Direct Catalytic Oxidation of Low-Concentration Methane to Methanol in One Step on Ni-Promoted BiOCl Catalysts

Chen Zhu; Ge Guo; Wenzhi Li; Mingwei Wu; Yihang Jiang; Wenjian Wu; Hao Zhang

doi:10.1021/acsomega.2c08039

Direct Catalytic Oxidation of Low-Concentration Methane to Methanol in One Step on Ni-Promoted BiOCl Catalysts

ACS Omega. 2023 Mar 16;8(12):11220-11232. doi: 10.1021/acsomega.2c08039. eCollection 2023 Mar 28.

Authors

Chen Zhu¹, Ge Guo¹, Wenzhi Li^{1

2}, Mingwei Wu¹, Yihang Jiang¹, Wenjian Wu¹, Hao Zhang¹

Affiliations

¹ Laboratory of Basic Research in Biomass Conversion and Utilization, Department of Thermal Science and Energy Engineering, University of Science and Technology of China, Hefei 230026, China.
² Institute of Energy, Hefei Comprehensive National Science Center, Hefei 230031, China.

Abstract

The direct oxidation of low-concentration methane (CH₄) to methanol (CH₃OH) is often regarded as the "holy grail". However, it still is very difficult and challenging to oxidize methane to methanol in one step. In this work, we present a new approach to directly oxidize CH₄ to generate CH₃OH in one step by doping non-noble metal Ni sites on bismuth oxychloride (BiOCl) equipped with high oxygen vacancies. Thereinto, the conversion rate of CH₃OH can reach 39.07 μmol/(g_cat·h) under 420 °C and flow conditions on the basis of O₂ and H₂O. The crystal morphology structure, physicochemical properties, metal dispersion, and surface adsorption capacity of Ni-BiOCl were explored, and the positive effect on the oxygen vacancy of the catalyst was proved, thus improving the catalytic performance. Furthermore, in situ diffuse reflectance infrared Fourier transform spectroscopy (DRIFTS) was also performed to study the surface adsorption and reaction process of methane to methanol in one step. Results demonstrate that the key to keep good activity lies in the oxygen vacancies of unsaturated Bi atoms, which can adsorb and active CH₄ and to produce methyl groups and adsorbing hydroxyl groups in methane oxidation process. This study broadens the application of oxygen-deficient catalysts in the catalytic conversion of CH₄ to CH₃OH in one step, which provides a new perspective on the role of oxygen vacancies in improving the catalytic performance of methane oxidation.