arXiv subjects

M. Warner

Publications and source records attributed to M. Warner.

17 recordsLinked to original sources

arXiv2024

Abatement of Ionizing Radiation for Superconducting Quantum Devices

Ionizing radiation has been shown to reduce the performance of superconducting quantum circuits. In this report, we evaluate the expected contributions of different sources of ambient radioactivity for typical superconducting qubit experiment platforms. Our assessment of radioactivity inside a typical cryostat highlights the importance of selecting appropriate materials for the experiment components nearest to qubit devices, such as packaging and electrical interconnects. We present a shallow underground facility (30-meter water equivalent) to reduce the flux of cosmic rays and a lead shielded cryostat to abate the naturally occurring radiogenic gamma-ray flux in the laboratory environment. We predict that superconducting qubit devices operated in this facility could experience a reduced rate of correlated multi-qubit errors by a factor of approximately 20 relative to the rate in a typical above-ground, unshielded facility. Finally, we outline overall design improvements that would be required to further reduce the residual ionizing radiation rate, down to the limit of current generation direct detection dark matter experiments.

quant-ph↗

arXiv2021

Metric mechanics with non-trivial topology: actuating irises, cylinders and evertors

Liquid crystal elastomers contract along their director on heating and recover on cooling, offering great potential as actuators and artificial muscles. If a flat sheet is programmed with a spatially varying director pattern, it will actuate into a curved surface, allowing the material to act as a strong machine such as a grabber or lifter. Here we study the actuation of programmed annular sheets which, owing to their central hole, can sidestep constraints on area and orientation. We systematically catalogue the set of developable surfaces encodable via axisymmetric director patterns, and uncover several qualitatively new modes of actuation, including cylinders, irises, and everted surfaces in which the inner boundary becomes the outer boundary after actuation. We confirm our designs with a combination of experiments and numerics. Many of our actuators can re-attain their initial inner or outer radius upon completing actuation, making them particularly promising, as they can avoid potentially problematic stresses in their activated state even when fixed onto a frame or pipe.

cond-mat.soft↗

arXiv2021

Shape programming lines of concentrated Gaussian curvature

Liquid crystal elastomers (LCEs) can undergo large reversible contractions along their nematic director upon heating or illumination. A spatially patterned director within a flat LCE sheet thus encodes a pattern of contraction on heating, which can morph the sheet into a curved shell, akin to how a pattern of growth sculpts a developing organism. Here we consider, theoretically, numerically and experimentally, patterns constructed from regions of radial and circular director, which, in isolation, would form cones and anticones. The resultant surfaces contain curved ridges with sharp V-shaped cross-sections, associated with the boundaries between regions in the patterns. Such ridges may be created in positively and negatively curved variants and, since they bear Gauss curvature (quantified here via the Gauss-Bonnet theorem), they cannot be flattened without energetically prohibitive stretch. Our experiments and numerics highlight that, although such ridges cannot be flattened isometrically, they can deform isometrically by trading the (singular) curvature of the V angle against the (finite) curvature of the ridge line. Furthermore, in finite thickness sheets, the sharp ridges are inevitably non-isometrically blunted to relieve bend, resulting in a modest smearing out of the encoded singular Gauss curvature. We close by discussing the use of such features as actuating linear features, such as probes, tongues and limbs, and highlighting the similarities between these patterns of shape change and those found during the morphogenesis of several biological systems.

cond-mat.soft↗

arXiv2014

Sub-nanometer resolution in three-dimensional magnetic-resonance imaging of individual dark spins

Magnetic resonance imaging (MRI) has revolutionized biomedical science by providing non-invasive, three-dimensional biological imaging. However, spatial resolution in conventional MRI systems is limited to tens of microns, which is insufficient for imaging on molecular and atomic scales. Here we demonstrate an MRI technique that provides sub-nanometer spatial resolution in three dimensions, with single electron-spin sensitivity. Our imaging method works under ambient conditions and can measure ubiquitous 'dark' spins, which constitute nearly all spin targets of interest and cannot otherwise be individually detected. In this technique, the magnetic quantum-projection noise of dark spins is measured using a single nitrogen-vacancy (NV) magnetometer located near the surface of a diamond chip. The spatial distribution of spins surrounding the NV magnetometer is imaged with a scanning magnetic-field gradient. To evaluate the performance of the NV-MRI technique, we image the three-dimensional landscape of dark electronic spins at and just below the diamond surface and achieve an unprecedented combination of resolution (0.8 nm laterally and 1.5 nm vertically) and single-spin sensitivity. Our measurements uncover previously unidentified electronic spins on the diamond surface, which can potentially be used as resources for improved magnetic imaging of samples proximal to the NV-diamond sensor. This three-dimensional NV-MRI technique is immediately applicable to diverse systems including imaging spin chains, readout of individual spin-based quantum bits, and determining the precise location of spin labels in biological systems.

