Elasticity-driven Nanoscale Texturing in Complex Electronic Materials

Finescale probes of many complex electronic materials have revealed a non-uniform nanoworld of sign-varying textures in strain, charge and magnetization, forming meandering ribbons, stripe segments or droplets. We introduce and simulate a Ginzburg-Landau model for a structural transition, with strains coupling to charge and magnetization. Charge doping acts as a local stress that deforms surrounding unit cells without generating defects. This seemingly innocuous constraint of elastic `compatibility', in fact induces crucial anisotropic long-range forces of unit-cell discrete symmetry, that interweave opposite-sign competing strains to produce polaronic elasto-magnetic textures in the composite variables. Simulations with random local doping below the solid-solid transformation temperature reveal rich multiscale texturing from induced elastic fields: nanoscale phase separation, mesoscale intrinsic inhomogeneities, textural cross-coupling to external stress and magnetic field, and temperature-dependent percolation. We describe how this composite textured polaron concept can be valuable for doped manganites, cuprates and other complex electronic materials.Comment: Preprin

Electronic phase separation in the rare earth manganates, (La1-xLnx)0.7Ca0.3MnO3 (Ln = Nd, Gd and Y)

All the three series of manganates showsaturation magnetization characteristic of ferromagnetism, with the ferromagnetic Tc decreasing with increasing in x up to a critical value of x, xc (xc = 0.6, 0.3, 0.2 respectively for Nd, Gd, Y). For x > xc, the magnetic moments are considerably smaller showing a small increase around TM, the value of TM decreasing slightly with increase in x or decrease in . The ferromagnetic compositions (x xc) show insulator-metal (IM) transitions, while the compositions with x > xc are insulating. The magnetic and electrical resistivity behavior of these manganates is consistent with the occurrence of phase separation in the compositions around xc, corresponding to a critical average radius of the A-site cation, , of 1.18 A. Both Tc and TIM increase linearly when < rA > > or x xc as expected of a homogenous ferromagnetic phase. Both Tc and TM decrease linearly with the A-site cation size disorder at the A-site as measured by the variance s2. Thus, an increase in s2 favors the insulating AFM state. Percolative conduction is observed in the compositions with > < rAc >. Electron transport properties in the insulating regime for x > xc conforms to the variable range hopping mechanism. More interestingly, when x > xc, the real part of dielectric constant (e') reaches a high value (104-106) at ordinary temperatures dropping to a very small (~500) value below a certain temperature, the value of which decreases with decreasing frequency.Comment: 27 pages; 11 figures, Submitted to J.Phys:Condens Matte

ARPES: A probe of electronic correlations

Angle-resolved photoemission spectroscopy (ARPES) is one of the most direct methods of studying the electronic structure of solids. By measuring the kinetic energy and angular distribution of the electrons photoemitted from a sample illuminated with sufficiently high-energy radiation, one can gain information on both the energy and momentum of the electrons propagating inside a material. This is of vital importance in elucidating the connection between electronic, magnetic, and chemical structure of solids, in particular for those complex systems which cannot be appropriately described within the independent-particle picture. Among the various classes of complex systems, of great interest are the transition metal oxides, which have been at the center stage in condensed matter physics for the last four decades. Following a general introduction to the topic, we will lay the theoretical basis needed to understand the pivotal role of ARPES in the study of such systems. After a brief overview on the state-of-the-art capabilities of the technique, we will review some of the most interesting and relevant case studies of the novel physics revealed by ARPES in 3d-, 4d- and 5d-based oxides.Comment: Chapter to appear in "Strongly Correlated Systems: Experimental Techniques", edited by A. Avella and F. Mancini, Springer Series in Solid-State Sciences (2013). A high-resolution version can be found at: http://www.phas.ubc.ca/~quantmat/ARPES/PUBLICATIONS/Reviews/ARPES_Springer.pdf. arXiv admin note: text overlap with arXiv:cond-mat/0307085, arXiv:cond-mat/020850

A brief discussion of the magnetocaloric effect in thin films of manganite doped with chromium

In this work we report on the magnetocaloric effect of La2/3Ca1/3MnO3 (LCMO) and La2/3Ca1/3Mn0.94Cr0.06O3 (LCMCrO) manganite thin films grown by DC magnetron sputtering on LaAlO3 (100) substrates. X-ray diffraction shows that both doped and undoped films crystallize in the orthorhombic structure. Magnetic measurements show a decrease in both the Curie temperature, TC , and the saturation magnetization, MS , for the LCMCrO sample. The change in the magnetic entropy (?Sm ) was extracted from hysteresis loops at different temperatures around the ferromagnetic to paramagnetic transition, displaying a maximum of entropy change (?Sm ) max near TC in both films. Moreover, a shift in (?Sm ) max toward temperatures above TC with increasing magnetic field and a broadening of the entropy change curve were observed. Results of refrigeration cooling power show a lower efficiency for LCMCrO. In order to obtain a local insight into the magnetic interactions of these films, measurements of X-ray absorption spectroscopy and X-ray magnetic circular dichroism (XMCD) were performed. XMCD suggests that an antiferromagnetic coupling between Mn4+ - Mn3+ is favored with Cr3+ incorporation, which reduces the Mn L 2,3 XMCD signal and results in a decrease of MS and (?Sm ) max in LCMCrO films. © Published under licence by IOP Publishing Ltd