Engineering Lewis‐Acid Defects on ZnO Quantum Dots by Trace Transition‐Metal Single Atoms for High Glycerol‐to‐Glycerol Carbonate Conversion

Author:

Butburee Teera123ORCID,Prasert Ampawan1ORCID,Rungtaweevoranit Bunyarat1ORCID,Khemthong Pongtanawat1ORCID,Mano Poobodin1ORCID,Youngjan Saran1ORCID,Phanthasri Jakkapop1ORCID,Namuangruk Supawadee1ORCID,Faungnawakij Kajornsak1ORCID,Zhang Lijuan2ORCID,Jin Ping34ORCID,Liu Huifang3ORCID,Wang Feng3ORCID

Affiliation:

1. National Nanotechnology Center (NANOTEC) National Science and Technology Development Agency (NSTDA) 111 Thailand Science Park Pathum Thani 12120 Thailand

2. Shanghai Synchrotron Radiation Facility (SSRF) Shanghai Advanced Research Institute (SARI) Chinese Academy of Sciences (CAS) 239 Zhangheng Rd., New Pudong District Shanghai 201204 P. R. China

3. State Key Laboratory of Catalysis (SKLC) Dalian National Laboratory for Clean Energy (DNL) Dalian Institute of Chemical Physics (DICP) Chinese Academy of Sciences (CAS) 457 Zhongshan Road Dalian 116023 P. R. China

4. University of Chinese Academy of Sciences (UCAS) Beijing 100049 P. R. China

Abstract

AbstractEfficient conversion of biomass wastes into valuable chemicals has been regarded as a sustainable approach for green and circular economy. Herein, a highly efficient catalytic conversion of glycerol (Gly) into glycerol carbonate (GlyC) by carbonylation with the commercially available urea is presented using low‐cost transition metal single atoms supported on zinc oxide quantum dots (M1‐ZnO QDs) as a catalyst without using any solvent. A facile one‐step wet chemical synthesis allows various types of metal single atoms to simultaneously dope and introduce Lewis‐acid defects in the ZnO QD structure. It is found that doping with a trace amount of isolated metal atoms greatly boosts the catalytic activity with Gly conversion of 90.7%, GlyC selectivity of 100.0%, and GlyC yield of 90.6%. Congruential results from both Density Functional Theory (DFT) and in situ Diffuse Reflectance Infrared Fourier Transform Spectroscopy (in situ DRIFTS) studies reveal that the superior catalytic performance can be attributed to the enriched Lewis acid sites that endow optimal adsorption, formation of the intermediate for coupling between urea and Gly, and desorption of GlyC. Moreover, the tiny size of ZnO QDs efficiently promotes the accessibility of these active sites to the reactants.

Funder

National Research Council of Thailand

Publisher

Wiley

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