Thermogalvanic and Thermocapacitive Behavior of Superabsorbent Hydrogels for Combined Low-Temperature Thermal Energy Conversion and Harvesting

被引:34
作者
Buckingham, Mark A. [1 ]
Zhang, Shuai [2 ]
Liu, Yuqing [2 ]
Chen, Jun [2 ]
Marken, Frank [3 ]
Aldous, Leigh [1 ]
机构
[1] Kings Coll London, Dept Chem, London SE1 1DB, England
[2] Univ Wollongong, ARC Ctr Excellence Electromat Sci, Intelligent Polymer Res Inst, AIIM Facil, Wollongong, NSW 2500, Australia
[3] Univ Bath, Dept Chem, Bath BA2 7AY, Avon, England
基金
中国国家自然科学基金; 英国工程与自然科学研究理事会; 澳大利亚研究理事会;
关键词
thermoelectrochemistry; thermogalvanic; thermocapacitance; gelled electrolyte; energy harvesting; REDOX COUPLE; NATURAL-CONVECTION; POWER-GENERATION; N-TYPE; CELLS; ELECTROLYTES; HEAT; THERMOELECTROCHEMISTRY; SUPERCAPACITORS;
D O I
10.1021/acsaem.1c02060
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Around two-thirds of the energy generated by the society is lost as waste heat. Thermogalvanic cells can continuously convert thermal energy directly into electrical energy. Conversely, thermocapacitors can convert and store thermal energy as thermocapacitance. Here, we report two superabsorbent monolithic polymer hydrogel matrices designed through vessel-templated synthesis, which act as soft host materials for extremely high concentrations of redox-active ions, namely, [Fe(CN)(6)](3-/4-) and Fe2+/3+. These highly charged superabsorbent hydrogels were found to improve both electrocatalysis and ohmic resistance of the hosted redox couples, preventing electrolyte leakage, and enable the ability to perform both thermogalvanic conversion and thermocapacitive storage. An unoptimized maximum thermogalvanic power density was observed at ca. 95 mW m(-2) (Delta T of 20 K), on par with other reported gelled systems. An optimized thermocapacitance density of ca. 220 F cm(-2) was achieved, which is 15-fold higher than the highest previously reported. These novel systems therefore present new possibilities in both the harvesting and storage of low-grade waste thermal energy.
引用
收藏
页码:11204 / 11214
页数:11
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