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Electrochemical Characteristics and Li+ Ion Intercalation Kinetics of Dual-Phase Li4Ti5O12/Li2TiO3 Composite in the Voltage Range 0–3 V
Li4Ti5O12, Li2TiO3, and dual-phase Li4Ti5O12/Li2TiO3 composite were prepared by sol–gel method with average particle size of 1, 0.3, and 0.4 μm, respectively. Though Li2TiO3 is electrochemically inactive, the rate capability of Li4Ti5O12/Li2TiO3 is comparable to that of Li4Ti5O12 at different curren...
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Published in: | Journal of physical chemistry. C 2016-05, Vol.120 (18), p.9553-9561 |
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container_title | Journal of physical chemistry. C |
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creator | Bhatti, Humaira S Anjum, Dalaver H Ullah, Shafiq Ahmed, Bilal Habib, Amir Karim, Altaf Hasanain, S. K |
description | Li4Ti5O12, Li2TiO3, and dual-phase Li4Ti5O12/Li2TiO3 composite were prepared by sol–gel method with average particle size of 1, 0.3, and 0.4 μm, respectively. Though Li2TiO3 is electrochemically inactive, the rate capability of Li4Ti5O12/Li2TiO3 is comparable to that of Li4Ti5O12 at different current rates. Li4Ti5O12/Li2TiO3 also shows a good rate performance of 90 mA h g–1 at a high rate of 10 C in the voltage range 1–3 V, attributable to increased interfaces in the composite. While Li4Ti5O12 delivers a capacity retention of 88.6% at 0.2 C over 50 cycles, Li4Ti5O12/Li2TiO3 exhibits no capacity fading at 0.2 C (40 cycles) and a capacity retention of 98.45% at 0.5 C (50 cycles). This highly stable cycling performance is attributed to the contribution of Li2TiO3 in preventing the undesirable reaction of Li4Ti5O12 with the electrolyte during cycling. Cyclic voltammetric curves of Li4Ti5O12/Li2TiO3 in the 0–3 V range exhibit two anodic peaks at 1.51 and 0.7–0.0 V, indicating two modes of lithium intercalation into the lattice sites of active material. Owing to enhanced intercalation/deintercalation kinetics in 0–3 V, the composite electrode delivers a superior rate performance of 203 mAh/g at 2.85 C and 140 mAh/g at 5.7 C with good reversible capacity retention over 100 cycles. |
doi_str_mv | 10.1021/acs.jpcc.5b12114 |
format | article |
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K</creator><creatorcontrib>Bhatti, Humaira S ; Anjum, Dalaver H ; Ullah, Shafiq ; Ahmed, Bilal ; Habib, Amir ; Karim, Altaf ; Hasanain, S. K</creatorcontrib><description>Li4Ti5O12, Li2TiO3, and dual-phase Li4Ti5O12/Li2TiO3 composite were prepared by sol–gel method with average particle size of 1, 0.3, and 0.4 μm, respectively. Though Li2TiO3 is electrochemically inactive, the rate capability of Li4Ti5O12/Li2TiO3 is comparable to that of Li4Ti5O12 at different current rates. Li4Ti5O12/Li2TiO3 also shows a good rate performance of 90 mA h g–1 at a high rate of 10 C in the voltage range 1–3 V, attributable to increased interfaces in the composite. While Li4Ti5O12 delivers a capacity retention of 88.6% at 0.2 C over 50 cycles, Li4Ti5O12/Li2TiO3 exhibits no capacity fading at 0.2 C (40 cycles) and a capacity retention of 98.45% at 0.5 C (50 cycles). This highly stable cycling performance is attributed to the contribution of Li2TiO3 in preventing the undesirable reaction of Li4Ti5O12 with the electrolyte during cycling. Cyclic voltammetric curves of Li4Ti5O12/Li2TiO3 in the 0–3 V range exhibit two anodic peaks at 1.51 and 0.7–0.0 V, indicating two modes of lithium intercalation into the lattice sites of active material. Owing to enhanced intercalation/deintercalation kinetics in 0–3 V, the composite electrode delivers a superior rate performance of 203 mAh/g at 2.85 C and 140 mAh/g at 5.7 C with good reversible capacity retention over 100 cycles.