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Understanding charge storage in Nb2CTx MXene as an anode material for lithium ion batteries
MXenes represent an emerging family of two-dimensional materials of transition metal carbides/carbonitrides terminated with functional groups like –O, –OH, and –F on the chemically active surface of MX slabs. As a member of the family, Nb2CTx exhibits superior lithium storage capacity over most of t...
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Published in: | Physical chemistry chemical physics : PCCP 2021-10, Vol.23 (40), p.23173-23183 |
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creator | Cheng, Renfei Hu, Tao Wang, Zuohua Yang, Jinxing Dai, Ruqiao Wang, Weizhen Cui, Cong Liang, Yan Zhang, Chao Li, Cuiyu Wang, Hailong Lu, Hongxia Yang, Zhiqing Zhang, Hongwang Wang, Xiaohui |
description | MXenes represent an emerging family of two-dimensional materials of transition metal carbides/carbonitrides terminated with functional groups like –O, –OH, and –F on the chemically active surface of MX slabs. As a member of the family, Nb2CTx exhibits superior lithium storage capacity over most of the other MXenes as anode materials in lithium-ion batteries (LIBs). However, an in-depth understanding of the charge storage mechanism is still lacking so far. Here, through combining complementary experiments and density functional theory calculations, we provide insights into the (de)lithiation process. Specifically, Nb2CTx with dominant –O functional groups stores charge as a result of changes in the oxidation states of both transition metals Nb and O, which is supported by Bader charge analysis showing a significant change in the oxidation states of Nb and O upon lithiation. As monitored by ex situ X-ray diffraction, the interlayer spacing of Nb2CTx changes slightly upon lithium ion (de)intercalation, corresponding to a volume change of only 2.3% with a near zero-strain feature. By coupling with a LiFePO4/C cathode, the full cell presents superior rate capability and cycling stability as well. The insights into the charge storage mechanism of Nb2CTx in this work provide useful guidance for the rational design of MXene-based anode materials for high-performance LIBs. |
doi_str_mv | 10.1039/d1cp03070a |
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As a member of the family, Nb2CTx exhibits superior lithium storage capacity over most of the other MXenes as anode materials in lithium-ion batteries (LIBs). However, an in-depth understanding of the charge storage mechanism is still lacking so far. Here, through combining complementary experiments and density functional theory calculations, we provide insights into the (de)lithiation process. Specifically, Nb2CTx with dominant –O functional groups stores charge as a result of changes in the oxidation states of both transition metals Nb and O, which is supported by Bader charge analysis showing a significant change in the oxidation states of Nb and O upon lithiation. As monitored by ex situ X-ray diffraction, the interlayer spacing of Nb2CTx changes slightly upon lithium ion (de)intercalation, corresponding to a volume change of only 2.3% with a near zero-strain feature. By coupling with a LiFePO4/C cathode, the full cell presents superior rate capability and cycling stability as well. The insights into the charge storage mechanism of Nb2CTx in this work provide useful guidance for the rational design of MXene-based anode materials for high-performance LIBs.</description><identifier>ISSN: 1463-9076</identifier><identifier>EISSN: 1463-9084</identifier><identifier>DOI: 10.1039/d1cp03070a</identifier><language>eng</language><publisher>Cambridge: Royal Society of Chemistry</publisher><subject>Anodes ; Carbon nitride ; Density functional theory ; Electrode materials ; Functional groups ; Interlayers ; Lithium ; Lithium-ion batteries ; Metal carbides ; MXenes ; Niobium ; Oxidation ; Rechargeable batteries ; Storage batteries ; Storage capacity ; Transition metals ; Two dimensional materials</subject><ispartof>Physical chemistry chemical physics : PCCP, 2021-10, Vol.23 (40), p.23173-23183</ispartof><rights>Copyright Royal Society of Chemistry 