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Light-induced halide segregation limits the bandgap tunability of mixed-halide perovskites for tandem photovoltaics. Here we report that light-induced halide segregation is strain-activated in MAPb(I 1−x Br x ) 3 with Br concentration below approximately 50%, while it is intrinsic for Br concentration over approximately 50%. Free-standing single crystals of CH 3 NH 3 Pb(I 0.65 Br 0.35 ) 3 (35%Br) do not show halide segregation until uniaxial pressure is applied. Besides, 35%Br single crystals grown on lattice-mismatched substrates (e.g. single-crystal CaF 2 ) show inhomogeneous segregation due to heterogenous strain distribution. Through scanning probe microscopy, the above findings are successfully translated to polycrystalline thin films. For 35%Br thin films, halide segregation selectively occurs at grain boundaries due to localized strain at the boundaries; yet for 65%Br films, halide segregation occurs in the whole layer. We close by demonstrating that only the strain-activated halide segregation (35%Br/45%Br thin films) could be suppressed if the strain is properly released via additives (e.g. KI) or ideal substrates (e.g. SiO 2 ). Mixed-halide perovskites are of interest for photovoltaic devices, but light-induced halide segregation obstructs bandgap tuning and is not fully understood. Here the authors study the effects of strain and iodide/bromide ratio on light-induced halide segregation in mixed-halide perovskites.

We report an ultra-short-pulse laser welding process that allows one to consistently weld Borofloat® 33 glass to aluminum with a shear strength above 50 MPa. We explored the morphology of the welding seam and quantified the quality of the bonding by statistically determining the shear strength with more than 30 samples. The results of the shear strength tests indicate that the intrinsic shear strength of the aluminum serves as the upper limit of the glass-to-metal bond.

In this study, 1393-B3 based borate bioactive glasses (BGs) undoped and doped with 1 wt% zinc (ZnBG), cerium (CeBG), or silver (AgBG) were prepared and were incorporated into gelatin/PCL (GEL/PCL) electrospun fibers for neural tissue engineering applications. Particle sizes of the prepared BGs were 3.1, 10.6, 14.6, and 3.7 µm for undoped BG, ZnBG, AgBG, and CeBG, respectively. Aligned electrospun fibers were prepared with 5 wt% of BG particles to produce 5BG/PCL/GEL, 5ZnBG/PCL/GEL, 5AgBG/PCL/GEL and 5CeBG/PCL/GEL fibers. Random 5CeBG/PCL/GEL fibers were also prepared for comparison. A rise in fiber diameter was measured for BG-incorporated fibers compared to PCL/GEL fibers. Mechanical tests on the fibers indicated ultimate tensile strength values of 1–3.5 MPa, the range of mechanical properties of neural tissue. Cell culture studies were carried out with the NG108-15 cell line. Cell alignment was observed on the electrospun fibers on day 2. On days 1 and 2, the optical density was higher for ZnBG/PCL/GEL, CeBG/PCL/GEL, and AgBG/PCL/GEL than for BG/PCL/GEL fibers. On day 4, undoped BG-containing nanofibers had higher optical density compared to those containing doped BGs. This result could be due to a slower release rate of boron from the pure BG/PCL/GEL fiber mat. Overall, within the studied range, all fiber mats were found to be suitable for neural tissue engineering in terms of neural cell compatibility and mechanical properties. In the future, a wider range of ion doping must be considered to fully comprehend the potential of such ion-releasing fibers for neural regeneration. Graphical Abstract

The influence of stress on the phase boundaries of polycrystalline lead-free perovskite (1 − x)Ba(Zr0.2Ti0.8)O3–x(Ba0.7Ca0.3)TiO3 (x = 0.4, 0.5, and 0.6) was characterized through the temperature- and stress-dependent small-signal dielectric and piezoelectric response from − 150 to 200 °C under uniaxial compressive stress up to − 75 MPa. For all three compositions, the phase transition temperatures separating the rhombohedral, orthorhombic, tetragonal, and cubic phases were shifted to higher temperatures with an increase in the uniaxial mechanical loading, corresponding to a significant decrease in the dielectric and piezoelectric responses. Additional stress-dependent relative permittivity measurements up to − 260 MPa were conducted at four different constant temperatures (− 10, 10, 25, and 40 °C), revealing significant increases in the dielectric response, making these materials interesting for tunable dielectric applications. Furthermore, the stress-induced shift in phase transition temperatures was confirmed by in situ combined temperature- and stress-dependent Raman spectroscopy measurements under different constant uniaxial loads within the temperature range from 30 to 130 °C.

