4.8 Article

Ni-based catalysts derived from layered-double-hydroxide nanosheets for efficient photothermal CO2 reduction under flow-type system

期刊

NANO RESEARCH
卷 14, 期 12, 页码 4828-4832

出版社

TSINGHUA UNIV PRESS
DOI: 10.1007/s12274-021-3436-6

关键词

photothermal CO2 hydrogenation; Ni-based catalysts; layered double hydroxide; photocatalysis; solar-to-fuel

资金

  1. National Key Projects for Fundamental Research and Development of China [2018YFB1502002, 2017YFA0206904, 2017YFA0206900]
  2. National Natural Science Foundation of China [51825205, 51772305, 21871279, 21902168, 52072382]
  3. Beijing Natural Science Foundation [2191002, 2194089]
  4. Strategic Priority Research Program of the Chinese Academy of Sciences [XDB17000000]
  5. Royal Society-Newton Advanced Fellowship [NA170422]
  6. International Partnership Program of Chinese Academy of Sciences [GJHZ1819, GJHZ201974]
  7. K. C. Wong Education Foundation
  8. Central China Normal University [2020YBZZ019]
  9. Youth Innovation Promotion Association of the CAS
  10. Open Fund of the Key Laboratory of Thermal Management and Energy Utilization of Aircraft, Ministry of Industry and Information Technology, Nanjing University of Aeronautics and Astronautics [CEPE2020014]

向作者/读者索取更多资源

The study successfully fabricated a series of Ni-based catalysts for efficient conversion of CO2 to methane via photothermal CO2 reduction. The Ni-600 catalyst exhibited high CO2 conversion rate, methane production rate, and long-term stability, offering new potential for sustainable conversion and utilization of CO2.
Photothermal CO2 reduction is an efficient and sustainable catalytic path for CO2 treatment. Here, we successfully fabricated a novel series of Ni-based catalysts (Ni-x) via H-2 reduction of NiAl-layered double hydroxide nanosheets at temperatures (x) ranging from 300 to 600 degrees C. With the increase of the reduction temperature, the methane generation rate of the Ni-x catalyst for photothermal CO2 hydrogenation gradually increased under ultraviolet-visible-infrared (UV-vis-IR) irradiation in a flow-type system. The Ni-600 catalyst showed a CO2 conversion of 78.4%, offering a CH4 production rate of 278.8 mmol.g(-1)h(-1), with near 100% selectivity and 100 h long-term stability. Detailed characterization analyses showed metallic Ni nanoparticles supported on amorphous alumina are the catalytically active phase for CO2 methanation. This study provides a possibility for large-scale conversion and utilization of CO2 from a sustainable perspective.

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