scholarly journals Reducing the Self-Discharge Rate of Supercapacitors by Suppressing Electron Transfer in the Electric Double Layer

Author(s):  
Mingwei Shi ◽  
Zailei Zhang ◽  
Man Zhao ◽  
Xianmao Lu ◽  
Zhong Lin (Z.L.) Wang

Abstract Designing supercapacitors with suppressed self-discharge for long-term energy storage has been a challenge. In this work, we demonstrate that substantially reduced self-discharge rate can be achieved by using highly concentrated electrolytes. Specifically, when supercapacitors with 14 M LiCl electrolyte are charged to 0.80 V, the open circuit voltage (OCV) drops to 0.65 V in 24 h. In stark contrast, when the electrolyte concentration is reduced to 1 M, the OCV drops from 0.80 to 0.65 V within only 0.3 h, which was 80 times faster than that with 14 M LiCl. Decreased OCV decay rate at high electrolyte concentration is also confirmed for supercapacitors with different electrolytes (e.g., LiNO3) or at higher charging voltages (1.60 V). The slow self-discharge in highly concentrated electrolyte can be largely attributed to impeded electron transfer between the electrodes and electrolyte due to the formation of hydration clusters and reduced amount of free water molecules, thereby faradaic reactions that cause fast self-discharge are reduced. Our study not only supports the newly revised model about the formation of electric double layer with the inclusion of electron transfer, but also points a direction for substantially reducing the self-discharge rate of supercapacitors.

2020 ◽  
Vol 142 (35) ◽  
pp. 14940-14946 ◽  
Author(s):  
Rachel E. Bangle ◽  
Jenny Schneider ◽  
Daniel T. Conroy ◽  
Bruno M. Aramburu-Trošelj ◽  
Gerald J. Meyer

MRS Advances ◽  
2016 ◽  
Vol 1 (22) ◽  
pp. 1619-1624 ◽  
Author(s):  
Anishkumar Manoharan ◽  
Z. Ryan Tian ◽  
Simon S. Ang

ABSTRACTA method for synthesizing and structuring 2D-MoS2/rGO (molybdenum disulfide/reduced graphene oxide) nanocomposite-based electric double layer capacitor (EDLC) that has a slower discharge rate and higher energy density than rGO-based EDLC (RG-EDLC) is reported. The rGO electrode and the nanocomposite were characterized using powder XRD and SEM for their physical and structural properties. Cyclic voltammetry (CV) was used to analyze the electrochemical behavior of the EDLCs. A maximum current density at which the MoS2/rGO nanocomposite-based EDLC (MRG-EDLC) can charge and discharge was 2.5 A/g, while it was 1A/g for the RG-EDLC. The specific capacitance of the MRG-EDLC was 14.52 F/g at 0.5 A/g with an energy density of 8.06 Wh/kg.


2015 ◽  
Vol 17 (2) ◽  
pp. 928-932 ◽  
Author(s):  
Stanisław Lamperski ◽  
Monika Płuciennik ◽  
Christopher W. Outhwaite

The transition of the solvent primitive model electrolyte differential capacitance from a minimum to a maximum, at fixed total packing fraction, occurs at a higher electrolyte concentration than that of the restricted primitive model electrolyte.


2016 ◽  
Vol 20 (2) ◽  
pp. 441-458 ◽  
Author(s):  
Manman Ma ◽  
Shuangliang Zhao ◽  
Zhenli Xu

AbstractThe differential capacitance of electric double-layer capacitors is studied by developing a generalized model of the self-consistent Gaussian field theory. This model includes many-body effects of particles near the interface such as ionic sizes, the order of water alignment and electrostatic correlations, and thus can present more accurate predictions of the electric double-layer structure and hence the capacitance than traditional continuum theories. Analytical simplification of the model and efficient numerical method are introduced, in particular, the approximation of the self-Green's function which describes the self energy of a mobile ion. We show that, when the applied voltage on interfaces is small the dielectric effect of the electrode materials plays an important role. For large voltage, this effect is screened, but the dielectric saturation due to the alignment of the nearby water is shown to be essential. For 2:1 electrolytes, abnormal enhancement on the capacitance due to the dielectric electrode is observed, which is due to the interplay of the image charge effect and Born solvation energy in the self energy of ions.


Energies ◽  
2020 ◽  
Vol 13 (4) ◽  
pp. 783 ◽  
Author(s):  
Roberto de Fazio ◽  
Donato Cafagna ◽  
Giorgio Marcuccio ◽  
Paolo Visconti

This paper aims to study the limitations and performances of the main energy storage devices commonly used in energy harvesting applications, namely super-capacitors (SC) and lithium polymer (LiPo) batteries. The self-discharge phenomenon is the main limitation to the employment of SCs to store energy for a long time, thus reducing efficiency and autonomy of the energy harvesting system. Therefore, the analysis of self-discharge trends was carried out for three different models of commercial SCs, describing the phenomenon in terms of self-discharge rate and internal resistance. In addition, physical interpretations concerning the self-discharge mechanism based on the experimental data are provided, thus explaining the two super-imposed phenomena featured by distinct time constants. Afterwards, the dependence of self-discharge phenomenon from the charging time duration (namely, SCs charged at 5 V and then kept under charge for one or five hours) was analyzed; by comparing the voltage drop during the self-discharge process, a self-discharge reduction for longer charging durations was obtained and the physical interpretation provided (at best −6.8% after 24 h and −13.4% after 120 h). Finally, self-discharge trends of two commercial 380 mAh LiPo batteries (model LW 752035) were acquired and analyzed; the obtained results show an open circuit voltage reduction of only 0.59% in the first 24 h and just 1.43% after 124 h.


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