4.6 Article

Water-in-Acid Gel Polymer Electrolyte Realized through a Phosphoric Acid-Enriched Polyelectrolyte Matrix toward Solid-State Supercapacitors

期刊

ACS SUSTAINABLE CHEMISTRY & ENGINEERING
卷 6, 期 10, 页码 12630-12640

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acssuschemeng.8b01175

关键词

Supercapacitor; Polyaniline; Gel polymer electrolyte; Water-in-acid electrolyte; Phosphoric acid; Concentrated electrolytes; Polyelectrolyte; Noncovalent interactions

资金

  1. University Grants Commission (UGC), New Delhi
  2. Council of Scientific and Industrial Research (CSIR), New Delhi [TLP003526]

向作者/读者索取更多资源

A new concept of water-in-acid gel polymer electrolytes (GPEs) is introduced. The simple and scalable UV-light-assisted synthesis of a copolymer matrix possessing polyelectrolyte behavior, followed by swelling in minimally diluted H3PO4 (15.1 M/88 wt % aqueous solution), effects formation of a high proton-conducting, self-standing, and mechanically stable polyelectrolyte GPE (PGPE). Retention of high mechanical stability despite the presence of a large amount of liquid species makes it a promising candidate for replacing conventional GPEs. The high proton conductivity (9.8 X 10(-2) S cm(-1)) of the PGPE at an ambient temperature of 303 K is attributed to the high concentration of the conducting species present in the polymer matrix. The PGPE-based polyaniline (PANI) supercapacitor device (PANI-1) with a mass loading of 1 mg cm(-2) exhibits a high specific gravimetric capacitance of 385 F g(-1) at a current density of 0.25 mA cm(-2). At the same current density, the PANI-5 device retains high gravimetric and areal capacitance values of 258 F g(-1) and 1288 mF cm(-2), respectively. The low equivalent series resistance value of 0.78 Omega (for the PANI-5 device) further proves the excellent electrode-electrolyte interface formed by the water-in-acid GPE. A 100% capacitance retention even after 9000 continuous charge-discharge cycles strongly indicates the feasibility of adopting water-in-acid GPEs in future supercapacitors.

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