Zhiwen Pan

Kinetics of Decelerated Melting

Abstract Melting presents one of the most prominent phenomena in condensed matter science. Its microscopic understanding, however, is still fragmented, ranging from simplistic theory to the observation of melting point depressions. Here, a multimethod experimental approach is combined with computational simulation to study the microscopic mechanism of melting between these two extremes. Crystalline structures are exploited in which melting occurs into a metastable liquid close to its glass transition temperature. The associated sluggish dynamics concur with real‐time observation of homogeneous melting. In‐depth information on the structural signature is obtained from various independent spectroscopic and scattering methods, revealing a step‐wise nature of the transition before reaching the liquid state. A kinetic model is derived in which the first reaction step is promoted by local instability events, and the second is driven by diffusive mobility. Computational simulation provides further confirmation for the sequential reaction steps and for the details of the associated structural dynamics. The successful quantitative modeling of the low‐temperature decelerated melting of zeolite crystals, reconciling homogeneous with heterogeneous processes, should serve as a platform for understanding the inherent instability of other zeolitic structures, as well as the prolific and more complex nanoporous metal–organic frameworks.

Boson peak, heterogeneity and intermediate-range order in binary SiO 2 -Al 2 O 3 glasses

In binary aluminosilicate liquids and glasses, heterogeneity on intermediate length scale is a crucial factor for optical fiber performance, determining the lower limit of optical attenuation and Rayleigh scattering, but also clustering and precipitation of optically active dopants, for example, in the fabrication of high-power laser gain media. Here, we consider the low-frequency vibrational modes of such materials for assessing structural heterogeneity on molecular scale. We determine the vibrational density of states VDoS g(ω) using low-temperature heat capacity data. From correlation with low-frequency Raman spectroscopy, we obtain the Raman coupling coefficient. Both experiments allow for the extraction of the average dynamic correlation length as a function of alumina content. We find that this value decreases from about 3.9 nm to 3.3 nm when mildly increasing the alumina content from zero (vitreous silica) to 7 mol%. At the same time, the average inter-particle distance increases slightly due to the presence of oxygen tricluster species. In accordance with Loewensteinian dynamics, this proves that mild alumina doping increases structural homogeneity on molecular scale.

Local Deformation of Glasses is Mediated by Rigidity Fluctuation on Nanometer Scale

Abstract Microscopic deformation processes determine defect formation on glass surfaces and, thus, the materials resistance to mechanical failure. While the macroscopic strength of most glasses is not directly dependent on material composition, local deformation and flaw initiation are strongly affected by chemistry and atomic arrangement. Aside from empirical insight, however, the structural origin of the fundamental deformation modes remains largely unknown. Experimental methods that probe parameters on short or intermediate length‐scale such as atom–atom or superstructural correlations are typically applied in the absence of alternatives. Drawing on recent experimental advances, spatially resolved Raman spectroscopy is now used in the THz‐gap for mapping local changes in the low‐frequency vibrational density of states. From direct observation of deformation‐induced variations on the characteristic length‐scale of molecular heterogeneity, it is revealed that rigidity fluctuation mediates the deformation process of inorganic glasses. Molecular field approximations, which are based solely on the observation of short‐range (interatomic) interactions, fail in the prediction of mechanical behavior. Instead, glasses appear to respond to local mechanical contact in a way that is similar to that of granular media with high intergranular cohesion.

Ultrathin Fluidic Laminates for Large‐Area Façade Integration and Smart Windows

Buildings represent more than 40% of Europes energy demands and about one third of its CO2 emissions. Energy efficient buildings and, in particular, building skins have therefore been among the key priorities of international research agendas. Here, glass–glass fluidic devices are presented for large‐area integration with adaptive façades and smart windows. These devices enable harnessing and dedicated control of various liquids for added functionality in the building envelope. Combining a microstructured glass pane, a thin cover sheet with tailored mechanical performance, and a liquid for heat storage and transport, a flat‐panel laminate is generated with thickness adapted to a single glass sheet in conventional windows. Such multimaterial devices can be integrated with state‐of‐the‐art window glazings or façades to harvest and distribute thermal as well as solar energy by wrapping buildings into a fluidic layer. High visual transparency is achieved through adjusting the optical properties of the employed liquid. Also secondary functionality, such as chromatic windows, polychromatism, or adaptive energy uptake can be generated on part of the liquid.

Light extraction from fundamental modes in modulated waveguides for homogeneous side-emission

Dedicated control of axial light emission from light-guides enables a new generation of functional light sources for volumetric illumination. A primary challenge is to ensure homogeneous emission intensity across the full length of the device. Here, we introduce an approach towards homogeneously side-emitting waveguides which do not rely on imposing local scattering centers such as bubbles, micro-/nanoparticles, and rough or abrupt interfaces, but on modulated core radius. Previous quantitative studies of the relationship between structural parameters and radiation losses provide initial conditions for tailoring side-emission through core-diameter modulations, however, with strongly limited amplitude of modulation. We now employ and verify numerical simulation to overcome this limitation towards meter-long homogeneously side-emitting waveguides in which the amplitude of core-diameter modulation is of the same order of magnitude as the core diameter itself. Similar emission properties can be obtained through modulation of the core refractive index instead of the core diameter, or through a combination of both approaches. Using the present model, we deduce exemplary conditions for homogeneous side-emission in which the power flow within the waveguides decays linearly, what may present another interesting feature for applications beyond illumination.