Observational analysis achieves a hydrogen evolution rate of 14.2 mmol·g−1 in photocatalysts, indicating the role of plasmon-induced interfacial electric fields.
The design of photocatalysts capable of generating localized surface plasmon resonance (LSPR) effects represents a promising strategy for enhancing photocatalytic activity. However, the mechanistic role of plasmonic nanoparticles-induced interfacial electric fields in driving photocatalytic processes remains poorly understood. To produce a Schottky junction, varying amounts of Au nanoparticles widely utilized to broaden the light absorption were loaded onto ultrathin carbon nitride sheets (Au/UCN). The Au/UCN-20 Schottky junction exhibits exceptional photocatalytic activity, achieving a hydrogen evolution rate (14.2 mmol·g−1 over a 4 h period) while maintaining robust stability through five consecutive photocatalytic cycles. The LSPR activity of Au nanoparticles are responsible for the broadened light absorption spectrum of Au/UCN nanocomposites. The interfacial electric field generated at the Au /UCN heterojunction is proposed to enhance charge-transfer efficiency through Schottky barrier penetration of photocarriers, mediated by electric field-driven carrier migration, according to surface potential and finite-difference time-domain (FDTD). These findings uncover a previously obscured photocatalytic mechanism driven by LSPR-induced interfacial electric fields, pioneering a quantum-dot-directed strategy to precisely engineer charge dynamics in advanced photocatalysts via targeted manipulation of nanoscale electric field effects.
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Yu et al. (2025) studied this question.
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