Affiliations 

  • 1 School of Energy and Environment, City University of Hong Kong, Tat Chee Avenue, Kowloon, Hong Kong, China
  • 2 Multidisciplinary Platform of Advanced Engineering, Chemical Engineering Discipline, School of Engineering, Monash University, Jalan Lagoon Selatan, Bandar Sunway, 47500, Selangor, Malaysia
  • 3 Centre for Translational Atomaterials, Faculty of Science Engineering and Technology, Swinburne University of Technology, John Street, Hawthorn, VIC, 3122, Australia
  • 4 Particles and Catalysis Research Group, School of Chemical Engineering, The University of New South Wales, Sydney, NSW, 2052, Australia
  • 5 Department of Chemical Engineering, University College London, Torrington Place, London, WC1E 7JE, UK
Angew Chem Int Ed Engl, 2021 Apr 06;60(15):8455-8459.
PMID: 33368920 DOI: 10.1002/anie.202015735

Abstract

Improving the stability of cuprous oxide (Cu2 O) is imperative to its practical applications in artificial photosynthesis. In this work, Cu2 O nanowires are encapsulated by metal-organic frameworks (MOFs) of Cu3 (BTC)2 (BTC=1,3,5-benzene tricarboxylate) using a surfactant-free method. Such MOFs not only suppress the water vapor-induced corrosion of Cu2 O but also facilitate charge separation and CO2 uptake, thus resulting in a nanocomposite representing 1.9 times improved activity and stability for selective photocatalytic CO2 reduction into CH4 under mild reaction conditions. Furthermore, direct transfer of photogenerated electrons from the conduction band of Cu2 O to the LUMO level of non-excited Cu3 (BTC)2 has been evidenced by time-resolved photoluminescence. This work proposes an effective strategy for CO2 conversion by a synergy of charge separation and CO2 adsorption, leading to the enhanced photocatalytic reaction when MOFs are integrated with metal oxide photocatalyst.

* Title and MeSH Headings from MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.