</description><identifier>ISSN: 1932-7447</identifier><identifier>EISSN: 1932-7455</identifier><identifier>DOI: 10.1021/acs.jpcc.5b12114</identifier><language>eng</language><publisher>American Chemical Society</publisher><ispartof>Journal of physical chemistry. C, 2016-05, Vol.120 (18), p.9553-9561</ispartof><rights>Copyright © 2016 American Chemical Society</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>314,780,784,27924,27925</link.rule.ids></links><search><creatorcontrib>Bhatti, Humaira S</creatorcontrib><creatorcontrib>Anjum, Dalaver H</creatorcontrib><creatorcontrib>Ullah, Shafiq</creatorcontrib><creatorcontrib>Ahmed, Bilal</creatorcontrib><creatorcontrib>Habib, Amir</creatorcontrib><creatorcontrib>Karim, Altaf</creatorcontrib><creatorcontrib>Hasanain, S. K</creatorcontrib><title>Electrochemical Characteristics and Li+ Ion Intercalation Kinetics of Dual-Phase Li4Ti5O12/Li2TiO3 Composite in the Voltage Range 0–3 V</title><title>Journal of physical chemistry. C</title><addtitle>J. Phys. Chem. C</addtitle><description>Li4Ti5O12, Li2TiO3, and dual-phase Li4Ti5O12/Li2TiO3 composite were prepared by sol–gel method with average particle size of 1, 0.3, and 0.4 μm, respectively. Though Li2TiO3 is electrochemically inactive, the rate capability of Li4Ti5O12/Li2TiO3 is comparable to that of Li4Ti5O12 at different current rates. Li4Ti5O12/Li2TiO3 also shows a good rate performance of 90 mA h g–1 at a high rate of 10 C in the voltage range 1–3 V, attributable to increased interfaces in the composite. While Li4Ti5O12 delivers a capacity retention of 88.6% at 0.2 C over 50 cycles, Li4Ti5O12/Li2TiO3 exhibits no capacity fading at 0.2 C (40 cycles) and a capacity retention of 98.45% at 0.5 C (50 cycles). This highly stable cycling performance is attributed to the contribution of Li2TiO3 in preventing the undesirable reaction of Li4Ti5O12 with the electrolyte during cycling. Cyclic voltammetric curves of Li4Ti5O12/Li2TiO3 in the 0–3 V range exhibit two anodic peaks at 1.51 and 0.7–0.0 V, indicating two modes of lithium intercalation into the lattice sites of active material. Owing to enhanced intercalation/deintercalation kinetics in 0–3 V, the composite electrode delivers a superior rate performance of 203 mAh/g at 2.85 C and 140 mAh/g at 5.7 C with good reversible capacity retention over 100 cycles.</description><issn>1932-7447</issn><issn>1932-7455</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><sourceid/><recordid>eNo9kEtLw0AUhQdRsFb3LmevaedpkqXEqsVAREK34XZyY6akSclM925d-w_9JY61uLmPw-Ee7kfINWczzgSfg3Gzzc6YmV5zwbk6IROeShHFSuvT_1nF5-TCuQ1jWjIuJ-Rz0aHx42Ba3FoDHc1aGMF4HK3z1jgKfU1ze0OXQ0-XfdCDCbwN24vt8WAZGvqwhy56bcFhMKvS6oKLeW5FaQtJs2G7G5z1SG1PfYt0NXQe3pG-QR8q-_74knR1Sc4a6BxeHfuUlI-LMnuO8uJpmd3nEQiR-siIZs0RRXgA13dKihSVhqaOWSIYGtRGK5akCFwkmECjOGMirqGWaBRTckpu_84GYNVm2I99CKs4q34pVgcxUKyOFOUPcVBn2g</recordid><startdate>20160512</startdate><enddate>20160512</enddate><creator>Bhatti, Humaira S</creator><creator>Anjum, Dalaver