Herein we develop an approach for optically controlling receptor tension. This is achieved using optomechanical actuator nanoparticles that are controlled with non-invasive near-infrared light. Illumination leads to particle collapse, delivering piconewton forces to specific cell surface receptors with high spatial and temporal resolution. As a proof-of-concept, we applied optomechanical actuation to trigger integrin-based focal adhesion formation, cell protrusion and migration, as well as T cell receptor activation.

A connection between continuum and atomic description of interface thermal conductanceThe majority of intuition on phonon transport has been derived from studies of homogenous crystalline solids, where the atomic composition and structure are periodic. For this specific class of materials, the solutions to the equations of motions for the atoms (in the harmonic limit) result in plane wave modulated velocity fields for the normal modes of vibration. However, it has been known for several decades that whenever a system lacks periodicity, either compositional or structural, the normal modes of vibration can still be determined (in the harmonic limit), but the solutions take on different characteristics and many modes may not be plane wave modulated. Previous work has classified the types of vibrations into three primary categories, namely, propagons, diffusions, and locons. One can use the participation ratio to distinguish locons, from propagons and diffusons, which measures the extent to which a mode is localized. However, distinguishing between propagons and diffusons has remained a challenge, since both are spatially delocalized. Here, we present a new method that quantifies the extent to which a mode's character corresponds to a propagating mode, e.g., exhibits plane wave modulation. This then allows for clear and quantitative distinctions between propagons and diffusons. By resolving this issue quantitatively, one can now automate the classification of modes for any arbitrary material or structure, subject to a single constraint that the atoms must vibrate stably around their respective equilibrium sites. Several example test cases are studied including crystalline silicon and germanium, crystalline silicon with different defect concentrations, as well as amorphous silicon, germanium, and silica. Published by AIP Publishing.

As the cost of renewable energy falls below fossil fuels, the most important challenge to enable widespread sustainable power generation has become making renewables dispatchable. Low cost energy storage can provide this dispatchability, but there is no clear technology that can meet the need. Pumped hydroelectric and compressed air storage have low costs, but they are geographically constrained. Similarly, lithium-ion batteries are becoming ubiquitous, but even their lower bounding asymptote cost is too high to enable cost-competitive dispatchable renewables. Here, we introduce a concept based on thermal energy grid storage (TEGS) using a multijunction photovoltaic heat engine (MPV) with promising initial experimental results that could meet the low cost required to enable cost competitive dispatchable renewables. The approach exploits an important tradeoff between the accession of an extremely low cost per unit energy stored, by storing heat instead of electricity directly, while paying the penalty of a lower round trip efficiency. To understand why this tradeoff is advantageous, we first introduce a framework for evaluating storage technologies that treats round trip efficiency (RTE) as a variable, in addition to cost per unit energy stored (CPE) and cost per unit power (CPP). It is from this perspective that the TEGS-MPV concept offers a compelling economic proposition.

Current understanding of phonons treats them as plane waves/quasi-particles of atomic vibration that propagate and scatter. The problem is that conceptually, when any level of disorder is introduced, whether compositional or structural, the character of vibrational modes in solids changes, yet nearly all theoretical treatments continue to assume phonons are still waves. For example, the phonon contributions to alloy thermal conductivity (TC) rely on this assumption and are most often computed from the virtual crystal approximation (VCA). Good agreement is obtained in some cases, but there are many instances where it fails-both quantitatively and qualitatively. Here, we show that the conventional theory and understanding of phonons requires revision, because the critical assumption that all phonons/normal modes resemble plane waves with well-defined velocities is no longer valid when disorder is introduced. Here we show, surprisingly, that the character of phonons changes dramatically within the first few percent of impurity concentration, beyond which phonons more closely resemble the modes found in amorphous materials. We then utilize a different theory that can treat modes with any character and experimentally confirm its new insights.

A high temperature thermophotovoltaic (TPV) system is modeled and its system level performance is assessed in the context of concentrated solar power (CSP) with thermal energy storage (TES). The model includes treatment of the emitter and the heat transfer fluid that draws thermal energy from the TES, which then allows for identification and prioritization of the most important TPV cell/module level properties that should be optimized to achieve maximum performance. The upper limiting efficiency for an idealized system is then calculated, which shows that TPV with TES may one day have the potential to become competitive with combined cycle turbines, but could also offer other advantages that would give CSP an advantage over fossil based alternatives. The system concept is enabled by the usage of liquid metal as a high temperature heat transfer and TES fluid. The system concept combines the great economic advantages of TES with the potential for low cost and high performance derived from TPV cells fabricated on reusable substrates, with a high reflectivity back reflector for photon recycling.

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