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Synthetic, Structural, and Electrochemical Study of Monoclinic Na4Ti5O12 as a Sodium-Ion Battery Anode Material
The monoclinic phase of Na4Ti5O12 (M-Na4Ti5O12) has been investigated as a potential sodium-ion battery anode material. In contrast to the previously investigated trigonal phase (T-Na4Ti5O12), M-Na4Ti5O12 has continuous two-dimensional (2D) channels with partially occupied Na sites, providing broade...
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Published in: | Chemistry of materials 2014-12, Vol.26 (24), p.7067-7072 |
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container_issue | 24 |
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container_title | Chemistry of materials |
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creator | Naeyaert, Pierre J. P Avdeev, Maxim Sharma, Neeraj Yahia, Hamdi Ben Ling, Chris D |
description | The monoclinic phase of Na4Ti5O12 (M-Na4Ti5O12) has been investigated as a potential sodium-ion battery anode material. In contrast to the previously investigated trigonal phase (T-Na4Ti5O12), M-Na4Ti5O12 has continuous two-dimensional (2D) channels with partially occupied Na sites, providing broader pathways and more space for the intercalation of excess sodium. Electrochemical measurements show that it exhibits a comparable or higher reversible capacity than T-Na4Ti5O12. Neutron powder diffraction reveals the preferred sites and occupancies of the excess sodium. In situ synchrotron X-ray diffraction under electrochemical cycling shows that the crystal lattice undergoes strongly anisotropic volume changes during cycling. |
doi_str_mv | 10.1021/cm5035358 |
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P ; Avdeev, Maxim ; Sharma, Neeraj ; Yahia, Hamdi Ben ; Ling, Chris D</creator><creatorcontrib>Naeyaert, Pierre J. P ; Avdeev, Maxim ; Sharma, Neeraj ; Yahia, Hamdi Ben ; Ling, Chris D</creatorcontrib><description>The monoclinic phase of Na4Ti5O12 (M-Na4Ti5O12) has been investigated as a potential sodium-ion battery anode material. In contrast to the previously investigated trigonal phase (T-Na4Ti5O12), M-Na4Ti5O12 has continuous two-dimensional (2D) channels with partially occupied Na sites, providing broader pathways and more space for the intercalation of excess sodium. Electrochemical measurements show that it exhibits a comparable or higher reversible capacity than T-Na4Ti5O12. Neutron powder diffraction reveals the preferred sites and occupancies of the excess sodium. In situ synchrotron X-ray diffraction under electrochemical cycling shows that the crystal lattice undergoes strongly anisotropic volume changes during cycling.</description><identifier>ISSN: 0897-4756</identifier><identifier>EISSN: 1520-5002</identifier><identifier>DOI: 10.1021/cm5035358</identifier><language>eng</language><publisher>American Chemical Society</publisher><ispartof>Chemistry of materials, 2014-12, Vol.26 (24), p.7067-7072</ispartof><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>314,780,784,27924,27925</link.rule.ids></links><search><creatorcontrib>Naeyaert, Pierre J. 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P</creatorcontrib><creatorcontrib>Avdeev, Maxim</creatorcontrib><creatorcontrib>Sharma, Neeraj</creatorcontrib><creatorcontrib>Yahia, Hamdi Ben</creatorcontrib><creatorcontrib>Ling, Chris D</creatorcontrib><jtitle>Chemistry of materials</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Naeyaert, Pierre J. P</au><au>Avdeev, Maxim</au><au>Sharma, Neeraj</au><au>Yahia, Hamdi Ben</au><au>Ling, Chris D</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Synthetic, Structural, and Electrochemical Study of Monoclinic Na4Ti5O12 as a Sodium-Ion Battery Anode Material</atitle><jtitle>Chemistry of materials</jtitle><addtitle>Chem. Mater</addtitle><date>2014-12-23</date><risdate>2014</risdate><volume>26</volume><issue>24</issue><spage>7067</spage><epage>7072</epage><pages>7067-7072</pages><issn>0897-4756</issn><eissn>1520-5002</eissn><abstract>The monoclinic phase of Na4Ti5O12 (M-Na4Ti5O12) has been investigated as a potential sodium-ion battery anode material. In contrast to the previously investigated trigonal phase (T-Na4Ti5O12), M-Na4Ti5O12 has continuous two-dimensional (2D) channels with partially occupied Na sites, providing broader pathways and more space for the intercalation of excess sodium. Electrochemical measurements show that it exhibits a comparable or higher reversible capacity than T-Na4Ti5O12. Neutron powder diffraction reveals the preferred sites and occupancies of the excess sodium. In situ synchrotron X-ray diffraction under electrochemical cycling shows that the crystal lattice undergoes strongly anisotropic volume changes during cycling.</abstract><pub>American Chemical Society</pub><doi>10.1021/cm5035358</doi><tpages>6</tpages></addata></record> |
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title | Synthetic, Structural, and Electrochemical Study of Monoclinic Na4Ti5O12 as a Sodium-Ion Battery Anode Material |
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