Pt1Bi Single-Atom Alloy for a Coupled Photocatalytic CO2 Reduction and Aryl Olefin Oxidation System

No Thumbnail Available

Access rights

embargoedAccess

URL

Journal Title

Journal ISSN

Volume Title

A1 Alkuperäisartikkeli tieteellisessä aikakauslehdessä
This publication is imported from Aalto University research portal.
View publication in the Research portal (opens in new window)
Embargo ends: 2025-10-11

Other link related to publication (opens in new window)

Date

2024-11-01

Major/Subject

Mcode

Degree programme

Language

en

Pages

11

Series

ACS Catalysis, Volume 14, issue 21, pp. 15935-15945

Abstract

Solar-driven CO2 reduction provides a promising strategy to produce fuels and value-added chemicals, while the efficiency and economy of the system are often limited by the coupled oxidation half-reaction. Here, we develop a synergistic system coupling photocatalytic CO2 reduction to CO and aryl olefin oxidation to aryl ketone with a high-efficiency and improved atom economy over a TiOx-supported Pt1Bi single-atom alloy photocatalyst. Combined experimental and computational studies elucidate the spontaneous electron transfer from Bi to Pt in the dark, which is enhanced under light radiation. Density functional theory calculations reveal that the oxidation process of aryl olefin favors the protonation of CO2 and the dissociation of COOH* to CO*, and Bi facilitates CO2 protonation and CO desorption on the Pt site. The generation rate of CO reaches 391 μmol g-1 h-1 with an electron selectivity of 91.4% using alpha-methylstyrene as the substrate, and the yield of the acetophenone product is 449 μmol g-1 h-1 with a 95.5% selectivity.

Description

Publisher Copyright: © 2024 American Chemical Society.

Keywords

aryl olefin, bimetallic catalyst, photocatalytic CO reduction, selective oxidation, single-atom alloy

Other note

Citation

Bai, P, Zhao, Y & Li, Y 2024, ' Pt 1 Bi Single-Atom Alloy for a Coupled Photocatalytic CO 2 Reduction and Aryl Olefin Oxidation System ', ACS Catalysis, vol. 14, no. 21, pp. 15935-15945 . https://doi.org/10.1021/acscatal.4c02868