2021</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,777,781,27905,27906</link.rule.ids></links><search><creatorcontrib>Cheng, Renfei</creatorcontrib><creatorcontrib>Hu, Tao</creatorcontrib><creatorcontrib>Wang, Zuohua</creatorcontrib><creatorcontrib>Yang, Jinxing</creatorcontrib><creatorcontrib>Dai, Ruqiao</creatorcontrib><creatorcontrib>Wang, Weizhen</creatorcontrib><creatorcontrib>Cui, Cong</creatorcontrib><creatorcontrib>Liang, Yan</creatorcontrib><creatorcontrib>Zhang, Chao</creatorcontrib><creatorcontrib>Li, Cuiyu</creatorcontrib><creatorcontrib>Wang, Hailong</creatorcontrib><creatorcontrib>Lu, Hongxia</creatorcontrib><creatorcontrib>Yang, Zhiqing</creatorcontrib><creatorcontrib>Zhang, Hongwang</creatorcontrib><creatorcontrib>Wang, Xiaohui</creatorcontrib><title>Understanding charge storage in Nb2CTx MXene as an anode material for lithium ion batteries</title><title>Physical chemistry chemical physics : PCCP</title><description>MXenes represent an emerging family of two-dimensional materials of transition metal carbides/carbonitrides terminated with functional groups like –O, –OH, and –F on the chemically active surface of MX slabs. As a member of the family, Nb2CTx exhibits superior lithium storage capacity over most of the other MXenes as anode materials in lithium-ion batteries (LIBs). However, an in-depth understanding of the charge storage mechanism is still lacking so far. Here, through combining complementary experiments and density functional theory calculations, we provide insights into the (de)lithiation process. Specifically, Nb2CTx with dominant –O functional groups stores charge as a result of changes in the oxidation states of both transition metals Nb and O, which is supported by Bader charge analysis showing a significant change in the oxidation states of Nb and O upon lithiation. As monitored by ex situ X-ray diffraction, the interlayer spacing of Nb2CTx changes slightly upon lithium ion (de)intercalation, corresponding to a volume change of only 2.3% with a near zero-strain feature. By coupling with a LiFePO4/C cathode, the full cell presents superior rate capability and cycling stability as well. The insights into the charge storage mechanism of Nb2CTx in this work provide useful guidance for the rational design of MXene-based anode materials for high-performance LIBs.</description><subject>Anodes</subject><subject>Carbon nitride</subject><subject>Density functional theory</subject><subject>Electrode materials</subject><subject>Functional groups</subject><subject>Interlayers</subject><subject>Lithium</subject><subject>Lithium-ion batteries</subject><subject>Metal carbides</subject><subject>MXenes</subject><subject>Niobium</subject><subject>Oxidation</subject><subject>Rechargeable batteries</subject><subject>Storage batteries</subject><subject>Storage capacity</subject><subject>Transition metals</subject><subject>Two dimensional materials</subject><issn>1463-9076</issn><issn>1463-9084</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><recordid>eNpdjk9LAzEUxIMoWKsXP0HAi5fVl81umhxl8R9UvbQgeChvN2_blG1SN1nw47tF8SAMzMD8GIaxSwE3AqS5taLZg4QZ4BGbiELJzIAujv_yTJ2ysxi3ACBKISfsY-kt9TGht86vebPBfk08ptDj6M7z1zqvFl_85Z08cYwc_ahgie8wUe-w423oeefSxg077oLnNaZDQ_GcnbTYRbr49SlbPtwvqqds_vb4XN3Ns_34KmUWQRJpKo0Bo8ZssdFayFYqNKq2BGRKoTAXCEKZoshNU7fatKXJRW21nLLrn919Hz4Himm1c7GhrkNPYYirvNSgDEglR_TqH7oNQ-_HdwdKSiPFDOQ36Blhgg</recordid><startdate>20211020</startdate><enddate>20211020</enddate><creator>Cheng, Renfei</creator><creator>Hu, Tao</creator><creator>Wang, Zuohua</creator><creator>Yang, Jinxing</creator><creator>Dai, Ruqiao</creator><creator>Wang, Weizhen</creator><creator>Cui, Cong</creator><creator>Liang, Yan</creator><creator>Zhang, Chao</creator><creator>Li, Cuiyu</creator><creator>Wang, Hailong</creator><creator>Lu, Hongxia</creator><creator>Yang, Zhiqing</creator><creator>Zhang, Hongwang</creator><creator>Wang, Xiaohui</creator><general>Royal Society of Chemistry</general><scope>7SR</scope><scope>7U5</scope><scope>8BQ</scope><scope>8FD</scope><scope>JG9</scope><scope>L7M</scope><scope>7X8</scope></search><sort><creationdate>20211020</creationdate><title>Understanding charge storage in Nb2CTx MXene as an anode material for lithium ion batteries</title><author>Cheng, Renfei ; Hu, Tao ; Wang, Zuohua ; Yang, Jinxing ; Dai, Ruqiao ; Wang, Weizhen ; Cui, Cong ; Liang, Yan ; Zhang, Chao ; Li, Cuiyu ; Wang, Hailong ; Lu, Hongxia ; Yang, Zhiqing ; Zhang, Hongwang ; Wang, Xiaohui</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-p146t-da03ee8e59909603edac8813f36a96bde0e9516a21a01694429cbf89f5921bd83</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Anodes</topic><topic>Carbon