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Covalent-bond-enhanced photocatalytic hydrogen evolution of C3N4/CoPx with L-cysteine molecule as bridging ligands

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Abstract Serious interface carrier recombination leads to moderated photocatalytic performance of carbon nitride (C3N4), and the realization of their strongly covalent bonding with co-catalysts can efficiently inhibit this. In this… Click to show full abstract

Abstract Serious interface carrier recombination leads to moderated photocatalytic performance of carbon nitride (C3N4), and the realization of their strongly covalent bonding with co-catalysts can efficiently inhibit this. In this article, C3N4 nanosheets are first functionalized with L-cysteine molecules to form C-SH bonds, and then the photodeposited CoPx NPs are covalently bonded with C3N4 with L-cysteine molecules as bridging ligands, which can efficiently reduce the C3N4/CoPx interface impedance. Their optimal hydrogen evolution rate and apparent quantum efficiency at 420 nm are 4.12 mmolg-1h-1 and 3.74%, respectively, which are 17.2 and 13.9 times that C3N4/CoPx reference without L-cysteine bridging ligands, mainly due to the reduced C3N4/CoPx interface impedance. This work proposes a general solution to inhibit interface carrier recombination in nanocomposites by introduction of bridging ligands.

Keywords: copx; cysteine; bridging ligands; c3n4 copx; hydrogen evolution

Journal Title: Applied Surface Science
Year Published: 2021

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