TY - JOUR
T1 - A non-alkoxide sol-gel method for the preparation of homogeneous nanocrystalline powders of la 0.85Sr 0.15MnO 3
AU - Chervin, Christopher N.
AU - Clapsaddle, Brady J.
AU - Chiu, Hsiang Wei
AU - Gash, Alexander E.
AU - Satcher, Joe H.
AU - Kauzlarich, Susan M.
PY - 2006/4/4
Y1 - 2006/4/4
N2 - Homogeneous, nanocrystalline Lai 1-xSr xMnO 3 (LSM) powders, with x ∼ 0.15, were synthesized with the epoxide addition sol-gel method. Through this simple technique, sol-gel materials were prepared from methanolic solutions of metal chlorides without the need for alkoxides, polymeric gel agents, or elaborate reaction schemes. The gels were dried in ambient conditions, resulting in mesoporous xerogels with networked nanostructures interconnecting particulate regions. Calcination of the dried gels resulted in the crystallization of single-phase LSM by 700 °C, after decomposition of intermediate hydroxide, chloride, and oxychloride compounds. SEM analysis indicated that the calcined powders were nanocrystalline and consisted of discrete particles, free of hard agglomeration. The average crystallite size and equivalent spherical diameter determined from XRD line broadening and BET analysis, respectively, were in good agreement with the SEM results (∼100 nm). The activation energies for the electronic conductivity from 1000 to 400 °C of sintered LSM xerogels were from 0.13 to 0.15 eV, in excellent agreement with previous reported results for LSM with x ∼ 0.15.
AB - Homogeneous, nanocrystalline Lai 1-xSr xMnO 3 (LSM) powders, with x ∼ 0.15, were synthesized with the epoxide addition sol-gel method. Through this simple technique, sol-gel materials were prepared from methanolic solutions of metal chlorides without the need for alkoxides, polymeric gel agents, or elaborate reaction schemes. The gels were dried in ambient conditions, resulting in mesoporous xerogels with networked nanostructures interconnecting particulate regions. Calcination of the dried gels resulted in the crystallization of single-phase LSM by 700 °C, after decomposition of intermediate hydroxide, chloride, and oxychloride compounds. SEM analysis indicated that the calcined powders were nanocrystalline and consisted of discrete particles, free of hard agglomeration. The average crystallite size and equivalent spherical diameter determined from XRD line broadening and BET analysis, respectively, were in good agreement with the SEM results (∼100 nm). The activation energies for the electronic conductivity from 1000 to 400 °C of sintered LSM xerogels were from 0.13 to 0.15 eV, in excellent agreement with previous reported results for LSM with x ∼ 0.15.
UR - http://www.scopus.com/inward/record.url?scp=33646096996&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=33646096996&partnerID=8YFLogxK
U2 - 10.1021/cm052301j
DO - 10.1021/cm052301j
M3 - Article
AN - SCOPUS:33646096996
VL - 18
SP - 1928
EP - 1937
JO - Chemistry of Materials
JF - Chemistry of Materials
SN - 0897-4756
IS - 7
ER -