You need JavaScript to view this

Thin copper phosphide films as conversion anode for lithium-ion battery applications

Abstract

Air stable copper phosphide of thicknesses (0.2, 0.4 μm) was synthesized over copper plates (of 10 mm diameter) by hybrid electrochemical deposition and low temperature solid-state reaction. Stoichiometric amount of red phosphorus (P) were sprayed over electrodeposited copper and followed by annealing at 250 °C under inert gas atmosphere for different durations (5 h, 7 h and 12 h). During this process, phosphorus particles diffuse by excavating into the copper deposits, producing holes, where the Cu{sub 3}P crystallites nucleate and lead to conglomeration of several agglomerates and hence resulted in non-homogeneous morphology. A small extend of Cu{sub 3}P oxidation occurs over the film's top surface. X-ray diffraction (XRD) patterns confirm that the layer to be pure Cu{sub 3}P. Scanning electron microscopy (FEG-SEM) reveals a porous microstructure consisting of agglomerated particles with ∼10 μm size. The as-prepared carbon-free Cu{sub 3}P electrodes exhibited significantly improved capacity retention and rate capability characteristics over 40 cycles when electrochemically tested against lithium at constant 20 μA/cm{sup 2} rendering it as possible negative electrode for high energy density lithium-ion battery (LiB) applications.
Authors:
Chandrasekar, M. S.; [1]  Mitra, Sagar [1] 
  1. Electrochemical Energy Laboratory, Department of Energy Science and Engineering, Indian Institute of Technology Bombay, Mumbai 400076 (India)
Publication Date:
Mar 01, 2013
Product Type:
Journal Article
Resource Relation:
Journal Name: Electrochimica Acta; Journal Volume: 92; Other Information: Copyright (c) 2013 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.; Country of input: International Atomic Energy Agency (IAEA)
Subject:
37 INORGANIC, ORGANIC, PHYSICAL AND ANALYTICAL CHEMISTRY; ANODES; CONGLOMERATES; COPPER; COPPER PHOSPHIDES; DEPOSITS; ELECTRIC BATTERIES; ELECTRODEPOSITION; ENERGY DENSITY; ENERGY STORAGE; HYBRIDIZATION; LITHIUM IONS; MICROSTRUCTURE; OXIDATION; PHOSPHORUS; SCANNING ELECTRON MICROSCOPY; SOLIDS; X-RAY DIFFRACTION
OSTI ID:
22238674
Country of Origin:
United Kingdom
Language:
English
Other Identifying Numbers:
Journal ID: ISSN 0013-4686; CODEN: ELCAAV; Other: PII: S0013-4686(13)00021-2; TRN: GB14R4056059763
Availability:
Available from http://dx.doi.org/10.1016/j.electacta.2012.12.136
Submitting Site:
INIS
Size:
page(s) 47-54
Announcement Date:
Jun 12, 2014

Citation Formats

Chandrasekar, M. S., and Mitra, Sagar. Thin copper phosphide films as conversion anode for lithium-ion battery applications. United Kingdom: N. p., 2013. Web. doi:10.1016/J.ELECTACTA.2012.12.136.
Chandrasekar, M. S., & Mitra, Sagar. Thin copper phosphide films as conversion anode for lithium-ion battery applications. United Kingdom. https://doi.org/10.1016/J.ELECTACTA.2012.12.136
Chandrasekar, M. S., and Mitra, Sagar. 2013. "Thin copper phosphide films as conversion anode for lithium-ion battery applications." United Kingdom. https://doi.org/10.1016/J.ELECTACTA.2012.12.136.
@misc{etde_22238674,
title = {Thin copper phosphide films as conversion anode for lithium-ion battery applications}
author = {Chandrasekar, M. S., and Mitra, Sagar}
abstractNote = {Air stable copper phosphide of thicknesses (0.2, 0.4 μm) was synthesized over copper plates (of 10 mm diameter) by hybrid electrochemical deposition and low temperature solid-state reaction. Stoichiometric amount of red phosphorus (P) were sprayed over electrodeposited copper and followed by annealing at 250 °C under inert gas atmosphere for different durations (5 h, 7 h and 12 h). During this process, phosphorus particles diffuse by excavating into the copper deposits, producing holes, where the Cu{sub 3}P crystallites nucleate and lead to conglomeration of several agglomerates and hence resulted in non-homogeneous morphology. A small extend of Cu{sub 3}P oxidation occurs over the film's top surface. X-ray diffraction (XRD) patterns confirm that the layer to be pure Cu{sub 3}P. Scanning electron microscopy (FEG-SEM) reveals a porous microstructure consisting of agglomerated particles with ∼10 μm size. The as-prepared carbon-free Cu{sub 3}P electrodes exhibited significantly improved capacity retention and rate capability characteristics over 40 cycles when electrochemically tested against lithium at constant 20 μA/cm{sup 2} rendering it as possible negative electrode for high energy density lithium-ion battery (LiB) applications.}
doi = {10.1016/J.ELECTACTA.2012.12.136}
journal = []
volume = {92}
journal type = {AC}
place = {United Kingdom}
year = {2013}
month = {Mar}
}