Aditya Sharma , Manas Nasit , Nitin Kumar Gautam , Shalendra Kumar , Ranjeet Brajpuriya , B.H. Lee , S.O. Won , Mayora Varshney , Nishima Chaddha , H.J. Shin
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摘要

我们采用固态反应法制备了 LiGa5O8 样品(在 800 ℃ 和 1300 ℃ 下退火),并对其电化学特性进行了研究。X 射线衍射 (XRD) 结果证实了尖晶石结构在 1300 ℃ 时的稳定性。扫描电子显微镜(SEM)结果表明 LiGa5O8 复合物形成了花瓣状形态。800 ℃退火的样品由 41.5 Å 和 72.3 Å 的两个不同孔隙组成,比表面积较大,为 0.982 m2/g。1300 ⁰C退火样品的比表面积为 0.433 m2/g,只有一个大小为 48.5 Å 的孔隙。根据富含氧化还原特征的 CV 曲线和来自 GCD 结果的伪电容充放电特性,比电容为 107.6 F/g (扫描速率为 5 mV/s) 和 141.8 F/g (电流密度为 1 A/g) 。LiGa5O8 -1300 样品的比电容较小,分别为 84.4 F/g(扫描速率为 5 mV/s)和 97.2 F/g(电流密度为 1 A/g),这是因为在次表面积和孔隙的花瓣处发生了较差的吸附/解吸和锂化/脱锂化反应。LiGa5O8-800 和 LiGa5O8-1300 样品在 3000 次循环中的保持率分别为 77% 和 70%。我们的研究结果为探索新型、经济、稳定的能量存储设备氧化物系统铺平了道路。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Petals morphology formation and pseudocapacitive properties of LiGa5O8 ceramics
The LiGa5O8 samples have been prepared using the solid-state reaction method (annealed at 800 ⁰C and 1300 ⁰C) and investigated for electrochemical properties. X-ray diffraction (XRD) results confirmed the spinel structure stability up to 1300 ⁰C. Scanning electron microscopy (SEM) results convey petals-like morphology formation in the LiGa5O8 compounds. The 800 ⁰C annealed sample consists of two different pores of 41.5 Å and 72.3 Å with a larger specific surface area of 0.982 m2/g. The 1300 ⁰C annealed sample obeys a specific surface area of 0.433 m2/g and a single pore of the size of 48.5 Å. The redox feature-rich CV curves and the pseudo-capacitance charging/discharging characteristics from GCD results have offered a specific capacitance of ∼107.6 F/g (at a scan rate of 5 mV/s) and 141.8 F/g (at a current density of 1 A/g), respectively, for LiGa5O8-800 sample. The LiGa5O8 −1300 sample could exhibit lesser specific capacitance of 84.4 F/g (at 5 mV/s scan rate) and 97.2 F/g (at a current density of 1 A/g) due to the inferior adsorption/desorption and lithiation/delithiation reactions at the petals of subordinate surface area and pores. LiGa5O8-800 and LiGa5O8-1300 samples have exhibited 77 % and 70 % retention up to 3000 cycles. Our results pave the way to explore new, cost-effective, and stable oxide systems for energy storage devices.
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