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Self-Assembled Flexible and Integratable 3D Microtubular Asymmetric Supercapacitors
2019, Li, F., Wang, J., Liu, L., Qu, J., Li, Y., Bandari, V.K., Karnaushenko, D., Becker, C., Faghih, M., Kang, T., Baunack, S., Zhu, M., Zhu, F., Schmidt, O.G.
The rapid development of microelectronics has equally rapidly increased the demand for miniaturized energy storage devices. On-chip microsupercapacitors (MSCs), as promising power candidates, possess great potential to complement or replace electrolytic capacitors and microbatteries in various applications. However, the areal capacities and energy densities of the planar MSCs are commonly limited by the low voltage window, the thin layer of the electrode materials and complex fabrication processes. Here, a new-type three-dimensional (3D) tubular asymmetric MSC with small footprint area, high potential window, ultrahigh areal energy density, and long-term cycling stability is fabricated with shapeable materials and photolithographic technologies, which are compatible with modern microelectronic fabrication procedures widely used in industry. Benefiting from the novel architecture, the 3D asymmetric MSC displays an ultrahigh areal capacitance of 88.6 mF cm−2 and areal energy density of 28.69 mW h cm−2, superior to most reported interdigitated MSCs. Furthermore, the 3D tubular MSCs demonstrate remarkable cycling stability and the capacitance retention is up to 91.8% over 12 000 cycles. It is believed that the efficient fabrication methodology can be used to construct various integratable microscale tubular energy storage devices with small footprint area and high performance for miniaturized electronics.
In-situ and ex-situ measurements of thermal conductivity of supercapacitors
2014, Hauge, H.H., Presser, V., Burheim, O.
Thermal signature of supercapacitors are investigated in-situ and ex-situ using commercial supercapacitors. Regarding the in-situ method, four supercapacitors were connected in series, with thermocouples embedded between the supercapacitors. As the applied current was increased, the temperature measured at the intrinsic positions also increased. When cycling at a current density of 0.11Acm-2 the centre temperature increased by 14K compared to the stack surface temperature. This is an important figure as literature states that an increase of 10K leads to a corresponding decrease in the lifetime by a factor of 2. Using the obtained temperature profiles, the effective thermal conductivity of the stack was found to vary between 0.5WK-1m-1 and 1.0WK-1m-1, depending on the compaction of the stack. For the ex-situ measurements, the thermal conductivity and the thicknesses of the supercapacitor material layers were measured individually in order to determine the corresponding thermal conductivity of the stack. When using this method an effective thermal conductivity of the stack of 0.53 ± 0.06WK-1m-1 was obtained. The analysis also demonstrated that the main contributor to the thermal resistivity and conductivity of the supercapacitor construction is the electrodes. This demonstrates that when managing heat from supercapacitors it is important to focus on the thermal conductivity of the components materials.
Tin/vanadium redox electrolyte for battery-like energy storage capacity combined with supercapacitor-like power handling
2016, Lee, Juhan, Krüner, Benjamin, Tolosa, Aura, Sathyamoorthi, Sethuraman, Kim, Daekyu, Choudhury, Soumyadip, Seo, Kum-Hee, Presser, Volker
We introduce a high performance hybrid electrochemical energy storage system based on an aqueous electrolyte containing tin sulfate (SnSO4) and vanadyl sulfate (VOSO4) with nanoporous activated carbon. The energy storage mechanism of this system benefits from the unique synergy of concurrent electric double-layer formation, reversible tin redox reactions, and three-step redox reactions of vanadium. The hybrid system showed excellent electrochemical properties such as a promising energy capacity (ca. 75 W h kg−1, 30 W h L−1) and a maximum power of up to 1.5 kW kg−1 (600 W L−1, 250 W m−2), exhibiting capacitor-like galvanostatic cycling stability and a low level of self-discharging rate.
Emulsion soft templating of carbide-derived carbon nanospheres with controllable porosity for capacitive electrochemical energy storage
2015, Oschatz, Martin, Zeiger, Marco, Jaeckel, Nicolas, Strubel, Patrick, Borchardt, Lars, Reinhold, Romy, Nickel, Winfried, Eckert, Jürgen, Presser, Volker, Kaskel, Stefan
A new approach to produce carbide-derived carbon nanospheres of 20-200 nm in diameter based on a novel soft-templating technique is presented. Platinum catalysis is used for the cross-linking of liquid (allylhydrido)polycarbosilane polymer chains with para-divinylbenzene within oil-in-water miniemulsions. Quantitative implementation of the pre-ceramic polymer can be achieved allowing precise control over the resulting materials. After pyrolysis and high-temperature chlorine treatment, resulting particles offer ideal spherical shape, very high specific surface area (up to 2347 m^2/g^-1), and large micro/mesopore volume (up to 1.67 cm^3/g^-1). The internal pore structure of the nanospheres is controllable by the composition of the oil phase within the miniemulsions. The materials are highly suitable for electrochemical double-layer capacitors with high specific capacitances in aqueous 1 M Na2SO4 solution (110 F/g^-1) and organic 1 M tetraethylammonium tetrafluoroborate in acetonitrile (130 F/g^-1).