Li2S is the final product of lithiation of sulfur cathodes in lithium-sulfur (Li-S) batteries. In this work, we study formation and diffusion of defects in Li2S. It is found that for a wide range of voltages (referenced to metal Li) between 0.17 V and 2.01 V, positively charged interstitial Li (Li+) is the most favorable defect type with a fixed formation energy of 1.02 eV. The formation energy of negatively charged Li vacancy () is also constant, and it is only 0.13 eV higher than that of Li+. For a narrow range of voltages between 0.00 V and 0.17 V, the formation energy of neutral S vacancy is the lowest and it decreases with decreasing the cell voltage. The energy barrier for Li+ diffusion (0.45 eV), which takes place via an exchange mechanism, is 0.18 eV higher than that for (0.27 eV), which takes place via a single vacancy hopping. Considering formation energies and diffusion barriers, we find that ionic conductivity in Li2S is due to both Li+ and , but the latter mechanism being slightly more favorable.
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23 May 2016
Research Article|
May 26 2016
Thermodynamics and kinetics of defects in Li2S
Ashkan Moradabadi;
Ashkan Moradabadi
1Institut für Materialwissenschaft, Fachgebiet Materialmodellierung,
Technische Universität Darmstadt
, Jovanka-Bontschits-Str. 2, 64287 Darmstadt, Germany
2Institut für Chemie und Biochemie,
Freie Universität Berlin
, Takustr. 3, 14195 Berlin, Germany
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Payam Kaghazchi
Payam Kaghazchi
a)
2Institut für Chemie und Biochemie,
Freie Universität Berlin
, Takustr. 3, 14195 Berlin, Germany
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a)
Electronic mail: [email protected]
Appl. Phys. Lett. 108, 213906 (2016)
Article history
Received:
December 02 2015
Accepted:
May 11 2016
Citation
Ashkan Moradabadi, Payam Kaghazchi; Thermodynamics and kinetics of defects in Li2S. Appl. Phys. Lett. 23 May 2016; 108 (21): 213906. https://doi.org/10.1063/1.4952434
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