Synthesis of LiNixMn2-xO4 by low-temperature solid-state reaction and its microstructure

Open

D. Purwaningsih, R. Roto, H. Sutrisno

2016 IOP Conference Series: Materials Science and Engineering Vol. 107 Issue 1 Conference paper Cited by 1 SDG 12 Quartile

Abstract

This study aims to synthesis the Ni-doped LiNixMn2-xO4 (x = 0; 0.02; 0.04; 0.06; 08; 0.1) by low temperature solid-state reaction. The microstructure of the product was evaluated based on the mole ratio of Ni/Mn of the precursors. The structural analysis of LiNixMn2-xO4 was analyzed by x-ray diffraction equipped with the Direct Method of win PLOTR package program and Diamond. It was found that doping with Ni could change the size, crystallinity and microstructure of LiNixMn2-xO4. The LiNixMn2-xO4 solids have a cubic structure with a space group of Fd3m. The increase in the doping content does not affect the structure. The particle size of the products is about 150-500 nm. The crystallinity of the solids tends to increase with the increase in Ni content. However, the increase of Ni content in the product causes the lattice parameters of the unit cell to decrease. © Published under licence by IOP Publishing Ltd.

Affiliations

Department of Chemistry, Faculty of Mathematics and Natural Sciences, Gadjah Mada University, Sekip Utara BLS 21, Yogyakarta, 55584, Indonesia; Department of Chemistry Education, Faculty of Mathematics and Natural Sciences, Yogyakarta State University, Jl. Colombo 1, Yogyakarta, 55281, Indonesia

Research at a Glance

Premium content — register to unlock

Research at a Glance

Register to unlock

Topics & SDG Alignment

Premium content — register to unlock

Topics & SDG Alignment

Register to unlock

Collaboration

Premium content — register to unlock

Collaboration

Register to unlock

Author Profile (Selected)

Premium content — register to unlock

Author Profile (Selected)

Register to unlock

References Overview

Premium content — register to unlock

References Overview

Register to unlock

Journal & Source

Premium content — register to unlock

Journal & Source

Register to unlock

Metadata & Integrity

Premium content — register to unlock

Metadata & Integrity

Register to unlock