Abstract
Photoelectrochemical cells face fundamental performance-stability trade-offs that conventional synthesis approaches cannot overcome. This perspective demonstrates how physical vapor deposition delivers orders of magnitude higher energies (103–105meV/atom) compared to chemical-based methods (∼25–60 meV/atom), enabling precise stoichiometric and structural control in multinary metal-oxide photoelectrodes. However, optimal crystallization requires high-temperature postprocessing exceeding substrate’s limits. Rapid-photonic-annealing achieves heating-rates of 102–107versus ∼0.01–1 K/s for conventional conduction/convection heating, creating thermal-nonequilibrium conditions that enable high-temperature crystallization while preserving substrate integrity with dramatically reduced energy consumption and enhanced processing versatility. This synergistic combination of energetic deposition with ultrafast annealing produces superior films with reduced grain-boundary density, minimized defects, and enhanced crystallinity. Case-studies of metal-oxides demonstrate enhanced photoelectrochemical stability and performance compared to conventional processing routes. Proof-of-concept SnWO4validation achieves phase-pure crystallization within several milliseconds─six-orders-of-magnitude faster than furnace annealing. This framework represents a paradigm-shift, simultaneously addressing efficiency, stability, and scalability requirements for practical photoelectrochemical systems.
| Original language | English |
|---|---|
| Pages (from-to) | 17363-17379 |
| Number of pages | 17 |
| Journal | Journal of Physical Chemistry C |
| Volume | 129 |
| Issue number | 39 |
| DOIs | |
| State | Published - 2 Oct 2025 |
Bibliographical note
Publisher Copyright:© 2025 American Chemical Society
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This output contributes to the following UN Sustainable Development Goals (SDGs)
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SDG 7 Affordable and Clean Energy
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