Effect of Octahedral Connectivity on the Negative Thermal Expansion of SrZrS3.

Sulfide perovskites (ABX3) are under increasing investigation for use in photovoltaic, optoelectronic, dielectric, and thermoelectric devices due to their favorable band gaps, dynamical properties, environmental stability, and structural diversity. A key material parameter to optimize in such devices is the constituent materials' coefficient of thermal expansion (CTE) in order to minimize thermomechanical stress during fabrication and operation. This can be done by avoiding materials that have large CTE mismatch or by compensating positive thermal expansion by including materials with negative thermal expansion (NTE). Here, we evaluate the CTE of (edge-connected) α- and (corner-connected) ß-SrZrS3 with density functional theory and the self-consistent quasiharmonic approximation. We find that both materials exhibit positive thermal expansion at 0 GPa and host pressure-induced negative thermal expansion. The ß phase has a smaller CTE (37 × 10-6 K-1) at room temperature and ambient pressure and also has a larger NTE response under pressure due to its more flexible corner-connected framework structure. We use our findings to suggest that corner-shared motifs should be prioritized over edge- or face-shared octahedral networks to maximize NTE arising from vibrational (phononic) mechanisms.

Computationally Directed Discovery of MoBi2.

Incorporating bismuth, the heaviest element stable to radioactive decay, into new materials enables the creation of emergent properties such as permanent magnetism, superconductivity, and nontrivial topology. Understanding the factors that drive Bi reactivity is critical for the realization of these properties. Using pressure as a tunable synthetic vector, we can access unexplored regions of phase space to foster reactivity between elements that do not react under ambient conditions. Furthermore, combining computational and experimental methods for materials discovery at high-pressures provides broader insight into the thermodynamic landscape than can be achieved through experiment alone, informing our understanding of the dominant chemical factors governing structure formation. Herein, we report our combined computational and experimental exploration of the Mo-Bi system, for which no binary intermetallic structures were previously known. Using the ab initio random structure searching (AIRSS) approach, we identified multiple synthetic targets between 0-50 GPa. High-pressure in situ powder X-ray diffraction experiments performed in diamond anvil cells confirmed that Mo-Bi mixtures exhibit rich chemistry upon the application of pressure, including experimental realization of the computationally predicted CuAl2-type MoBi2 structure at 35.8(5) GPa. Electronic structure and phonon dispersion calculations on MoBi2 revealed a correlation between valence electron count and bonding in high-pressure transition metal-Bi structures as well as identified two dynamically stable ambient pressure polymorphs. Our study demonstrates the power of the combined computational-experimental approach in capturing high-pressure reactivity for efficient materials discovery.

Pb2 BO3 I: A Borate Iodide with the Largest Second-Harmonic Generation (SHG) Response in the KBe2 BO3 F2 (KBBF) Family of Nonlinear Optical (NLO) Materials.

Borate halides are an ideal materials class from which to design high-performance nonlinear optical (NLO) materials. Currently, borate fluorides, chlorides, and bromides are extensively investigated while borate iodide materials discovery remains rare because of the perceived synthetic challenges. We report a new borate iodide, Pb2 BO3 I, synthesized by a straightforward hydrothermal method. The Pb2 BO3 I chemical formula conceals that the compound exhibits a structure similar to the well-established KBe2 BO3 F2 (KBBF), which we show supports the highest second-harmonic generation (SHG) at 1064 nm in the KBBF family, 10 × KH2 PO4 (KDP), arising from the inclusion of Pb2+ and I- and the crystal chemistry. Our work shows that KBBF-related compounds can be synthesized incorporating iodide and exhibit superior NLO responses.

Beryllium-Free ß-Rb2 Al2 B2 O7 as a Possible Deep-Ultraviolet Nonlinear Optical Material Replacement for KBe2 BO3 F2.

A new beryllium-free deep-ultraviolet (DUV) nonlinear optical (NLO) material, ß-Rb2 Al2 B2 O7 (ß-RABO), has been synthesized and characterized. The chiral nonpolar acentric material shows second-harmonic generation (SHG) activity at both 1064 and 532 nm with efficiencies of 2×KH2 PO4 and 0.4×ß-BaB2 O4 , respectively, and exhibits a short absorption edge below 200 nm. ß-Rb2 Al2 B2 O7 has a three-dimensional structure of corner-shared Al(BO3 )3 O polyhedra. The discovery of ß-RABO shows that through careful synthesis and characterization, replacement of KBe2 BO3 F2 (KBBF) by a Be-free DUV NLO material is possible.

Interlayer magnetophononic coupling in MnBi2Te4.

The emergence of magnetism in quantum materials creates a platform to realize spin-based applications in spintronics, magnetic memory, and quantum information science. A key to unlocking new functionalities in these materials is the discovery of tunable coupling between spins and other microscopic degrees of freedom. We present evidence for interlayer magnetophononic coupling in the layered magnetic topological insulator MnBi2Te4. Employing magneto-Raman spectroscopy, we observe anomalies in phonon scattering intensities across magnetic field-driven phase transitions, despite the absence of discernible static structural changes. This behavior is a consequence of a magnetophononic wave-mixing process that allows for the excitation of zone-boundary phonons that are otherwise 'forbidden' by momentum conservation. Our microscopic model based on density functional theory calculations reveals that this phenomenon can be attributed to phonons modulating the interlayer exchange coupling. Moreover, signatures of magnetophononic coupling are also observed in the time domain through the ultrafast excitation and detection of coherent phonons across magnetic transitions. In light of the intimate connection between magnetism and topology in MnBi2Te4, the magnetophononic coupling represents an important step towards coherent on-demand manipulation of magnetic topological phases.

