4.8 Article

Ultra-thin Two-Dimensional Trimetallic Metal-Organic Framework for Photocatalytic Reduction of CO2

Journal

ACS CATALYSIS
Volume 12, Issue 5, Pages 3238-3248

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acscatal.1c05984

Keywords

photocatalysis; metal-organic framework; carbon dioxide reduction; two-dimensional structure; metal doping

Funding

  1. National Natural Science Foundation of China [22122113]
  2. National Key R&D Program of China [2021YFB4000405]

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In this study, an ultra-thin two-dimensional trimetallic metal-organic framework nanosheet was successfully synthesized and used as a photocatalyst for CO2 reduction. The nanosheet exhibited high catalytic activity and selectivity, and Zr and Cu doping were found to enhance its performance.
Photocatalytic reduction of carbon dioxide (CO2) into high-value chemicals is a very effective way to solve the greenhouse effect, improve the utilization ratio of resources, and cope with the energy crisis. However, the low catalytic activity and poor product selectivity of the catalyst have been largely restricting its large-scale application. Herein, we successfully synthesized an ultra-thin two-dimensional trimetallic metal-organic framework (NiZrCu-BDC) nanosheet as a photocatalyst for CO2 reduction, and the average thickness of NiZrCu-BDC is about 4 nm. The NiZrCu-BDC nanosheet has the ability to reduce CO2 to methanol (41.05 mu mol h(-1) g(-1)) and ethanol (36.62 mu mol h(-1) g(-1)), and the turnover frequency of NiZrCu-BDC is 34 times more than that of NiZr-BDC. Zr and Cu doping enables enrichment of Ni surface charges to promote CO2 chemisorption, and the ultra-thin structure can shorten the electron transport path. Meanwhile, the electron density of Ni catalytical sites in NiZrCu-BDC is enhanced by doping Cu and Zr to facilitate COOH* and CHO formation, which are deemed as key species for CO2 reduction reactions to liquid products. This work provides further insights into the photocatalytic reduction of CO2 based on the multi-metal-organic framework.

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