Indium Oxide as a Superior Catalyst for Methanol Synthesis by CO2 Hydrogenation

被引:940
|
作者
Martin, Oliver [1 ]
Martin, Antonio J. [1 ]
Mondelli, Cecilia [1 ]
Mitchell, Sharon [1 ]
Segawa, Takuya F. [2 ]
Hauert, Roland [3 ]
Drouilly, Charlotte [4 ]
Curulla-Ferre, Daniel [4 ]
Perez-Ramirez, Javier [1 ]
机构
[1] ETH, Dept Chem & Appl Biosci, Inst Chem & Bioengn, Vladimir Prelog Weg 1, CH-8093 Zurich, Switzerland
[2] ETH, Dept Chem & Appl Biosci, Phys Chem Lab, Vladimir Prelog Weg 2, CH-8093 Zurich, Switzerland
[3] Swiss Fed Labs Mat Sci & Technol, Empa, Uberlandstr 129, CH-8600 Dubendorf, Switzerland
[4] Total Res & Technol Feluy, Zone Ind Feluy C, B-7181 Seneffe, Belgium
关键词
CO2; hydrogenation; indium oxide; methanol synthesis; oxygen vacancies; zirconium oxide; WATER-GAS SHIFT; REFORMING ACTIVITY; IN2O3; ADSORPTION; RESONANCE; KINETICS; SITE; DFT; ZNO;
D O I
10.1002/anie.201600943
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Methanol synthesis by CO2 hydrogenation is attractive in view of avoiding the environmental implications associated with the production of the traditional syngas feedstock and mitigating global warming. However, there still is a lack of efficient catalysts for such alternative processes. Herein, we unveil the high activity, 100% selectivity, and remarkable stability for 1000 h on stream of In2O3 supported on ZrO2 under industrially relevant conditions. This strongly contrasts to the benchmark Cu-ZnO-Al2O3 catalyst, which is unselective and experiences rapid deactivation. In-depth characterization of the In2O3-based materials points towards a mechanism rooted in the creation and annihilation of oxygen vacancies as active sites, whose amount can be modulated in situ by co-feeding CO and boosted through electronic interactions with the zirconia carrier. These results constitute a promising basis for the design of a prospective technology for sustainable methanol production.
引用
收藏
页码:6261 / 6265
页数:5
相关论文
共 50 条
  • [21] Hydrogenation of CO2 to methanol over Cu/ZnCr catalyst
    Xiong, Shuhao
    Lian, Yun
    Xie, Hong
    Liu, Bing
    FUEL, 2019, 256
  • [22] Hydrogenation of CO2 to methanol over Cu/AlCeO catalyst
    Li, Shaozhong
    Guo, Limin
    Ishihara, Tatsumi
    CATALYSIS TODAY, 2020, 339 : 352 - 361
  • [23] Application of solid solution catalyst in the hydrogenation of CO2 to methanol
    Na, Wei
    Zuo, Junyi
    Yang, Xuelei
    Zhang, Pingyao
    Wen, Jianlin
    Gao, Wengui
    Jingxi Huagong/Fine Chemicals, 2021, 38 (12): : 2415 - 2421
  • [24] Recent Advances of Indium Oxide-Based Catalysts for CO2 Hydrogenation to Methanol: Experimental and Theoretical
    Cai, Dongren
    Cai, Yanmei
    Tan, Kok Bing
    Zhan, Guowu
    MATERIALS, 2023, 16 (07)
  • [25] Effect of CO on methanol synthesis from CO2 hydrogenation
    Li, JT
    Zhang, WD
    Au, CT
    ACTA PHYSICO-CHIMICA SINICA, 1998, 14 (03) : 275 - 277
  • [26] Influence of Indium as a Promoter on the Stability and Selectivity of the Nanocrystalline Cu/CeO2 Catalyst for CO2 Hydrogenation to Methanol
    Sharma, Sachin Kumar
    Paul, Bappi
    Pal, Rohan Singh
    Bhanja, Piyali
    Banerjee, Arghya
    Samanta, Chanchal
    Bal, Rajaram
    ACS APPLIED MATERIALS & INTERFACES, 2021, 13 (24) : 28201 - 28213
  • [27] Effect of Mixed Crystal Phase Control of Indium-Based Catalyst on the Reaction of CO2 Hydrogenation to Methanol
    Wang, Yu
    Li, Hongwei
    Wu, Yu
    Hu, Zhihai
    Shiyou Xuebao, Shiyou Jiagong/Acta Petrolei Sinica (Petroleum Processing Section), 2024, 40 (04): : 983 - 992
  • [28] A theoretical study for methanol synthesis by CO2 hydrogenation
    Kakumoto, T
    Watanabe, T
    CATALYSIS TODAY, 1997, 36 (01) : 39 - 44
  • [29] Methanol Synthesis from CO2 Hydrogenation over CuZnCeTi Mixed Oxide Catalysts
    Chang, Kuan
    Wang, Tiefeng
    Chen, Jingguang G.
    INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH, 2019, 58 (19) : 7922 - 7928
  • [30] Inverse Oxide/Metal Catalysts for CO2 Hydrogenation to Methanol
    Kapiamba, Kashala Fabrice
    Otor, Hope O.
    Viamajala, Sridhar
    Alba-Rubio, Ana C.
    ENERGY & FUELS, 2022, 36 (19) : 11691 - 11711