4.6 Article

Engineering Co Nanoparticles Supported on Defect MoS2-x for Mild Deoxygenation of Lignin-Derived Phenols to Arenes

Journal

ACS ENERGY LETTERS
Volume 5, Issue 4, Pages 1330-1336

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acsenergylett.0c00411

Keywords

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Funding

  1. National Key R&D Program of China [2019YFC1905302]
  2. National Natural Science Foundation of China [21776236, 21676225, 21721004, 21878288, 21690083]
  3. Natural Science Foundation of Hunan Province [2018JJ2384]
  4. Scientific Research Fund of Hunan Provincial Education Department [19A478]
  5. Engineering Research Centre of Chemical Process Simulation and Optimization of Ministry of Education
  6. Hunan Key Laboratory of Environment-Friendly Chemical Process Integrated Technology

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To enhance the catalytic activity and temper the reaction conditions in the hydrodeoxygenation (HDO) of lignin-derived phenols to arenes, a Co-MoS2-x catalyst was proposed and prepared via a facile strategy. Co oxide was synthesized via a solvothermal method, adsorbed at the edge of MoS2-x, and finally reduced to metallic Co via an in situ spontaneous interfacial redox reaction to form Co-MoS2-x. In the HDO of 4-methylphenol, a 97.4% conversion with toluene selectivity up to 99.6% is obtained at the hitherto lowest reaction temperature of 120 degrees C. This catalyst also exhibits good versatility in catalyzing HDO of different lignin monomers and even lignin bio-oil into arenes. Notably, CoMoS2-x is very stable in the HDO reusability study: no deactivation was observed after recycling eight times. The high HDO activity of CoMoS2-x is attributed to the formation of a metal-vacancy interface and electronic transfer from Co to MoS2-x according to the characterization results and theoretical analysis.

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