar University (IQ), Chettinad Academy of Research and Education (IN), Trường ĐH Nguyễn Tất Thành (VN), University of Ha'il (SA), Shoolini University (IN), Saveetha University (IN)
Openalex Percentile: Top 27%
Advanced Photocatalysis Techniques
0.73
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