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At least 1,441 records · Page 80

Monoatomic orbital-based one-dimensional topological crystalline insulator

The bulk-boundary correspondence in topological crystalline insulators (TCIs) links the topological properties of the bulk to robust observables on the edges, e.g., the existence of robust edge modes or fractional charge. In one dimension, TCIs protected by reflection symmetry have been realized in a variety of systems in which each unit cell has spatially distributed degrees of freedom (SDOF). However, these realizations exhibit sensitivity of the resulting edge modes to variations in edge termination and to the local breaking of the protective spatial symmetries by inhomogeneity. Here we demonstrate topologically protected edge states in a monoatomic, orbital-based TCI that mitigates both of these issues. By collapsing all SDOF within the unit cell to a singular point in space, we eliminate the ambiguity in unit-cell definition and hence remove a prominent source of boundary termination variability. The topological observables are also more tolerant to disorder in the orbital energies. To validate this concept, we experimentally realize a lattice of mechanical resonators where each resonator acts as an “atom” that harbors two key orbital degrees of freedom having opposite reflection parity. Finally, our measurements of this system provide direct visualization of the sp-hybridization between orbital modes that leads to a nontrivial band inversion in the bulk.

75 CONDENSED MATTER PHYSICS, SUPERCONDUCTIVITY AND↗

Polymorphous band structure model of gapping in the antiferromagnetic and paramagnetic phases of the Mott insulators MnO, FeO, CoO, and NiO

The existence of band gaps in both the antiferromagnetic (AFM) and paramagnetic (PM) phases of the classic NaCl-structure Mott insulators MnO, FeO, CoO, and NiO is traditionally viewed and taught as a manifestation of strong correlation whereby insulation results from electrons moving across the lattice forming states with doubly occupied d orbitals on certain atomic sites and empty d orbitals on other sites. Within such theories, the gap of the AFM and PM phases of these oxides emerges even in the absence of spatial symmetry breaking. The need for such a correlated picture is partially based on the known failure of the commonly used band models for the PM phase that assume for such a spin disordered state the macroscopically averaged NaCl structure, where all transition metal (TM) sites are symmetry-equivalent (a monomorphous description), producing a gapless PM state with zero magnetic moments, in sharp conflict with experiment. Here, we seek to understand the minimum theoretical description needed to capture the leading descriptors of ground state Mott insulation in the classic, 3d monoxide Mott systems—gapping and moment formation in the AFM and PM phase. As noted by previous authors, the spin-ordered AFM phase in these materials already shows in band theory a significant band gap when one doubles the NaCl unit cell by permitting different potentials for transition-metal atoms with different spins. For the spin-disordered PM phase, we allow analogously larger NaCl-type supercells where each TM site can have different spin direction and local bonding environments (i.e., disordered), yet the total spin is zero. Such a polymorphous description has the flexibility to acquire symmetry-breaking energy-lowering patterns that can lift the degeneracy of the d orbitals and develop large on-site magnetic moments without violating the global, averaged NaCl symmetry. Electrons are exchanged between spin-up and spin-down bands to create closed-shell insulating configurations that lend themselves to a single determinental description. It turns out that such a polymorphous description of the structure within the single-determinant, mean-field, Bloch periodic band structure approach (based on DFT+U) allows large on-site magnetic moments to develop spontaneously, leading to significant (1–3 eV) band gaps and large local moments in the AFM and PM phases of the classic NaCl-structure Mott insulators MnO, FeO, CoO, and NiO in agreement with experiment. We adapt to the spin disordered polymorphous configurations the “special quasirandom structure” (SQS) construct known from the theory of disordered substitutional alloys whereby supercell approximants which represent the best random configuration average (not individual snapshots) for finite (64, 216 atoms, or larger) supercells of a given lattice symmetry are constructed. We conclude that the basic features of these paradigmatic Mott insulators can be approximated by the physics included in energy-lowering symmetry broken DFT.

