4.8 Article

A Top-Down Templating Strategy toward Functional Porous Carbons

Journal

SMALL
Volume 18, Issue 26, Pages -

Publisher

WILEY-V C H VERLAG GMBH
DOI: 10.1002/smll.202201838

Keywords

fuel cells; oxygen reduction reaction; porous carbons; single-atom catalysts; top-down templating

Funding

  1. National Key Research and Development Program of China [2018YFA0702001]
  2. National Natural Science Foundation of China [22071225]
  3. Fundamental Research Funds for the Central Universities [WK2060190103]
  4. Hefei National Synchrotron Radiation Laboratory [KY2060000175]
  5. Collaborative Innovation Program of Hefei Science Center of CAS [2021HSC-CIP015]

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This paper presents a top-down templating strategy for the synthesis of functional porous carbon materials with high porosity and desired chemical functionalities. The porosity and heteroatom doping of the carbon materials can be controlled by varying the organic precursors and metal oxides. The strategy is also applicable for the preparation of carbon-based single-atom catalysts with iron-nitrogen sites.
Nanostructured carbon materials with high porosity and desired chemical functionalities are of immense interest because of their wide application potentials in catalysis, environment, and energy storage. Herein, a top-down templating strategy is presented for the facile synthesis of functional porous carbons, based on the direct carbonization of diverse organic precursors with commercially available metal oxide powders. During the carbonization, the metal oxide powders can evolve into nanoparticles that serve as in situ templates to introduce nanopores in carbons. The porosity and heteroatom doping of the prepared carbon materials can be engineered by varying the organic precursors and/or the metal oxides. It is further demonstrated that the top-down templating strategy is applicable to prepare carbon-based single-atom catalysts with iron-nitrogen sites, which exhibit a high power density of 545 mW cm(-2) in a H-2-air proton exchange membrane fuel cell.

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