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Jiyeob Kim

Publications and source records attributed to Jiyeob Kim.

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Heterogeneous field response of hierarchical polar laminates in relaxor ferroelectrics

Relaxor ferroelectrics are a class of materials that are widely perceived as deriving their exotic properties from structural heterogeneities. Understanding the microscopic origin of the superior electromechanical response requires knowledge not only concerning the formation of polar nanodomains (PNDs) built from individual atoms but more importantly the spatial distribution of PNDs over longer distances. The mesoscale PND arrangement is shaped by the interactions between these domains and, in turn, dictates the electric-field driven PND response directly relevant to the macroscopic material properties. Here, we show the emergence of mesoscale lattice order that we name "polar laminates" in the canonical relaxor ferroelectric 0.68PbMg$_{1/3}$Nb$_{2/3}$O$_{3}$-0.32PbTiO$_{3}$ (PMN-0.32PT) using X-ray coherent nano-diffraction. These laminates are nematic with a size of ~350 nm and arise from the staggered arrangement of ~13 nm monoclinic PNDs along the <110> of the pseudocubic lattice. The spatial distribution of c-axis strain is directly correlated with the tilting of the PNDs and is most prominent between the laminates. Further operando nano-diffraction studies demonstrate heterogeneous electric-field-driven responses. The most active regions tend to reside inside the laminates while the spatial pinning centers are between the laminates. This observation reveals the hierarchical assembly of lattice order as a novel form of electron and lattice self-organization in heterogenous materials and establishes the role of such mesoscale spatial arrangement in connecting the nanoscale heterogeneity and macroscopic material properties. These findings provide a guiding principle for the design and optimization of future relaxors and may shed light on the existence of similar behavior in a wide range of quantum and functional materials.

cond-mat.mtrl-sci

Large magnetoelectric coupling in multiferroic oxide heterostructures assembled via epitaxial lift-off

The strain dependent functional properties of epitaxial transition metal oxide films can be significantly modified via substrate selection. However, large lattice mismatches preclude dislocation-free epitaxial growth on ferroelectric substrates, whose strain states are modified by applied electric fields. Here we overcome this mismatch problem by depositing an epitaxial film of ferromagnetic La0.7Sr0.3MnO3 on a single crystal substrate of well lattice matched SrTiO3 via a film of SrRuO3 that we subsequently dissolved, permitting the transfer of unstrained La0.7Sr0.3MnO3 to a ferroelectric substrate of 0.68Pb(Mg1/3Nb2/3)O3 0.32PbTiO3 in a different crystallographic orientation. Ferroelectric domain switching, and a concomitant ferroelectric phase transition, produced large non volatile changes of magnetization that were mediated by magnetic domain rotations at locations defined by the microstructure - as revealed via high resolution vector maps of magnetization constructed from photoemission electron microscopy data, with contrast from x-ray magnetic circular dichroism. In future, our method may be exploited to control functional properties in dislocation free epitaxial films of any composition.

cond-mat.mtrl-sci

Multi-site exchange enhanced barocaloric response in Mn$_{3}$NiN

We have studied the barocaloric effect (BCE) in the geometrically frustrated antiferromagnet Mn$_{3}$NiN across the Néel transition temperature. Experimentally we find a larger barocaloric entropy change by a factor of 1.6 than that recently discovered in the isostructural antiperovskite Mn$_{3}$GaN despite greater magnetovolume coupling in the latter. By fitting experimental data to theory we show that the larger BCE of Mn$_{3}$NiN originates from multi-site exchange interactions amongst the local Mn magnetic moments and their coupling with itinerant electron spins. Using this framework, we discuss the route to maximise the BCE in the wider Mn$_{3}$AN family.

cond-mat.str-el