#TITLE_ALTERNATIVE#

• Main Author: Rusli NIM: 20504020, Rolan
• Format: Theses
• Language: Indonesia
• Online Access: https://digilib.itb.ac.id/gdl/view/9142
• Institution: Institut Teknologi Bandung

Abstract: <br /> <br /> <br /> <br /> <br /> Most of studies in Aurivillius oxide have been synthesized of Aurivillius oxides with d cation as B cation. Recently, attempts to substitute d with do cation at perovskite layered has been started. In this work attempt to substitute (Ti4+) with (Fe3+) has been carried out. Aurivillius oxides Sr2Bi4Ti5xFexOis, Sr2+0,5XBi4Ti5XFeXO18, Pb2Bi5Ti5FeO21 and Pb3Bi5Ti6FeO24 have been synthesized using the solid state reaction method. X-ray Diffraction powder data were refined using Le Bail method implemented in Rietica. Sr2Bi4Ti5XFeXO18, and Sr2+o,5xBi4Ti5XFeXO18 oxides have space group B2cb, Z = 4; whilst Pb2Bi5Ti5FeO21 and Pb3Bi5Ti6FeO24 oxides have space group A21am, Z = 4 and I4/mmm, Z = 2. The random substitution of cation Fe3+ at Ti4+ position in these Aurivillius oxides was showed by the increase of lattice volume and magnetic moment in these oxides with increasing Fe substitution. The results of atomic simulation indicate that there were goal agreements between the simulated and experimental structural parameter for several Aurivillius oxides like Bi2Mo025Wo.75O6, Bi2. Bi2 L (x = 0-1), ABi2Ta2O9 (A = Sr, Ba, Ca), AASr2XBi2Nb2TiO12 (A = Ba, Ca; and x = 0, 0.5), and Bi5Ti1,5W1.5O15, with the differences less than 0.03 %. Yoder Flora equation can be used to determine lattice energy of Aurivillius oxides.