In this study, the photoluminescence (PL) behavior of two aluminosilicate glass series containing alkali-niobates ranging from 0.4 to 20 mol% was investigated. The glasses exhibit an intense visible emission centered at ~18,400 cm−1 for the peralkaline series and at higher energies (~19,300 cm−1) for the metaluminous glasses. However, the photoluminescence emission intensity varies significantly with the niobate content and the bulk chemistry. PL and fluorescence lifetime measurements indicate that the broad emission bands result from the overlap of different niobate populations, whose distribution changes with niobate content. The distinct PL behavior in the two glass series was related to the structural evolution of the niobate units upon niobium addition. An enhancement of the visible emission was observed for a higher fraction of distorted [NbO6] units. Eu-doping was carried out as a structural probe of the glass network, and also to determine if these glasses could be used as potential rare earth element (REE) activators. The crystal field strength around Eu ions is strongly dependent on the bulk chemistry and the niobate content. Furthermore, the peralkaline series showed energy transfer from the host [NbO6] to Eu3+, confirming the feasibility of exploring niobate glasses and glass-ceramics as lanthanide ion-activated luminescent materials. In addition, glass-ceramics (GCs) containing alkali-niobate phases with a perovskite-like structure were developed and studied to verify the optical performance of these materials. It was verified that the bulk chemistry influences crystallization behavior, and also the photoluminescence response. The transparent GC from the metaluminous series exhibits a quenching of the Eu3+ emission, whereas an enhanced emission intensity is observed for the peralkaline GC. The latter shows a strong excitation-dependent PL emission, suggesting energy transfer and migration of electronic excitation from one Eu population to another. Additionally, Eu3+ emissions arising from the D15 and D25 excited states were observed, highlighting the low phonon energy achievable in niobo-aluminosilicate hosts.

The room temperature aerosol deposition method is especially promising for the rapid deposition of ceramic thick films, making it interesting for functional components in energy, mobility, and telecommunications applications. Despite this, a number of challenges remain, such as an enhanced electrical conductivity and internal residual stresses in as-deposited films. In this work, a novel technique that integrates a sacrificial water-soluble buffer layer was used to fabricate freestanding ceramic thick films, which allows for direct observation of the film without influence of the substrate or prior thermal treatment. Here, the temperature-dependent chemical and structural relaxation phenomena in freestanding BaTiO3 films were directly investigated by characterizing the thermal expansion properties and temperature-dependent crystal structure as a function of oxygen partial pressure, where a clear nonlinear, hysteretic contraction was observed during heating, which is understood to be influenced by lattice defects. As such, aliovalent doping and atmosphere-dependent annealing experiments were used to demonstrate the influence of local chemical redistribution and oxygen vacancies on the thermal expansion, leading to insight into the origin of the high room temperature conductivity of as-deposited films as well as greater insight into the influence of the induced chemical, structural, and microstructural changes in room temperature deposited functional ceramic thick films.

