Back to Search Start Over

Screening of 29 transition metal doped Ni loaded BN catalyzed dry reforming of methane reaction and the mechanism study of anti-carbon deposition.

Authors :
Zhao, Weiling
Meng, Yue
Huang, Zhiling
Xie, Bo
Ni, Zheming
Xia, Shengjie
Source :
Molecular Catalysis. Nov2024, Vol. 568, pN.PAG-N.PAG. 1p.
Publication Year :
2024

Abstract

• Ni loaded BN (Ni/BN) and transition metal doped Ni loaded BN (TM Ni/BN) were constructed. • 29 kinds of TM were screened for the effects on DRM catalytic performance and mechanism. • TM atoms have electron-unfilled d orbitals, which can promote the interaction between CO 2 and TM Ni/BN. • TM Ni/BN (TM = V, Mo, Ru) were screened to further catalyzing the whole DRM reactions. • Carbon deposition mechanism was further studied, and V Ni/BN performed the best. In the context of carbon peaking and carbon neutrality goals, dry reforming of methane (DRM) is attracting attention for its ability to convert greenhouse gases into synthesis gas with economic and environmental benefits. However, the commercialization of DRM has been limited by catalyst sintering and carbon deposition. In this work, Ni loaded BN (Ni/BN) and transition metal doped Ni loaded BN (TM Ni/BN) structures were constructed by density functional theory (DFT) in this work. 29 kinds of TM were screened for the effects on DRM catalytic performance and mechanism. It shows that TM have electron-unfilled d orbitals, which can promote the interaction between CO 2 and TM Ni/BN. After stability analysis of TM Ni/BN and adsorption calculation of CO 2 and CH 4 , three structures of TM Ni/BN (TM = V, Mo, Ru) were screened to further catalyze the DRM reaction. The carbon deposition problem was analyzed from the reaction mechanistic point of view. And it was further determined that the V Ni/BN structure performed the best. In summary, Ni and TM bimetallic catalysts were designed, and TM was screened comprehensively to provide some theoretical references for exploring the DRM reaction mechanism and realizing the goal of reducing carbon and increasing the source. [Display omitted] [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
24688231
Volume :
568
Database :
Academic Search Index
Journal :
Molecular Catalysis
Publication Type :
Academic Journal
Accession number :
179557764
Full Text :
https://doi.org/10.1016/j.mcat.2024.114497