Cargando…

Boosting the Electrochemical Performance of Li(1.2)Mn(0.54)Ni(0.13)Co(0.13)O(2) by Atomic Layer-Deposited CeO(2) Coating

[Image: see text] It has been demonstrated that atomic layer deposition (ALD) provides an initially safeguarding, uniform ultrathin film of controllable thickness for lithium-ion battery electrodes. In this work, CeO(2) thin films were deposited to modify the surface of lithium-rich Li(1.2)Mn(0.54)N...

Descripción completa

Detalles Bibliográficos
Autores principales: Gao, Yan, Patel, Rajankumar L., Shen, Kuan-Yu, Wang, Xiaofeng, Axelbaum, Richard L., Liang, Xinhua
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2018
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6641259/
https://www.ncbi.nlm.nih.gov/pubmed/31457937
http://dx.doi.org/10.1021/acsomega.7b01922
_version_ 1783436739688267776
author Gao, Yan
Patel, Rajankumar L.
Shen, Kuan-Yu
Wang, Xiaofeng
Axelbaum, Richard L.
Liang, Xinhua
author_facet Gao, Yan
Patel, Rajankumar L.
Shen, Kuan-Yu
Wang, Xiaofeng
Axelbaum, Richard L.
Liang, Xinhua
author_sort Gao, Yan
collection PubMed
description [Image: see text] It has been demonstrated that atomic layer deposition (ALD) provides an initially safeguarding, uniform ultrathin film of controllable thickness for lithium-ion battery electrodes. In this work, CeO(2) thin films were deposited to modify the surface of lithium-rich Li(1.2)Mn(0.54)Ni(0.13)Co(0.13)O(2) (LRNMC) particles via ALD. The film thicknesses were measured by transmission electron microscopy. For electrochemical performance, ∼2.5 nm CeO(2) film, deposited by 50 ALD cycles (50Ce), was found to have the optimal thickness. At a 1 C rate and 55 °C in a voltage range of 2.0−4.8 V, an initial capacity of 199 mAh/g was achieved, which was 8% higher than that of the uncoated (UC) LRNMC particles. Also, 60.2% of the initial capacity was retained after 400 cycles of charge–discharge, compared to 22% capacity retention of UC after only 180 cycles of charge–discharge. A robust kinetic of electrochemical reaction was found on the CeO(2)-coated samples at 55 °C through electrochemical impedance spectroscopy. The conductivity of 50Ce was observed to be around 3 times higher than that of UC at 60–140 °C. The function of the CeO(2) thin-film coating was interpreted as being to increase substrate conductivity and to block the dissolution of metal ions during the charge–discharge process.
format Online
Article
Text
id pubmed-6641259
institution National Center for Biotechnology Information
language English
publishDate 2018
publisher American Chemical Society
record_format MEDLINE/PubMed
spelling pubmed-66412592019-08-27 Boosting the Electrochemical Performance of Li(1.2)Mn(0.54)Ni(0.13)Co(0.13)O(2) by Atomic Layer-Deposited CeO(2) Coating Gao, Yan Patel, Rajankumar L. Shen, Kuan-Yu Wang, Xiaofeng Axelbaum, Richard L. Liang, Xinhua ACS Omega [Image: see text] It has been demonstrated that atomic layer deposition (ALD) provides an initially safeguarding, uniform ultrathin film of controllable thickness for lithium-ion battery electrodes. In this work, CeO(2) thin films were deposited to modify the surface of lithium-rich Li(1.2)Mn(0.54)Ni(0.13)Co(0.13)O(2) (LRNMC) particles via ALD. The film thicknesses were measured by transmission electron microscopy. For electrochemical performance, ∼2.5 nm CeO(2) film, deposited by 50 ALD cycles (50Ce), was found to have the optimal thickness. At a 1 C rate and 55 °C in a voltage range of 2.0−4.8 V, an initial capacity of 199 mAh/g was achieved, which was 8% higher than that of the uncoated (UC) LRNMC particles. Also, 60.2% of the initial capacity was retained after 400 cycles of charge–discharge, compared to 22% capacity retention of UC after only 180 cycles of charge–discharge. A robust kinetic of electrochemical reaction was found on the CeO(2)-coated samples at 55 °C through electrochemical impedance spectroscopy. The conductivity of 50Ce was observed to be around 3 times higher than that of UC at 60–140 °C. The function of the CeO(2) thin-film coating was interpreted as being to increase substrate conductivity and to block the dissolution of metal ions during the charge–discharge process. American Chemical Society 2018-01-24 /pmc/articles/PMC6641259/ /pubmed/31457937 http://dx.doi.org/10.1021/acsomega.7b01922 Text en Copyright © 2018 American Chemical Society This is an open access article published under an ACS AuthorChoice License (http://pubs.acs.org/page/policy/authorchoice_termsofuse.html) , which permits copying and redistribution of the article or any adaptations for non-commercial purposes.
spellingShingle Gao, Yan
Patel, Rajankumar L.
Shen, Kuan-Yu
Wang, Xiaofeng
Axelbaum, Richard L.
Liang, Xinhua
Boosting the Electrochemical Performance of Li(1.2)Mn(0.54)Ni(0.13)Co(0.13)O(2) by Atomic Layer-Deposited CeO(2) Coating
title Boosting the Electrochemical Performance of Li(1.2)Mn(0.54)Ni(0.13)Co(0.13)O(2) by Atomic Layer-Deposited CeO(2) Coating
title_full Boosting the Electrochemical Performance of Li(1.2)Mn(0.54)Ni(0.13)Co(0.13)O(2) by Atomic Layer-Deposited CeO(2) Coating
title_fullStr Boosting the Electrochemical Performance of Li(1.2)Mn(0.54)Ni(0.13)Co(0.13)O(2) by Atomic Layer-Deposited CeO(2) Coating
title_full_unstemmed Boosting the Electrochemical Performance of Li(1.2)Mn(0.54)Ni(0.13)Co(0.13)O(2) by Atomic Layer-Deposited CeO(2) Coating
title_short Boosting the Electrochemical Performance of Li(1.2)Mn(0.54)Ni(0.13)Co(0.13)O(2) by Atomic Layer-Deposited CeO(2) Coating
title_sort boosting the electrochemical performance of li(1.2)mn(0.54)ni(0.13)co(0.13)o(2) by atomic layer-deposited ceo(2) coating
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6641259/
https://www.ncbi.nlm.nih.gov/pubmed/31457937
http://dx.doi.org/10.1021/acsomega.7b01922
work_keys_str_mv AT gaoyan boostingtheelectrochemicalperformanceofli12mn054ni013co013o2byatomiclayerdepositedceo2coating
AT patelrajankumarl boostingtheelectrochemicalperformanceofli12mn054ni013co013o2byatomiclayerdepositedceo2coating
AT shenkuanyu boostingtheelectrochemicalperformanceofli12mn054ni013co013o2byatomiclayerdepositedceo2coating
AT wangxiaofeng boostingtheelectrochemicalperformanceofli12mn054ni013co013o2byatomiclayerdepositedceo2coating
AT axelbaumrichardl boostingtheelectrochemicalperformanceofli12mn054ni013co013o2byatomiclayerdepositedceo2coating
AT liangxinhua boostingtheelectrochemicalperformanceofli12mn054ni013co013o2byatomiclayerdepositedceo2coating