Abstract
The body-centered cubic (bcc) polymorph of NaCB11H12 has been stabilized at room temperature by high-energy mechanical milling. Temperature-dependent electrochemical impedance spectroscopy shows an optimum at 45-min milling time, leading to an rt conductivity of 4 mS cm-1. Mechanical milling suppresses an order-disorder phase transition in the investigated temperature range. Nevertheless, two main regimes can be identified, with two clearly distinct activation energies. Powder X-ray diffraction and 23Na solid-state NMR reveal two different Na+ environments, which are partially occupied, in the bcc polymorph. The increased number of available sodium sites w.r.t. ccp polymorph raises the configurational entropy of the bcc phase, contributing to a higher ionic conductivity. Mechanical treatment does not alter the oxidative stability of NaCB11H12. Electrochemical test on a symmetric cell (Na|NaCB11H12|Na) without control of the stack pressure provides a critical current density of 0.12 mA cm-2, able to fully charge/discharge a 120 mA h g-1 specific capacity positive electrode at the rate of C/2.
| Original language | English |
|---|---|
| Pages (from-to) | 61346-61356 |
| Number of pages | 11 |
| Journal | ACS Applied Materials and Interfaces |
| Volume | 13 |
| Issue number | 51 |
| DOIs | |
| Publication status | Published - 29 Dec 2021 |
Bibliographical note
Funding Information:F.M., M.B., and R.C. received funding from the University of Geneva.
Publisher Copyright:
© 2021 American Chemical Society.
Funding
F.M., M.B., and R.C. received funding from the University of Geneva.
Keywords
- boron chemistry
- hydroborate
- mechanical milling
- Nasuperionic conductor
- NaCBH
- solid electrolyte