Insights into the Surface Electronic Structure and Catalytic Activity of InO x /Au(111) Inverse Catalysts for CO2 Hydrogenation to Methanol

被引:1
作者
Reddy, Kasala Prabhakar [1 ]
Tian, Yi [2 ]
Ramirez, Pedro J. [3 ,4 ]
Islam, Arephin [1 ]
Lim, Hojoon [5 ]
Rui, Ning [1 ]
Xie, Yilin [6 ]
Hunt, Adrian [5 ]
Waluyo, Iradwikanari [5 ]
Rodriguez, Jose A. [1 ,2 ]
机构
[1] Brookhaven Natl Lab, Chem Div, Upton, NY 11973 USA
[2] SUNY Stony Brook, Dept Chem, Stony Brook, NY 11794 USA
[3] Univ Cent Venezuela, Fac Ciencias, Caracas 1020A, Venezuela
[4] Zoneca CENEX, R&D Labs, Monterrey 64770, Mexico
[5] Brookhaven Natl Lab, Natl Synchrotron Light Source 2, Upton, NY 11973 USA
[6] Brown Univ, Dept Chem, Providence, RI 02912 USA
来源
ACS CATALYSIS | 2024年 / 14卷 / 22期
关键词
indium oxide nanostructures; gold; oxide-metalInterface; CO2; hydrogenation; methanolproduction; METAL-OXIDE INTERFACE; SELECTIVE HYDROGENATION; STRUCTURE SENSITIVITY; MODEL CATALYSTS; CHEMISTRY; KINETICS; SITES; PD; ADSORPTION; REACTIVITY;
D O I
10.1021/acscatal.4c05837
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The direct conversion of carbon dioxide (CO2) into methanol (CH3OH) via low-temperature hydrogenation is crucial for recycling anthropogenic CO2 emissions and producing fuels or high value chemicals. Nevertheless, it continues to be a great challenge due to the trade-off between selectivity and catalytic activity. For CO2 hydrogenation, In2O3 catalysts are known for their high CH3OH selectivity. Subsequent studies explored depositing metals on In2O3 to enhance CO2 conversion. Despite extensive research on metal (M) supported In2O3 catalysts, the role of In-M alloys and M/In2O3 interfaces in CO2 activation and CH3OH selectivity remains unclear. In this work, we have examined the behavior of In/Au(111) alloys and InOx/Au(111) inverse systems during CO2 hydrogenation using synchrotron-based ambient-pressure X-ray photoelectron spectroscopy (AP-XPS) and catalytic tests in a batch reactor. Indium forms alloys with Au(111) after deposition. The In-Au(111) alloys display high reactivity toward CO2 and can dissociate the molecule at room temperature to generate InOx nanostructures. At very low coverages of In (<= 0.05 ML), the InOx nanostructures are not stable under CO2 hydrogenation conditions and the active In-Au(111) alloys produces mainly CO and little methanol. An increase in indium coverage to 0.3 ML led to stable InOx nanostructures under CO2 hydrogenation conditions. These InOx/Au(111) catalysts displayed a high selectivity (similar to 80%) toward CH3OH production and an activity for CO2 conversion that was at least 10 times larger than that of plain In2O3 or Cu(111) and Cu/ZnO(0001) benchmark catalysts. The results of AP-XPS show that InOx/Au(111) produces methanol via methoxy intermediates. Inverse oxide/metal catalysts containing InOx open up a possibility for improving CO2 -> CH3OH conversion in processes associated with the control of environmental pollution and the production of high value chemicals.
引用
收藏
页码:17148 / 17158
页数:11
相关论文
共 50 条
  • [41] The Mechanism of CO and CO2 Hydrogenation to Methanol over Cu-Based Catalysts
    Studt, Felix
    Behrens, Malte
    Kunkes, Edward L.
    Thomas, Nygil
    Zander, Stefan
    Tarasov, Andrey
    Schumann, Julia
    Frei, Elias
    Varley, Joel B.
    Abild-Pedersen, Frank
    Norskov, Jens K.
    Schloegl, Robert
    CHEMCATCHEM, 2015, 7 (07) : 1105 - 1111
  • [42] Indium-based Catalysts for CO2 Hydrogenation to Methanol: Key Aspects for Catalytic Performance
    Wesner, Anne
    Kampe, Philipp
    Herrmann, Nick
    Eller, Sebastian
    Ruhmlieb, Charlotte
    Albert, Jakob
    CHEMCATCHEM, 2023, 15 (24)
  • [43] Catalytic systems for hydrogenation of CO2 to methanol
    Tedeeva, Marina A.
    Kustov, Alexander L.
    Batkin, Alexander M.
    Garifullina, Cholpan
    Zalyatdinov, Albert A.
    Yang, Dan
    Dai, Yihu
    Yang, Yanhui
    Kustov, Leonid M.
    MOLECULAR CATALYSIS, 2024, 566
  • [44] Structure Sensitivity of an Atomic Co-Promoted In2O3 Catalyst toward CO2 Hydrogenation to Methanol
    Dang, Shanshan
    Ding, Xiaoya
    Li, Jinying
    Chang, Junchao
    Zhang, Zhenzhou
    Gao, Peng
    Tu, Weifeng
    Han, Yifan
    ACS CATALYSIS, 2025, 15 (05): : 3967 - 3979
  • [45] Catalytic Hydrogenation of CO2 to Methanol: A Review
    Ren, Menghao
    Zhang, Yanmin
    Wang, Xuan
    Qiu, Hengshan
    CATALYSTS, 2022, 12 (04)
  • [46] CO2 Hydrogenation to Methanol on Indium Oxide-Supported Rhenium Catalysts: The Effects of Size
    Shen, Chenyang
    Sun, Kaihang
    Zou, Rui
    Wu, Qinglei
    Mei, Donghai
    Liu, Chang-jun
    ACS CATALYSIS, 2022, 12 (20) : 12658 - 12669
  • [47] CO2 hydrogenation to methanol over Cu-In intermetallic catalysts: Effect of reduction temperature
    Shi, Zhisheng
    Tan, Qingqing
    Tian, Chao
    Pan, Yu
    Sun, Xuewei
    Zhang, Jinxin
    Wu, Dongfang
    JOURNAL OF CATALYSIS, 2019, 379 : 78 - 89
  • [48] CO2 Hydrogenation to Methanol on Supported Au Catalysts under Moderate Reaction Conditions: Support and Particle Size Effects
    Hartadi, Yeusy
    Widmann, Daniel
    Behm, R. Juergen
    CHEMSUSCHEM, 2015, 8 (03) : 456 - 465
  • [49] Pd/ZnO catalysts for direct CO2 hydrogenation to methanol
    Bahruji, Hasliza
    Bowker, Michael
    Hutchings, Graham
    Dimitratos, Nikolaos
    Wells, Peter
    Gibson, Emma
    Jones, Wilm
    Brookes, Catherine
    Morgan, David
    Lalev, Georgi
    JOURNAL OF CATALYSIS, 2016, 343 : 133 - 146
  • [50] CO2 hydrogenation selectivity shift over In-Co binary oxides catalysts: Catalytic mechanism and structure-property relationship
    Li, Longtai
    Yang, Bin
    Gao, Biao
    Wang, Yifu
    Zhang, Lingxia
    Ishihara, Tatsumi
    Qi, Wei
    Guo, Limin
    CHINESE JOURNAL OF CATALYSIS, 2022, 43 (03) : 862 - 876