nitride</topic><topic>Density functional theory</topic><topic>Electrode materials</topic><topic>Functional groups</topic><topic>Interlayers</topic><topic>Lithium</topic><topic>Lithium-ion batteries</topic><topic>Metal carbides</topic><topic>MXenes</topic><topic>Niobium</topic><topic>Oxidation</topic><topic>Rechargeable batteries</topic><topic>Storage batteries</topic><topic>Storage capacity</topic><topic>Transition metals</topic><topic>Two dimensional materials</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Cheng, Renfei</creatorcontrib><creatorcontrib>Hu, Tao</creatorcontrib><creatorcontrib>Wang, Zuohua</creatorcontrib><creatorcontrib>Yang, Jinxing</creatorcontrib><creatorcontrib>Dai, Ruqiao</creatorcontrib><creatorcontrib>Wang, Weizhen</creatorcontrib><creatorcontrib>Cui, Cong</creatorcontrib><creatorcontrib>Liang, Yan</creatorcontrib><creatorcontrib>Zhang, Chao</creatorcontrib><creatorcontrib>Li, Cuiyu</creatorcontrib><creatorcontrib>Wang, Hailong</creatorcontrib><creatorcontrib>Lu, Hongxia</creatorcontrib><creatorcontrib>Yang, Zhiqing</creatorcontrib><creatorcontrib>Zhang, Hongwang</creatorcontrib><creatorcontrib>Wang, Xiaohui</creatorcontrib><collection>Engineered Materials Abstracts</collection><collection>Solid State and Superconductivity Abstracts</collection><collection>METADEX</collection><collection>Technology Research Database</collection><collection>Materials Research Database</collection><collection>Advanced Technologies Database with Aerospace</collection><collection>MEDLINE - Academic</collection><jtitle>Physical chemistry chemical physics : PCCP</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Cheng, Renfei</au><au>Hu, Tao</au><au>Wang, Zuohua</au><au>Yang, Jinxing</au><au>Dai, Ruqiao</au><au>Wang, Weizhen</au><au>Cui, Cong</au><au>Liang, Yan</au><au>Zhang, Chao</au><au>Li, Cuiyu</au><au>Wang, Hailong</au><au>Lu, Hongxia</au><au>Yang, Zhiqing</au><au>Zhang, Hongwang</au><au>Wang, Xiaohui</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Understanding charge storage in Nb2CTx MXene as an anode material for lithium ion batteries</atitle><jtitle>Physical chemistry chemical physics : PCCP</jtitle><date>2021-10-20</date><risdate>2021</risdate><volume>23</volume><issue>40</issue><spage>23173</spage><epage>23183</epage><pages>23173-23183</pages><issn>1463-9076</issn><eissn>1463-9084</eissn><abstract>MXenes represent an emerging family of two-dimensional materials of transition metal carbides/carbonitrides terminated with functional groups like –O, –OH, and –F on the chemically active surface of MX slabs. As a member of the family, Nb2CTx exhibits superior lithium storage capacity over most of the other MXenes as anode materials in lithium-ion batteries (LIBs). However, an in-depth understanding of the charge storage mechanism is still lacking so far. Here, through combining complementary experiments and density functional theory calculations, we provide insights into the (de)lithiation process. Specifically, Nb2CTx with dominant –O functional groups stores charge as a result of changes in the oxidation states of both transition metals Nb and O, which is supported by Bader charge analysis showing a significant change in the oxidation states of Nb and O upon lithiation. As monitored by ex situ X-ray diffraction, the interlayer spacing of Nb2CTx changes slightly upon lithium ion (de)intercalation, corresponding to a volume change of only 2.3% with a near zero-strain feature. By coupling with a LiFePO4/C cathode, the full cell presents superior rate capability and cycling stability as well. The insights into the charge storage mechanism of Nb2CTx in this work provide useful guidance for the rational design of MXene-based anode materials for high-performance LIBs.</abstract><cop>Cambridge</cop><pub>Royal Society of Chemistry</pub><doi>10.1039/d1cp03070a</doi><tpages>11</tpages></addata></record> |
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subjects | Anodes Carbon nitride Density functional theory Electrode materials Functional groups Interlayers Lithium Lithium-ion batteries Metal carbides MXenes Niobium Oxidation Rechargeable batteries Storage batteries Storage capacity Transition metals Two dimensional materials |
title | Understanding charge storage in Nb2CTx MXene as an anode material for lithium ion batteries |
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