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Title: Direct synthesis of LiNi1/3Co1/3Mn1/3O2 from nitrateprecursors

Abstract

Two novel methods for synthesis of the title compound directly from metal nitrates are described. Phase-pure materials are produced when precursors are calcined between 600 and 1000 C, with little to no ion mixing exhibited for products heated to 900 C or above. The electrochemical characteristics of these materials depended upon calcination temperature and synthesis method, with results comparable to a commercial sample for the materials made at high temperatures in a one-step process without combustion. The sample prepared by combustion also exhibited very stable capacity retention upon cycling.

Authors:
;
Publication Date:
Research Org.:
Lawrence Berkeley National Lab. (LBNL), Berkeley, CA (United States)
Sponsoring Org.:
USDOE. Assistant Secretary for Energy Efficiency andRenewable Energy. Office of the FreedomCAR and Vehicle TechnologiesProgram
OSTI Identifier:
860309
Report Number(s):
LBNL-54969
R&D Project: 500301; BnR: VT0301030; TRN: US200524%%83
DOE Contract Number:  
DE-AC02-05CH11231
Resource Type:
Journal Article
Journal Name:
Electrochemistry Communications
Additional Journal Information:
Journal Volume: 6; Journal Issue: 8; Related Information: Journal Publication Date: 08/2004
Country of Publication:
United States
Language:
English
Subject:
25 ENERGY STORAGE; CALCINATION; CAPACITY; COMBUSTION; NITRATES; RETENTION; SYNTHESIS

Citation Formats

Patoux, Sebastien, and Doeff, Marca M. Direct synthesis of LiNi1/3Co1/3Mn1/3O2 from nitrateprecursors. United States: N. p., 2004. Web. doi:10.1016/j.elecom.2004.05.024.
Patoux, Sebastien, & Doeff, Marca M. Direct synthesis of LiNi1/3Co1/3Mn1/3O2 from nitrateprecursors. United States. https://doi.org/10.1016/j.elecom.2004.05.024
Patoux, Sebastien, and Doeff, Marca M. 2004. "Direct synthesis of LiNi1/3Co1/3Mn1/3O2 from nitrateprecursors". United States. https://doi.org/10.1016/j.elecom.2004.05.024. https://www.osti.gov/servlets/purl/860309.
@article{osti_860309,
title = {Direct synthesis of LiNi1/3Co1/3Mn1/3O2 from nitrateprecursors},
author = {Patoux, Sebastien and Doeff, Marca M},
abstractNote = {Two novel methods for synthesis of the title compound directly from metal nitrates are described. Phase-pure materials are produced when precursors are calcined between 600 and 1000 C, with little to no ion mixing exhibited for products heated to 900 C or above. The electrochemical characteristics of these materials depended upon calcination temperature and synthesis method, with results comparable to a commercial sample for the materials made at high temperatures in a one-step process without combustion. The sample prepared by combustion also exhibited very stable capacity retention upon cycling.},
doi = {10.1016/j.elecom.2004.05.024},
url = {https://www.osti.gov/biblio/860309}, journal = {Electrochemistry Communications},
number = 8,
volume = 6,
place = {United States},
year = {Wed Apr 28 00:00:00 EDT 2004},
month = {Wed Apr 28 00:00:00 EDT 2004}
}