While the influence of silicate oxide glass composition on its chemical durability is increasingly known, the contribution of structure only is less well understood, yet is crucial for an accurate description of aqueous alteration mechanisms. The effect of structural disorder can be investigated by varying the thermal history of the glass. Furthermore, the structural changes generated by self-irradiation in nuclear glasses can be compared with those induced by fast quenching. In the context of deep geological disposal of vitreous matrices, it is then challenging to address the structural impact on glass durability. Here, a borosilicate glass, the International Simple Glass, was fiberized to obtain a rapidly quenched sample. The quenching rate and fictive temperature were evaluated from in situ Raman and Brillouin spectroscopies. Multinuclear nuclear magnetic resonance was used to obtain insight into the effect of quenching on the pristine and altered glass structure. Higher bond angle distribution and lower mixing of alkalis were observed in the fast quenched glass. Some of AlO 4 groups are then Ca-compensated, while a part of BO 4 is transformed into BO 3 units. The structural modifications increase the hydrolysis of the silicate network occurring in the forward rate regime at 90 °C by a factor of 1.4–1.8 depending on the pH value. Residual rate regime is similarly affected, more significantly at the beginning of the experiments conducted in silica saturated solutions. These findings prove that the reactivity of glass remains controlled by its structure under the various alteration regimes. Glass durability: Studying structure The structural changes induced by the rapid quenching of borosilicate glasses and their effects on chemical durability have been studied. Understanding how, and how fast, borosilicate glasses degrade is of great importance because they are often used as containment matrices for the disposal of radioactive waste. However, understanding how glass structure affects durability can be troublesome because both structural and compositional factors must be accounted for and are difficult to deconvolute. Now, a team, led by Frédéric Angeli at the CEA, Marcoule, France, have shown, using various spectroscopic techniques, how the effects of structural disorder can be investigated by varying the thermal history of a glass. The results show that this methodology can be used to investigate radiation damage in nuclear glasses, the effects of which are similar to those of quenching.

Glass welding by ultra-short puled lasers is known to exhibit a strongly localized heat affected zone, thereby allowing the fusion welding of glass parts with thermally sensitive components nearby. Moreover, the shape of the refractive index change induced by the thermomechanical gradients has an impact on the laser beam propagation into the molten zone and could cause e.g. an eventual focus shift or deteriorate the beam quality. While the temperature of the heat affected zone can be estimated by simulations, measurements of the Raman shift or thermography cameras, the shape of the temperature and stress gradients cannot be completely recovered by the aforementioned techniques due to specific limitations. In this work we present an interferometric approach to measure a 2-dimensional change of the refractive index around the molten zone before, during and after welding. Moreover comparisons between phase distribution inside the cold and unmodified glass with the hot and modified as well as cold and modified glass make it possible to estimate the thermal and the stress-induced refractive index modifications around the molten zone separately. Keywords: pump-probe, glass, ultra-short pulsed lasers, refractive index, phase, welding, laser processing, thermal evolution

Europium-doped magnesium tellurite glasses were prepared using melt quenching techniques and attenuated total reflection (ATR) spectroscopy was used to study the glass structure. The glass transition temperature increased with increasing MgO content. Eu2+ and Eu3+ emissions were studied using photoluminescence spectroscopy (PL). The broad emission of Eu2+ ions centered at approximately 485 nm was found to decrease in intensity with increasing MgO content, while the Eu3+ emission was enhanced. The Eu3+ emission lay within the red orange range and its decay time was found to increase with increasing MgO content. Different excitation wavelengths were used to adjust Eu2+ to Eu3+ emissions to reach white light emission. The white light emission was obtained for the sample with the lowest MgO content under excitation in the near-UV range.

Thermal evolutions of calcium-tungstate-borate glasses were investigated for the development of luminescent glass-ceramics by using Eu3+ dopant in a borate glass matrix with calcium tungstate, which was expected to have a combined character of glass and ceramics. This study revealed that single-phase precipitation of CaWO4 crystals in borate glass matrix was possible by heat-treatment at a temperature higher than glass transition temperature Tg for (100−x) (33CaO-67B2O3)−xCa3WO6 (x = 8−15 mol%). Additionally, the crystallization of CaWO4 was found by Raman spectroscopy due to the formation of W=O double bondings of WO4 tetrahedra in the pristine glass despite starting with the higher calcium content of Ca3WO6. Eu3+ ions were excluded from the CaWO4 crystals and positioned in the borate glass phase as a stable site for them, which provided local environments in higher symmetry around Eu3+ ions.