Abstract

We develop a model of latch-mediated spring actuated (LaMSA) systems relevant to comparative biomechanics and bioinspired design. The model contains five components: two motors (muscles), a spring, a latch, and a load mass. One motor loads the spring to store elastic energy and the second motor subsequently removes the latch, which releases the spring and causes movement of the load mass. We develop freely available software to accompany the model, which provides an extensible framework for simulating LaMSA systems. Output from the simulation includes information from the loading and release phases of motion, which can be used to calculate kinematic performance metrics that are important for biomechanical function. In parallel, we simulate a comparable, directly actuated system that uses the same motor and mass combinations as the LaMSA simulations. By rapidly iterating through biologically relevant input parameters to the model, simulated kinematic performance differences between LaMSA and directly actuated systems can be used to explore the evolutionary dynamics of biological LaMSA systems and uncover design principles for bioinspired LaMSA systems. As proof of principle of this concept, we compare a LaMSA simulation to a directly actuated simulation that includes either a Hill-type force-velocity trade-off or muscle activation dynamics, or both. For the biologically-relevant range of parameters explored, we find that the muscle force-velocity trade-off and muscle activation have similar effects on directly actuated performance. Including both of these dynamic muscle properties increases the accelerated mass range where a LaMSA system outperforms a directly actuated one.

Abstract

We compare the low-strain mechanical properties of bottlebrush elastomers (BBEs) synthesized using ring-opening metathesis and free radical polymerization. Through comparison of experimentally measured elastic moduli and those predicted by an ideal, affine model, we evaluate the efficiency of our networks in forming stress-supporting strands. This comparison allowed us to develop a structural efficiency ratio that facilitates the prediction of mechanical properties relative to polymerization chemistry (e.g., softer BBEs when polymerizing under dilute conditions). This work highlights the impact that polymerization chemistry has on the structural efficiency ratio and the resultant mechanical properties of BBEs with identical side chains, providing another “knob” by which to control polymer network properties.

Abstract

The mechanical properties of glassy polymer thin films change as film thickness decreases below the average polymer molecule size. These changes have been associated with a reduction in interchain entanglements due to confinement and an increase in molecular mobility from the mobile surface layer. Here, using experiments and simulations, we determine how entanglements and surface mobility each individually impact the failure behavior of a glassy polymer film as the film becomes confined. We utilize a custom-built uniaxial tensile tester for ultrathin films and dark-field optical microscopy to characterize the complete stress−strain response and the associated strain localizations for ultrathin polystyrene films of varying thicknesses (h = 10 to 150 nm) for a range of molecular weights Mn of 61 to 2135 kDa. To directly correlate the changes in the molecular network to changes in the failure properties of ultrathin films, we perform nonequilibrium molecular dynamics simulations on N = 250, N = 60, with h = 10 to 30 films. From our results, accounting for both the changes in entanglements and mobility, we propose a semiempirical model that captures the failure response in both simulated and experimental glassy polymer thin films.

Abstract

One of the most versatile sources for entangled photons are emitters that interact via more than one tunable mechanism. Here, we demonstrate how hybridization and dipole-dipole interactions---potentially simultaneously available in colloidal quantum dots and molecular aggregates---leveraged in conjunction can couple simple, well understood emitters into composite emitters with flexible control over the level structure. We show that cascade decay through carefully designed level structures can result in emission of frequency-entangled photons with Bell states and three-photon GHZ states as example cases. These results pave the way toward rational design of quantum optical emitters of entangled photons.

Abstract

Hot spotting in photovoltaic (PV) panels causes physical damage, power loss, reduced lifetime reliability, and increased manufacturing costs. The problem arises routinely in defect-free standard panels; any string of cells that receives uneven illumination can develop hot spots, and the temperature rise often exceeds 100°C in conventional monocrystalline-silicon panels despite on-panel bypass diodes, the standard mitigation technique. Bypass diodes limit the power dissipated in a cell subjected to reverse bias, but they do not prevent hot spots from forming. An alternative control method has been suggested by Kernahan that senses in real time the dynamic conductance \(|\mathrm{d}I/\mathrm{d}V|\) of a string of cells and adjusts its operating current so that a partially shaded cell is never forced into reverse bias. We start by exploring the behavior of individual illuminated PV cells when externally forced into reverse bias. We observe that cells can suffer significant heating and structural damage, with desoldering of cell-tabbing and discolorations on the front cell surface. Then we test PV panels and confirm Kernahan's proposed panel-level solution that anticipates and prevents hot spots in real time. Simulations of cells and panels confirm our experimental observations and provide insights into both the operation of Kernahan's method and panel performance.

