Electrochemical interfaces and solvation dynamics in calcium-ion battery probed by the operando soft x-ray spectroscopy
ORAL · Invited
Abstract
The solvation of an electrolyte near the electrolyte/electrode interphase dictates the charge transfer efficiency and therefore affects the performance of a battery. However, current understanding regarding this interphase was limited due to the lack of direct interphase probing approaches under in-situ/operando conditions. In the operando soft x-ray spectroscopy characterization of interfacial phenomena in energy materials and devices, it has been found that the microstructure and composition of materials as well as the microstructure evolution process have a great influence on performances in a variety of fields, e.g., energy conversion and energy storage materials, chemical and catalytic processes.
In this report, using operando x-ray absorption spectroscopy and resonant soft x-ray scattering through a patterned e-chip, the solvation of a calcium organic electrolyte was investigated under operando conditions. The disruption of the solvation structure by a secondary anion or cation were evaluated using the methodologies developed, which will guide the design of electrolytes for future energy storage. The strategy of these new methodologies developed will also benefit the investigation of catalysis at interphases and electrochemical microenvironments in general.
In this report, using operando x-ray absorption spectroscopy and resonant soft x-ray scattering through a patterned e-chip, the solvation of a calcium organic electrolyte was investigated under operando conditions. The disruption of the solvation structure by a secondary anion or cation were evaluated using the methodologies developed, which will guide the design of electrolytes for future energy storage. The strategy of these new methodologies developed will also benefit the investigation of catalysis at interphases and electrochemical microenvironments in general.
*This work was supported by the Joint Center for Energy Storage Research, an Energy Innovation Hub funded by the U.S. Department of Energy. The soft x-ray spectroscopy and scattering experiments were performed on beamlines 8.0.1, 7.3.1, and 11.0.1.2 at the Advanced Light Source. Funding: This research used resources of the Advanced Light Source, the Molecular Foundry, and the National Energy Research Scientific Computing Center, the DOE Office of Science User Facilities under contract no. DE-AC02-05CH11231. K. Q. and M. T. acknowledge support from NSF (CHE-1665284).
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Presenters
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Jinghua Guo
- Lawrence Berkeley National Laboratory