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.
Authors
- Pankaj Raizada (ORCID: https://orcid.org/0000-0003-1758-7461)
- Archana Singh (ORCID: https://orcid.org/0000-0002-0203-084X)
- Krishna Kumar Yadav (ORCID: https://orcid.org/0000-0002-4228-2726)
- Duc Anh Dinh (ORCID: https://orcid.org/0000-0002-3762-5245)
- Van‐Huy Nguyen (ORCID: https://orcid.org/0000-0001-8556-1955)
- Xuan‐Cuong Luu
- Maha Awjan Alreshidi (ORCID: https://orcid.org/0009-0003-9232-1839)
- Balvinder Kaur (ORCID: https://orcid.org/0000-0002-3078-1106)
Institutions
- 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)
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