Source abstract
Abstract
The electrochemical production of H 2 O 2 via the two-electron oxygen-reduction reaction (2e – ORR) has been actively studied using systems with atomically dispersed metal–nitrogen–carbon (M–N–C) structures. However, the development of well-defined M–N–C structures that restrict the migration and agglomeration of single-metal sites remains elusive. Herein, we demonstrate a Langmuir–Blodgett (LB) monolayer of cobalt phthalocyanine (CoPc) on monolayer graphene (LB CoPc/G) as a single-metal catalyst for the 2e – ORR. The as-prepared CoPc LB monolayer has a β-form crystalline structure with a lattice space for the facile adsorption of oxygen molecules on the cobalt active sites. The CoPc LB monolayer system provides highly exposed Co atoms in a well-defined structure without agglomeration, resulting in significantly improved catalytic activity, which is manifested by a very high H 2 O 2 production rate per catalyst (31.04 mol g cat –1 h –1 ) and TOF (36.5 s –1 ) with constant production stability for 24 hours. To the best of our knowledge, the CoPc LB monolayer system exhibits the highest H 2 O 2 production rate per active site. This fundamental study suggests that an LB monolayer of molecules with single-metal atoms as a well-defined structure works for single-atom catalysts.
Source: openalex_inverted_index · Quality: baseline
Affiliations
Department of Chemistry, Ulsan National Institute of Science and Technology (UNIST), 50 UNIST-gil, Ulsan 44919, Republic of Korea
School of Energy and Chemical Engineering, Ulsan National Institute of Science and Technology (UNIST), 50 UNIST-gil, Ulsan 44919, Republic of Korea
Department of Chemistry, Seoul National University, Seoul 08826, Republic of Korea
Department of Chemistry, College of Science, Kyung Hee University, 26 Kyungheedae-ro, Dongdaemun-gu, Seoul 02447, Republic of Korea
Funding
National Research Foundation of Korea