arXiv subjects

G. Aeppli

Publications and source records attributed to G. Aeppli.

At least 37 records · Page 2Linked to original sources

arXiv2008

Nanomechanical detection of antibiotic-mucopeptide binding in a model for superbug drug resistance

The alarming growth of the antibiotic-resistant superbugs methicillin-resistant Staphylococcus aureus (MRSA) and vancomycin-resistant Enterococcus (VRE) is driving the development of new technologies to investigate antibiotics and their modes of action. We report the label-free detection of vancomycin binding to bacterial cell wall precursor analogues (mucopeptides) on cantilever arrays, with 10 nM sensitivity and at clinically relevant concentrations in blood serum. Differential measurements quantified binding constants for vancomycin-sensitive and vancomycin-resistant mucopeptide analogues. Moreover, by systematically modifying the mucopeptide density we gain new insights into the origin of surface stress. We propose that stress is a product of a local chemical binding factor and a geometrical factor describing the mechanical connectivity of regions affected by local binding in terms of a percolation process. Our findings place BioMEMS devices in a new class of percolative systems. The percolation concept will underpin the design of devices and coatings to significantly lower the drug detection limit and may also impact on our understanding of antibiotic drug action in bacteria.

physics.bio-ph↗

arXiv2008

Macroscopic signature of protected spins in a dense frustrated magnet

The inability of systems of interacting objects to satisfy all constraints simultaneously leads to frustration. A particularly important consequence of frustration is the ability to access certain protected parts of a system without disturbing the others. For magnets such "protectorates" have been inferred from theory and from neutron scattering, but their practical consequences have been unclear. We show that a magnetic analogue of optical hole-burning can address these protected spin clusters in a well-known, geometrically frustrated Heisenberg system, gadolinium gallium garnet. Our measurements additionally provide a resolution of a famous discrepancy between the bulk magnetometry and neutron diffraction results for this magnetic compound.

cond-mat.mtrl-sci↗

arXiv2008

Doping a semiconductor to create an unconventional metal

Landau Fermi liquid theory, with its pivotal assertion that electrons in metals can be simply understood as independent particles with effective masses replacing the free electron mass, has been astonishingly successful. This is true despite the Coulomb interactions an electron experiences from the host crystal lattice, its defects, and the other ~1022/cm3 electrons. An important extension to the theory accounts for the behaviour of doped semiconductors1,2. Because little in the vast literature on materials contradicts Fermi liquid theory and its extensions, exceptions have attracted great attention, and they include the high temperature superconductors3, silicon-based field effect transistors which host two-dimensional metals4, and certain rare earth compounds at the threshold of magnetism5-8. The origin of the non-Fermi liquid behaviour in all of these systems remains controversial. Here we report that an entirely different and exceedingly simple class of materials - doped small gap semiconductors near a metal-insulator transition - can also display a non-Fermi liquid state. Remarkably, a modest magnetic field functions as a switch which restores the ordinary disordered Fermi liquid. Our data suggest that we have finally found a physical realization of the only mathematically rigourous route to a non-Fermi liquid, namely the 'undercompensated Kondo effect', where there are too few mobile electrons to compensate for the spins of unpaired electrons localized on impurity atoms9-12.

cond-mat.str-el↗

arXiv2008

Molecular Thin Films: a New Type of Magnetic Switch

The design and fabrication of materials that exhibit both semiconducting and magnetic properties for spintronics and quantum computing has proven difficult. Important starting points are high-purity thin films as well as fundamental theoretical understanding of the magnetism. Here we show that small molecules have great potential in this area, due to ease of insertion of localised spins in organic frameworks and both chemical and structural purity. In particular, we demonstrate that archetypal molecular semiconductors, namely the metal phthalocyanines (Pc), can be readily fabricated as thin film quantum antiferromagnets, important precursors to a solid state quantum computer. Their magnetic state can be switched via fabrication steps which modify the film structure, offering practical routes into information processing. Theoretical calculations show that a new mechanism, which is the molecular analogue of the interactions between magnetic ions in metals, is responsible for the magnetic states. Our combination of theory and experiments opens the field of organic thin film magnetic engineering.

