Credit: ZHU Feng, Md Shafiqul Islam, ZHOU Lin, et al.
On April 14th, Prof. MA Cheng from the University of Science and Technology of China (USTC) of the Chinese Academy of Sciences (CAS) and his colleagues made an important discovery on the mechanism of Li-ion migration in solid electrolytes for batteries. They observed a new type of microscopic feature that can significantly influence ionic transport.
Solid electrolyte is the key component in enabling the safe, energy-dense all-solid-state batteries. Before highly conductive solid electrolytes can be developed in a knowledge-based manner, the mechanism behind Li-ion migration must be thoroughly understood. In many materials, the success of this task lies in whether the “non-periodic features” can be well understood, because such features frequently cause orders of magnitude change in ionic conductivity. At present, only two types of non-periodic features, i.e., grain boundaries and point defects, were considered in most studies.
MA’s team discovered an additional type of non-periodic feature that profoundly affects ionic transport. Using aberration-corrected transmission electron microscopy, they spotted a large number of single-atom-layer defects in a prototype solid electrolyte Li0.33La0.56TiO3. In contrast to other well-known non-periodic features, the observed defect is essentially a single-atom-layer compound that emerges only on a limited number of atomic planes. Because of the symmetry of these planes, differently oriented defects almost always form closed loops.
“There are actually many of such defect loops in the material, but it is very difficult to observe them,” said the first author ZHU Feng, who is currently a Ph.D. student of USTC. “They are visible only along certain orientations. Besides, due to their extremely small thickness and the distraction from other coexisting microstructures, the presence of these defects can hardly be noticed. This might explain why they have not been reported until now.”
The observed defects were found to exhibit an atomic configuration that completely forbids Li-ion migration across the defect layer. As a result, when such defects form a closed loop, Li ions can neither enter nor exit the volume inside, and this part of material is thus excluded from the overall ionic transport. The volume isolated this way is as large as ~15%, which can lead to 1-2 orders of magnitude reduction in ionic conductivity.
“The defect loop is acting as Li-ion traps: it prevents the Li ions within the enclosed volume from escaping,” said Prof. MA Cheng from USTC, the lead author of the study. “As such, although the defects themselves are only one-atom thin, they still can ‘kill’ very large volumes of the solid electrolyte, making them non-conductive.”
The scientists coined a term called “single-atom-layer trap” (SALT) to describe this unique feature. Its discovery points out that non-periodic features other than grain boundaries and point defects may also greatly alter ionic transport, and that similar study is urgently needed in other solid electrolytes. The reviewer of Nature Communications spoke very highly of the scientific significance of this work: “This was an exciting manuscript to read, reporting on a very novel observation.” “I would … expect that it stirs up quite some discussion both in the solid electrolyte/solid-state battery field as well as generally in the material science and electron microscopy communities.”
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The study was published on Nature Communications, entitled “Single-atom-layer traps in a solid electrolyte for lithium batteries”.
Prof. MA Cheng’s collaborators include Prof. MO Yifei from University of Maryland, Prof. NAN Cewen from Tsinghua University, and Prof. LUO Jun from Tianjin University of Technology.
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