36 MATERIALS SCIENCE↗

The Ammonia-Hydrogen System under Pressure

Binary mixtures of hydrogen and ammonia were compressed in diamond anvil cells to 15 GPa at room temperature over a range of compositions. The phase behavior was characterized using optical microscopy, Raman spectroscopy, and synchrotron X-ray diffraction. Below 1.2 GPa we observed two-phase coexistence between liquid ammonia and fluid hydrogen phases with limited solubility of hydrogen within the ammonia-rich phase. Complete immiscibility was observed subsequent to the freezing of ammonia phase III at 1.2 GPa, although hydrogen may become metastably trapped within the disordered face-centered-cubic lattice upon rapid solidification. For all compositions studied, the phase III to phase IV transition of ammonia occurred at ~3.8 GPa and hydrogen solidified at ~5.5 GPa, transition pressures equivalent to those observed for the pure components. A P-x phase diagram for the NH 3 -H 2 system is proposed on the basis of these observations with implications for planetary ices, molecular compound formation, and possible hydrogen storage materials.

08 HYDROGEN↗

Temperature-dependent conformations of exciton-coupled Cy3 dimers in double-stranded DNA

Understanding the properties of electronically interacting molecular chromophores, which involve internally coupled electronic-vibrational motions, is important to the spectroscopy of many biologically relevant systems. In this paper, we apply linear absorption, circular dichroism, and two-dimensional fluorescence spectroscopy to study the polarized collective excitations of excitonically coupled cyanine dimers (Cy3) 2 that are rigidly positioned within the opposing sugar-phosphate backbones of the double-stranded region of a double-stranded (ds)–single-stranded (ss) DNA fork construct. We show that the exciton-coupling strength of the (Cy3) 2 -DNA construct can be systematically varied with temperature below the ds–ss DNA denaturation transition. We interpret spectroscopic measurements in terms of the Holstein vibronic dimer model, from which we obtain information about the local conformation of the (Cy3) 2 dimer, as well as the degree of static disorder experienced by the Cy3 monomer and the (Cy3) 2 dimer probe locally within their respective DNA duplex environments. The properties of the (Cy3) 2 -DNA construct we determine suggest that it may be employed as a useful model system to test fundamental concepts of protein-DNA interactions and the role of electronic-vibrational coherence in electronic energy migration within exciton-coupled bio-molecular arrays.

37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CH↗

The highly disordered Zintl phase Ca 10 GdCdSb 9 – New example of a p-type semiconductor with remarkable thermoelectric properties

Ca 10 GdCdSb 9 is a new Zintl phase with a large unit cell volume (~2500 Å 3 ) and a very complex, disordered structure, which can drive the realization of ultralow thermal conductivity in this material. The measured Seebeck coefficient, α, for single-crystalline Ca 10 GdCdSb 9 approaches 350 μV/K at 600 K. The experimentally determinedelectrical resistivity of Ca 10 GdCdSb 9 is very low, leading to a remarkably high-power factor PF of 23.2 μW/cm·K 2 at 460 K. Furthermore, the extraordinary PF value in this material, higher than those of the currently known state-of-the-art materials within the same temperature range, suggests that the Ca 10 RECdSb 9 material system (RE = rare earth metal) could serve as a viable playground to harnessing new efficient thermoelectric generators.

36 MATERIALS SCIENCE↗

Structure and expression of a novel compact myelin protein – Small VCP-interacting protein (SVIP)

Highlights: •SVIP (small p97/VCP-interacting protein) co-localizes with myelin basic protein (MBP) in compact myelin. •We determined that SVIP is an intrinsically disordered protein (IDP). •The helical content of SVIP increases dramatically during its interaction with negatively charged lipid membrane. •This study provides structural insight into interactions between SVIP and myelin membranes. -- Abstract: SVIP (small p97/VCP-interacting protein) was initially identified as one of many cofactors regulating the valosin containing protein (VCP), an AAA+ ATPase involved in endoplasmic-reticulum-associated protein degradation (ERAD). Our previous study showed that SVIP is expressed exclusively in the nervous system. In the present study, SVIP and VCP were seen to be co-localized in neuronal cell bodies. Interestingly, we also observed that SVIP co-localizes with myelin basic protein (MBP) in compact myelin, where VCP was absent. Furthermore, using nuclear magnetic resonance (NMR) and circular dichroism (CD) spectroscopic measurements, we determined that SVIP is an intrinsically disordered protein (IDP). However, upon binding to the surface of membranes containing a net negative charge, the helical content of SVIP increases dramatically. These findings provide structural insight into interactions between SVIP and myelin membranes.

