4.8 Article

Stereodefined Codoping of sp-N and S Atoms in Few-Layer Graphdiyne for Oxygen Evolution Reaction

Journal

JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
Volume 141, Issue 18, Pages 7240-7244

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/jacs.8b13695

Keywords

-

Funding

  1. National Key Research and Development Program of China [2016YFB0600903]
  2. National Natural Science Foundation of China [21590795, 21820102002]
  3. Scientific Instrument Developing Project of the Chinese Academy of Sciences [YZ201623]
  4. Queensland-Chinese Academy of Sciences Collaborative Science Fund [122111KYSB20170001]
  5. Chinese Academy of Sciences (CAS) Interdisciplinary Innovation Team

Ask authors/readers for more resources

Developing metal-free catalysts with high catalytic activity for oxygen evolution reaction (OER) is essentially important for energy and environment-related techniques. Compared with individual element doping, doping carbon materials with multiple heteroelements has more advantages for enhancing the OER performance. However, doped sites for the different atoms are highly uncontrollable under the reported methods, which hinder the deeper understanding on the relationship between structure and property, and also limit the enhancement of catalytic activity. Our latest research has reported a method to site-controlled introducing a new form of nitrogen atoms, i.e. sp-hybridized nitrogen (sp-N), into graphdiyne, showing its potential advantages in OER catalysis. Since the sites of sp-N atoms are defined in graphdiyne, and the doping sites for S atoms are well understood, the relative position between N and S can be further defined. It gives us a chance to understand deeply the mechanism in the N, S heteroelements doped metal-free catalyst. Experimental results present that the codoping of sp-N and S atoms brought an excellent OER performance with low overpotential and high current density owning to the effectively synergistic effect of the stereodefined heteroatoms.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.8
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available