TY - CHAP
T1 - A Comparison Study on Structural Properties in La0.7Ca0.2Sr0.1MnO3 Compound Synthesized by Solid-State, Sol-Gel, and Wet-Mixing Methods
AU - Nehan, Phahul Z.Z.
AU - Vitayaya, Okvarahireka
AU - Munazat, Dicky R.
AU - Naibaho, Marzuki
AU - Manawan, Maykel T.E.
AU - Darminto,
AU - Kurniawan, Budhy
N1 - Publisher Copyright:
© 2025 Trans Tech Publications Ltd. All Rights Reserved.
PY - 2025
Y1 - 2025
N2 - In this research, we have tried to investigate the effects of the synthesis methods on structural properties in La0.7Ca0.2Sr0.1MnO3 compound synthesized using solid-state, sol-gel, and wet-mixing methods. All samples were measured with several measurements, such as X-ray diffraction (XRD), scanning electron microscope-energy dispersive X-ray (SEM-EDX), and Fourier transform infrared spectroscopy (FTIR). Our XRD analysis reveals a single phase without impurity and confirms the presence of orthorhombic structures with Pnma space group. Additionally, the average crystal size of La0.7Ca0.2Sr0.1MnO3 compound by using solid-state, sol-gel, and wet-mixing methods exhibits values of 112.51, 91.33, and 88.75 nm. For the morphological structure analysis, we have carried out SEM analysis, which shows a decreasing value of grain size average of 1.70, 0.91, and 0.81 μm for solid-state, sol-gel, and wet-mixing methods samples, respectively, which have a similar trend with values of the average crystal size. The FTIR measurement confirms the presence of the internal bending mode of MnO6 and asymmetric stretching mode of MnO6 at a band around 518.16 - 524.24 and 548.68 - 616.57 cm-1, respectively.
AB - In this research, we have tried to investigate the effects of the synthesis methods on structural properties in La0.7Ca0.2Sr0.1MnO3 compound synthesized using solid-state, sol-gel, and wet-mixing methods. All samples were measured with several measurements, such as X-ray diffraction (XRD), scanning electron microscope-energy dispersive X-ray (SEM-EDX), and Fourier transform infrared spectroscopy (FTIR). Our XRD analysis reveals a single phase without impurity and confirms the presence of orthorhombic structures with Pnma space group. Additionally, the average crystal size of La0.7Ca0.2Sr0.1MnO3 compound by using solid-state, sol-gel, and wet-mixing methods exhibits values of 112.51, 91.33, and 88.75 nm. For the morphological structure analysis, we have carried out SEM analysis, which shows a decreasing value of grain size average of 1.70, 0.91, and 0.81 μm for solid-state, sol-gel, and wet-mixing methods samples, respectively, which have a similar trend with values of the average crystal size. The FTIR measurement confirms the presence of the internal bending mode of MnO6 and asymmetric stretching mode of MnO6 at a band around 518.16 - 524.24 and 548.68 - 616.57 cm-1, respectively.
KW - Ceramic
KW - Comparison Synthesis Method
KW - Perovskite Manganite
KW - X-ray Diffraction
UR - https://www.scopus.com/pages/publications/105009237521
U2 - 10.4028/p-X4BrmP
DO - 10.4028/p-X4BrmP
M3 - Chapter
AN - SCOPUS:105009237521
T3 - Materials Science Forum
SP - 45
EP - 54
BT - Materials Science Forum
PB - Trans Tech Publications Ltd
ER -