cond-mat.mtrl-sci↗

arXiv2008

Mesoscopic Phase Coherence in a Quantum Spin Fluid

Mesoscopic quantum phase coherence is important because it improves the prospects for handling quantum degrees of freedom in technology. Here we show that the development of such coherence can be monitored using magnetic neutron scattering from a one-dimensional spin chain Y2BaNiO5, a quantum spin fluid where no classical, static magnetic order is present. In the cleanest samples, the quantum coherence length is 20 nm, almost an order of magnitude larger than the classical antiferromagnetic correlation length of 3 nm. We also demonstrate that the coherence length can be modified by static and thermally activated defects in a quantitatively predictable manner.

cond-mat.str-el↗

arXiv2008

Ferromagnet in a continuously tuneable random field

The Random-Field Ising Model (RFIM) has been extensively studied as a model system for understanding the effects of disorder in magnets. Since the late 1970s, there has been a particular focus on realizations of the RFIM in site-diluted antiferromagnets. We observe random-field effects in the dilute dipole-coupled ferromagnet $\mathrm{LiHo}_x\mathrm{Y}_{1-x}\mathrm{F}_4$. In the presence of a magnetic field transverse to the Ising axis ($H_t$), the behavior of $\mathrm{LiHo}_x\mathrm{Y}_{1-x}\mathrm{F}_4$ becomes increasingly dominated by the influence of random-field terms in the effective Hamiltonian. This is seen experimentally in the shape of the ferromagentic-paramagnetic phase boundary and in changes to the critical exponents near the classical critical point. We find that above the classical critical point the magnetic susceptibility diverges as $H_t\to0$, and that the susceptibility both above and below the classical critical point can be collapsed onto a single universal curve using a modified Curie law which explicitly incorporates random-field contributions. The discovery of a ferromagnetic realization of the RFIM opens the door to investigation of the random-field problem with the wide variety of techniques available for probing ferromagnets, including the ability to examine both the statics and dynamics of the random-field problem. It also allows studying the effects of controlled amounts of randomness on the dynamics of domain pinning and the energetics of domain reversal.

cond-mat.dis-nn↗

arXiv2007

Quantum dynamics and entanglement of spins on a square lattice

Bulk magnetism in solids is fundamentally quantum mechanical in nature. Yet in many situations, including our everyday encounters with magnetic materials, quantum effects are masked, and it often suffices to think of magnetism in terms of the interaction between classical dipole moments. Whereas this intuition generally holds for ferromagnets, even as the size of the magnetic moment is reduced to that of a single electron spin (the quantum limit), it breaks down spectacularly for antiferromagnets, particularly in low dimensions. Considerable theoretical and experimental progress has been made in understanding quantum effects in one-dimensional quantum antiferromagnets, but a complete experimental description of even simple two-dimensional antiferromagnets is lacking. Here we describe a comprehensive set of neutron scattering measurements that reveal a non-spin-wave continuum and strong quantum effects, suggesting entanglement of spins at short distances in the simplest of all two-dimensional quantum antiferromagnets, the square lattice Heisenberg system.

cond-mat.str-el↗

arXiv2007

Pressure-Tuned Spin and Charge Ordering in an Itinerant Antiferromagnet

Elemental chromium orders antiferromagnetically near room temperature, but the ordering temperature can be driven to zero by applying large pressures. We combine diamond anvil cell and synchrotron x-ray diffraction techniques to measure directly the spin and charge order in the pure metal at the approach to its quantum critical point. Both spin and charge order are suppressed exponentially with pressure, well beyond the region where disorder cuts off such a simple evolution, and they maintain a harmonic scaling relationship over decades in scattering intensity. By comparing the development of the order parameter with that of the magnetic wavevector, it is possible to ascribe the destruction of antiferromagnetism to the growth in electron kinetic energy relative to the underlying magnetic exchange interaction.

cond-mat.str-el↗

arXiv2007

Quantum Projection in an Ising Spin Liquid

A transverse magnetic field is used to scan the diagonal and off-diagonal susceptibility of the uniaxial quantum magnet, $\text{LiHo}_{0.045}\text{Y}_{0.955}\text{F}_4$. Clusters of strongly-coupled spins act as the primary source for the response functions, which result from a field-induced quantum projection of the system into a classically forbidden (meaning non-Ising) regime. Calculations based on spin pairs reproduce only some features of the data and fail to predict the measured off-diagonal response, providing evidence of a multi-spin collective state.

