TY - JOUR
T1 - Operando Observations and First-Principles Calculations of Reduced Lithium Insertion in Au-Coated LiMn 2 O 4
AU - Bassett, Kimberly L.
AU - Warburton, Robert E.
AU - Deshpande, Siddharth
AU - Fister, Timothy T.
AU - Ta, Kim
AU - Esbenshade, Jennifer L.
AU - Kinaci, Alper
AU - Chan, Maria K.Y.
AU - Wiaderek, Kamila M.
AU - Chapman, Karena W.
AU - Greeley, Jeffrey P.
AU - Gewirth, Andrew A.
N1 - Funding Information:
K.L.B. and R.E.W. contributed equally to this work. This research was supported as part of the Center for Electrochemical Energy Science, an Energy Frontier Research Center funded by the U.S. Department of Energy (DOE), Office of Science, and Basic Energy Sciences (BES). Use of the Center for Nanoscale Materials was supported by the U.S. Department of Energy, Office of Science, and Office of Basic Energy Sciences, under Contract No. DE-AC02-06CH11357. This research used resources of the National Energy Research Scientific Computing Center and a DOE Office of Science User Facility supported by the Office of Science of the U.S. Department of Energy under Contract No. DE-AC02-05CH11231. This research used resources of the Advanced Photon Source, a U.S. Department of Energy (DOE) Office of Science User Facility operated for the DOE Office of Science by Argonne National Laboratory under Contract No. DE-AC02-06CH11357. The authors thank Wenqian Xu at the Advanced Photon Source 17-BM Beamline for his advice and thoughtful comments. K.L.B. acknowledges support from the National Science Foundation Graduate Research Fellowship Program under Grant No. DGE-1144245.
Funding Information:
K.L.B. and R.E.W. contributed equally to this work. This research was supported as part of the Center for Electrochemical Energy Science, an Energy Frontier Research Center funded by the U.S. Department of Energy (DOE), Office of Science, and Basic Energy Sciences (BES). Use of the Center for Nanoscale Materials was supported by the U.S. Department of Energy, Office of Science, and Office of Basic Energy Sciences, under Contract No. DE-AC02-06CH11357. This research used resources of the National Energy Research Scientific Computing Center and a DOE Office of Science User Facility supported by the Office of Science of the U.S. Department of Energy under Contract No. DE-AC02-05CH11231. This research used resources of the Advanced Photon Source, a U.S. Department of Energy (DOE) Office of Science User Facility operated for the DOE?Office of Science by Argonne National Laboratory under Contract No. DE-AC02-06CH11357. The authors thank Wenqian Xu at the Advanced Photon Source 17-BM Beamline for his advice and thoughtful comments. K.L.B. acknowledges support from the National Science Foundation Graduate Research Fellowship Program under Grant No. DGE-1144245.
Publisher Copyright:
© 2019 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim
PY - 2019/2/22
Y1 - 2019/2/22
N2 - The deposition of protective coatings on the spinel LiMn 2 O 4 (LMO) lithium-ion battery cathode is effective in reducing Mn dissolution from the electrode surface. Although protective coatings positively affect LMO cycle life, much remains to be understood regarding the interface formed between these coatings and LMO. Using operando powder X-ray diffraction with Rietveld refinement, it is shown that, in comparison to bare LMO, the lattice parameter of a model Au-coated LMO cathode is significantly reduced upon relithiation. Less charge passes through Au-coated LMO in comparison to bare LMO, suggesting that the reduced lattice parameter is associated with decreased Li + solubility in the Au-coated LMO. Density functional theory calculations show that a more Li + -deficient near-surface is thermodynamically favorable in the presence of the Au coating, which may further stabilize these cathodes through suppressing formation of the Jahn–Teller distorted Li 2 Mn 2 O 4 phase at the surface. Electronic structure and chemical bonding analyses show enhanced hybridization between Au and LMO for delithiated surfaces leading to partial oxidation of Au upon delithiation. This study suggests that, in addition to transition metal dissolution from electrode surfaces, protective coating design must also balance potential energy effects induced by charge transfer at the electrode-coating interface.
AB - The deposition of protective coatings on the spinel LiMn 2 O 4 (LMO) lithium-ion battery cathode is effective in reducing Mn dissolution from the electrode surface. Although protective coatings positively affect LMO cycle life, much remains to be understood regarding the interface formed between these coatings and LMO. Using operando powder X-ray diffraction with Rietveld refinement, it is shown that, in comparison to bare LMO, the lattice parameter of a model Au-coated LMO cathode is significantly reduced upon relithiation. Less charge passes through Au-coated LMO in comparison to bare LMO, suggesting that the reduced lattice parameter is associated with decreased Li + solubility in the Au-coated LMO. Density functional theory calculations show that a more Li + -deficient near-surface is thermodynamically favorable in the presence of the Au coating, which may further stabilize these cathodes through suppressing formation of the Jahn–Teller distorted Li 2 Mn 2 O 4 phase at the surface. Electronic structure and chemical bonding analyses show enhanced hybridization between Au and LMO for delithiated surfaces leading to partial oxidation of Au upon delithiation. This study suggests that, in addition to transition metal dissolution from electrode surfaces, protective coating design must also balance potential energy effects induced by charge transfer at the electrode-coating interface.
KW - density functional theory
KW - lithium manganese oxide
KW - lithium-ion batteries
KW - operando X-ray diffraction
KW - protective coatings
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U2 - 10.1002/admi.201801923
DO - 10.1002/admi.201801923
M3 - Article
AN - SCOPUS:85060163262
SN - 2196-7350
VL - 6
JO - Advanced Materials Interfaces
JF - Advanced Materials Interfaces
IS - 4
M1 - 1801923
ER -