{"title":"Petals morphology formation and pseudocapacitive properties of LiGa5O8 ceramics","authors":"Aditya Sharma , Manas Nasit , Nitin Kumar Gautam , Shalendra Kumar , Ranjeet Brajpuriya , B.H. Lee , S.O. Won , Mayora Varshney , Nishima Chaddha , H.J. Shin","doi":"10.1016/j.nxmate.2025.100521","DOIUrl":null,"url":null,"abstract":"<div><div>The LiGa<sub>5</sub>O<sub>8</sub> 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 LiGa<sub>5</sub>O<sub>8</sub> 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 m<sup>2</sup>/g. The 1300 ⁰C annealed sample obeys a specific surface area of 0.433 m<sup>2</sup>/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 LiGa<sub>5</sub>O<sub>8</sub>-800 sample. The LiGa<sub>5</sub>O<sub>8</sub> −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. LiGa<sub>5</sub>O<sub>8</sub>-800 and LiGa<sub>5</sub>O<sub>8</sub>-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.</div></div>","PeriodicalId":100958,"journal":{"name":"Next Materials","volume":"7 ","pages":"Article 100521"},"PeriodicalIF":0.0000,"publicationDate":"2025-02-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Next Materials","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2949822825000395","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
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.