60 APPLIED LIFE SCIENCES↗

Neuroprotection trek--the next generation: neuromodulation I. Techniques--deep brain stimulation, vagus nerve stimulation, and transcranial magnetic stimulation

Neuromodulation denotes controlled electrical stimulation of the central or peripheral nervous system. The three forms of neuromodulation described in this paper-deep brain stimulation, vagus nerve stimulation, and transcranial magnetic stimulation-were chosen primarily for their demonstrated or potential clinical usefulness. Deep brain stimulation is a completely implanted technique for improving movement disorders, such as Parkinson's disease, by very focal electrical stimulation of the brain-a technique that employs well-established hardware (electrode and pulse generator/battery). Vagus nerve stimulation is similar to deep brain stimulation in being well-established (for the treatment of refractory epilepsy), completely implanted, and having hardware that can be considered standard at the present time. Vagus nerve stimulation differs from deep brain stimulation, however, in that afferent stimulation of the vagus nerve results in diffuse effects on many regions throughout the brain. Although use of deep brain stimulation for applications beyond movement disorders will no doubt involve placing the stimulating electrode(s) in regions other than the thalamus, subthalamus, or globus pallidus, the use of vagus nerve stimulation for applications beyond epilepsy-for example, depression and eating disorders-is unlikely to require altering the hardware significantly (although stimulation protocols may differ). Transcranial magnetic stimulation is an example of an external or non-implanted, intermittent (at least given the current state of the hardware) stimulation technique, the clinical value of which for neuromodulation and neuroprotection remains to be determined.

Review, Tutorial↗

Simultaneous Stabilization of LiNi 0.76 Mn 0.14 Co 0.10 O 2 Cathode and Lithium Metal Anode by Lithium Bis(oxalato)borate as Additive

Abstract The long‐term cycling performance, rate capability, and voltage stability of lithium (Li) metal batteries with LiNi 0.76 Mn 0.14 Co 0.10 O 2 (NMC76) cathodes is greatly enhanced by lithium bis(oxalato)borate (LiBOB) additive in the LiPF 6 ‐based electrolyte. With 2 % LiBOB in the electrolyte, a Li∥NMC76 cell is able to achieve a high capacity retention of 96.8 % after 200 cycles at C/3 rate (1 C=200 mA g −1 ), which is the best result reported for a Ni‐rich NMC cathode coupled with Li metal anode. The significantly enhanced electrochemical performance can be ascribed to the stabilization of both the NMC76 cathode/electrolyte and Li‐metal‐anode/electrolyte interfaces. The LiBOB‐containing electrolyte not only facilitates the formation of a more compact solid–electrolyte interphase on the Li metal surface, it also forms a enhanced cathode electrolyte interface layer, which efficiently prevents the corrosion of the cathode interface and mitigates the formation of the disordered rock‐salt phase after cycling. The fundamental findings of this work highlight the importance of recognizing the dual effects of electrolyte additives in simultaneously stabilizing both cathode and anode interfaces, so as to enhance the long‐term cycle life of high‐energy‐density battery systems.

Zhao, Wengao↗

Dependence of Morphology, Shear Modulus, and Conductivity on the Composition of Lithiated and Magnesiated Single-Ion-Conducting Block Copolymer Electrolytes

Single-ion-conducting block copolymers are of considerable interest as electrolytes for battery systems, as they eliminate overpotentials due to concentration gradients. In this study, we characterize a library of poly(ethylene oxide) (PEO)-based diblock copolymers where the second block is poly(styrene-4-sulfonyltrifluoromethylsulfonyl)imide with either cation: univalent lithium or divalent magnesium counterions (PEO-PSLiTFSI or PEO-P[(STFSI) 2 Mg]). The PEO chain length is held fixed in this study. Polymers were synthesized in matched pairs that were identical in all aspects except for the identity of the counterion. Using rheology, SAXS, DSC, and AC impedance spectroscopy, we show that the dependence of morphology, modulus, and conductivity on composition in these charged copolymer systems is fundamentally different from uncharged block copolymers. At a given frequency and temperature, the shear moduli of the magnesiated copolymer systems were approximately 3-4 orders of magnitude higher than those of the matched lithiated pair. The shear moduli of all of the lithiated copolymers showed liquid-like rheological features while the magnesiated copolymers did not. All of the lithiated copolymers were completely disordered (homogeneous), consistent with the observed rheological properties. As expected, the moduli of the lithiated copolymers increased with increasing volume fraction of the ion-containing block (Φ PSTFSI ), and the conductivity decreased with Φ PSTFSI . However, the magnesiated copolymers followed a distinct trend. We show that this was due to the presence of microphase separation in the regime 0.21 ≤ Φ PSTFSI ≤ 0.36, and the tendency for microphase separation became weaker with increasing Φ PSTFSI . In conclusion, the magnesiated copolymer with Φ PSTFSI = 0.38 was homogeneous. The morphological, rheological, and conductivity properties of these systems are governed by the affinity of the cations for PEO chains; homogeneous systems are obtained when the cations migrate from the ion-containing block to PEO.

