Correlating X-ray absorption spectra and ultraviolet photoelectron spectra to understand magnetic and transport properties of charge-ordered perovskite manganites

被引:2
|
作者
Dwivedi, G. D. [1 ,2 ]
Kumawat, S. M. [1 ,2 ]
Shyu, W. S. [1 ,2 ]
Chien, Y. H. [1 ,2 ]
Su, P. F. [1 ,2 ]
Huang, Z. H. [1 ,2 ]
Haw, S. C. [3 ]
Chen, J. M. [3 ]
Chou, H. [1 ,2 ]
Chatterjee, S. [4 ]
机构
[1] Natl Sun Yat Sen Univ, Dept Phys, Kaohsiung 80424, Taiwan
[2] Natl Sun Yat Sen Univ, Ctr Crystal Res, Kaohsiung 80424, Taiwan
[3] Natl Synchrotron Radiat Res Ctr, Hsinchu 30076, Taiwan
[4] Indian Inst Technol Banaras Hindu Univ, Dept Phys, Varanasi 221005, India
关键词
Charge-ordering; Magneto-resistance; Electronic structure; Ultraviolet photoelectron spectroscopy; X-ray absorption spectroscopy; ELECTRONIC-STRUCTURE; NEUTRON-DIFFRACTION; RARE-EARTH; THIN-FILMS; TRANSITION; MAGNETORESISTANCE; FIELD; CA; MAGNETOTRANSPORT; PR1-XCAXMNO3;
D O I
10.1016/j.apsusc.2021.151131
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
X-ray absorption spectra and ultraviolet photoelectron spectra have been used to compare the electronic structures of (La0.6Pr0.4)(0.65)Ca0.35MnO3 and (La0.4Pr0.6)(0.65)Ca0.35MnO3 systems to understand their magnetic and transport properties. Structural analysis showed that increased Pr-substitution triggers expansion in apical Mn-O bond lengths, which eventually causes narrowing of the e(g) band width. (La0.6Pr0.4)(0.65)Ca0.35MnO3 exhibits ferromagnetic ordering below 215 K and shows semiconductor to metal transition around 212 K, while (La0.4Pr0.6)(0.65)Ca0.35MnO3 exhibit complex magnetic behaviour and also show local semiconductor to metal transition around 95 K before re-entering into semiconducting region again below 80 K. A slight change in the slope of resistivity around 220 K and four orders increase in resistivity indicates presence of charge-ordering in (La0.4Pr0.6)(0.65)Ca0.35MnO3. Moreover, (La0.4Pr0.6)(0.65)Ca0.35MnO3 exhibits similar to 100% magneto-resistance. X-ray absorption studies of Mn-L-2,L-3 edge and O -K edge reveal the onset of Mn3+-Mn4+ charge-ordering in (La0.4Pr0.6)(0.65)Ca0.35MnO3 at room temperature. O-K edge spectra exhibits an increased spectral intensity of O2p-Mn3d(eg) states near Fermi-level for (La0.4Pr0.6)(0.65)Ca0.35MnO3, which reflects the number of unoccupied eg states. Valence band ultraviolet photoemission spectroscopy study revealed that Mn3d(e(g)) states of (La0.6Pr0.4)(0.65)Ca0.35MnO3 extends into conduction band by crossing-over the Fermi-level. On the other hand, (La0.4Pr0.6)(0.65)Ca0.35MnO3 exhibits no electronic state at Fermi-level explaining stronger semiconducting nature of x = 0.6 system than x = 0.4 near room temperature.
引用
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页数:10
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