Cargando…
Intensifying Electrochemical Activity of Ti(3)C(2)T(x) MXene via Customized Interlayer Structure and Surface Chemistry
MXene, a new intercalation pseudocapacitive electrode material, possesses a high theoretical capacitance for supercapacitor application. However, limited accessible interlayer space and active sites are major challenges to achieve this high capacitance in practical application. In order to stimulate...
Autores principales: | , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10421071/ https://www.ncbi.nlm.nih.gov/pubmed/37570746 http://dx.doi.org/10.3390/molecules28155776 |
_version_ | 1785088875359633408 |
---|---|
author | Hu, Minmin Chen, Lihong Jing, Yunqi Zhu, Yuanyuan Dai, Jun Meng, Alan Sun, Changlong Jia, Jin Li, Zhenjiang |
author_facet | Hu, Minmin Chen, Lihong Jing, Yunqi Zhu, Yuanyuan Dai, Jun Meng, Alan Sun, Changlong Jia, Jin Li, Zhenjiang |
author_sort | Hu, Minmin |
collection | PubMed |
description | MXene, a new intercalation pseudocapacitive electrode material, possesses a high theoretical capacitance for supercapacitor application. However, limited accessible interlayer space and active sites are major challenges to achieve this high capacitance in practical application. In order to stimulate the electrochemical activity of MXene to a greater extent, herein, a method of hydrothermal treatment in NaOH solution with reducing reagent-citric acid is first proposed. After this treatment, the gravimetric capacitance of MXene exhibits a significant enhancement, about 250% of the original value, reaching 543 F g(−1) at 2 mV s(−1). This improved electrochemical performance is attributed to the tailoring of an interlayer structure and surface chemistry state. An expanded and homogenized interlayer space is created, which provides enough space for electrolyte ions storage. The –F terminations are replaced with O-containing groups, which enhances the hydrophilicity, facilitating the electrolyte’s accessibility to MXene’s surface, and makes MXene show stronger adsorption for electrolyte ion-H(+), providing sufficient electrochemical active sites. The change in terminations further leads to the increase in Ti valence, which becomes more prone to reduction. This work establishes full knowledge of the rational MXene design for electrochemical energy storage applications. |
format | Online Article Text |
id | pubmed-10421071 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-104210712023-08-12 Intensifying Electrochemical Activity of Ti(3)C(2)T(x) MXene via Customized Interlayer Structure and Surface Chemistry Hu, Minmin Chen, Lihong Jing, Yunqi Zhu, Yuanyuan Dai, Jun Meng, Alan Sun, Changlong Jia, Jin Li, Zhenjiang Molecules Article MXene, a new intercalation pseudocapacitive electrode material, possesses a high theoretical capacitance for supercapacitor application. However, limited accessible interlayer space and active sites are major challenges to achieve this high capacitance in practical application. In order to stimulate the electrochemical activity of MXene to a greater extent, herein, a method of hydrothermal treatment in NaOH solution with reducing reagent-citric acid is first proposed. After this treatment, the gravimetric capacitance of MXene exhibits a significant enhancement, about 250% of the original value, reaching 543 F g(−1) at 2 mV s(−1). This improved electrochemical performance is attributed to the tailoring of an interlayer structure and surface chemistry state. An expanded and homogenized interlayer space is created, which provides enough space for electrolyte ions storage. The –F terminations are replaced with O-containing groups, which enhances the hydrophilicity, facilitating the electrolyte’s accessibility to MXene’s surface, and makes MXene show stronger adsorption for electrolyte ion-H(+), providing sufficient electrochemical active sites. The change in terminations further leads to the increase in Ti valence, which becomes more prone to reduction. This work establishes full knowledge of the rational MXene design for electrochemical energy storage applications. MDPI 2023-07-31 /pmc/articles/PMC10421071/ /pubmed/37570746 http://dx.doi.org/10.3390/molecules28155776 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Hu, Minmin Chen, Lihong Jing, Yunqi Zhu, Yuanyuan Dai, Jun Meng, Alan Sun, Changlong Jia, Jin Li, Zhenjiang Intensifying Electrochemical Activity of Ti(3)C(2)T(x) MXene via Customized Interlayer Structure and Surface Chemistry |
title | Intensifying Electrochemical Activity of Ti(3)C(2)T(x) MXene via Customized Interlayer Structure and Surface Chemistry |
title_full | Intensifying Electrochemical Activity of Ti(3)C(2)T(x) MXene via Customized Interlayer Structure and Surface Chemistry |
title_fullStr | Intensifying Electrochemical Activity of Ti(3)C(2)T(x) MXene via Customized Interlayer Structure and Surface Chemistry |
title_full_unstemmed | Intensifying Electrochemical Activity of Ti(3)C(2)T(x) MXene via Customized Interlayer Structure and Surface Chemistry |
title_short | Intensifying Electrochemical Activity of Ti(3)C(2)T(x) MXene via Customized Interlayer Structure and Surface Chemistry |
title_sort | intensifying electrochemical activity of ti(3)c(2)t(x) mxene via customized interlayer structure and surface chemistry |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10421071/ https://www.ncbi.nlm.nih.gov/pubmed/37570746 http://dx.doi.org/10.3390/molecules28155776 |
work_keys_str_mv | AT huminmin intensifyingelectrochemicalactivityofti3c2txmxeneviacustomizedinterlayerstructureandsurfacechemistry AT chenlihong intensifyingelectrochemicalactivityofti3c2txmxeneviacustomizedinterlayerstructureandsurfacechemistry AT jingyunqi intensifyingelectrochemicalactivityofti3c2txmxeneviacustomizedinterlayerstructureandsurfacechemistry AT zhuyuanyuan intensifyingelectrochemicalactivityofti3c2txmxeneviacustomizedinterlayerstructureandsurfacechemistry AT daijun intensifyingelectrochemicalactivityofti3c2txmxeneviacustomizedinterlayerstructureandsurfacechemistry AT mengalan intensifyingelectrochemicalactivityofti3c2txmxeneviacustomizedinterlayerstructureandsurfacechemistry AT sunchanglong intensifyingelectrochemicalactivityofti3c2txmxeneviacustomizedinterlayerstructureandsurfacechemistry AT jiajin intensifyingelectrochemicalactivityofti3c2txmxeneviacustomizedinterlayerstructureandsurfacechemistry AT lizhenjiang intensifyingelectrochemicalactivityofti3c2txmxeneviacustomizedinterlayerstructureandsurfacechemistry |