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Advancing energy storage and supercapacitor applications through the development of Li+-doped MgTiO3 perovskite nano-ceramics.
Magar, Hend S; Mansour, A M; Hammad, Ali B Abou.
Afiliação
  • Magar HS; Applied Organic Chemistry Department, National Research Centre (NRC), 33 El­Bohouth St., Dokki, 12622, Cairo, Egypt.
  • Mansour AM; Solid State Physics Department, Physics Research Institute, National Research Centre, 33 El Bohouth St., Dokki, 12622, Giza, Egypt.
  • Hammad ABA; Solid State Physics Department, Physics Research Institute, National Research Centre, 33 El Bohouth St., Dokki, 12622, Giza, Egypt. abohmad2@yahoo.com.
Sci Rep ; 14(1): 1849, 2024 Jan 22.
Article em En | MEDLINE | ID: mdl-38253766
ABSTRACT
Perovskite oxide materials, specifically MgTiO3 (MT) and Li-doped MgTiO3 (MTxLi), were synthesized via a sol-gel method and calcination at 800 °C. This study explores the impact of varying Li doping levels (x = 0, 0.01, 0.05, and 0.1) on the crystalline structure and properties of MgTiO3. X-ray diffraction analysis revealed a well-defined rhombohedral MgTiO3 phase. Optical diffuse reflectance measurements provided insights into energy gap values, refractive index, and dielectric constant. Li+ doping enhanced the electrical properties of MgTiO3, with a notable phase transition observed at 50 °C. The study investigated impedance and AC conductivity under varying temperature and frequency conditions (25-120 °C, 4 Hz to 8 MHz). Electrochemical analysis through cyclic voltammetry and electrochemical impedance spectroscopy confirmed highly electrocatalytic properties for MTxLi, particularly when modified onto screen-printed electrodes. This work not only advances the understanding of Li-doped MgTiO3 nanostructures but also highlights their significant potential for direct electrochemical applications, particularly in the realm of energy storage.

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article