When a spatially uniform temperature change is imposed on a solid with more than one phase, or on a polycrystal of a single, non-cubic phase (showing anisotropic expansion-contraction), the resulting thermal strain is inhomogeneous (non-affine). Thermal cycling induces internal stresses, leading to structural and property changes that are usually deleterious. Glasses are the solids that form on cooling a liquid if crystallization is avoided--they might be considered the ultimate, uniform solids, without the microstructural features and defects associated with polycrystals. Here we explore the effects of cryogenic thermal cycling on glasses, specifically metallic glasses. We show that, contrary to the null effect expected from uniformity, thermal cycling induces rejuvenation, reaching less relaxed states of higher energy. We interpret these findings in the context that the dynamics in liquids become heterogeneous on cooling towards the glass transition, and that there may be consequent heterogeneities in the resulting glasses. For example, the vibrational dynamics of glassy silica at long wavelengths are those of an elastic continuum, but at wavelengths less than approximately three nanometres the vibrational dynamics are similar to those of a polycrystal with anisotropic grains. Thermal cycling of metallic glasses is easily applied, and gives improvements in compressive plasticity. The fact that such effects can be achieved is attributed to intrinsic non-uniformity of the glass structure, giving a non-uniform coefficient of thermal expansion. While metallic glasses may be particularly suitable for thermal cycling, the non-affine nature of strains in glasses in general deserves further study, whether they are induced by applied stresses or by temperature change.

The discovery of lead-free hybrid double perovskites provides a viable approach in the search for stable and environmentally benign photovoltaic materials as alternatives to lead-containing systems such as MAPbX 3 (X = Cl, Br, or I). Following our recent reports of (MA) 2 KBiCl 6 and (MA) 2 TlBiBr 6 , we have now synthesized a hybrid double perovskite, (MA) 2 AgBiBr 6 , that has a low band gap of 2.02 eV and is relatively stable and nontoxic. Its electronic structure and mechanical and optical properties are investigated with a combination of experimental studies and density functional theory calculations.

IN A SEARCH FOR LEAD-FREE MATERIALS THAT COULD BE USED AS ALTERNATIVES TO THE HYBRID PEROVSKITES, (MA)PbX 3 , in photovoltaic applications, we have discovered a hybrid double perovskite, (MA) 2 KBiCl 6 , which shows striking similarities to the lead analogues. Spectroscopic measurements and nanoindentation studies are combined with density functional calculations to reveal the properties of this interesting system.The light-harvesting, semiconducting hybrid inorganic-organic perovskites (HIOPs) have recently attracted a great deal of attention in the photovoltaic community, with their solar cell efficiencies rising from ~4% to over 20% in just six years. 1, 2 The most extensively studied materials are the lead-containing systems, APbX 3 , where A is alkyl ammonium cation (e.g. CH 3 NH 3 + (methylammonium, MA) or NH 2 CHNH 2 + (formamidinium, FA)) and X is Cl -, Bror I -. However, the toxicity of lead to the environment could become a major drawback in their commercialization and the quest for lead-free alternatives is therefore attracting a lot of attention. Other group IV metals such as Ge and Sn are being explored, but the chemical instability of Sn 2+ and Ge 2+ presents challenges for their practical utilization. 3,4 Alternatively, the replacement of Pb 2+ by isoelectronic ions also seems attractive because the strong light absorption and long carrier life-times exhibited by MAPbX 3 are believed to be related to the 6s 2 6p 0 electronic configuration of Pb 2+ . 5 While Tl + is also toxic, Bi 3+ is an interesting option because coordination complexes of bismuth are used in over-the-counter medicines such as Pepto-Bismol. 6 However, this strategy poses challenges because Bi 3+ has a different valence state from Pb 2+ and cannot therefore be simply substituted into phases such as (MA)PbX 3 . In the present work, we show that the incorporation of Bi 3+ into a HIOP can be achieved by synthesizing a hybrid double perovskite of general formula (MA) 2 M I M III X 6 .There has been significant recent progress in the incorporation of Bi 3+ into hybrid perovskiterelated halides. For example, (MA) 3 Bi 2 I 9 can be readily obtained by using a synthetic route analogous to that used for MAPbI 3 , 7 and an ammonium bismuth iodide phase, (NH 4 ) 3 Bi 2 I 9 , was recently reported to show a bandgap of 2.04eV. 8 A number of alkali metal systems of

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Spontaneous strains for the ␣ ↔ ␤ transition in quartz were determined from lattice parameter data collected by X-ray powder diffraction and neutron powder diffraction over the temperature range ϳ5-1340 K. These appear to be compatible with previous determinations of the order parameter variation in ␣ quartz only if there is a non-linear relationship between the individual strains and the square of the order parameter. An expanded form of the 2-4-6 Landau potential usually used to describe the phase transition was developed to account for these strains and to permit calculation of the elastic constant variations. Calibration of the renormalized coefficients of the basic 2-4-6 potential, using published heat capacity data, provides a quantitative description of the excess free energy, enthalpy, entropy, and heat capacity. Values of the unrenormalized coefficients in the Landau expansion that include all the strain-order parameter coupling coefficients were used to calculate variations of the elastic constants. Values of the bare elastic constants were extracted from published elasticity data for ␤ quartz. Calculated variations of C 11 and C 12 match their observed variations closely, implying that the extended Landau expansion provides a good representation of macroscopic changes within the (001) plane of quartz. Agreement was not as close for C 33 , suggesting that other factors may influence the strain parallel to [001]. The geometrical mechanism for the transition involves both rotations and shearing of SiO 4 tetrahedra, with each coupled differently to the driving order parameter. Only the shearing part of the macroscopic distortions appears to show the same temperature dependence as other properties that scale with Q 2. Coupling between the strain and the order parameter provides the predominant stabilization energy for ␣ quartz and is also responsible for the first-order character of the transition.