Large Exchange Coupling Between Localized Spins and Topological Bands in MnBi2 Te4.

Magnetism in topological materials creates phases exhibiting quantized transport phenomena with potential technological applications. The emergence of such phases relies on strong interaction between localized spins and the topological bands, and the consequent formation of an exchange gap. However, this remains experimentally unquantified in intrinsic magnetic topological materials. Here, this interaction is quantified in MnBi2 Te4 , a topological insulator with intrinsic antiferromagnetism. This is achieved by optically exciting Bi-Te p states comprising the bulk topological bands and interrogating the consequent Mn 3d spin dynamics, using a multimodal ultrafast approach. Ultrafast electron scattering and magneto-optic measurements show that the p states demagnetize via electron-phonon scattering at picosecond timescales. Despite being energetically decoupled from the optical excitation, the Mn 3d spins, probed by resonant X-ray scattering, are observed to disorder concurrently with the p spins. Together with atomistic simulations, this reveals that the exchange coupling between localized spins and the topological bands is at least 100 times larger than the superexchange interaction, implying an optimal exchange gap of at least 25 meV in the surface states. By quantifying this exchange coupling, this study validates the materials-by-design strategy of utilizing localized magnetic order to manipulate topological phases, spanning static to ultrafast timescales.

Polarization Dependence of Water Adsorption to CH3NH3PbI3 (001) Surfaces.

The instability of organometal halide perovskites when in contact with water is a serious challenge to their feasibility as solar cell materials. Although studies of moisture exposure have been conducted, an atomistic understanding of the degradation mechanism is required. Toward this goal, we study the interaction of water with the (001) surfaces of CH3NH3PbI3 under low and high water concentrations using density functional theory. We find that water adsorption is heavily influenced by the orientation of the methylammonium cations close to the surface. We demonstrate that, depending on methylammonium orientation, the water molecule can infiltrate into the hollow site of the surface and get trapped. Controlling dipole orientation via poling or interfacial engineering could thus enhance its moisture stability. No direct reaction between the water and methylammonium molecules is seen. Furthermore, calculations with an implicit solvation model indicate that a higher water concentration may facilitate degradation through increased lattice distortion.

Ferroelectric Domain Wall Induced Band Gap Reduction and Charge Separation in Organometal Halide Perovskites.

Organometal halide perovskites have been intensely studied in the past 5 years, inspired by their certified high photovoltaic power conversion efficiency. Some of these materials are room-temperature ferroelectrics. The presence of switchable ferroelectric domains in methylammonium lead triiodide, CH3NH3PbI3, has recently been observed via piezoresponse force microscopy. Here, we focus on the structural and electronic properties of ferroelectric domain walls in CH3NH3PbX3 (X = Cl, Br, I). We find that organometal halide perovskites can form both charged and uncharged domain walls due to the flexible orientational order of the organic molecules. The electronic band gaps for domain structures possessing 180 and 90° walls are estimated with density functional theory. It is found that the presence of charged domain walls will significantly reduce the band gap by 20-40%, while the presence of uncharged domain walls has no substantial impact on the band gap. We demonstrate that charged domain walls can serve as segregated channels for the motions of charge carriers. These results highlight the importance of ferroelectric domain walls in hybrid perovskites for photovoltaic applications and suggest a possible avenue for device optimization through domain patterning.

First-Principles Calculation of the Bulk Photovoltaic Effect in CH3NH3PbI3 and CH3NH3PbI(3-x)Cl(x).

Hybrid halide perovskites exhibit nearly 20% power conversion efficiency, but the origin of their high efficiency is still unknown. Here, we compute the shift current, a dominant mechanism of the bulk photovoltaic (PV) effect for ferroelectric photovoltaics, in CH3NH3PbI3 and CH3NH3PbI(3-x)Cl(x) from first-principles. We find that these materials give approximately three times larger shift current PV response to near-IR and visible light than the prototypical ferroelectric photovoltaic BiFeO3. The molecular orientations of CH3NH3⁺ can strongly affect the corresponding PbI3 inorganic frame so as to alter the magnitude of the shift current response. Specifically, configurations with dipole moments aligned in parallel distort the inorganic PbI3 frame more significantly than configurations with near-net-zero dipole, yielding a larger shift current response. Furthermore, we explore the effect of Cl substitution on shift current and find that Cl substitution at the equatorial site induces a larger response than does substitution at the apical site.

Theoretical Model of Oxidative Adsorption of Water on a Highly Reduced Reconstructed Oxide Surface.

Highly reduced surface reconstructions of BaTiO3 (001) have been found to be composed of a TiO2 surface covered with Ti adatoms occupying surface interstitial sites. We predict the reactivity of these highly oxophilic and reduced surface Ti species through density functional theory, where we calculate the adsorption of H2O on the (√5 × âˆš5)R26.6° TiO2-Ti3/5 reconstruction. H2O serves as the primary O source and oxidizing agent. We demonstrate that H2O oxidizes some of the Ti adatoms, shifting their occupied 3d states to the surface conduction band edge. We find that, due to the high concentration of reduced Ti species on the surface, a dissociative adsorption of water on the reconstructed surface can also lead to the formation of surface hydrides, which serve as a precursor for H2 evolution. This suggests that the reconstructed surface may be an attractive single-phase hydrogen evolution catalyst.