cond-mat.other↗

arXiv2007

Direct measurement of antiferromagnetic domain fluctuations

Measurements of magnetic noise emanating from ferromagnets due to domain motion were first carried out nearly 100 years ago and have underpinned much science and technology. Antiferromagnets, which carry no net external magnetic dipole moment, yet have a periodic arrangement of the electron spins extending over macroscopic distances, should also display magnetic noise, but this must be sampled at spatial wavelengths of order several interatomic spacings, rather than the macroscopic scales characteristic of ferromagnets. Here we present the first direct measurement of the fluctuations in the nanometre-scale spin- (charge-) density wave superstructure associated with antiferromagnetism in elemental Chromium. The technique used is X-ray Photon Correlation Spectroscopy, where coherent x-ray diffraction produces a speckle pattern that serves as a "fingerprint" of a particular magnetic domain configuration. The temporal evolution of the patterns corresponds to domain walls advancing and retreating over micron distances. While the domain wall motion is thermally activated at temperatures above 100K, it is not so at lower temperatures, and indeed has a rate which saturates at a finite value - consistent with quantum fluctuations - on cooling below 40K. Our work is important because it provides an important new measurement tool for antiferromagnetic domain engineering as well as revealing a fundamental new fact about spin dynamics in the simplest antiferromagnet.

cond-mat.str-el↗

arXiv2006

Microscopic and Macroscopic Signatures of Antiferromagnetic Domain Walls

Magnetotransport measurements on small single crystals of Cr, the elemental antiferromagnet, reveal the hysteretic thermodynamics of the domain structure. The temperature dependence of the transport coefficients is directly correlated with the real-space evolution of the domain configuration as recorded by x-ray microprobe imaging, revealing the effect of antiferromagnetic domain walls on electron transport. A single antiferromagnetic domain wall interface resistance is deduced to be of order $5\times10^{-5}\mathrm{μΩ\cdot cm^{2}}$ at a temperature of 100 K.

cond-mat.mtrl-sci↗

arXiv2006

Three-dimensionality of field-induced magnetism in a high-temperature superconductor

Many physical properties of high-temperature (high-Tc) superconductors are two-dimensional phenomena derived from their square planar CuO2 building blocks. This is especially true of the magnetism from the copper ions. As mobile charge carriers enter the CuO2 layers, the antiferromagnetism of the parent insulators, where each copper spin is antiparallel to its nearest neighbours1, evolves into a fluctuating state where the spins show tendencies towards magnetic order of a longer periodicity. For certain charge carrier densities, quantum fluctuations are sufficiently suppressed to yield static long-period order2,3,4,5,6, and external magnetic fields also induce such order7,8,9,10,11,12. Here we show that in contrast to the chemically-controlled order in superconducting samples, the field-induced order in these same samples is actually three-dimensional, implying significant magnetic linkage between the CuO2 planes. The results are important because they show that there are three-dimensional magnetic couplings which survive into the superconducting state, and coexist with the crucial inter-layer couplings responsible for three-dimensional superconductivity. Both types of coupling will straighten the vortex lines, implying that we have finally established a direct link between technical superconductivity, which requires zero electrical resistance in an applied magnetic field and depends on vortex dynamics, and the underlying antiferromagnetism of the cuprates.

cond-mat.str-el↗

arXiv2005

Suppressed reflectivity due to spin-controlled localization in a magnetic semiconductor

The narrow gap semiconductor FeSi owes its strong paramagnetism to electron-correlation effects. Partial Co substitution for Fe produces a spin-polarized doped semiconductor. The spin-polarization causes suppression of the metallic reflectivity and increased scattering of charge carriers, in contrast to what happens in other magnetic semiconductors, where magnetic order reduces the scattering. The loss of metallicity continues progressively even into the fully polarized state, and entails as much as a 25% reduction in average mean-free path. We attribute the observed effect to a deepening of the potential wells presented by the randomly distributed Co atoms to the majority spin carriers. This mechanism inverts the sequence of steps for dealing with disorder and interactions from that in the classic Al'tshuler Aronov approach - where disorder amplifies the Coulomb interaction between carriers - in that here, the Coulomb interaction leads to spin polarization which in turn amplifies the disorder-induced scattering.

