Novel Insights on the Metal-Support Interactions of Pd/ZrO2 Catalysts on CH4 Oxidation

被引:10
|
作者
Li, Junhua [1 ]
Li, Qi [1 ]
Wang, Ya [2 ]
Si, Wenzhe [1 ]
Peng, Yue [1 ]
机构
[1] Tsinghua Univ, Sch Environm, State Key Joint Lab Environm Simulat & Pollut Cont, Beijing 100084, Peoples R China
[2] Univ Sci & Technol Beijing, Sch Energy & Environm Engn, Beijing 100083, Peoples R China
基金
北京市自然科学基金; 中国国家自然科学基金;
关键词
CH4; oxidation; metal-support interaction; electron transfer; Pd particle morphology; reaction mechanism; METHANE COMBUSTION; ACTIVE CATALYST; PARTICLE-SIZE; PD CATALYSTS; SPECTROSCOPY; ADSORPTION; MORPHOLOGY; OXIDES; OXYGEN; HYDRODEOXYGENATION;
D O I
10.1021/acsami.2c18716
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
With the environmental harm of unburnt CH4 in natural gas vehicle exhaust, oxidizing CH4 to CO2 over catalysts at low temperatures becomes an exigent issue. Supported Pd catalysts possess higher CH4 activity than other noble metal catalysts. A series of Pd/ZrO2 catalysts were synthesized to research the potential relationship among Pd particle morphology, electron transfer, CH4 oxidation mechanism, and catalytic activity. Characterizations show that the ratio of PdOx facets to edge/corner sites on four catalysts increases in the order of PZ85 approximate to PZ40 < PZ55 < PZ70 because of the difference in content of surface -OH groups, and this order turns out to be the same as that of electron transfer intensity, revealing the degree of metal-support interactions. This kind of metal-support interaction in PZ70 can be helpful to accelerate CH4 combustion via promoting the break of the C-H bond and dissociation of CO3* according to density functional theory studies. T90 of the PZ70 catalyst with optimum catalytic activity reaches 331 degrees C.
引用
收藏
页码:7959 / 7968
页数:10
相关论文
共 50 条
  • [1] Metal-support interactions in Fe/ZrO2 catalysts for hydrogenation of CO
    Chen, KD
    Fan, YN
    Yan, QJ
    [J]. JOURNAL OF CATALYSIS, 1997, 167 (02) : 573 - 575
  • [2] Oxidation of CH4 and CO2 reforming of CH4 over Rh/ZrO2 catalysts with different metal dispersions
    Ito, S
    Nagashima, K
    Araki, R
    Yarimizu, T
    Kameoka, S
    Kunimori, K
    [J]. NIPPON KAGAKU KAISHI, 2000, (08) : 561 - 566
  • [4] The role of metal-support interactions in CO2 reforming of CH4
    Bradford, MCJ
    Vannice, MA
    [J]. CATALYSIS TODAY, 1999, 50 (01) : 87 - 96
  • [5] Elucidation of Active Sites for CH4 Catalytic Oxidation over Pd/CeO2 Via Tailoring Metal-Support Interactions
    Chen, Shiyuan
    Li, Songda
    You, Ruiyang
    Guo, Ziyi
    Wang, Fei
    Li, Guanxing
    Yuan, Wentao
    Zhu, Beien
    Gao, Yi
    Zhang, Ze
    Yang, Hangsheng
    Wang, Yong
    [J]. ACS CATALYSIS, 2021, 11 (09) : 5666 - 5677
  • [6] Oxygen Vacancy-Induced Metal-Support Interactions in AuPd/ZrO2 Catalysts for Boosting 5-Hydroxymethylfurfural Oxidation
    Chen, Yao
    Sun, Lu
    Li, Yiwang
    Cao, Yu
    Guan, Wen
    Pan, Jianming
    Zhang, Zehui
    Zhang, Yunlei
    [J]. INORGANIC CHEMISTRY, 2023, 62 (37) : 15277 - 15292
  • [7] Metal-support interactions during the CO2 reforming of CH4 over model TiOx/Pt catalysts
    M.C.J. Bradford
    M.A. Vannice
    [J]. Catalysis Letters, 1997, 48 : 31 - 38
  • [8] Electronic metal-support interactions and their promotional effect on CO2 methanation on Ru/ZrO2 catalysts
    Chen, Shilong
    Abdel-Mageed, Ali M.
    Li, Mengru
    Cisneros, Sebastian
    Bansmann, Joachim
    Rabeah, Jabor
    Brueckner, Angelika
    Gross, Axel
    Behm, R. Juergen
    [J]. JOURNAL OF CATALYSIS, 2021, 400 : 407 - 420
  • [9] Metal-support interactions during the CO2 reforming of CH4 over model TiOx/Pt catalysts
    Bradford, MCJ
    Vannice, MA
    [J]. CATALYSIS LETTERS, 1997, 48 (1-2) : 31 - 38
  • [10] Boosting toluene deep oxidation by tuning metal-support interaction in MOF-derived Pd@ZrO2 catalysts: The role of interfacial interaction between Pd and ZrO2
    Bi, Fukun
    Ma, Shuting
    Gao, Bin
    Liu, Baolin
    Huang, Yuandong
    Qiao, Rong
    Zhang, Xiaodong
    [J]. FUEL, 2024, 357