cond-mat.mes-hall↗

arXiv2011

Elasticity of Polydomain Liquid Crystal Elastomers

We model polydomain liquid-crystal elastomers by extending the neo-classical soft and semi-soft free energies used successfully to describe monodomain samples. We show that there is a significant difference between polydomains cross-linked in homogeneous high symmetry states then cooled to low symmetry polydomain states and those cross-linked directly in the low symmetry polydomain state. For example, elastomers cross-linked in the isotropic state then cooled to a nematic polydomain will, in the ideal limit, be perfectly soft, and with the introduction of non-ideality, will deform at very low stress until they are macroscopically aligned. The director patterns observed in them will be disordered, characteristic of combinations of random deformations, and not disclination patterns. We expect these samples to exhibit elasticity significantly softer than monodomain samples. Polydomains cross-linked in the nematic polydomain state will be mechanically harder and contain characteristic schlieren director patterns. The models we use for polydomain elastomers are spatially heterogeneous, so rather than solving them exactly we elucidate this behavior by bounding the energies using Taylor-like (compatible test strain fields) and Sachs (constant stress) limits extended to non-linear elasticity. Good agreement is found with experiments that reveal the supersoft response of some polydomains. We also analyze smectic polydomain elastomers and propose that polydomain SmC* elastomers cross-linked in the SmA monodomain state are promising candidates for low field electrical actuation.

cond-mat.soft↗

arXiv2009

On the physical basis for the nematic rubber elastic free energy

We discuss why it is physical to keep terms in the nematic rubber elastic free energy that reflect the order parameter dependence of the natural size of the network polymers. We address a point of difficulty in some mathematical approaches to this problem.

cond-mat.soft↗

arXiv2008

Mechanical switching of ferro-electric rubber

At the A to C transition, smectic elastomers have recently been observed to undergo $\sim$35% spontaneous shear strains. We first explicitly describe how strains of up to twice this value could be mechanically or electrically induced in Sm-$C$ elastomers by rotation of the director on a cone around the layer normal at various elastic costs depending on constraints. Secondly, for typical sample geometries, we give the various microstructures in Sm-$C$ akin to those seen in nematic elastomers under distortions with constraints. It is possible to give explicit results for the nature of the textures. Chiral Sm-$C$ elastomers are ferro-electric. We calculate how the polarization could be mechanically reversed by large, hard or soft strains of the rubber, depending upon sample geometry.

cond-mat.soft↗

arXiv2008

Smectic-$A$ elastomers with weak director anchoring

Experimentally it is possible to manipulate the director in a (chiral) smectic-$A$ elastomer using an electric field. This suggests that the director is not necessarily locked to the layer normal, as described in earlier papers that extended rubber elasticity theory to smectics. Here, we consider the case that the director is weakly anchored to the layer normal assuming that there is a free energy penalty associated with relative tilt between the two. We use a recently developed weak-anchoring generalization of rubber elastic approaches to smectic elastomers and study shearing in the plane of the layers, stretching in the plane of the layers, and compression and elongation parallel to the layer normal. We calculate, inter alia, the engineering stress and the tilt angle between director and layer normal as functions of the applied deformation. For the latter three deformations, our results predict the existence of an instability towards the development of shear accompanied by smectic-$C$-like order.

cond-mat.soft↗

arXiv2008

Bleaching and stimulated recovery of dyes and of photo-cantilevers

We examine how intense optical beams can penetrate deeply into highly absorbing media by a non-linear, photo-bleaching process. The role of stimulated recovery to the dye ground state can be important and is delineated. This analysis of non-linear absorption processes is applicable in general to situations where chromophores are irradiated, for instance in biology. We examine the implications for the bending of cantilevers made of heavily dye-loaded nematic photo-solids, that is nematic glasses and elastomers that have large mechanical reactions to light. In particular we describe the bending of cantilevers sufficiently absorbing that they would not bend if Beer's Law were applicable. We quantify the role of optically-generated heat in determining the mechanical response and conclude that in general it is minor in importance compared with optical effects.

cond-mat.soft↗

arXiv2008

The dynamics of non-linear optical absorption

On traversing materials with absorbing dyes, weak optical beams develop a Beer (exponential) profile, while intense beams develop a spatially initially linear and then finally an exponential profile. This anomalous, deep penetration due to photo-bleaching of surface layers is important for heavy dye-loading and intense beams, for instance in photo-actuation. We address the problem of the evolution in time from initial Beer's Law to deeply penetrating optical profiles in dyes. Our solution of the coupled, non-linear, partial differential equations governing the spatio-temporal decay of the Poynting flux and the non-linear dynamics of the \textit{trans-cis} conversion is applicable to general systems of photo-active molecules under intense irradiation, for instance in biology, in spectroscopy and in opto-mechanical devices.

