Outstanding performance of activated graphene based supercapacitors in ionic liquid electrolyte from –50 to 80°C Wan-Yu Tsai, Rongying Lin, Shanthi Murali, Li Li Zhang, John K. Mcdonough, Rodney S. Ruoff, Pierre-Louis Taberna, Yury Gogotsi, Patrice Simon To cite this version: Wan-Yu Tsai, Rongying Lin, Shanthi Murali, Li Li Zhang, John K. Mcdonough, et al.. Outstanding performance of activated graphene based supercapacitors in ionic liquid electrolyte from –50 to 80°C. Nano Energy, Elsevier, 2013, vol. 2 (n° 3), pp. 403-411. 10.1016/j.nanoen.2012.11.006. hal- 01154261 HAL Id: hal-01154261 https://hal.archives-ouvertes.fr/hal-01154261 Submitted on 21 May 2015 HAL is a multi-disciplinary open access L’archive ouverte pluridisciplinaire HAL, est archive for the deposit and dissemination of sci- destinée au dépôt et à la diffusion de documents entific research documents, whether they are pub- scientifiques de niveau recherche, publiés ou non, lished or not. The documents may come from émanant des établissements d’enseignement et de teaching and research institutions in France or recherche français ou étrangers, des laboratoires abroad, or from public or private research centers. publics ou privés. Open Archive TOULOUSE Archive Ouverte (OATAO) OATAO is an open access repository that collects the work of Toulouse researchers and makes it freely available over the web where possible. This is an author-deposited version published in : http://oatao.univ-toulouse.fr/ Eprints ID : 13894 To link to this article : DOI:10.1016/j.nanoen.2012.11.006 URL : http://dx.doi.org/10.1016/j.nanoen.2012.11.006 To cite this version : Tsai, Wan-Yu and Lin, Rongying and Murali, Shanthi and Zhang, Li Li and McDonough, John K. and Ruoff, Rodney S. and Taberna, Pierre-Louis and Gogotsi, Yury and Simon, Patrice Outstanding performance of activated graphene based supercapacitors in ionic liquid electrolyte from −50 to 80°C. (2013) Nano Energy, vol. 2 (n° 3). pp. 403-411. ISSN 2211-2855 Any correspondance concerning this service should be sent to the repository administrator: [email protected] Outstanding performance of activated graphene based supercapacitors in ionic liquid electrolyte from À50 to 80 1C Wan-Yu Tsaia, Rongying Lina, Shanthi Muralic, Li Li Zhangc, John K. McDonoughd, Rodney S. Ruoffc, Pierre-Louis Tabernaa, Yury Gogotsid,n, Patrice Simona,b,nn aUniversite Paul Sabatier, CIRIMAT UMR CNRS 5085, 118 route de Narbonne, 31062 Toulouse, France bReseau sur le Stockage Electrochimique de l’Energie (RS2E), FR CNRS 3459, France cDepartment of Mechanical Engineering and the Materials Science and Engineering Program, The University of Texas at Austin, One University Station C2200, Austin, TX 78712, United States dDepartment of Materials Science and Engineering & A.J. Drexel Nanotechnology Institute, Drexel University, 3141 Chestnut St., Philadelphia, PA 19104, United States KEYWORDS Abstract Electrochemical High specific surface area (SSA 2000 m2/g) porous KOH-activated microwave exfoliated graphite capacitors; oxide (‘a-MEGO’) electrodes have been tested in a eutectic mixture of ionic liquids (1:1 by weight Activated graphene; or molar ratio N-methyl-N-propylpiperidinium bis(fluorosulfonyl)imide (PIP13-FSI) and N-butyl-N- Ionic liquid mixture; methylpyrrolidinium bis(fluorosulfonyl)imide (PYR -FSI)) as electrolyte for supercapacitor appli- Wide temperature 14 cations. By optimizing the carbon/electrolyte system, outstanding capacitive performance range has been achieved with high capacitance (up to 180 F/g) and wide electrochemical window (up to 3.5 V) over a wide temperature range from À50 1Cto801C. This is the first demonstration of a carbon–ionic liquid system capable of delivering capacitance in excess of 100 F/g below room temperature. The excellent electrochemical response of the proposed couple shows that optimization of the carbon/electrolyte interface is of great importance for improving capacitive energy storage. Introduction Electrochemical double layer capacitors (EDLCs), also known as supercapacitors, store electrical charges between electrode materials and electrolyte ions by electrostatic http://dx.doi.org/10.1016/j.nanoen.2012.11.006 attractions. Supercapacitors had their debut mainly in CMOS first appeared with the discovery by Wilkes et al. in 1982 of memory back-up and are now widely used in power electro- a MeEtImCl/AlCl3 molten salt mixture that was liquid over a nics for peak power shaving and back-up supplies (as wide range of compositions and to temperatures as low as support for power disruption). Today, one of the most À98 1C for a composition of 67% AlCl3 [20]. Other binary promising applications is their use in transportation (in systems have been investigated by Hou et al. [21] using hybrid-electric vehicles (HEVs) in particular) for harvesting imidazolium-based ILs with organic salts. Every et al. [22] braking energy and for faster start-up of the engine [1–3]. reported a eutectic mixture of pure ILs (mixing ethyl- Their increasing use for energy storage is due to a number of methyl-immidazolium tri-fluorosulfonyl-imide (EMI-TFSI) À factors including (i) their high power densities (410 kW/kg), and EMI-CF3SO3 (triflate)) with no evidence of a melting (ii) moderate energy density (5–6 Wh/kg), (iii) that they can point, indeed only a glass transition was observed. be fully charged/discharged in a matter of seconds [4,5], (iv) Pyrrolidinium-based mixtures with TFSI-FSI-based ILs were the cost competitiveness of the materials that they are also found by differential scanning calorimetry to form comprised of, (v) high charge/discharge efficiency, and (vi) eutectic mixtures [23]. Deeper eutectics (À95 1C) were their high cycle life, which is generally longer than the life of however observed to be mainly in mixtures of a common the device being powered. cation with two different anions compared to eutectics Generally, EDLCs are made up of two symmetrical acti- (À25 1C) in mixtures of a common anion with two different vated carbon electrodes that display symmetric charge/ cations. Other binary systems include IL–LiX mixtures as discharge power capability over the complete range of electrolytes for battery applications [24–26]. Henderson potential operation (i.e., from the maximum rated voltage et al. [24] reported decreasing the eutectic temperatures to near zero). Carbon/carbon supercapacitors can be used of pyrrolidinium-based ILs by using different alkyl chain over the complete voltage range without damage for at lengths and Li salt concentrations. least 1 million cycles [6]. Carbon-based electrodes are of As reported before, we have designed IL mixtures with great interest because they are light, of moderate cost, exactly the same anion (FSI) but two different cations: abundant, easy to process, and possess high electronic piperidinium (PIP) and pyrrolidinium (PYR) [27]. These conductivity and high specific surface area (yielding high cations have the same molecular weight and the same charge storage). A variety of different carbon nanostruc- number of atoms of the same nature, with the only tures can be produced that have very high surface areas and difference being their cation molecular structure, namely a wide variety of physical properties, which allows targeting a five-member (piperidinium) or six-member (pyrrolidinium) of different types of applications. Templated carbons [7], heterocycle. Methyl+propyl substituent groups (total of carbide-derived carbons (CDCs) [8–10], ‘onion-like’ carbons 4 carbons on side chains) are used for synthesizing the PIP- (OLCs) [11], carbon fabrics (cloth, fibers) [12], nanotubes based cation and methyl+butyl substituent groups (total of [13], activated graphene [14] and nanohorns [15] have been 5 carbons on side chains) for synthesizing the PYR-based used as electrodes for EDLC applications [16]. cation. The concept is to maintain similar intermolecular Batteries have much higher energy densities (up to interactions due to the similar constituent atoms of the 250 Wh/kg for Li-ion) than current commercial supercapa- two cations, while also increasing disorder and asymmetry citors (5 Wh/kg) [17]. One approach to increase energy among the cations to hinder lattice formation to lower density of supercapacitors is with ionic liquid electrolytes the melting point, but still maintaining good miscibility. À that offer better electrochemical stability than that of the Amongst common anions such as hexafluorophosphate (PF6 ), À À aqueous (1.23 V) and organic (2.7 V) electrolytes currently tetrafluoroborate (BF4 ), bis(trifluorosulfonyl)imide (TFSI ) used. Ionic liquids (IL) – salts (mainly, organic) that are and bis(fluorosulfonyl)imide (FSIÀ) anions, the imides (TFSIÀ À À liquid at room temperature – are being explored as electro- and FSI ) have emerged as popular alternatives to the PF6 À À À lytes for Electrical Energy Storage (EES) systems owing to and BF4 anions due to the susceptibility of the PF6 and BF4 their high thermal (up to 350 1C) and electrochemical (up to anions to hydrolysis, leading to the production of hazardous 6 V) stability [18]. Their high heat capacity, a large cohesive hydrogen fluoride [28–32]. This is why hydrophobic TFSIÀ and energy, and negligible vapor pressure at elevated tempera- FSIÀ anions are increasingly being studied as electrolytes for tures make them safe and non-flammable electrolytes. This energy storage [33–35]. The FSIÀ ion has been selected to be is especially important in energy storage applications when the anion for the electrolyte used in this study due to its devices need to perform under extreme temperature con- generally higher conductivity and lower viscosity as compared ditions that can raise/cause safety issues. The raison d’etreˆ to the TFSIÀ ionwhenpairedwiththesamecation[36], for exploring eutectic mixtures of ionic liquids is their large because of the smaller size and hence higher mobility of the stable liquidus temperature range (the span of tempera- FSIÀ ion. Cations were chosen by comparing their stability. The tures between the freezing point and boiling point of a electrochemical stability of commonly used cations of ILs liquid, such as from À80 1CtoZ250 1C).