Identifying the Metallic State of Rh Catalyst on Boron Nitride during Partial Oxidation of Methane by Using the Product Molecule as the Infrared Probe

• Published in: Catalysts Vol. 12; no. 10; p. 1146
• Main Authors: Yao, Jikang, Xu, Yuanjie, Yang, Hua, Ren, Zhuangzhuang, Wu, Lizhi, Tang, Yu
• Format: Journal Article
• Language: English
• Published: Basel MDPI AG 01.10.2022
• Subjects: Boron; Boron nitride; Carbon; Catalysts; Chemical reactions; Drift; DRIFTS; Fourier transforms; High temperature; Infrared instruments; Infrared spectroscopy; Methane; Nanoparticles; Oxidation; partial oxidation of methane; Photoelectrons; Pore size; Raman spectroscopy; Reforming; Rhodium; Spectrum analysis; syngas; Synthesis gas; Transition metals; X ray photoelectron spectroscopy
• ISSN: 2073-4344; 2073-4344
• DOI: 10.3390/catal12101146

The partial oxidation of methane (POM) is a promising method for converting methane to syngas. The transition metal supported on boron nitride (BN) has recently been studied as part of a catalog of emerging catalysts. However, the chemical state of the metal supported on BN during methane reforming is still in debate. In this work, we report a rhodium catalyst on boron nitride (Rh/BN) for the POM, with exceptional activity and long-term stability at 600 °C for 230 h. The Rh/BN catalyst was investigated by X-ray diffraction, X-ray photoelectron spectroscopy, Raman spectroscopy, transmission electron microscopy, and diffuse reflectance infrared Fourier transformed spectroscopy (DRIFTS). As revealed by in situ DRIFTS, the infrared band (2020 cm−1) of the product molecule, CO, adsorbed on the Rh, as the probe confirms the metallic state of Rh during the POM reaction. In addition, the results of in situ DRIFTS indicate that the reactive gaseous environment would react with the catalyst to form B-OH and B-H, which synergistically boost the POM activity.