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      Thermal charging of supercapacitors: a perspective

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          Abstract

          A change in temperature can modify the ion density near the electrode surface, and create a potential difference across a supercapacitor.

          Abstract

          Thermally-induced self-charging of electrochemical capacitors is a recently reported phenomenon, whereby a change in the temperature of a supercapacitor can lead to the generation of a voltage difference across the device. The temperature change is induced for all the device or only some of its components, unaided by or in combination with other voltage-inducing effects. This phenomenon is based on old and known physical concepts, whose use for energy generation became possible due to the advent of nanomaterials. The purpose of this article is to present the research conducted on this phenomenon, and offer a prospective direction for further progress in the field. First, we briefly introduce the existing heat-to-electricity conversion technologies, and their underlying principles. Then, we examine the main thermally-induced phenomena occurring in the environment of an ionic electrolyte, and/or a solid–liquid interface. After that, we review the studies conducted on thermally-induced self-charging in electrochemical capacitors, and the performance factors investigated so far. Finally, we present the future prospects of this field in the form of questions to address, additional factors to inspect, and materials of potential benefit for the design of thermally-chargeable supercapacitors.

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          Most cited references168

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          Materials for electrochemical capacitors.

          Electrochemical capacitors, also called supercapacitors, store energy using either ion adsorption (electrochemical double layer capacitors) or fast surface redox reactions (pseudo-capacitors). They can complement or replace batteries in electrical energy storage and harvesting applications, when high power delivery or uptake is needed. A notable improvement in performance has been achieved through recent advances in understanding charge storage mechanisms and the development of advanced nanostructured materials. The discovery that ion desolvation occurs in pores smaller than the solvated ions has led to higher capacitance for electrochemical double layer capacitors using carbon electrodes with subnanometre pores, and opened the door to designing high-energy density devices using a variety of electrolytes. Combination of pseudo-capacitive nanomaterials, including oxides, nitrides and polymers, with the latest generation of nanostructured lithium electrodes has brought the energy density of electrochemical capacitors closer to that of batteries. The use of carbon nanotubes has further advanced micro-electrochemical capacitors, enabling flexible and adaptable devices to be made. Mathematical modelling and simulation will be the key to success in designing tomorrow's high-energy and high-power devices.
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            Materials science. Where do batteries end and supercapacitors begin?

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              Anomalous increase in carbon capacitance at pore sizes less than 1 nanometer.

              Carbon supercapacitors, which are energy storage devices that use ion adsorption on the surface of highly porous materials to store charge, have numerous advantages over other power-source technologies, but could realize further gains if their electrodes were properly optimized. Studying the effect of the pore size on capacitance could potentially improve performance by maximizing the electrode surface area accessible to electrolyte ions, but until recently, no studies had addressed the lower size limit of accessible pores. Using carbide-derived carbon, we generated pores with average sizes from 0.6 to 2.25 nanometer and studied double-layer capacitance in an organic electrolyte. The results challenge the long-held axiom that pores smaller than the size of solvated electrolyte ions are incapable of contributing to charge storage.
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                Author and article information

                Contributors
                Journal
                SEFUA7
                Sustainable Energy & Fuels
                Sustainable Energy Fuels
                Royal Society of Chemistry (RSC)
                2398-4902
                2017
                2017
                : 1
                : 7
                : 1457-1474
                Affiliations
                [1 ]Shenzhen Engineering Lab for Supercapacitor Materials
                [2 ]Shenzhen Key Laboratory for Advanced Materials
                [3 ]Department of Material Science and Engineering
                [4 ]Shenzhen Graduate School
                [5 ]Harbin Institute of Technology
                Article
                10.1039/C7SE00239D
                c77c4e56-c2b9-47e7-aa67-b7d7e844c8e3
                © 2017
                History

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