Please use this identifier to cite or link to this item: http://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/9593
Title: On the atomic structure of monolayer V4C3Tz and the study of charge storage processes in an acidic electrolyte using SPEIS and in-situ X-ray absorption spectroscopy
Authors: Mendoza-Sanchez, Beatriz
LADOLE, ATHARVA H.
Samperio-Niembro, Enrique
Mangold, Stefan
Knapp, Michael
Tseng, Eric N.
Persson, Per O. A.
Douard, Camille
Shuck, Christopher E.
Brousse, Thierry
Dept. of Chemistry
Keywords: V4C3Tz
MXene
Atomic structure
Monolayer
Supercapacitors
Charge storage processes
In situ XAS
2024
Issue Date: Aug-2024
Publisher: Elsevier B.V.
Citation: Energy Storage Materials, 71, 103566.
Abstract: Monolayer V4C3Tz is synthesized and its atomic structure is studied using high-end transmission electron microscopy. X-Ray diffraction reveals key 3D to 2D crystal transformations as a V4AlC3 crystal is transformed into V4C3Tz in synthesis processes. The charge storage properties of V4C3Tz film electrodes are investigated for supercapacitor applications in 3 M H2SO4. V4C3Tz film electrodes shows an excellent capacitance of up to 469.6 F g−1 and 845.7 F cm−3, rate performance up to 30 A g−1 and cycling stability up to 10,000 cycles. A combination of electrochemical kinetics/mass transport models, staircase potentio-electrochemical impedance spectroscopy and in situ X-Ray absorption spectroscopy reveals, for the first time for this MXene, the underlying charge storage mechanisms, consisting of double layer capacitance, pseudocapacitance and a minor contribution from mass transport-controlled processes. The latter two implying a outstanding redox activity superior to Ti-based MXenes. The stability in standard environments, mechanical flexibility and the demonstrated excellent charge storage performance of V4C3Tz makes it one of the best candidates for supercapacitor applications, especially in miniaturized devices.
URI: https://doi.org/10.1016/j.ensm.2024.103566
http://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/9593
ISSN: 2405-8297
2405-8289
Appears in Collections:JOURNAL ARTICLES

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