4.8 Article

Colloidal Co single-atom catalyst: a facile synthesis strategy and high catalytic activity for hydrogen generation

期刊

GREEN CHEMISTRY
卷 22, 期 4, 页码 1269-1274

出版社

ROYAL SOC CHEMISTRY
DOI: 10.1039/c9gc03477c

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资金

  1. National Natural Science Foundation of China [51672194, 51702241]
  2. Program for Innovative Teams of Outstanding Young and Middle-aged Researchers in the Higher Education Institutions of Hubei Province [T201602]
  3. Key Program of Natural Science Foundation of Hubei Province, China [2017CFA004]
  4. Special Project of Central Government for Local Science and Technology Development of Hubei Province [2019ZYYD076]
  5. Doctoral Fund Project of Henan Polytechnic University [B2019-40]
  6. Open Foundation of the State Key Laboratory of Refractories and Metallurgy [G201904]

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Developing highly active single-atom catalysts is one of the most significant issues for future renewable energy technologies. Here we present a facile but effective and efficient strategy for synthesizing colloidal Co single-atom catalysts with excellent catalytic activity using a copolymer, poly(isobutylene-alt-maleic anhydride) (ISOBAM-104), as a stabilizing agent. The catalytic activity of the as-prepared colloidal single-atom catalyst for hydrogen generation from hydrolysis of KBH4 in an alkaline solution was as high at about 14 300 mL-H-2 min(-1) g-Co-1, which was even higher than that of its Pt, Pd or Rh counterpart. Such a high catalytic activity of the colloidal catalyst was attributable to the in situ formed and well-stabilized Co single-atoms whose existence was confirmed by aberration-corrected high-angle annular dark-field scanning transmission electron microscopy. Moreover, quantum chemical calculations reveal that ISOBAM-104 has a higher binding energy with the Co catalyst than with the well-known conventional protective agents, including poly(N-vinyl-2-pyrrolidone), starch, carboxymethylcellulose sodium, polyvinyl alcohol, sodium polyacrylate and polyethylene glycol. In addition, the use of as-prepared Co catalysts resulted in a much lowered barrier for the dissociation reaction of BH4- than in the cases of using Pt, Pd and Rh counterpart catalysts.

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