| Literature DB >> 31674103 |
Ming-Xi Chen1, Mengzhao Zhu1, Ming Zuo1, Sheng-Qi Chu2, Jing Zhang2, Yuen Wu1, Hai-Wei Liang1, Xinliang Feng3.
Abstract
The development of metal-N-C materials as efficient non-precious metal (NPM) catalysts for catalysing the oxygen reduction reaction (ORR) as alternatives to platinum is important for the practical use of proton exchange membrane fuel cells (PEMFCs). However, metal-N-C materials have high structural heterogeneity. As a result of their high-temperature synthesis they often consist of metal-Nx sites and graphene-encapsulated metal nanoparticles. Thus it is hard to identify the active structure of metal-N-C catalysts. Herein, we report a low-temperature NH4 Cl-treatment to etch out graphene-encapsulated nanoparticles from metal-N-C catalysts without destruction of co-existing atomically dispersed metal-Nx sites. Catalytic activity is much enhanced by this selective removal of metallic nanoparticles. Accordingly, we can confirm the spectator role of graphene-encapsulated nanoparticles and the pivotal role of metal-Nx sites in the metal-N-C materials for ORR in the acidic medium.Entities:
Keywords: Fe-N-C; active sites; encapsulated nanoparticles; fuel cells; oxygen reduction reaction (ORR)
Year: 2019 PMID: 31674103 DOI: 10.1002/anie.201912275
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336