4.6 Article

Vapour phase conversion of metal oxalates to metal phosphide nanostructures and their use as anode in rechargeable Li, Na and K-ion batteries

期刊

ELECTROCHIMICA ACTA
卷 388, 期 -, 页码 -

出版社

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.electacta.2021.138643

关键词

Metal phosphides; Anode; Li-ion; Na-ion; K-ion batteries; Vapour phase conversion

资金

  1. Department of Science and Technology, India [DST/TMD/MES/2k17/11, DST/TMD/MES/2k18/225]
  2. Ramanujan Fellowship from Science and engineering research board [SB/S2/RJN-100/2014]
  3. [MES-17]
  4. [MES-18]

向作者/读者索取更多资源

A simple vapor-phase conversion method was used to convert metal oxalates into metal phosphide nanostructures, which showed good performance in various alkali ion batteries with reversible specific capacity under different cycling conditions.
We report a simple, vapour-phase conversion of two prominent metal oxalates into metal phosphide nanostructures (CoP and FeP) and their application in three alkali ion batteries (Li, Na and K). This method was a low temperature, scalable, single step conversion process using metal oxalates and sodium hypophosphite as originators. Apart from the vapour phase conversion reaction mechanism, structural, morphological, surface chemical, thermo-gravimetric and surface area analysis of these metal phosphides were also carried out. The metal phosphides was imaged using transmission electron microscopy which revealed a macroporous sheet like morphology for CoP and a mesoporous frame work for FeP particles which was further confirmed by BET. CoP and FeP nanostructures delivered reversible specific capacity of 265 and 360 mAh/g respectively for lithium ion battery at a current density of 250 mA/g for 500 cycles. For sodium ion battery, at a current density of 100 mA/g, CoP and FeP exhibited a specific capacity of 122 and 216 mAh/g respectively. For potassium ion battery, CoP and FeP exhibited a specific capacity of 73 and 113 mAh/g for 100 cycles. The alkali ion storage performances correlated well with their physicochemical and electrochemical properties while the surface and bulk storage contributions were also explored. 0 2021 Elsevier Ltd. All rights reserved.

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