cond-mat.str-el↗

arXiv2005

Charge ordering, stripes and phase separation in manganese perovskite oxides: an STM/STS study

A microscopic characterisation of the phase transitions associated with colossal magnetoresistance (CMR) in manganese perovskite oxides is a very important ingredient in the quest of understanding its underlying mechanism. Scanning tunneling microscopy (STM) is most suitable to investigate some of their reported hallmarks, including charge ordering, lattice distortions, and electronic phase separation. Here we investigate Bi1-XCaXMnO3 (BCMO) with x=0.76. At this composition, BCMO develops an insulating charge-ordered phase upon cooling, whose study as a function of temperature will allow identifying atomic scale characteristics of the metal-insulator phase transition (MIT). We observe distinct atomic scale phases at temperatures above and below the MIT, with very different electronic and structural characteristics. Combining STM micrographs and current-voltage tunneling characteristics, we find that charge ordering correlates both with the local conduction state (metallic or insulating) and the local structural order. Furthermore, STM shows coexistence of these phases as expected for a first order phase transition.

cond-mat.str-el↗

arXiv2005

Polarons and confinement of electronic motion to two dimensions in a layered transition metal oxide

A very remarkable feature of the layered transition metal oxides (TMOs), whose most famous members are the high-temperature superconductors (HTSs), is that even though they are prepared as bulk three-dimensional single crystals, they display hugely anisotropic electrical and optical properties, seeming to be insulating perpendicular to the layers and metallic within them. This is the phenomenon of confinement, a concept at odds with the conventional theory of solids and recognized as due to magnetic and electron-lattice interactions in the layers which must be overcome at a substantial energy cost if electrons are to be transferred between layers. The associated energy gap or 'pseudogap' is particularly obvious in experiments where charge is moved perpendicular to the planes, most notably scanning tunneling microscopy (STM) and polarized infrared spectroscopy. Here, using the same experimental tools, we show that there is a second family of TMOs - the layered manganites La2-2xSr1+2xMn2O7 (LSMO) - with even more extreme confinement and pseudogap effects. The data, which are the first to resolve atoms in any metallic manganite, demonstrate quantitatively that because they are attached to polarons - lattice and spin textures within the planes -, it is equally difficult to remove carriers from the planes via vacuum tunneling into a conventional metallic tip, as it is for them to move between Mn-rich layers within the material itself.

cond-mat.str-el↗

arXiv2005

Quantum Phase Transition of a Magnet in a Spin Bath

The excitation spectrum of a model magnetic system, LiHoF$_4$, has been studied using neutron spectroscopy as the system is tuned to its quantum critical point by an applied magnetic field. The electronic mode softening expected for a quantum phase transition is forestalled by hyperfine coupling to the nuclear spins. We show that interactions with the nuclear spin bath control the length scale over which the excitations can be entangled. This generic result limits how far it is possible to approach intrinsic electronic quantum criticality.

cond-mat.other↗

arXiv2004

Ferromagnetism makes a doped semiconductor less shiny

Magnetic semiconductors have attracted interest because of the question of how a magnetic metal can be derived from a paramagnetic insulator. Here our approach is to carrier dope insulating FeSi and we show that the magnetic half-metal which emerges has unprecedented optical properties, unlike those of other low carrier density magnetic metals. All traces of the semiconducting gap of FeSi are obliterated and the material is unique in being less reflective in the ferromagnetic than in the paramagnetic state, corresponding to larger rather than smaller electron scattering in the ordered phase.

cond-mat.str-el↗

arXiv2004

Universal Dispersive Excitations in the High-Temperature Superconductors

High-resolution neutron scattering experiments on optimally doped La$_{2-x}$Sr$_x$CuO$_4$ have been performed which reveal that the magnetic excitations are dispersive. The dispersion is found to be the same as in the YBa$_2$Cu$_3$O$_{6+x}$ family, and is quantitatively related to that observed with charge sensitive probes. The excitations are also found to broaden rapidly with increasing energy, forming a continuum at higher energy, and bear a remarkable resemblance to multi-particle excitations observed in low-dimensional antiferromagnets and some magnetic metals. The magnetic correlations are two dimensional, and so rule out the simplest scenarios where the copper oxide planes are subdivided into weakly interacting one-dimensional magnets.

cond-mat.supr-con↗