Abstract

Designing solid-state electrolytes for proton batteries at moderate temperatures is challenging as most solid-state proton conductors suffer from poor moldability and thermal stability. Crystal–glass transformation of coordination polymers (CPs) and metal–organic frameworks (MOFs) via melt-quenching offers diverse accessibility to unique properties as well as processing abilities. Here, we synthesized a glassy-state CP, [Zn3(H2PO4)6(H2O)3](1,2,3-benzotriazole), that exhibited a low melting temperature (114 °C) and a high anhydrous single-ion proton conductivity (8.0 × 10−3 S cm−1 at 120 °C). Converting crystalline CPs to their glassy-state counterparts via melt-quenching not only initiated an isotropic disordered domain that enhanced H+ dynamics, but also generated an immersive interface that was beneficial for solid electrolyte applications. Finally, we demonstrated the first example of a rechargeable all-solid-state H+ battery utilizing the new glassy-state CP, which exhibited a wide operating-temperature range of 25 to 110 °C.

Highlights

  • The proton (H+) has a diameter of 0.84 fm and is localized in the solid state.[1]

  • Converting crystalline coordination polymers (CPs) to their glassy-state counterparts via melt-quenching initiated an isotropic disordered domain that enhanced H+ dynamics, and generated an immersive interface that was beneficial for solid electrolyte applications

  • single-crystal X-ray diffraction (SC-XRD) analysis of 1a provided its chemical formula, [Zn3(H2PO4)6(H2O)3](BTA), and it was found to exist as a onedimensional (1D) chain along the a-axis (Fig. 1)

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Summary

Introduction

The proton (H+) has a diameter of 0.84 fm and is localized in the solid state.[1]. We synthesized a glassy-state CP, [Zn3(H2PO4)6(H2O)3](1,2,3-benzotriazole), that exhibited a low melting temperature (114 C) and a high anhydrous single-ion proton conductivity (8.0 Â 10À3 S cmÀ1 at 120 C).

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