Highly Conductive, Mechanically Robust, and Electrochemically Inactive TiC/C Nanofiber Scaffold for High-Performance Silicon Anode Batteries
KAUST Grant NumberKUS-l1-001-12
Online Publication Date2011-10-11
Print Publication Date2011-10-25
Permanent link to this recordhttp://hdl.handle.net/10754/598501
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AbstractSilicon has a high specific capacity of 4200 mAh/g as lithium-ion battery anodes, but its rapid capacity fading due to >300% volume expansion and pulverization presents a significant challenge for practical applications. Here we report a core-shell TiC/C/Si inactive/active nanocomposite for Si anodes demonstrating high specific capacity and excellent electrochemical cycling. The amorphous silicon layer serves as the active material to store Li+, while the inactive TiC/C nanofibers act as a conductive and mechanically robust scaffold for electron transport during the Li-Si alloying process. The core-shell TiC/C/Si nanocomposite anode shows ∼3000 mAh g-1 discharge capacity and 92% capacity retention after 100 charge/discharge cycles. The excellent cycling stability and high rate performance could be attributed to the tapering of the nanofibers and the open structure that allows facile Li ion transport and the high conductivity and mechanical stability of the TiC/C scaffold. © 2011 American Chemical Society.
CitationYao Y, Huo K, Hu L, Liu N, Cha JJ, et al. (2011) Highly Conductive, Mechanically Robust, and Electrochemically Inactive TiC/C Nanofiber Scaffold for High-Performance Silicon Anode Batteries. ACS Nano 5: 8346–8351. Available: http://dx.doi.org/10.1021/nn2033693.
SponsorsThis work was partially supported by the Assistant Secretary for Energy Efficiency and Renewable Energy, Office of Vehicle Technologies of the U.S. Department of Energy, under Contract No. DE-AC02-05CH11231, Subcontract No. 6951379 under the Batteries for Advanced Transportation Technologies (BATT) Program. A portion of this work is also supported by the Department of Energy, Office of Basic Energy Sciences, Division of Materials Sciences and Engineering, under Contract DE-AC02-76SF0051, through the SLAC National Accelerator Laboratory LDRD project. Y.C. acknowledges support from the King Abdullah University of Science and Technology Investigator Award (No. KUS-l1-001-12). K.H. acknowledges support from National Natural Science Foundation of China (No. 50902104), City University of Hong Kong Strategic Research Grant No. 7008009, and China Scholarship Council (No. 2010842443).
PublisherAmerican Chemical Society (ACS)
CollectionsPublications Acknowledging KAUST Support
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