Mechanism for Al2O3 Atomic Layer Deposition on LiMn2O4 from In Situ Measurements and Ab Initio Calculations

Lin Chen, Robert E. Warburton, Kan Sheng Chen, Joseph A. Libera, Christopher Johnson, Zhenzhen Yang, Mark C Hersam, Jeffrey P. Greeley, Jeffrey W. Elam

Research output: Contribution to journalArticle

4 Citations (Scopus)

Abstract

Here, we elucidate the mechanism for Al2O3 atomic layer deposition (ALD) on LiMn2O4 (LMO) cathodes for lithium-ion batteries by using in situ and ex situ experimental characterization coupled with density functional theory (DFT) calculations. We demonstrate that not only does Al2O3 coat the LMO, but the Al heteroatom of the trimethylaluminum (TMA) precursor also dopes to interstitial sites on the LMO surface, thereby reducing the oxidation state of near-surface Mn ions. DFT calculations further suggest facile transfer of methyl groups from the TMA precursor to oxygen atoms on the LMO surface, which blocks adsorption sites for subsequent TMA adsorption. These predictions are supported by quartz crystal microbalance experiments demonstrating inhibited growth below ten ALD Al2O3 cycles, suggesting that sub-monolayer coverages of alumina are present on the LMO surface in the early stages of film growth. In comparison with fully conformal films, these sub-monolayer coatings show enhanced electrochemical capacity when cycled in coin cells. There is great demand for rechargeable battery electrodes with improved energy density and cycle life. Although protective coatings deposited on lithium-ion electrodes show enhanced performance, many of the mechanistic details at the electrode-coating interface remain elusive. In this work, Al2O3 was grown on spinel LiMn2O4, a model cathode for studying the transition-metal-loss problem that plagues many promising cathode materials. We employed a suite of in situ and ex situ techniques, along with theoretical calculations, to elucidate mechanisms of Al2O3 growth by atomic layer deposition on LiMn2O4. The ALD Al2O3 reaction is multi-faceted in that it involves precursor decomposition, Al doping, Mn redox, and non-uniform film growth, each of which contributes to observed trends in electrochemical performance. The fundamental understanding demonstrated in this work provides insights toward rational tuning of electrode interfaces for enhanced electrochemical performance. Deposition of protective coatings on lithium-ion battery electrode materials has been shown to enhance electrochemical capacity retention. Despite this, little is understood regarding the nature of the interface formed between the protective coating and the electrode. Here, we report a detailed mechanism for Al2O3 atomic layer deposition on LiMn2O4. We find that the initial stages of Al2O3 ALD on LiMn2O4 lead to sub-monolayer deposits that enhance electrochemical performance.

Original languageEnglish
Pages (from-to)2418-2435
Number of pages18
JournalChem
Volume4
Issue number10
DOIs
Publication statusPublished - Oct 11 2018

Fingerprint

Atomic layer deposition
in situ measurement
Electrodes
electrode
coating
Protective coatings
lithium
Monolayers
Cathodes
Film growth
ion
Lithium
Ions
Density functional theory
Growth
Adsorption
Coatings
Secondary batteries
adsorption
Quartz crystal microbalances

Keywords

  • atomic layer deposition
  • coating and doping in LMO and NMC
  • fundamental understanding
  • SDG7: Affordable and clean energy

ASJC Scopus subject areas

  • Chemistry(all)
  • Biochemistry
  • Environmental Chemistry
  • Chemical Engineering(all)
  • Biochemistry, medical
  • Materials Chemistry

Cite this

Chen, L., Warburton, R. E., Chen, K. S., Libera, J. A., Johnson, C., Yang, Z., ... Elam, J. W. (2018). Mechanism for Al2O3 Atomic Layer Deposition on LiMn2O4 from In Situ Measurements and Ab Initio Calculations. Chem, 4(10), 2418-2435. https://doi.org/10.1016/j.chempr.2018.08.006

Mechanism for Al2O3 Atomic Layer Deposition on LiMn2O4 from In Situ Measurements and Ab Initio Calculations. / Chen, Lin; Warburton, Robert E.; Chen, Kan Sheng; Libera, Joseph A.; Johnson, Christopher; Yang, Zhenzhen; Hersam, Mark C; Greeley, Jeffrey P.; Elam, Jeffrey W.

In: Chem, Vol. 4, No. 10, 11.10.2018, p. 2418-2435.

Research output: Contribution to journalArticle

Chen, L, Warburton, RE, Chen, KS, Libera, JA, Johnson, C, Yang, Z, Hersam, MC, Greeley, JP & Elam, JW 2018, 'Mechanism for Al2O3 Atomic Layer Deposition on LiMn2O4 from In Situ Measurements and Ab Initio Calculations', Chem, vol. 4, no. 10, pp. 2418-2435. https://doi.org/10.1016/j.chempr.2018.08.006
Chen, Lin ; Warburton, Robert E. ; Chen, Kan Sheng ; Libera, Joseph A. ; Johnson, Christopher ; Yang, Zhenzhen ; Hersam, Mark C ; Greeley, Jeffrey P. ; Elam, Jeffrey W. / Mechanism for Al2O3 Atomic Layer Deposition on LiMn2O4 from In Situ Measurements and Ab Initio Calculations. In: Chem. 2018 ; Vol. 4, No. 10. pp. 2418-2435.
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AU - Johnson, Christopher

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N2 - Here, we elucidate the mechanism for Al2O3 atomic layer deposition (ALD) on LiMn2O4 (LMO) cathodes for lithium-ion batteries by using in situ and ex situ experimental characterization coupled with density functional theory (DFT) calculations. We demonstrate that not only does Al2O3 coat the LMO, but the Al heteroatom of the trimethylaluminum (TMA) precursor also dopes to interstitial sites on the LMO surface, thereby reducing the oxidation state of near-surface Mn ions. DFT calculations further suggest facile transfer of methyl groups from the TMA precursor to oxygen atoms on the LMO surface, which blocks adsorption sites for subsequent TMA adsorption. These predictions are supported by quartz crystal microbalance experiments demonstrating inhibited growth below ten ALD Al2O3 cycles, suggesting that sub-monolayer coverages of alumina are present on the LMO surface in the early stages of film growth. In comparison with fully conformal films, these sub-monolayer coatings show enhanced electrochemical capacity when cycled in coin cells. There is great demand for rechargeable battery electrodes with improved energy density and cycle life. Although protective coatings deposited on lithium-ion electrodes show enhanced performance, many of the mechanistic details at the electrode-coating interface remain elusive. In this work, Al2O3 was grown on spinel LiMn2O4, a model cathode for studying the transition-metal-loss problem that plagues many promising cathode materials. We employed a suite of in situ and ex situ techniques, along with theoretical calculations, to elucidate mechanisms of Al2O3 growth by atomic layer deposition on LiMn2O4. The ALD Al2O3 reaction is multi-faceted in that it involves precursor decomposition, Al doping, Mn redox, and non-uniform film growth, each of which contributes to observed trends in electrochemical performance. The fundamental understanding demonstrated in this work provides insights toward rational tuning of electrode interfaces for enhanced electrochemical performance. Deposition of protective coatings on lithium-ion battery electrode materials has been shown to enhance electrochemical capacity retention. Despite this, little is understood regarding the nature of the interface formed between the protective coating and the electrode. Here, we report a detailed mechanism for Al2O3 atomic layer deposition on LiMn2O4. We find that the initial stages of Al2O3 ALD on LiMn2O4 lead to sub-monolayer deposits that enhance electrochemical performance.

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