TY - JOUR
T1 - Potentials in Li-Ion Batteries Probed by Operando Ambient Pressure Photoelectron Spectroscopy
AU - Källquist, Ida
AU - Ericson, Tove
AU - Lindgren, Fredrik
AU - Chen, Heyin
AU - Shavorskiy, Andrey
AU - Maibach, Julia
AU - Hahlin, Maria
PY - 2022/2/9
Y1 - 2022/2/9
N2 - The important electrochemical processes in a battery happen at the solid/liquid interfaces. Operando ambient pressure photoelectron spectroscopy (APPES) is one tool to study these processes with chemical specificity. However, accessing this crucial interface and identifying the interface signal are not trivial. Therefore, we present a measurement setup, together with a suggested model, exemplifying how APPES can be used to probe potential differences over the electrode/electrolyte interface, even without direct access to the interface. Both the change in electron electrochemical potential over the solid/liquid interface, and the change in Li chemical potential of the working electrode (WE) surface at Li-ion equilibrium can be probed. Using a Li4Ti5O12 composite as a WE, our results show that the shifts in kinetic energy of the electrolyte measured by APPES can be correlated to the electrochemical reactions occurring at the WE/electrolyte interface. Different shifts in kinetic energy are seen depending on if a phase transition reaction occurs or if a single phase is lithiated. The developed methodology can be used to evaluate charge transfer over the WE/electrolyte interface as well as the lithiation/delithiation mechanism of the WE.
AB - The important electrochemical processes in a battery happen at the solid/liquid interfaces. Operando ambient pressure photoelectron spectroscopy (APPES) is one tool to study these processes with chemical specificity. However, accessing this crucial interface and identifying the interface signal are not trivial. Therefore, we present a measurement setup, together with a suggested model, exemplifying how APPES can be used to probe potential differences over the electrode/electrolyte interface, even without direct access to the interface. Both the change in electron electrochemical potential over the solid/liquid interface, and the change in Li chemical potential of the working electrode (WE) surface at Li-ion equilibrium can be probed. Using a Li4Ti5O12 composite as a WE, our results show that the shifts in kinetic energy of the electrolyte measured by APPES can be correlated to the electrochemical reactions occurring at the WE/electrolyte interface. Different shifts in kinetic energy are seen depending on if a phase transition reaction occurs or if a single phase is lithiated. The developed methodology can be used to evaluate charge transfer over the WE/electrolyte interface as well as the lithiation/delithiation mechanism of the WE.
KW - ambient pressure photoelectron spectroscopy
KW - electrochemical potential
KW - electrochemistry
KW - Li-ion battery
KW - operando
KW - photoelectron spectroscopy
KW - solid/liquid interface
UR - http://www.scopus.com/inward/record.url?scp=85124443232&partnerID=8YFLogxK
U2 - 10.1021/acsami.1c12465
DO - 10.1021/acsami.1c12465
M3 - Article
C2 - 35099928
AN - SCOPUS:85124443232
VL - 14
SP - 6465
EP - 6475
JO - ACS Applied Materials and Interfaces
JF - ACS Applied Materials and Interfaces
SN - 1944-8244
IS - 5
ER -