37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CH↗

Tuning Block Polymer Structure, Properties, and Processability for the Design of Efficient Nanostructured Materials Systems

Block polymers (BPs) are ideal building blocks for nanoporous membranes, microelectronics templates, energy storage devices, and other technologies. For these systems, precise control over morphology, properties, and processability are essential to optimize performance. The Epps group has used a multidisciplinary approach to control BP nanostructure ordering and orientations, order-disorder and glass transition temperatures, and mechanical and transport properties through the informed manipulation of BP effective segregation strengths and interfacial energetics. For example, alterations in macromolecular interactions between BP chains were achieved through the introduction of composition gradients between copolymer blocks or by adding dopants. In thin films, high-throughput approaches were designed to modify and characterize substrate-polymer interactions, and solvent annealing techniques were developed to facilitate nanoscale alignment and ordering. Finally, by manipulating BP interfacial energetics to gain exquisite tunability of nanostructures and materials' properties, the group is accelerating the development of next-generation BPs that will be harnessed to fabricate inexpensive, efficient, and high-performance devices.

37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CH↗

Magnetic and Magnetoresistive Behavior of the Ferromagnetic Heavy Fermion YbNi{sub 2}

We present a study on the magnetic susceptibility χ(T) and electrical resistance, as a function of temperature and magnetic field R(T, H), of the ferromagnetic heavy fermion YbNi{sub 2}. The X-ray diffraction analysis shows that the synthesized polycrystalline samples crystallizes in the cubic Laves phase structure C15, with a spatial group Fd 3-bar m. The magnetic measurements indicate a ferromagnetic behavior with transition temperature at 9 K. The electrical resistance is metallic-like at high temperatures and no signature of Kondo effect was observed. In the ferromagnetic state, the electrical resistance can be justified by electron-magnon scattering considering the existence of an energy gap in the magnonic spectrum. The energy gap was determined for various applied magnetic fields. Magnetoresistance as a function of applied magnetic field, subtracted from the R(T, H) curves at several temperatures, is negative from 2 K until about 40 K for all applied magnetic fields. The negative magnetoresistance originates from the suppression of magnetic disorder by the magnetic field.

75 CONDENSED MATTER PHYSICS, SUPERCONDUCTIVITY AND↗

Vortex Dynamic Phases in Type II Superconducting Strips with Regular and Flattened Triangular Pinning Arrays

The dynamic behavior of vortices in type II superconducting infinite strips is simulated with two types of triangular pinning lattices: the regular one and a flattened triangular array that mimics the vortex lattice in a superconducting strip in the absence of a pinning array. The calculations were made at zero temperature and perpendicular magnetic field. The size effects are investigated for several strip widths maintaining the density and size of pinning centers unchanged. A driving force is applied in the infinite direction to analyze the depinning process and the different dynamic regimes. For the regular triangular pinning lattice, we found that there is a great richness of vortex dynamical phases because depending on strip width, part of the vortices may stabilize in different interstitial positions and the depinning process depends on the commensurability of each vortex chain. For the flattened triangular lattice, the system exhibits one ordered moving phase for narrower strips and two moving phases for the larger strip. As the transport force increases, vortices in the larger strip go from a disordered to an ordered phase. Moreover, the flattened lattice shows a much higher critical depinning force than the regular one due to commensurability effects.

