4.6 Article

Ultralow Rh Bimetallic Catalysts with High Catalytic Activity for the Hydrogenation of N-Ethylcarbazole

期刊

ACS SUSTAINABLE CHEMISTRY & ENGINEERING
卷 9, 期 15, 页码 5260-5267

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acssuschemeng.0c08270

关键词

Hydrogen storage; Bimetallic catalyst; Low cost; Hydrogenation; N-Ethylcarbazole

资金

  1. NSFC [22078354, 21776295]
  2. Youth Innovation Promotion Association, Chinese Academy of Sciences [2017355]
  3. Shanghai Functional Platform for Innovation Low Carbon Technology

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This study successfully developed a gamma-Al2O3-supported Rh-Ni bimetallic catalyst with only 0.1 wt % Rh, which exhibited excellent catalytic performance in the hydrogenation of NEC. Various characterizations confirmed that factors such as electron transfer between the bimetallic Rh-Ni nanoparticles structure, promotion of smaller Ni nanoparticles formation by Rh, and increased reducibility of loaded NiO contributed to the catalyst's outstanding activity. The research sheds light on a promising strategy for developing low-cost hydrogenation catalysts for LOHCs such as NEC.
Liquid organic hydrogen carrier (LOHC) has attracted a great deal of attention in recent years for its use in hydrogen storage. Supported Rh catalyst has been widely used in the hydrogenation reaction of the N-ethylcarbazole (NEC), one of the most promising LOHCs. However, the high Rh content is challenging because of its high cost. Herein, we successfully developed a gamma-Al2O3-supported Rh-Ni bimetallic catalyst with only 0.1 wt % Rh, which showed excellent catalytic performance in the hydrogenation of NEC with a high conversion of 99% and high selectivity of 98% in 2 h. Various characterizations such as high-angle annual dark-field scanning transmission electron microscopy images with phase mappings, X-ray photoelectron spectroscopy, H-2 temperature-programmed desorption, and in situ diffuse reflectance infrared Fourier transform spectroscopy confirmed that the excellent catalytic performance was ascribed to the following factors: (i) electron transfer between the bimetallic Rh-Ni nanoparticles (NPs) structure on the catalyst support; (ii) formation of smaller Ni NPs on the bimetallic Rh-Ni catalyst, which was promoted by Rh; (iii) increased reducibility of the loaded NiO during the catalyst preparation process as a result of the highly dispersed single Rh atom. Thus, the prepared catalyst with ultralow Rh content in this work still has outstanding catalytic activity and sheds light on a fruitful strategy for developing low-cost hydrogenation catalysts of NEC for hydrogen storage.

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