Direct and Indirect Interfacial Electron Transfer at a Plasmonic p-Cu7S4/CdS Heterojunction

ACS Nano. 2025 Jan 1. doi: 10.1021/acsnano.4c14556. Online ahead of print.

Abstract

Plasmonic semiconductors exhibit significant potential for harvesting near-IR solar energy, although their mechanisms of plasmon-induced hot electron transfer (HET) are poorly understood. We report a transient absorption study of plasmon-induced HET in p-Cu7S4/CdS type II heterojunctions. Near-IR excitation of the p-Cu7S4 plasmon band at ∼1400 nm leads to ultrafast HET into the CdS conduction band with a time constant of <150 fs and a quantum efficiency of ∼0.054%. The injected hot electrons remain in CdS with an amplitude-weighted average lifetime of 1.9 ± 0.5 ns, significantly longer than that in Au/CdS heterostructures, suggesting that plasmonic semiconductors can slow down charge recombination due to the presence of a bandgap. The excited near-IR plasmon does not decay by coupling to the interfacial charge transfer transition, likely due to its energy mismatch. This study provides a detailed mechanistic understanding and possible directions for improving plasmonic HET in plasmonic semiconductor heterojunctions.

Keywords: Cu7S4; heat transfer; hot electron transfer; nanorods; plasmonic semiconductor; type-II heterostructure.