4.8 Article

Titania-Supported Ni2P/Ni Catalysts for Selective Solar-Driven CO Hydrogenation

期刊

ADVANCED MATERIALS
卷 33, 期 36, 页码 -

出版社

WILEY-V C H VERLAG GMBH
DOI: 10.1002/adma.202103248

关键词

phosphidation; photothermal catalysis; solar-driven; value-added hydrocarbons

资金

  1. National Key Projects for Fundamental Research and Development of China [2018YFB1502002]
  2. National Natural Science Foundation of China [51825205, 51772305, 21902168]
  3. Beijing Natural Science Foundation [2191002]
  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. Youth Innovation Promotion Association of the CAS
  9. MacDiarmid Institute for Advanced Materials and Nanotechnology
  10. Energy Education Trust of New Zealand

向作者/读者索取更多资源

This research demonstrates a partial phosphidation strategy to prepare titania supported Ni2P/Ni photothermal catalysts, which can enhance the selectivity of multi-carbon products (C2+) in Fischer-Tropsch synthesis and efficiently harness solar energy for high value product production.
Solar-driven Fischer-Tropsch synthesis (FTS) holds great potential for the sustainable production of fuels from syngas and solar energy. However, the selectivity toward multi-carbon products (C2+) is often hampered by the difficulty in the regulation of transition metals acting as both light absorption units and active sites. Herein, a partial phosphidation strategy to prepare titania supported Ni2P/Ni catalysts for photothermal FTS is demonstrated. Under Xenon lamp or concentrated sunlight irradiation, the optimized catalyst shows a C2+ selectivity of 70% at a CO conversion of >20%. Conversely, nickel metal in the absence of Ni2P delivers negligible C2+ products (approximate to 1%) with methane being the major product (>90%). Structural characterization and density functional theory calculation reveal that the partial phosphidation allows exposed metallic Ni to be active for CO adsorption and activation, while the existence of Ni2P/Ni interface is responsible to inhibit CO methanation and promote C-C coupling of adsorbed *CH intermediates. This work introduces a novel phosphidation strategy for nickel-based photothermal catalysts in efficiently harnessing solar energy, and regulating the reaction pathways for CO hydrogenation to deliver high value products.

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