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author:

Xu, Y. (Xu, Y..) [1] | An, Z. (An, Z..) [2] | Yu, X. (Yu, X..) [3] | Yao, J. (Yao, J..) [4] | Lv, Q. (Lv, Q..) [5] | Yang, H. (Yang, H..) [6] | Lv, Z. (Lv, Z..) [7] | Guo, H. (Guo, H..) [8] | Jiang, Q. (Jiang, Q..) [9] | Liu, W. (Liu, W..) [10] | Wu, L. (Wu, L..) [11] (Scholars:吴立志) | Tan, L. (Tan, L..) [12] (Scholars:谭理) | Dai, Y. (Dai, Y..) [13] | Tang, Y. (Tang, Y..) [14] (Scholars:汤禹)

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Scopus

Abstract:

Strong metal-support interaction (SMSI) is a crucial factor that determines the structure and performance of a supported metal catalyst. Herein, the SMSI effect of Rh nanoparticle catalyst supported on h-BN is investigated in the dry reforming of methane (DRM) reactions with different CO2/CH4 ratios. The catalyst characterization results demonstrate that the SMSI effect allows the Rh nanoparticles to be encapsulated by BOx overlayers under DRM reaction conditions (CO2/CH4 = 1/1), which prevents the interaction between the reactants and metal centers for causing rapid deactivation. By increasing the partial pressure of CO2 (CO2/CH4 = 3/1), Rh/BN exhibits significantly enhanced activity and long-term stability in the DRM reaction. CO2 or H2O in the reactive atmosphere can effectively etch the BOx overlayers for steadily exposing the active Rh-BN interface sites, as evidenced by the characterization. This observation extends the understanding of the SMSI effect at the interfaces between metal and non-oxide support. © 2023 Elsevier Inc.

Keyword:

Boron nitride Carbon dioxide Dry reforming of methane Rhodium Strong metal-support interaction

Community:

  • [ 1 ] [Xu Y.]Institute of Molecule Catalysis and In-Situ/Operando Studies, College of Chemistry, Fuzhou University, Fuzhou, 350108, China
  • [ 2 ] [An Z.]Institute of Molecule Catalysis and In-Situ/Operando Studies, College of Chemistry, Fuzhou University, Fuzhou, 350108, China
  • [ 3 ] [Yu X.]State Key Laboratory of Coal Conversion, Institute of Coal Chemistry, Chinese-Academy of Sciences, Taiyuan, 030001, China
  • [ 4 ] [Yu X.]National Energy Center for Coal to Liquids, Synfuels China Co., Ltd., Beijing, 101400, China
  • [ 5 ] [Yu X.]SynCat@Beijing, Synfuels China Technology Co. Ltd., Beijing, 101407, China
  • [ 6 ] [Yao J.]Institute of Molecule Catalysis and In-Situ/Operando Studies, College of Chemistry, Fuzhou University, Fuzhou, 350108, China
  • [ 7 ] [Lv Q.]Institute of Molecule Catalysis and In-Situ/Operando Studies, College of Chemistry, Fuzhou University, Fuzhou, 350108, China
  • [ 8 ] [Yang H.]Institute of Molecule Catalysis and In-Situ/Operando Studies, College of Chemistry, Fuzhou University, Fuzhou, 350108, China
  • [ 9 ] [Lv Z.]National Energy Center for Coal to Liquids, Synfuels China Co., Ltd., Beijing, 101400, China
  • [ 10 ] [Guo H.]National Energy Center for Coal to Liquids, Synfuels China Co., Ltd., Beijing, 101400, China
  • [ 11 ] [Jiang Q.]Dalian Institute of Chemical Physics, Chinese Academy of Sciences, Dalian, 116023, China
  • [ 12 ] [Liu W.]Dalian Institute of Chemical Physics, Chinese Academy of Sciences, Dalian, 116023, China
  • [ 13 ] [Wu L.]Institute of Molecule Catalysis and In-Situ/Operando Studies, College of Chemistry, Fuzhou University, Fuzhou, 350108, China
  • [ 14 ] [Tan L.]Institute of Molecule Catalysis and In-Situ/Operando Studies, College of Chemistry, Fuzhou University, Fuzhou, 350108, China
  • [ 15 ] [Dai Y.]Institute of Advanced Synthesis, School of Chemistry and Molecular Engineering, Nanjing Tech University, Nanjing, 211816, China
  • [ 16 ] [Tang Y.]Institute of Molecule Catalysis and In-Situ/Operando Studies, College of Chemistry, Fuzhou University, Fuzhou, 350108, China

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Source :

Journal of Catalysis

ISSN: 0021-9517

Year: 2023

Volume: 427

6 . 5

JCR@2023

6 . 5 0 0

JCR@2023

ESI HC Threshold:39

JCR Journal Grade:1

CAS Journal Grade:2

Cited Count:

WoS CC Cited Count:

SCOPUS Cited Count: 12

ESI Highly Cited Papers on the List: 0 Unfold All

WanFang Cited Count:

Chinese Cited Count:

30 Days PV: 4

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