75 CONDENSED MATTER PHYSICS, SUPERCONDUCTIVITY AND↗

Crystal engineering in 3D: Converting nanoscale lamellar manganese oxide to cubic spinel while affixed to a carbon architecture

Here, by applying differential pair distribution function (DPDF) analyses to the energy–storage relevant MnOx/carbon system— but in a 3D architectural rather than powder–composite configuration—we can remove contributions of the carbon nanofoam paper scaffold and quantify the multiphasic oxide speciation as the nanoscale, disordered MnOx grafted to the carbon walls (MnOx@CNF) structurally rearranges in situ from birnessite AMnOx (A = Na + ; Li + ) to tetragonal Mn 3 O 4 to spinel LiMn 2 O 4 . The first reaction step involves topotactic exchange of interlayer Na + by Li + in solution followed by thermal treatments to crystal engineer the –10–nm–thick 2D layered oxide throughout the macroscale nanofoam paper into a spinel phase. The oxide remains affixed to the walls of the nanofoam throughout the phase transformations. The DPDF fits are improved by retention of one plane of birnessite–like oxide after conversion to spinel. We support the DPDF–derived assignments by X–ray photoelectron spectroscopy and Raman spectroscopy, the latter of which tracks how crystal engineering the oxide affects the disorder of the carbon substrate. We further benchmark MnOx@CNF with nonaqueous electrochemical measurements versus lithium as the oxide converts from X–ray–amorphous birnessite to interlayer-registered LiMnOx to spinel. The lamellar AMnOx displays pseudocapacitive electrochemical behavior, with a doubling of specific capacitance for the interlayer–registered LiMnOx, while the spinel LiMn 2 O 4 @CNF displays a faradaic electrochemical response characteristic of Li–ion insertion. Our results highlight the need for holistic understanding when crystal engineering an (atomistic) charge–storing phase within the (architectural) structure of practical electrodes.

36 MATERIALS SCIENCE↗

Origin of the crossover between a freezing and a structural transition at low concentration in the relaxor ferroelectric K 1-x Li x TaO 3

The origin of the relaxor behavior in K 1-x Li x TaO 3 (KLT) and other disordered perovskites is now recognized to be due to the reorientation of the polar nanodomains formed by the correlated dipoles of off-center ions. The collective dynamics of these systems evolve through several temperature stages. On decreasing temperature below the so-called Burns temperature T B , individual dipoles become correlated within nanosized regions. On further cooling, the slow dynamics of these polar regions allows local lattice distortions to take place and the formation of polar nanodomains at T* < T B . At still lower temperature, some relaxors undergo a phase transition while others do not. In KLT, there is a critical Li concentration x c = 0.022 above which the system undergoes a structural transition at T c , and below which it freezes in a dipole glass state at T f . To better understand the nature of this critical concentration, the changes that occur upon crossing it and the nature of the dipole glass state, the collective dynamics of KLT have been studied by dielectric spectroscopy and neutron diffraction for two Li concentrations (x = 0.026 and 0.018), close to but straddling the critical concentration x c . Two very different transitional behaviors are observed. Just below this critical concentration, KLT displays critical slowing down and the onset of freezing as seen in hydrogen-bonded molecular ferroelectrics, while just above this concentration, KLT undergoes a first-order structural transition.

36 MATERIALS SCIENCE↗

Dissipative Dynamics of a Harmonically Confined Bose-Einstein Condensate

We study the dissipation of the center of mass oscillation of a harmonically confined condensate in the presence of a disorder potential. An extension of the harmonic potential theorem allows one to formulate the dynamics from the point of view of an oscillating disorder potential. This formulation leads to a rigorous result for the damping rate in the limit of weak disorder.

71 CLASSICAL AND QUANTUM MECHANICS, GENERAL PHYSIC↗

Induced phase transformation in ionizable colloidal nanoparticles

Abstract Acid–base equilibria directly influence the functionality and behavior of particles in a system. Due to the ionizing effects of acid–base functional groups, particles will undergo charge exchange. The degree of ionization and their intermolecular and electrostatic interactions are controlled by varying the pH and salt concentration of the solution in a system. Although the pH can be tuned in experiments, it is hard to model this effect using simulations or theoretical approaches. This is due to the difficulty in treating charge regulation and capturing the cooperative effects in a colloidal suspension with Coulombic interaction. In this work, we analyze a suspension of ionizable colloidal particles via molecular dynamics (MD) simulations, along with Monte Carlo simulations for charge regulation (MC-CR) and derive a phase diagram of the system as a function of pH. It is observed that as pH increases, particles functionalized with acid groups change their arrangement from face-centered cubic (FCC) packing to a disordered state. We attribute these transitions to an increase in the degree of charge polydispersity arising from an increase in pH. Our work shows that charge regulation leads to amorphous solids in colloids when the mean nanoparticle charge is sufficiently high. Graphical abstract

