4.7 Article

Textile carbon network with enhanced areal capacitance prepared by chemical activation of cotton cloth

期刊

JOURNAL OF COLLOID AND INTERFACE SCIENCE
卷 553, 期 -, 页码 705-712

出版社

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.jcis.2019.06.048

关键词

Textile carbon network; Cotton cloth; Chemical activation; Capacitive performance; Solid-state supercapacitor

资金

  1. National Natural Science Foundation of China, China [51772181, 51605034, 51711540300, 61804009]
  2. 111 project [B14041]
  3. National Key Research and Development Program of China, China [2016YFA0202703]
  4. Hundred Talents Program of the Chinese Academy of Science, China
  5. State key laboratory of precision measuring technology and instruments (Tianjin University)

向作者/读者索取更多资源

Flexible all-solid-state supercapacitors are emerging as one of the most gratifying energy storage devices in the application of portable and wearable electronics. The design and fabrication of high-performance and flexible electrodes are crucial for an all-solid-state supercapacitor. Herein we report a free-standing textile carbon network composed of activated textile carbon (aTC) by thermal annealing of cotton cloth, followed by chemical activation with KOH. The aTC fibers remain the unique features of surface wrinkles and hollow tubular structure of the natural cotton fibers, together with the abundant micropores introduced by further chemical activation, making the specific surface area of the aTC-3 fibers reach 1075 m(2) g(-1) with a high electrical conductivity of 1506 S m(-1). When served as the supercapacitor electrode, the aTC-3 exhibits a specific capacitance as high as 1026 mF cm(-2) with a capacitance retention of 85% at 100 mA cm(-2) (868 mF cm(-2)), which is far superior to commercial carbon cloth. More interestingly, the long-range continuous structure enables aTC as electrode of solid-state supercapacitor, which delivers an outstanding mechanical flexibility without noticeable change of capacitive performance when folded at maximal angle of 180 degrees over 200 cycles. This work may benefit the low-cost mass production of carbon-based flexible electrodes for developing wearable electrochemical energy storage systems. (C) 2019 Elsevier Inc. All rights reserved.

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