A transversal low-cost pre-metallation strategy enabling ultrafast and stable metal ion capacitor technologies

Metal ion capacitors (MICs) are foreseen to be a complementary alternative of vital importance to current energy storage issues, coupling high energy density delivered by batteries with high power/long cycle life offered by supercapacitors. The prime issues in realising this technology are pre-metal...

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Published inEnergy & environmental science Vol. 13; no. 8; pp. 2441 - 2449
Main Authors Arnaiz, María, Shanmukaraj, Devaraj, Carriazo, Daniel, Bhattacharjya, Dhrubajyoti, Villaverde, Aitor, Armand, Michel, Ajuria, Jon
Format Journal Article
LanguageEnglish
Published Cambridge Royal Society of Chemistry 01.01.2020
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Summary:Metal ion capacitors (MICs) are foreseen to be a complementary alternative of vital importance to current energy storage issues, coupling high energy density delivered by batteries with high power/long cycle life offered by supercapacitors. The prime issues in realising this technology are pre-metallation and replacement of graphite electrodes that bring about an energy gain at the expense of power. Herein we present an easy-to-scale-up approach, combining activated carbon with a highly efficient and industrially compatible low-cost sacrificial salt (dimetal squarates) that can be used as a metal source for pre-metallation. Paired with a hard carbon electrode tailored to perform at high rates, lithium, sodium and potassium MICs are demonstrated. Furthermore, the successful fabrication of a lithium ion capacitor (LIC) pouch cell prototype with high energy at high power densities showing capacitance retention over 84% after 48 000 cycles validates the strategy. This breakthrough may trigger the easy and low-cost fabrication of LICs and significantly reduce technological barriers to market growth and consolidation. A low-cost pre-metallation strategy based on inorganic sacrificial salts that decompose on the first charge.
Bibliography:Electronic supplementary information (ESI) available. See DOI
10.1039/d0ee00351d
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ISSN:1754-5692
1754-5706
DOI:10.1039/d0ee00351d