The "In situ electrolyte" as a sustainable alternative for the realization of high-power devices

被引:1
|
作者
Sander, Miriam [1 ]
Magar, Sandesh Darlami [2 ,3 ]
Etter, Martin [4 ]
Balducci, Andrea [2 ,3 ]
Borchardt, Lars [1 ]
机构
[1] Ruhr Univ Bochum, Inorgan Chem 1, Univ Str 150, D-44801 Bochum, Germany
[2] Friedrich Schiller Univ, Inst Tech Chem & Environm Chem, Philosophenweg 7a, D-07743 Jena, Germany
[3] Friedrich Schiller Univ, Ctr Energy & Environm Chem Jena CEEC Jena, Philosophenweg 7a, D-07743 Jena, Germany
[4] Deutsch Elektronen Synchrotron DESY, Notkestr 85, D-22607 Hamburg, Germany
关键词
in situ electrolyte; pre-lithiation; salt loaded carbon; mechanochemistry; high-power devices; ION CAPACITORS; SOLVENT-FREE; LITHIUM METAL; HIGH-ENERGY; CARBON; SUPERCAPACITORS; GRAPHITE; GREEN; ANODE; GASIFICATION;
D O I
10.1002/cssc.202301746
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The "in situ electrolyte" displays a concept for electric double-layer- as well as metal-ion capacitors in which the by-products formed during carbon synthesis serve directly as electrolyte salt to minimize waste. In this work, the concept is applied for lithium- and sodium-based systems realizing EDLCs containing aqueous, "Water in Salt" (up to 1.8 V) as well as organic (2.4 V) electrolytes. Via the mechanochemical synthesis, carbon materials with surface areas up to 2000 m(2) g(-1) and an optimal amount of remaining by-product are designed from the renewable resource lignin. Different cation-anion combinations are enabled by further modification directly inside the pores creating imide-based salts which are tracked by synchrotron in situ XRD. By the addition of solvents, the EDLCs show good capacitances up to 21 F g(-1) combined with excellent rate performances and stabilities. Moreover, the LiTFSI loaded carbon as positive electrode introduces a new tunable lithium alternative for the pre-lithiation of Li-ion capacitors displaying a good rate performance and cyclability.
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页数:9
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