Pt nanocluster-Fe single atom pairs dual-regulate charge extraction and interfacial reaction for enhanced photoelectric response.
Ontology highlight
ABSTRACT: Energy level mismatches between semiconductors and cocatalysts often induce carrier recombination, limiting photocatalytic and photoelectrochemical (PEC) efficiency. Here, we integrate Pt nanocluster-Fe single-atom pairs with CuO to regulate both solid-solid and solid-liquid interfaces in PEC systems. Experimental and theoretical analyses reveal that an Ohmic contact at the CuO/Pt interface accelerates electron extraction, while Pt-to-Fe charge transfer enhances oxygen reduction at Fe sites, collectively boosting reaction kinetics. Leveraging this, we construct a PEC biosensor exploiting chelating effect of glyphosate on CuO to impede electron transfer, achieving a detection limit of 0.41 ng/mL. This interface engineering strategy advances cocatalyst design for enhanced energy conversion a
SUBMITTER: Chen Y
PROVIDER: S-EPMC11947233 | biostudies-literature | 2025 Mar
REPOSITORIES: biostudies-literature
ACCESS DATA