Significant Acceleration of Photocatalytic CO2 Reduction at the Gas‐Liquid Interface of Microdroplets**

Author:

Ge Qiuyue1,Liu Yangyang1ORCID,Li Kejian1,Xie Lifang1,Ruan Xuejun1,Wang Wei1,Wang Longqian1,Wang Tao1,You Wenbo1,Zhang Liwu123ORCID

Affiliation:

1. Department of Environmental Science and Engineering Fudan University Shanghai 200433 P. R. China

2. Shanghai Key Laboratory of Atmospheric Particle Pollution and Prevention Fudan University Shanghai 200433 P. R. China

3. Shanghai Institute of Pollution Control and Ecological Security Shanghai 200092 P. R. China

Abstract

AbstractSolar‐driven CO2 reduction reaction (CO2RR) is largely constrained by the sluggish mass transfer and fast combination of photogenerated charge carriers. Herein, we find that the photocatalytic CO2RR efficiency at the abundant gas‐liquid interface provided by microdroplets is two orders of magnitude higher than that of the corresponding bulk phase reaction. Even in the absence of sacrificial agents, the production rates of HCOOH over WO3 ⋅ 0.33H2O mediated by microdroplets reaches 2536 μmol h−1 g−1 (vs. 13 μmol h−1 g−1 in bulk phase), which is significantly superior to the previously reported photocatalytic CO2RR in bulk phase reaction condition. Beyond the efficient delivery of CO2 to photocatalyst surfaces within microdroplets, we reveal that the strong electric field at the gas‐liquid interface of microdroplets essentially promotes the separation of photogenerated electron‐hole pairs. This study provides a deep understanding of ultrafast reaction kinetics promoted by the gas‐liquid interface of microdroplets and a novel way of addressing the low efficiency of photocatalytic CO2 reduction to fuel.

Funder

National Natural Science Foundation of China

Natural Science Foundation of Shanghai

Publisher

Wiley

Subject

General Chemistry,Catalysis

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