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Cited 2 time in webofscience Cited 3 time in scopus
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Exploring the bifunctional electrocatalytic activity of tin sulfide decorated manganese iron oxide in alkaline and urea contaminated water

Authors
Justin Jesuraj, P.John, G.Navaneethan, M.Lee, Chang MinMun, JeonghoKang, Yong-CheolRyu, Seung Yoon
Issue Date
Sep-2024
Publisher
Elsevier B.V.
Keywords
Adsorption sites; Bifunctional electrode; Interfacial bonding; SnS decoration; Tafel slope
Citation
Inorganic Chemistry Communications, v.167, pp 1 - 7
Pages
7
Indexed
SCIE
SCOPUS
Journal Title
Inorganic Chemistry Communications
Volume
167
Start Page
1
End Page
7
URI
https://scholarworks.dongguk.edu/handle/sw.dongguk/26141
DOI
10.1016/j.inoche.2024.112686
ISSN
1387-7003
1879-0259
Abstract
Efficient, affordable, and stable electrocatalysts are pivotal for large-scale water splitting. Herein, we report an optimized decoration of tin sulfide (SnS) bundles on porous manganese ferrite (MnFe2O4) on nickel foam for enhancing the overall water splitting. This decoration yielded an interfacial Sn-O bond between MnFe2O4 and SnS, stabilized the structure, and provided optimistic adsorption energies for oxygen and hydrogen. The decorated electrode exhibited overpotentials of 383 mV for the oxygen evolution reaction (OER) and 127 mV for the hydrogen evolution reaction (HER) at 20 mA.cm−2. Moreover, the decorated sample demonstrated reduced overpotentials of 272 mV and 75 mV (at 20 mA cm−2) for OER and HER in urea-contaminated water. The augmented double layer capacitance (Cdl) electrochemical surface area (ECSA) and X-ray photoelectron spectroscopy (XPS) studies of the decorated sample corroborated the enhanced performances and effectiveness of the SnS decoration. Furthermore, SnS-decorated MnFe2O4 showed outstanding performance in a two-cell configuration with a cell voltage of 1.69 V and 1.52 V (@10 mA cm−2) under alkaline KOH and urea (0.33 M) electrolyte, respectively. Further, the chronoamperometry and post-X-ray photoelectron spectroscopy studies demonstrated the stability and promising potential of this electrode for future non-noble metal-based bifunctional catalytic applications. © 2024 Elsevier B.V.
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