journal article·2024-05-06Open access

NaMCl6 (M = Nb and Ta): A New Class of Sodium-Conducting Halide-Based Solid Electrolytes

Zheng Huang, Suguru Yoshida, Hirofumi Akamatsu, Katsuro Hayashi, Saneyuki Ohno

ACS Materials Letters· Volume 6· Issue 5

Abstract

Highly conductive solid electrolytes (SEs) are a prerequisite for developing all-solid-state batteries. Recently, Li-ion conducting halide-based SEs have attracted enormous attention owing to their electrochemical, mechanical, and transport properties. Despite the success of Li-ion conducting halides, the research on the Na analogue remains sparse, and the reported ionic conductivities are limited. In this study, we demonstrate the significantly improved ionic conductivity in Na M 5+ Cl 6 ( M 5+ = Nb, Ta) by extending the existing structural framework of the Na-ion conducting halides Na 3 M 3+ Cl 6 ( M 3+ = Y, Er) and Na 2 ZrCl 6 . Transport analysis reveals that the cation M rules the activation energies of the resulting phases. Given that M is pivotal, a further fine-tuning of M in Na M Cl 6 leads to a high ionic conductivity of 0.1 mS cm –1 at 30 °C, owing to a beneficial inductive effect and enhanced migration entropy. These discoveries will provide more design strategies for Na-ion conducting halide-based SEs.
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Research context

OpenAlex topics: Advanced Battery Materials and Technologies · Thermal Expansion and Ionic Conductivity · Inorganic Chemistry and Materials

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

Department of Applied Chemistry, Graduate School of Engineering, Kyushu University, 744 Motooka, Nishi-ku, Fukuoka 819-0395, Japan

Materials Research Institute, Pennsylvania State University, University Park, Pennsylvania 16802, United States

Institute of Multidisciplinary Research for Advanced Materials, Tohoku University, 2-1-1 Katahira, Aoba-ku, Sendai, Miyagi 980-8577, Japan

Funding

Toyota Physical and Chemical Research Institute · Japan Society for the Promotion of Science

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