Enhanced Electrochemical Performance of Ultracentrifugation-Derived nc-Li3VO4/MWCNT Composites for Hybrid Supercapacitors
Nanocrystalline Li3VO4 dispersed within multiwalled carbon nanotubes (MWCNTs) was prepared using an ultracentrifugation (uc) process and electrochemically characterized in Li-containing electrolyte. When charged and discharged down to 0.1 V vs Li, the material reached 330 mAh g–1 (per composite) at...
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| Veröffentlicht in: | ACS nano Jg. 10; H. 5; S. 5398 - 5404 |
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| Sprache: | Englisch |
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American Chemical Society
24.05.2016
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| ISSN: | 1936-0851, 1936-086X |
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| Abstract | Nanocrystalline Li3VO4 dispersed within multiwalled carbon nanotubes (MWCNTs) was prepared using an ultracentrifugation (uc) process and electrochemically characterized in Li-containing electrolyte. When charged and discharged down to 0.1 V vs Li, the material reached 330 mAh g–1 (per composite) at an average voltage of about 1.0 V vs Li, with more than 50% capacity retention at a high current density of 20 A g–1. This current corresponds to a nearly 500C rate (7.2 s) for a porous carbon electrode normally used in electric double-layer capacitor devices (1C = 40 mA g–1 per activated carbon). The irreversible structure transformation during the first lithiation, assimilated as an activation process, was elucidated by careful investigation of in operando X-ray diffraction and X-ray absorption fine structure measurements. The activation process switches the reaction mechanism from a slow “two-phase” to a fast “solid-solution” in a limited voltage range (2.5–0.76 V vs Li), still keeping the capacity as high as 115 mAh g–1 (per composite). The uc-Li3VO4 composite operated in this potential range after the activation process allows fast Li+ intercalation/deintercalation with a small voltage hysteresis, leading to higher energy efficiency. It offers a promising alternative to replace high-rate Li4Ti5O12 electrodes in hybrid supercapacitor applications. |
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| AbstractList | Nanocrystalline Li3VO4 dispersed within multiwalled carbon nanotubes (MWCNTs) was prepared using an ultracentrifugation (uc) process and electrochemically characterized in Li-containing electrolyte. When charged and discharged down to 0.1 V vs Li, the material reached 330 mAh g–1 (per composite) at an average voltage of about 1.0 V vs Li, with more than 50% capacity retention at a high current density of 20 A g–1. This current corresponds to a nearly 500C rate (7.2 s) for a porous carbon electrode normally used in electric double-layer capacitor devices (1C = 40 mA g–1 per activated carbon). The irreversible structure transformation during the first lithiation, assimilated as an activation process, was elucidated by careful investigation of in operando X-ray diffraction and X-ray absorption fine structure measurements. The activation process switches the reaction mechanism from a slow “two-phase” to a fast “solid-solution” in a limited voltage range (2.5–0.76 V vs Li), still keeping the capacity as high as 115 mAh g–1 (per composite). The uc-Li3VO4 composite operated in this potential range after the activation process allows fast Li+ intercalation/deintercalation with a small voltage hysteresis, leading to higher energy efficiency. It offers a promising alternative to replace high-rate Li4Ti5O12 electrodes in hybrid supercapacitor applications. |
| Author | Iwama, Etsuro Kawabata, Nozomi Nishio, Nagare Kisu, Kazuaki Simon, Patrice Miyamoto, Junichi Naoi, Katsuhiko Rozier, Patrick Naoi, Wako |
| AuthorAffiliation | Tokyo University of Agriculture & Technology Global Innovation Research Organization Advanced Capacitor Research Center Department of Applied Chemistry Division of Art and Innovative Technologies CIRIMAT Université de Toulouse, CNRS, INPT, UPS K&W Inc |
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| Keywords | hyperdispersion initial electrochemical activation Li3VO4 ultrafast charge storage varied energy efficiency ultracentrifugation |
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| Title | Enhanced Electrochemical Performance of Ultracentrifugation-Derived nc-Li3VO4/MWCNT Composites for Hybrid Supercapacitors |
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