Effective Formation of a Mn-ZIF-67 Nanofibrous Network via Electrospinning: An Active Electrocatalyst for OER in Alkaline Medium
- Authors
- Selvasundarasekar, Sam Sankar; Bijoy, T. K.; Kumaravel, Sangeetha; Karmakar, Arun; Madhu, Ragunath; Bera, Krishnendu; Nagappan, Sreenivasan; Dhandapani, Hariharan N.; Mersal, Gaber A. M.; Ibrahim, Mohamed M.; Sarkar, Debashish; Yusuf, Seikh Mohammad; Lee, Seung-Cheol; Kundu, Subrata
- Issue Date
- 2022-10
- Publisher
- American Chemical Society
- Citation
- ACS Applied Materials & Interfaces, v.14, no.41, pp.46581 - 46594
- Abstract
- Finding the active center in a bimetallic zeolite imidazolate framework (ZIF) is highly crucial for the electro-catalytic oxygen evolution reaction (OER). In the present study, we constructed a bimetallic ZIF system with cobalt and manganese metal ions and subjected it to an electrospinning technique for feasible fiber formation. The obtained nanofibers delivered a lower overpotential value of 302 mV at a benchmarking current density of 10 mA cm-2 in an electrocatalytic OER study under alkaline conditions. The obtained Tafel slope and charge-transfer resistance values were 125 mV dec-1 and 4 omega, respectively. The kinetics of the reaction is mainly attributed from the ratio of metals (Co and Mn) present in the catalyst. Jahn-Teller distortion reveals that the electrocatalytic active center on the Mn-incorporated ZIF-67 nanofibers (Mn-ZIF-67-NFs) was found to be Mn3+ along with the Mn2+ and Co2+ ions on the octahedral and tetrahedral sites, respectively, where Co2+ ions tend to suppress the distortion, which is well supported by density functional theory analysis, molecular orbital study, and magnetic studies.
- Keywords
- HYBRIDS; OXIDE; CO; NANOCOMPOSITES; NANOPARTICLES; OXYGEN EVOLUTION REACTION; MAGNETIC-PROPERTIES; WATER OXIDATION; PEROVSKITE; FRAMEWORK; electrocatalyst; electrospinning; zeolite imidazolate framework; oxygen evolution reaction; overpotential
- ISSN
- 1944-8244
- URI
- https://pubs.kist.re.kr/handle/201004/114471
- DOI
- 10.1021/acsami.2c12643
- Appears in Collections:
- KIST Article > 2022
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