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Register a new userPerfect and Stable Hybrid Glasses from Strong and Fragile Metal-Organic Framework Liquids
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Hybrid glasses connect emerging fields of metal-organic frameworks (MOFs) with the glass-formation, amorphization, and melting processes of these structurally diverse and chemically versatile systems. Most zeolites, including MOFs, amorphize around the glass transition, devitrifying and then melting at much higher temperatures. The relationship between the two processes has so far not been investigated. Herein we show how heating first results in a low density perfect glass, following an order-order transition, leading to a super-strong liquid of low fragility that dynamically controls MOF collapse. A subsequent order-disorder transition creates a high density liquid of greater fragility. After crystallization and melting, subsequent cooling results in a stable glass virtually identical to the high density phase. Furthermore, the wide-ranging melting temperatures of different MOFs suggest these can be differentiated by topology. Our research provides new insight into the stability and functionality of these novel ductile crystalline materials, including the possibility of melt-casting MOFs.
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Achieving large-area uniform two-dimensional (2D) metal-organic frameworks (MOFs) and controlling their electronic properties on inert surfaces is a big step towards future applications in electronic devices. Here we successfully fabricated a 2D monolayer Cu-dicyanoanthracene (DCA) MOF with long-range order on an epitaxial graphene surface. Its structural and electronic properties are studied by low-temperature scanning tunneling microscopy (STM) and spectroscopy (STS) complemented by density-functional theory (DFT) calculations. We demonstrate access to multiple molecular charge states in the 2D MOF using tip-induced local electric fields. We expect that a similar strategy could be applied to fabricate and characterize 2D MOFs with exotic, engineered electronic states.
The availability of ultrafast pulses of coherent hard x-rays from the Linac Coherent Light Source opens new opportunities for studies of atomic-scale dynamics in amorphous materials. Here we show that single ultrafast coherent x-ray pulses can be used to observe the speckle contrast in the high-angle diffraction from liquid Ga and glassy Ni2Pd2P and B2O3. We determine the thresholds above which the x-ray pulses disturb the atomic arrangements. Furthermore, high contrast speckle is observed in scattering patterns from the glasses integrated over many pulses, demonstrating that the source and optics are sufficiently stable for x-ray photon correlation spectroscopy studies of dynamics over a wide range of time scales.
Organic-inorganic coupling in the hybrid lead-halide perovskite is a central issue in rationalizing the outstanding photovoltaic performance of these emerging materials. Here we compare and contrast the evolution of structure and dynamics of the hybrid CH3NH3PbBr3 and the inorganic CsPbBr3 lead-halide perovskites with temperature, using Raman spectroscopy and single-crystal X-ray diffraction. Results reveal a stark contrast between their order-disorder transitions, abrupt for the hybrid whereas smooth for the inorganic perovskite. X-ray diffraction observes an intermediate incommensurate phase between the ordered and the disordered phases in CH3NH3PbBr3. Low-frequency Raman scattering captures the appearance of a sharp soft mode in the incommensurate phase, ascribed to the theoretically predicted amplitudon mode. Our work highlights the interaction between the structural dynamics of organic cation CH3NH3+ and the lead-halide framework, and unravels the competition between tendencies of the organic and inorganic moieties to minimize energy in the incommensurate phase of the hybrid perovskite structure.
This paper presents computer simulations of Cu$_x$Zr$_{100-x}$ $(x=36,50,64)$ in the liquid and glass phases. The simulations are based on the effective-medium theory (EMT) potentials. We find good invariance of both structure and dynamics in reduced units along the isomorphs of the systems. The state points studied involve a density variation of almost a factor of two and temperatures going from 1500 K to above 4000 K for the liquids and from 500 K to above 1500 K for the glasses. For comparison, results are presented also for similar temperature variations along isochores, showing little invariance. In general for a binary system the phase diagram has three axes: composition, temperature and pressure (or density). When isomorphs are present, there are effectively only two axes, and for a fixed composition just one. We conclude that the liquid and glass parts of the thermodynamic phase diagram of this metallic glass former at a fixed composition is effectively one-dimensional in the sense that many physical properties are invariant along the same curves, implying that in order to investigate the phase diagram, it is only necessary to go across these curves.
Colloidal particles, which are ubiquitous, have become ideal testing grounds for the structural glass transition (SGT) theories. In these systems glassy behavior is manifested as the density of the particles is increased. Thus, soft colloidal particles with varying degree of softness capture diverse glass forming properties, observed normally in molecular glasses. By performing Brownian dynamics simulations for a binary mixture of micron-sized charged colloidal suspensions, known to form Wigner glasses, we show that by tuning the softness of the potential, achievable by changing the monovalent salt concentration, there is a continuous transition between fragile to strong behavior. Remarkably, this is found in a system where the well characterized potential between the colloidal particles is isotropic. We also show that the predictions of the random first order transition (RFOT) theory quantitatively describes the universal features such as the growing correlation length, $xisim (phi_K/phi - 1)^{- u}$ with $ u = 2/3$ where $phi_K$, the analogue of the Kauzmann temperature, depends on the salt concentration. As anticipated by the RFOT predictions, we establish a causal relationship between the growing correlation length and a steep increase in the relaxation time and dynamic heterogeneity. The broad range of fragility observed in Wigner glasses is used to draw analogies with molecular glasses. The large variations in the fragility is found only when the temperature dependence of the viscosity is examined for a large class of diverse glass forming materials. In sharp contrast, this is vividly illustrated in a single system that can be experimentally probed. Our work also shows that the RFOT predictions are accurate in describing the dynamics over the entire density range, regardless of the fragility of the glasses, implying that the physics describing the SGT is universal.
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