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Achieving low thermal conductivity and good electrical properties is a crucial condition for thermal energy harvesting materials. Nanostructuring offers a very powerful tool to address both requirements: in nanostructured materials, boundaries preferentially scatter phonons compared to electrons. The search for low-thermal-conductivity nanostructures is typically limited to materials with simple crystal structures, such as silicon, because of the complexity arising from modeling branch- and wave vector- dependent nanoscale heat transport. Using the phonon mean-free-path (MFP) dependent Boltzmann transport equation, a model that overcomes this limitation, we compute thermal transport in 75 nanoporous half-Heusler compounds for different pore sizes. We demonstrate that the optimization of thermal transport in nanostructures should take into account both bulk thermal properties and geometry-dependent phonon suppression, two aspects that are typically engineered separately. In fact, our work predicts that, given a set of bulk materials and a system geometry, the ordering of the thermal conductivity of the nanostructure does not necessarily align with that of the bulk: We show that what dictates thermal transport is the interplay between the bulk MFP distribution and the nanostructuring length scale of the material. Finally, we derive a thermal transport model that enables fast systems screening within large bulk material repositories and a given geometry. Our study motivates the need for a holistic approach to engineering thermal transport and provides a method for high-throughput materials discovery.

Nanostructured materials exhibit low thermal conductivity because of the additional scattering due to phonon-boundary interactions. As these interactions are highly sensitive to the mean free path (MFP) of a given phonon mode, MFP distributions in nanostructures can be dramatically distorted relative to bulk. Here we calculate the MFP distribution in periodic nanoporous Si for different temperatures, using the recently developed MFP-dependent Boltzmann Transport Equation. After analyzing the relative contribution of each phonon branch to thermal transport in nanoporous Si, we find that at room temperature optical phonons contribute 18 % to heat transport, compared to 5% in bulk Si. Interestingly, we observe a steady thermal conductivity in the nanoporous materials over a temperature range 200 K < T < 300 K, which we attribute to the ballistic transport of acoustic phonons with long intrinsic MFP. These results, which are also consistent with a recent experimental study, shed light on the origin of the reduction of thermal conductivity in nanostructured materials, and could contribute to multiscale heat transport engineering, in which the bulk material and geometry are optimized concurrently.

Catalytic conversion of CO$_2$ into useful chemicals is an attractive alternative to expensive physical carbon sequestration methods. However, this approach is challenging because current chemical conversion methods employ high temperatures or pressures, thereby increasing cost and potentially leading to net carbon positive processes. In this paper, we examine the interface properties of ZnO(11$\bar{2}$0)/PbTiO$_3$ and its surface interaction with CO$_2$, CO and O. We show that the stoichiometry of the stable interface is dependent on the substrate polarization and can be controlled by changing the growth conditions. Using a model reaction, we demonstrate that a dynamically tuned catalysis schemes could enable significantly lower-energy approaches for CO$_2$ conversion.

We present an ab initio study of the (001) interfaces between two insulating perovskites, the polar LaAlO3 and the nonpolar SrTiO3. We observe an insulating-to-metallic transition above a critical LaAlO3 thickness. We explain that the high conductivity observed at the TiO2 /LaO interface and the lack of similar conductivity at the SrO/AlO2 interface are inherent in the atomic geometry of the system. A large interfacial hopping matrix element between cations causes the formation of a bound electron state at the TiO2 /LaO interface. This mechanism for the formation of interfacial bound states suggests a robust means for tuning conductivities at various oxide heterointerfaces., Comment: 4 pages, 3 figures and 1 table

We examine the application of short-circuit electrical boundary conditions in density functional theory calculations of ferroelectric thin films. Modeling PbTiO$_3$ films with Pt electrodes, we demonstrate that under periodic boundary conditions of supercells, short-circuit conditions for the electrodes are equivalently satisfied in two repeated slab geometries: a PbTiO$_3$/metal superlattice geometry and a periodic metal/PbTiO$_3$/metal/vacuum geometry, where the metal is Pt or SrRuO$_3$. We discuss the benefits of each geometry in the study of ferroelectricity in thin films., 5 pages, 3 figures, 2 tables

Using ab initio methods, we examine the the charge distribution at the interface of alpha-alumina-supported Pt films, and we consider the influence of this interface on CO adsorption. We demonstrate that a combination of electrostatic charge transfer and covalent bonding governs the interfacial interactions, and that these interactions play an important role in the metal reactivity. By modifying the interface and varying the Pt film thickness over a nanoscale range, CO adsorption can be significantly enhanced or diminished. These observations could be used to tune the reactivity of Pt particles.

Boundary-engineering in nanostructures has the potential to dramatically impact the development of materials for high- efficiency conversion of thermal energy directly into electricity. In particular, nanostructuring of semiconductors can lead to strong suppression of heat transport with little degradation of electrical conductivity. Although this combination of material properties is promising for thermoelectric materials, it remains largely unexplored. In this work, we introduce a novel concept, the directional phonon suppression function, to unravel boundary-dominated heat transport in unprecedented detail. Using a combination of density functional theory and the Boltzmann transport equation, we compute this quantity for nanoporous silicon materials. We first compute the thermal conductivity for the case with aligned circular pores, confirming a significant thermal transport degradation with respect to the bulk. Then, by analyzing the information on the directionality of phonon suppression in this system, we identify a new structure of rectangular pores with the same porosity that enables a four-fold decrease in thermal transport with respect to the circular pores. Our results illustrate the utility of the directional phonon suppression function, enabling new avenues for systematic thermal conductivity minimization and potentially accelerating the engineering of next-generation thermoelectric devices., United States. Dept. of Energy. Office of Basic Energy Sciences (DESC0001)

While thermal anisotropicity is a desirable materials property for many applications, including transverse thermoelectrics and thermal management in electronic devices, it remains elusive in practical natural compounds. In this work, we show how nanoporous materials with anisotropic pore lattices can be used as a platform for inducing strong heat transport directionality in isotropic materials. Using density functional theory and the phonon Boltzmann transport equation, we calculate the phonon-size effects and thermal conductivity of nanoporous silicon with different anisotropicpore lattices. Our calculations predict a strong directionality in the thermal conductivity, dictated by the difference in the pore-pore distances along the two Cartesian axes. As the space between pores along the direction of the applied temperature gradient represents the phonon bottleneck, an anisotropic pores lattice distortion induces directionality in heat transport. Using Fourier's law, we also compute diffusive heat transport for the same geometries obtaining significantly smaller anisotropicity, revealing the crucial role of phonon-size effects in tuning thermal transport directionality. Besides enhancing our understanding of nanoscale heat transport, our results demonstrate the promise of nanoporous materials for modulating anisotropy in thermal conductivity.