Enhanced Magnetotransport Properties of Ag-doped La0.7Ca0.3-xAgxMnO3 Polycrystalline Ceramics

The present report focuses on the successful synthesis of La 0.7 Ca 0.3− x Ag x MnO 3 ( x  = 0, 0.10, 0.15, 0.20, and 0.30) polycrystalline manganite samples through a soft chemical polymeric precursor route and subsequent impact of Ag doping and grain size on their magnetotransport features. X-ray...

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Veröffentlicht in:Journal of electronic materials 2023-10, Vol.52 (10), p.6425-6435
Hauptverfasser: Srivastava, Pankaj, Singh, Ashwani Kumar, Tyagi, Udai Prakash, Singh, Jai, Srivastava, Amit
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Sprache:eng
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Zusammenfassung:The present report focuses on the successful synthesis of La 0.7 Ca 0.3− x Ag x MnO 3 ( x  = 0, 0.10, 0.15, 0.20, and 0.30) polycrystalline manganite samples through a soft chemical polymeric precursor route and subsequent impact of Ag doping and grain size on their magnetotransport features. X-ray diffraction (XRD) and transmission electron microscopy (TEM) analyses reveal that Ag doping leads to a phase transformation from the orthorhombic phase to the rhombohedral phase (for x  ≥ 15%). Furthermore, it shows that the insulator–metal transition temperature (T IM ) and paramagnetic–ferromagnetic (PM-FM) transition temperature ( T C ) increase with Ag doping concentration and also with the sintering temperature. The prime factors leading to the enhancement with Ag doping are the well-known oxygenation effect by metallic Ag, which helps to improve the transport properties of La 1− x Ca x MnO 3 (LCMO) manganite, and the increase in the tolerance factor ( τ ), which in turn leads to the Mn-O-Mn bond angle and the structural disorder near the grain boundaries that weaken the double exchange. The room temperature magnetoresistance values are found to be higher for Ag-doped LCMO samples than for the pristine LCMO. The enhanced ferromagnetic ordering temperature along with low-field magnetoresistance (LFMR) of the as-synthesized Ag-doped LCMO polycrystalline ceramic indicate its potential for device fabrication.
ISSN:0361-5235
1543-186X
DOI:10.1007/s11664-023-10595-4