Atomic-scale origin of the large grain-boundary resistance in perovskite Li-ion-conducting solid electrolytes

2014 ◽  
Vol 7 (5) ◽  
pp. 1638 ◽  
Author(s):  
Cheng Ma ◽  
Kai Chen ◽  
Chengdu Liang ◽  
Ce-Wen Nan ◽  
Ryo Ishikawa ◽  
...  
Nano Energy ◽  
2019 ◽  
Vol 66 ◽  
pp. 104109 ◽  
Author(s):  
Hongli Wan ◽  
Jean Pierre Mwizerwa ◽  
Fudong Han ◽  
Wei Weng ◽  
Jing Yang ◽  
...  

2016 ◽  
Vol 18 (4) ◽  
pp. 3023-3031 ◽  
Author(s):  
Sangtae Kim ◽  
Seong K. Kim ◽  
Sergey Khodorov ◽  
Joachim Maier ◽  
Igor Lubomirsky

Combining the linear diffusion and resistivity ratio models, one can distinguish the grain boundary resistance related to space charge from the resistance from other sources.


2019 ◽  
Vol 31 (3) ◽  
pp. 707-713 ◽  
Author(s):  
Tushar Swamy ◽  
Xinwei Chen ◽  
Yet-Ming Chiang

2018 ◽  
Vol 140 (22) ◽  
pp. 7044-7044 ◽  
Author(s):  
James A. Dawson ◽  
Pieremanuele Canepa ◽  
Theodosios Famprikis ◽  
Christian Masquelier ◽  
M. Saiful Islam

Author(s):  
Mihails Kusnezoff ◽  
Dörte Wagner ◽  
Jochen Schilm ◽  
Christian Heubner ◽  
Björn Matthey ◽  
...  

AbstractCrystallization of highly ionic conductive N5 (Na5YSi4O12) phase from melted Na3+3x-1Y1-xPySi3-yO9 parent glass provides an attractive pathway for cost-effective manufacturing of Na-ion conducting thin electrolyte substrates. The temperature-dependent crystallization of parent glass results in several crystalline phases in the microstructure (N3 (Na3YSi2O7), N5 and N8 (Na8.1Y Si6O18) phases) as well as in rest glass phase with temperature dependent viscosity. The electrical properties of dense parent glass and of compositions densified and crystallized at 700 °C, 800 °C, 900 °C, 1000 °C, and 1100 °C are investigated by impedance spectroscopy and linked to their microstructure and crystalline phase content determined by Rietveld refinement. The parent glass has high isolation resistance and predominantly electrons as charge carriers. For sintering at ≥ 900 °C, sufficient N5 phase content is formed to exceed the percolation limit and form ion-conducting pathways. At the same time, the highest content of crystalline phase and the lowest grain boundary resistance are observed. Further increase of the sintering temperature leads to a decrease of the grain resistance and an increase of grain boundary resistance. The grain boundary resistance increases remarkably for samples sintered at 1100 °C due to softening of the residual glass phase and wetting of the grain boundaries. The conductivity of fully crystallized N5 phase (grain conductivity) is calculated from thorough impedance spectra analysis using its volume content estimated from Rietveld analysis, density measurements and assuming reasonable tortuosity to 2.8 10−3 S cm−1 at room temperature. The excellent conductivity and easy processing demonstrate the great potential for the use of this phase in the preparation of solid-state sodium electrolytes.


2019 ◽  
Author(s):  
James Dawson ◽  
Pieremanuele Canepa ◽  
Matthew Clarke ◽  
Theodosios Famprikis ◽  
Dibyajyoti Ghosh ◽  
...  

Solid electrolytes provide a route to the development of all-solid-state batteries that can potentially surpass the safety and performance of conventional liquid electrolyte-based devices. Sulfide solid electrolytes have received particular attention as a result of their high ionic conductivities. One of the main reasons for such high ionic conductivity is the apparently reduced grain boundary resistance of sulfide solid electrolytes compared to their oxide counterparts, but this is not fully established. Using two model electrolyte systems, Na3PS4 and Na3PO4, we apply a novel microscale simulation approach to analyze ionic transport in polycrystalline materials with various grain volumes. For Na3PO4, high grain boundary resistance is found, with the Na-ion conductivity decreasing with decreasing grain volume. For Na3PS4, the overall influence of grain boundaries is significantly reduced compared to the oxide. Detailed analysis reveals a minimal change in the local structures and Na-ion conduction mechanism between bulk and polycrystalline Na3PS4, whereas the change is far more substantial for Na3PO4, with evidence of over-coordination of Na ions at the grain boundaries. Our microscale approach helps to explain the fundamentally different influences of grain boundaries on ion transport in phosphate and thiophosphate solid electrolytes.


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