Abstract

The snap of a finger has been used as a form of communication and music for millennia across human cultures. However, a systematic analysis of the dynamics of this rapid motion has not yet been performed. Using high-speed imaging and force sensors, we analyse the dynamics of the finger snap. We discover that the finger snap achieves peak angular accelerations of \( 1.6 \times 10^{6\;\circ} \mathrm{s}^{-2} \) in 7 ms, making it one of the fastest recorded angular accelerations the human body produces (exceeding professional baseball pitches). Our analysis reveals the central role of skin friction in mediating the snap dynamics by acting as a latch to control the resulting high velocities and accelerations. We evaluate the role of this frictional latch experimentally, by covering the thumb and middle finger with different materials to produce different friction coefficients and varying compressibility. In doing so, we reveal that the compressible, frictional latch of the finger pads likely operates in a regime optimally tuned for both friction and compression. We also develop a soft, compressible friction-based latch-mediated spring actuated model to further elucidate the key role of friction and how it interacts with a compressible latch. Our mathematical model reveals that friction plays a dual role in the finger snap, both aiding in force loading and energy storage while hindering energy release. Our work reveals how friction between surfaces can be harnessed as a tunable latch system and provides design insight towards the frictional complexity in many robotic and ultrafast energy-release structures.

Abstract

In established theories of grain coarsening, grains disappear either by shrinking or by rotating as a rigid object to coalesce with an adjacent grain. Here we report a third mechanism for grain coarsening, in which a grain splits apart into two regions that rotate in opposite directions to match two adjacent grains’ orientations. We experimentally observe both conventional grain rotation and grain splitting in two-dimensional colloidal polycrystals. We find that grain splitting occurs via independently rotating “granules” whose shapes are determined by the underlying triangular lattices of the two merging crystal grains. These granules are so small that existing continuum theories of grain boundary energy are inapplicable, so we introduce a hard sphere model for the free energy of a colloidal polycrystal. We find that, during splitting, the system overcomes a free energy barrier before ultimately reaching a lower free energy when splitting is complete. Using simulated splitting events and a simple scaling prediction, we find that the barrier to grain splitting decreases as grain size decreases. Consequently, grain splitting is likely to play an important role in polycrystals with small grains. This discovery suggests that mesoscale models of grain coarsening may offer better predictions in the nanocrystalline regime by including grain splitting.

Abstract

We propose a program at B-factories of inclusive, multi-track displaced vertex searches, which are expected to be low background and give excellent sensitivity to non-minimal hidden sectors. Multi-particle hidden sectors often include long-lived particles (LLPs) which result from approximate symmetries, and we classify the possible decays of GeV-scale LLPs in an effective field theory framework. Considering several LLP production modes, including dark photons and dark Higgs bosons, we study the sensitivity of LLP searches with different number of displaced vertices per event and track requirements per displaced vertex, showing that inclusive searches can have sensitivity to a large range of hidden sector models that are otherwise unconstrained by current or planned searches.

From the Cover…

In this modern and distinctive textbook, Helliwell and Sahakian present classical mechanics as a thriving and contemporary field with strong connections to cutting-edge research topics in physics. Each part of the book concludes with a capstone chapter describing various key topics in quantum mechanics, general relativity, and other areas of modern physics, clearly demonstrating how they relate to advanced classical mechanics, and enabling students to appreciate the central importance of classical mechanics within contemporary fields of research. Numerous and detailed examples are interleaved with theoretical content, illustrating abstract concepts more concretely. Extensive problem sets at the end of each chapter further reinforce students' understanding of key concepts, and provide opportunities for assessment or self-testing. A detailed online solutions manual and lecture slides accompany the text for instructors. Often a flexible approach is required when teaching advanced classical mechanics, and, to facilitate this, the authors have outlined several paths instructors and students can follow through the book, depending on background knowledge and the length of their course.

Abstract

Biological membranes are composed of lipid bilayers that are often asymmetric with regards to the lipid composition and/or aqueous solvent they separate. Studying lipid asymmetry both experimentally and computationally is challenging. Molecular dynamics simulations of lipid bilayers with asymmetry are difficult due to finite system sizes and time scales accessible to simulations. Due to the very slow flip-flop rate for phospholipids, one must first choose how many lipids are on each side of the bilayer, but the resulting bilayer may be unstable (or metastable) due to differing tensile and compressive forces between leaflets. Here we use molecular dynamics simulations to investigate a number of different asymmetric membrane systems, both with atomistic and coarse-grained models. Asymmetries studied include differences in number of lipids, lipid composition (unsaturated and saturated tails and different headgroups), and chemical gradients between the aqueous phases. Extensive analysis of the bilayers’ properties such as area per lipid, density, and lateral pressure profiles are used to characterize bilayer asymmetry. We also address how cholesterol (which flip-flops relatively quickly) influences membrane asymmetries. Our results show how each leaflet is influenced by the other and can mitigate the structural changes to the bilayer overall structure. Cholesterol can respond to changes in bilayer asymmetry to alleviate some of the effect on the bilayer structure, but that will alter its leaflet distribution, which in turn affects its chemical potential. Ionic imbalances are shown to have a modest change in bilayer structure, despite large changes in the electrostatic potential. Bilayer asymmetry can also induce a modest electrostatic potential across the membrane. Our results highlight the importance of membrane asymmetry on bilayer properties, the influence of lipid headgroups, tails and cholesterol on asymmetry, and the ability of lipids to adapt to different environments.