Peeking across Grain Boundaries in a Solid-State Ionic Conductor
S Ganapathy (TU Delft - RST/Storage of Electrochemical Energy)
Chuang Yu (TU Delft - RST/Storage of Electrochemical Energy)
Ernst R.H. van Eck (Radboud Universiteit Nijmegen)
Marnix Wagemaker (TU Delft - RST/Storage of Electrochemical Energy)
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Abstract
The development of high-performance all-solid-state batteries relies on charge transport in solid electrolytes, where transport across grain boundaries often limits their bulk conductivity. The argyrodite Li
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X (X = Cl, Br) solid electrolyte has a high conductivity; however, macroscopic diffusion in this material involves complex jump processes, which leads to an underestimation of the activation energy. Using a comprehensive frequency- and temperature-dependent analysis of the spin-lattice relaxation rates, a complete estimation of Li self-diffusion is demonstrated. Another experimental challenge is quantifying the impact of grain boundaries on the total bulk conductivity. Li
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Cl and Li
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Br have identical crystalline structures, but with
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Li MAS NMR, their resonance peaks have different chemical shifts. Exploiting this with two-dimensional
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Li-
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Li exchange NMR on a mixture of Li
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Br and Li
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Cl, we observe Li exchange between particles of these two materials across grain boundaries, allowing direct and unambiguous quantification of this often limiting process in solid-state electrolytes.
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