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Title: | MAX Phase (Nb4AlC3) For Electrocatalysis Applications | Authors: | Gandara, Meriene Mladenović, Dušan Oliveira Martins, Marta de Jesus Rakocevic, Lazar Kruszynski de Assis, João Marcos Šljukić Paunković, Biljana Sarmento Gonçalves, Emerson |
Keywords: | capacitance;energy conversion;hydrogen evolution reaction;max phase (Nb4AlC3);oxygen reduction reaction | Issue Date: | Jul-2024 | Journal: | Small (Weinheim an der Bergstrasse, Germany) | Abstract: | In search for novel materials to replace noble metal-based electrocatalysts in electrochemical energy conversion and storage devices, special attention is given to a distinct class of materials, MAX phase that combines advantages of ceramic and metallic properties. Herein, Nb4AlC3 MAX phase is prepared by a solid-state mixing reaction and characterized morphologically and structurally by transmission and scanning electron microscopy with energy-dispersive X-ray spectroscopy, nitrogen-sorption, X-ray diffraction analysis, X-ray photoelectron and Raman spectroscopy. Electrochemical performance of Nb4AlC3 in terms of capacitance as well as for oxygen reduction reaction (ORR) and hydrogen evolution reaction (HER) is evaluated in different electrolytes. The specific capacitance Cs of 66.4, 55.0, and 46.0 F g-1 at 5 mV s-1 is determined for acidic, neutral and alkaline medium, respectively. Continuous cycling reveals high capacitance retention in three electrolyte media; moreover, increase of capacitance is observed in acidic and neutral media. The electrochemical impedance spectroscopy showed a low charge transfer resistance of 64.76 Ω cm2 that resulted in better performance for HER in acidic medium (Tafel slope of 60 mV dec-1). In alkaline media, the charge storage value in the double layer is 360 mF cm-2 (0.7 V versus reversible hydrogen electrode) and the best ORR performance of the Nb4AlC3 is achieved in this medium (Tafel slope of 126 mV dec-1). |
URI: | https://dspace.ffh.bg.ac.rs/handle/123456789/2325 | ISSN: | 16136810 | DOI: | 10.1002/smll.202310576 |
Appears in Collections: | Journal Article |
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