cond-mat.soft↗

arXiv2003

Reflectivity of cholesteric liquid crystals with spatially varying pitch

Solids with spatially varying photonic structure offer gaps to light of a wider range of frequencies than do simple photonic systems. We solve numerically the field distribution in a solid cholesteric with a linearly varying inverse pitch (helical wavevector) using equations we derive for the general case. The simple idea that the position where the Bragg condition is locally satisfied is where reflection takes place is only true in part. Here, reflection is due to a region where the waves are forced to become evanescent, and the rate of variation of structure determines over which distance the waves decay and therefore how complete reflection is. The approximate local Bragg-de Vries schemes are shown to break down in detail at the edges of the gap, and an analytical estimate is given for the transmission coefficient.

cond-mat.soft↗

arXiv2002

Uniaxial and biaxial soft deformations of nematic elastomers

We give a geometric interpretation of the soft elastic deformation modes of nematic elastomers, with explicit examples, for both uniaxial and biaxial nematic order. We show the importance of body rotations in this non-classical elasticity and how the invariance under rotations of the reference and target states gives soft elasticity (the Golubovic and Lubensky theorem). The role of rotations makes the Polar Decomposition Theorem vital for decomposing general deformations into body rotations and symmetric strains. The role of the square roots of tensors is discussed in this context and that of finding explicit forms for soft deformations (the approach of Olmsted).

cond-mat.soft↗

arXiv2001

Imprinted Networks as Chiral Pumps

We investigate the interaction between a chirally imprinted network and a solvent of chiral molecules. We find, a liquid crystalline polymer network is preferentially swollen by one component of a racemic solvent. This ability to separate is linked to the chiral order parameter of the network, and can be reversibly controlled via temperature or a mechanical deformation. It is maximal near the point at which the network loses its imprinted structure. One possible practical application of this effect would be a mechanical device for sorting mixed chiral molecules.

cond-mat.soft↗

arXiv2001

Linear hydrodynamics and viscoelasticity of nematic elastomers

We develop a continuum theory of linear viscoelastic response in oriented monodomain nematic elastomers. The expression for dissipation function is analogous to the Leslie-Ericksen version of anisotropic nematic viscosity; we propose the relations between the anisotropic rubber moduli and new viscous coefficients. A new dimensionless number is introduced, which describes the relative magnitude of viscous and rubber-elastic torques. In an elastic medium with an independently mobile internal degree of freedom, the nematic director with its own relaxation dynamics, the model shows a dramatic decrease in the dynamic modulus in certain deformation geometries. The degree to which the storage modulus does not altogether drop to zero is shown to be both dependent on frequency and to be proportional to the semi-softness, the non-ideality of a nematic network. We consider the most interesting geometry for the implementation of the theory, calculating the dynamic response to an imposed simple shear and making predictions for effective moduli and (exceptionally high) loss factors.

cond-mat.soft↗

arXiv2000

Untwisting of a cholesteric elastomer by a mechanical field

A mechanical strain field applied to a monodomain cholesteric elastomer will unwind the helical director distribution. There is an analogy with the classical problem of an electric field applied to a cholesteric liquid crystal, but with important differences. Frank elasticity is of minor importance unless the gel is very weak. The interplay is between director anchoring to the rubber elastic matrix and the external mechanical field. Stretching perpendicular to the helix axis induces the uniform unwound state via the elimination of sharp, pinned twist walls above a critical strain. Unwinding through conical director states occurs when the elastomer is stretched along the helical axis.

cond-mat.soft↗

arXiv1998

Electro-Mechanical Fredericks Effects in Nematic Gels

The solid nematic equivalent of the Fredericks transition is found to depend on a critical field rather than a critical voltage as in the classical case. This arises because director anchoring is principally to the solid rubbery matrix of the nematic gel rather than to the sample surfaces. Moreover, above the threshold field, we find a competition between quartic (soft) and conventional harmonic elasticity which dictates the director response. By including a small degree of initial director misorientation, the calculated field variation of optical anisotropy agrees well with the conoscopy measurements of Chang et al (Phys.Rev.E56, 595, 1997) of the electro-optical response of nematic gels.

cond-mat.soft↗

arXiv1995

Non-uniform deformations in liquid crystalline elastomers

We develop a molecular model of non-uniform deformations within the framework of liquid crystal rubber elasticity. We show that, similarly to the uniform case, the theory is not sensitive to the molecular details of polymer liquid crystal involved and the resulting elastic free energy is quite universal. The result of this work is the general expression for the free energy of deformations, which combines the effects of large non-symmetric affine strains in the rubbery network and gradients of curvature deformations of the director field, $F = λ^T (\nabla {n})^2 λ$. We derive the molecular expressions for the elastic constants governing non uniform deformations in the presence of elastic strains. They also depend on the polymer step length anisotropy and - most strikingly - have an overall {negative} sense. We therefore predict that in some circumstances, especially at large elastic deformations $λ$, these new terms may overpower the usual, positive Frank elastic moduli of the underlying nematic structure, as well as the coupling in nematic elastomers of uniform relative rotations of the director and the elastic matrix. In this event highly distorted polydomain textures n(r) would be favoured.

cond-mat↗