4.8 Article

Monolithic co-aerogels of carbon/titanium dioxide as three dimensional nanostructured electrodes for energy storage

期刊

JOURNAL OF POWER SOURCES
卷 218, 期 -, 页码 140-147

出版社

ELSEVIER
DOI: 10.1016/j.jpowsour.2012.06.070

关键词

Carbon aerogels; TiO2 aerogels; Sol-gel; Monolith; Lithium ion batteries

资金

  1. Army Research Office (ARO) [W911NF-04-D-0001]
  2. National Science Foundation (NSF) [EF-0830093]
  3. Environmental Protection Agency (EPA) under NSF [EF-0830093]
  4. Duke SMIF (Shared Materials Instrumentation Facilities)

向作者/读者索取更多资源

Conductive fillers, such as amorphous carbon, carbon nanotube and graphene etc., are generally mixed with nanostructured metal oxide materials to improve the performance of electrode materials in energy storage devices. However, the conductive framework that provides path for electric conduction does not normally form a well-connected and robust 3-D network to ensure optimized ions transport. Here, we report a convenient, inexpensive and scalable method for synthesizing hybrid carbon and titanium dioxide co-gels and co-aerogels to improve the electrochemical capacity by combining both the lithium insertion and the surface storage mechanisms in Li ion batteries (LIBs) anodes. A monolithic piece of a hybrid C/TiO2 co-aerogel can be directly used as an active electrode without the addition of binders, such as polyvinylidene fluoride (PVDF). As a result, the performance of LIB anodes using the hybrid co-aerogel is significantly improved over current LIBs based on carbon/titanium oxide composites. The reversible discharge capacity was stabilized at similar to 400 mAh g(-1) at a 168 mA g(-1) scan rate and an operating voltage between 3.0 and 0.05 V vs. Li+/Li with excellent cyclic capacity retention. This approach, however, is not limited to only C/TiO2 system but can be extended to other metal oxides to form co-gels with carbon to improve their potential use in numerous electrochemical, photocatalytic, and photoelectronic devices. (C) 2012 Elsevier B.V. All rights reserved.

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