36 MATERIALS SCIENCE↗

Physics of Life: A Model for Non-Newtonian Properties of Living Systems

This innovation proposes the reconciliation of the evolution of life with the second law of thermodynamics via the introduction of the First Principle for modeling behavior of living systems. The structure of the model is quantum-inspired: it acquires the topology of the Madelung equation in which the quantum potential is replaced with the information potential. As a result, the model captures the most fundamental property of life: the progressive evolution; i.e. the ability to evolve from disorder to order without any external interference. The mathematical structure of the model can be obtained from the Newtonian equations of motion (representing the motor dynamics) coupled with the corresponding Liouville equation (representing the mental dynamics) via information forces. All these specific non-Newtonian properties equip the model with the levels of complexity that matches the complexity of life, and that makes the model applicable for description of behaviors of ecological, social, and economical systems. Rather than addressing the six aspects of life (organization, metabolism, growth, adaptation, response to stimuli, and reproduction), this work focuses only on biosignature ; i.e. the mechanical invariants of life, and in particular, the geometry and kinematics of behavior of living things. Living things obey the First Principles of Newtonian mechanics. One main objective of this model is to extend the First Principles of classical physics to include phenomenological behavior on living systems; to develop a new mathematical formalism within the framework of classical dynamics that would allow one to capture the specific properties of natural or artificial living systems such as formation of the collective mind based upon abstract images of the selves and non-selves; exploitation of this collective mind for communications and predictions of future expected characteristics of evolution; and for making decisions and implementing the corresponding corrections if the expected scenario is different from the originally planned one. This approach postulates that even a primitive living species possesses additional, non-Newtonian properties that are not included in the laws of Newtonian or statistical mechanics. These properties follow from a privileged ability of living systems to possess a self-image (a concept introduced in psychology) and to interact with it. The proposed mathematical system is based on the coupling of the classical dynamical system representing the motor dynamics with the corresponding Liouville equation describing the evolution of initial uncertainties in terms of the probability density and representing the mental dynamics. The coupling is implemented by the information-based supervising forces that can be associated with self-awareness. These forces fundamentally change the pattern of the probability evolution, and therefore, lead to a major departure of the behavior of living systems from the patterns of both Newtonian and statistical mechanics. This innovation is meant to capture the signature of life based only on observable behavior, not on any biochemistry. This will not prevent the use of this model for developing artificial living systems, as well as for studying some general properties of behavior of natural, living systems.

Zak, Michail↗

Impact of nanostructuring on the magnetic and magnetocaloric properties of microscale phase-separated La 5/8–y Pr y Ca 3/8 MnO₃ manganites

Bulk manganites of the form La 5/8–y Pr y Ca 3/8 MnO₃ (LPCMO) exhibit a complex phase diagram due to coexisting charge-ordered antiferromagnetic (CO/AFM), charge-disordered paramagnetic (PM), and ferromagnetic (FM) phases. Because phase separation in LPCMO occurs on the microscale, reducing particle size to below this characteristic length is expected to have a strong impact on the magnetic properties of the system. Through a comparative study of the magnetic and magnetocaloric properties of single-crystalline (bulk) and nanocrystalline LPCMO (y=3/8) we show that the AFM, CO, and FM transitions seen in the single crystal can also be observed in the large particle sizes (400 and 150 nm), while only a single PM to FM transition is found for the small particles (55 nm). Magnetic and magnetocaloric measurements reveal that decreasing particle size affects the balance of competing phases in LPCMO and narrows the range of fields over which PM, FM, and CO phases coexist. The FM volume fraction increases with size reduction, until CO is suppressed below some critical size, ~100 nm. With size reduction, the saturation magnetization and field sensitivity first increase as long-range CO is inhibited, then decrease as surface effects become increasingly important. The trend that the FM phase is stabilized on the nanoscale is contrasted with the stabilization of the charge-disordered PM phase occurring on the microscale, demonstrating that in terms of the characteristic phase separation length, a few microns and several hundred nanometers represent very different regimes in LPCMO.

Bingham, N. S.↗