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The Study Of A Site Doping In Perovskite Manganite

Posted on:2009-11-21Degree:DoctorType:Dissertation
Country:ChinaCandidate:L S LingFull Text:PDF
GTID:1100360242495922Subject:Condensed matter physics
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The studies of transition-metal oxides with perovskite structure started in 1950's. In the recent ten.years, the renaissance of these materials is due to the exciting discovery of high- TC (high temperature superconductivity) in cuprates and CMR (colossal magnetoresistance ) effect in manganites. The CMR materials represented by manganites have attracted the major attention of researchers in recent years due to the fascinating properties such as colossal magnetoresistance, and the potential applications in magnetic devices, e.g., read and/or write heads for magnetic disk drives, magnetic refrigeration, magnetic random access memories as well as magnetic field sensors. These inspire people to investigate it and become one of the hot topics of present physical research. Most importantly, as a strongly correlated electron system, these materials also exhibit intriguing physical properties such as insulator-metal and/or structure transition induced by applied field or photo radiation, charge ordering, orbital ordering and phase separation etc. Once the micro mechanism of the CMR effect is fully elucidated, the progress in many fields of condensed matter physics will be definitely stimulated. In this dissertation, the author devoted his effort to the study of the properties and charge ordering in doped perovskite manganites by doping at A-site. The whole dissertation consists of five chapters.The chapter one: a brief overview of the progress of the perovskite manganites and related properties. This chapter devotes to a review of the magnetoresistance phenomena and related physical properties of perovskite manganites, such as the crystal structural, electronic configuration, magnetic property, electronic transport, charge ordering, phase separation. Some physics concept, such as double-exchange, Jahn-Teller effect, etc. are interpreted. This part is helping to build up a background for the research.The chapter two: The magnetic properties of Nd0.6Ln0.1Sr0.3MnO3 compositions (Ln = La, Pr, Gd, Dy) have been investigated thoroughly. The effect of (rA) is considered to be profound on the PM-FM phase transition in the manganites. The experiment results indicate that TC decreases with Ln changing from La to Gd due to the decreases of A> The abnormal increase of TC in Dy-composition with the smallest A> and largestσ2 is attributed to the large magnetic moment of Dy3+ ions. The rapid increase of magnetization below 30 K indicates directly the magnetic ordering of rare earth ions at A-site.The chapter three: The electrical and magnetic properties of highly doped manganite Gd0.4Ca0.6MnO3 with a relatively small A> have been investigated thoroughly. Through the M-T, M-H, and ESR measurements it is found that the magnetization in M-T curve originates from the paramagnetic contribution of disordered Mn ions at B-site and Gd3+ ions at A-site. The peculiar behavior of M-T curve below TCO originates from the remaining spin disordered Mn ions after the formation of charge-ordering phase in the manganite, and the AFM charge-ordering state is supposed to be a local short-range ordering state.The chapter four: We investigated the magnetic properties of the Pr0.5-xNdxSr0.5MnO3 (x = 0, 0.1, 0. 2, 0. 3, 0. 4, 0. 5) system. Since the two end samples Pr0.5Sr0.5MnO3 and Nd0.5Sr0.5MnO3 are A-type and CE-type AFM at low temperatures, respectively, due to their different orbital ordering d x2-y2 and d3x2-r2/d(3y2-r2), the magnetic structure of Pr0.5-xNdxSr0.5MnO3 is expected to be a mixture of A- and CE-type AFM. Our experiment results show that TC remains almost constant, while TN decreases dramatically as Pr3+ ions are replaced by Nd3+ ions. We suggest that this originates from the orbital ordering instability of the different magnetic structure type rather than from the ionic radius at the A-site.The chapter five: The electrical and magnetic properties of Ln0.4Ca0.6MnO3 compositions (Ln = La, Pr, Nd, Sm) have been investigated. The effect of A> on the charge-ordering behavior of the manganites is considered to be profound. The charge-ordering temperature TCO increases with decreasing A> , the antiferromagnetic charge-ordering state transforms from long-range into local short-range ordering and the magnetic behaviors for Ln = La, Pr, Nd, Sm are all different. Through the M-T, M-H, and electron spin resonance measurements, it is found that the magnetization in M-T curves comes from the paramagnetic contribution of disordered Mn ions at the B-site and magnetic ions at the A-site. The rise of TCO is attributed to the fact that eg electrons are localized by decreasing A>, and the different behavior of M-T curves below TCO originates from the number of remaining spin disordered Mn ions after the formation of the charge-ordering phase in the manganites.This work is supported by National Natural Science Foundation of China through Grant No. 10334090, No. 10504029, and the State Key Project of Fundamental Research, China, No. 2007CB925001, No. 001CB610604.
Keywords/Search Tags:perovskite mangnites, charge ordering, spin ordering, orbital ordering
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