H</creator><creator>Ullah, Shafiq</creator><creator>Ahmed, Bilal</creator><creator>Habib, Amir</creator><creator>Karim, Altaf</creator><creator>Hasanain, S. K</creator><general>American Chemical Society</general><scope/></search><sort><creationdate>20160512</creationdate><title>Electrochemical Characteristics and Li+ Ion Intercalation Kinetics of Dual-Phase Li4Ti5O12/Li2TiO3 Composite in the Voltage Range 0–3 V</title><author>Bhatti, Humaira S ; Anjum, Dalaver H ; Ullah, Shafiq ; Ahmed, Bilal ; Habib, Amir ; Karim, Altaf ; Hasanain, S. K</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a229t-c2fb1ee2053eb64329e45afd70820ece5c54089ea128e8af410027dad3ec4043</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Bhatti, Humaira S</creatorcontrib><creatorcontrib>Anjum, Dalaver H</creatorcontrib><creatorcontrib>Ullah, Shafiq</creatorcontrib><creatorcontrib>Ahmed, Bilal</creatorcontrib><creatorcontrib>Habib, Amir</creatorcontrib><creatorcontrib>Karim, Altaf</creatorcontrib><creatorcontrib>Hasanain, S. K</creatorcontrib><jtitle>Journal of physical chemistry. C</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Bhatti, Humaira S</au><au>Anjum, Dalaver H</au><au>Ullah, Shafiq</au><au>Ahmed, Bilal</au><au>Habib, Amir</au><au>Karim, Altaf</au><au>Hasanain, S. K</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Electrochemical Characteristics and Li+ Ion Intercalation Kinetics of Dual-Phase Li4Ti5O12/Li2TiO3 Composite in the Voltage Range 0–3 V</atitle><jtitle>Journal of physical chemistry. C</jtitle><addtitle>J. Phys. Chem. C</addtitle><date>2016-05-12</date><risdate>2016</risdate><volume>120</volume><issue>18</issue><spage>9553</spage><epage>9561</epage><pages>9553-9561</pages><issn>1932-7447</issn><eissn>1932-7455</eissn><abstract>Li4Ti5O12, Li2TiO3, and dual-phase Li4Ti5O12/Li2TiO3 composite were prepared by sol–gel method with average particle size of 1, 0.3, and 0.4 μm, respectively. Though Li2TiO3 is electrochemically inactive, the rate capability of Li4Ti5O12/Li2TiO3 is comparable to that of Li4Ti5O12 at different current rates. Li4Ti5O12/Li2TiO3 also shows a good rate performance of 90 mA h g–1 at a high rate of 10 C in the voltage range 1–3 V, attributable to increased interfaces in the composite. While Li4Ti5O12 delivers a capacity retention of 88.6% at 0.2 C over 50 cycles, Li4Ti5O12/Li2TiO3 exhibits no capacity fading at 0.2 C (40 cycles) and a capacity retention of 98.45% at 0.5 C (50 cycles). This highly stable cycling performance is attributed to the contribution of Li2TiO3 in preventing the undesirable reaction of Li4Ti5O12 with the electrolyte during cycling. Cyclic voltammetric curves of Li4Ti5O12/Li2TiO3 in the 0–3 V range exhibit two anodic peaks at 1.51 and 0.7–0.0 V, indicating two modes of lithium intercalation into the lattice sites of active material. Owing to enhanced intercalation/deintercalation kinetics in 0–3 V, the composite electrode delivers a superior rate performance of 203 mAh/g at 2.85 C and 140 mAh/g at 5.7 C with good reversible capacity retention over 100 cycles.</abstract><pub>American Chemical Society</pub><doi>10.1021/acs.jpcc.5b12114</doi><tpages>9</tpages></addata></record> |
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title | Electrochemical Characteristics and Li+ Ion Intercalation Kinetics of Dual-Phase Li4Ti5O12/Li2TiO3 Composite in the Voltage Range 0–3 V |
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