CROSS-DISCIPLINARY PHYSICS AND RELATED AREAS OF SCIENCE AND TECHNOLOGY |
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Electrochemical Behavior of Vanadium Carbide in Neutral Aqueous Electrolytes |
Chaofan Chen1, Di Pang1, Xiaotong Wang1, Gang Chen1,2, Fei Du1,2*, and Yu Gao1* |
1Key Laboratory of Physics and Technology for Advanced Batteries (Ministry of Education), College of Physics, Jilin University, Changchun 130012, China 2State Key Laboratory of Superhard Materials, College of Physics, Jilin University, Changchun 130012, China
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Cite this article: |
Chaofan Chen, Di Pang, Xiaotong Wang et al 2021 Chin. Phys. Lett. 38 058201 |
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Abstract The V$_{2}$C compound, belonging to the group of two-dimensional transition metal carbonitrides, or MXenes, has demonstrated a promising electrochemical performance in capacitor applications in acidic electrolytes; however, there is evidence to suggest that V$_{2}$C is unstable in an acidic environment. On the other hand, the performance of V$_{2}$C in neutral aqueous electrolytes is still moderate, and has not yet been systematically studied. The charge storage mechanism in a V$_{2}$C electrode, employed in neutral aqueous electrolytes, is investigated via cyclic voltammetry testing and in situ x-ray diffraction (XRD). Good specific capacitances are achieved, specifically 208 F/g in 0.5 M Li$_{2}$SO$_{4}$, 225 F/g in 1 M MgSO$_{4}$, 120 F/g in 1M Na$_{2}$SO$_{4}$, and 104 F/g in 0.5 M K$_{2}$SO$_{4}$. Using in situ XRD, we observe that, during the charge and discharge process, the $c$-lattice parameter shrinks or expands by up to 0.25 Å in MgSO$_{4}$, and 0.29 Å in Li$_{2}$SO$_{4}$ which demonstrates the intercalation/de-intercalation of cations into the $d$-V$_{2}$C layer.
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Received: 10 January 2021
Published: 02 May 2021
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Fund: Supported by the Science & Technology Department of Jilin Province (Grant Nos. 20180101199JC and 20180101204JC), and Jilin Province/Jilin University Co-construction Project-Funds for New Materials (SXGJSF2017-3). |
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