| JOURNAL OF POWER SOURCES | 卷:293 |
| Structural manipulation approaches towards enhanced sodium ionic conductivity in Na-rich antiperovskites | |
| Article | |
| Wang, Yonggang1,2,3  Wang, Qingfei1  Liu, Zhenpu1  Zhou, Zhengyang2  Li, Shuai3  Zhu, Jinlong3  Zou, Ruqiang1  Wang, Yingxia2  Lin, Jianhua2  | |
| [1] Peking Univ, Coll Engn, Beijing 100871, Peoples R China | |
| [2] Peking Univ, Coll Chem & Mol Engn, State Key Lab Rare Earth Mat Chem & Applicat, Beijing 100871, Peoples R China | |
| [3] Univ Nevada, Dept Phys & Astron, Las Vegas, NV 89154 USA | |
| 关键词: Antiperovskite; Solid electrolyte; Sodium ionic conductor; Superionic; | |
| DOI : 10.1016/j.jpowsour.2015.06.002 | |
| 来源: Elsevier | |
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【 摘 要 】
High-performance solid electrolytes are critical for realizing all-solid-state batteries with enhanced safety and cycling efficiency. However, currently available candidates (sulfides and the NASICON-type ceramics) still suffer from drawbacks such as inflammability, high-cost and unfavorable machinability. Here we present the structural manipulation approaches to improve the sodium ionic conductivity in a series of affordable Na-rich antiperovskites. Experimentally, the whole solid solutions of Na3OX (X = Cl, Br, I) are synthesized via a facile and timesaving route from the cheapest raw materials (Na, NaOH and NaX). The materials are nonflammable, suitable for thermoplastic processing due to low melting temperatures (<300 degrees C) without decomposing. Notably, owing to the flexibility of perovskite-type structure, it's feasible to control the local structure features by means of size-mismatch substitution and unequivalent-doping for a favorable sodium ionic diffusion pathway. Enhancement of sodium ionic conductivity by 2 magnitudes is demonstrated by these chemical tuning methods. The optimized sodium ionic conductivity in Na2.9Sr0.05OBr0.6I0.4 bulk samples reaches 1.9 x 10(-3) S/cm at 200 degrees C and even higher at elevated temperature. We believe further chemical tuning efforts on Na-rich antiperovskites will promote their performance greatly for practical all-solid state battery applications. (C) 2015 Elsevier B.V. All rights reserved.
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| 10_1016_j_jpowsour_2015_06_002.pdf | 1518KB |
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