Optimization of active sites by sulfurization of the core–shell ZIF 67@ZIF 8 for rapid oxygen reduction kinetics in acidic media
- Authors
- Lee, Jung Su; Rajan, Hashikaa; Christy, Maria; Yi, Sung Chul
- Issue Date
- Mar-2021
- Publisher
- Elsevier Ltd
- Keywords
- Metal organic frameworks; Zeolitic imidazolate frameworks; Oxygen reduction reaction; Sulfurization; Reaction kinetics
- Citation
- International Journal of Hydrogen Energy, v.46, no.18, pp.10739 - 10748
- Indexed
- SCIE
SCOPUS
- Journal Title
- International Journal of Hydrogen Energy
- Volume
- 46
- Number
- 18
- Start Page
- 10739
- End Page
- 10748
- URI
- https://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/1368
- DOI
- 10.1016/j.ijhydene.2020.12.159
- ISSN
- 0360-3199
- Abstract
- Achieving a highly active cathode surface with extremely efficient electrocatalysts for oxygen reduction kinetics is a fundamental necessity for durable fuel cells. Developing such active materials into desirable nanostructures is crucial in the pursuit of electrocatalysis. A facile preparation of cobalt decorated nitrogen and sulfur co-doped carbon nanostructures (Co-NSC) with the added advantage of Zeolitic imidazolate frameworks (ZIF), ZIF 67@ZIF 8 is reported here. The as-prepared Co, N, S, co-doped carbon (Co-NSC) electrocatalyst comes under platinum group metal-free (PGM-free) catalysts which intends to replace the scarce and highly expensive commercial Pt catalysts. Facile preparation of the Co-NSC catalyst that is scalable, low cost and highly ORR active makes the material advantageous. Co-doping sulfur has dramatically enhanced the intrinsic catalytic activity of the catalyst, and the degree of variation in sulfurization greatly influences the overall catalytic property. Co-NSC 200 with high sulfur doping exhibit a positively shifted onset potential of 0.81 V, and a high yielding current density of 5.5 mA cm(-2) at 20 mV s(-1).
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