4.5 Article

Sodium Insertion into Fe[Fe(CN)6] Framework Prepared by Microwave-Assisted Co-Precipitation

Journal

CHEMELECTROCHEM
Volume 10, Issue 8, Pages -

Publisher

WILEY-V C H VERLAG GMBH
DOI: 10.1002/celc.202201070

Keywords

Berlin green; Insertion; Prussian blue analogs; Batteries; X-ray absorption spectroscopy

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In this study, iron hexacyanoferrate nanoparticles were synthesized using a microwave-assisted co-precipitation method, showing a specific capacity of 120 mAh g(-1) and a capacity retention of 84.8% over 100 cycles at 20 mA g(-1) current, as well as a capacity of 80 mAh g(-1) at 10 C rate. Ex-situ X-ray absorption spectroscopy (XAS) revealed some irreversibility and changes in Fe-C and Fe-N bond lengths during the initial charge/discharge cycle, which were attributed to electrode activation processes and partly explained the observed capacity fading.
Prussian blue analogues (PBAs) are interesting materials for Na electrochemical insertion, owing to their ease of synthesis, rigid open framework and large interstitial space. In this work, iron hexacyanoferrate nanoparticles, Fe-III[Fe-III(CN)(6)], also known as Berlin green (BG), where both Fe centers are in the Fe(III) configuration, have been synthesized by an easy microwave assisted co-precipitation method, with an average particle size of around 44 nm. The BG nanoparticles exhibited a 120 mAh g(-1) specific capacity with a capacity retention of 84.8 % over 100 cycles at 20 mA g(-1) current and up to 80 mAh g(-1) at 10 C rate. The initial charge and discharge processes were fully investigated by ex-situ X-ray absorption spectroscopy (XAS). The XAS results reveal that there is some irreversibility in the initial electrochemical processes and the Fe-C and Fe-N bond lengths change during the first charge/discharge cycle. This effect was attributed to BG electrode activation processes, and partly explained the observed capacity fading.

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