Neutron diffraction measurements on liquid ammonia at two temperature states on the liquid-vapor coexistence curve are presented. Three isotropic mixtures of hydrogenated and deuterated ammonia have been studied and the three radial atom–atom distribution functions extracted at 213 K and 273 K. The comparison of the experimental results with the partial radial distribution functions for orientationally uncorrelated molecules, shows some evidence for hydrogen bonding in liquid ammonia but this is much less pronounced than that found in water under ambient conditions.
Graphene and its related materials have attracted much interest in sensing applications because of their optimized ratio between active surface and bulk volume. In particular, several forms of oxidized graphene have been studied to optimize the sensing efficiency, sometimes moving away from practical solutions to boost performance. In this paper, we propose a practical, high-sensitivity, and easy to fabricate gas sensor based on high quality graphene oxide (GO), and we give the rationale to the high performance of the device. The device is fabricated by drop-casting water-dispersed single-layer GO flakes on standard 30 μm spaced interdigitated Pt electrodes. The exceptional size of the GO flakes (27 μm mean size and ∼500 μm maximum size) allows single GO flake to bridge adjacent electrodes. A typical p-type response is observed by testing the device in both reducing and oxidizing environments. The specific response to NO 2 is studied by varying the operating temperature and the gas concentration. Sensing activity is demonstrated to be mainly mediated by the oxygen functional groups. A 20 ppb detection limit is measured. Besides illustrating a simple and efficient approach to gas sensing, this work is an example of the versatility of graphene oxide, accomplishing tasks that are complementary to graphene.
Raman spectra of La(0.75)Ca(0.25)MnO(3) have been collected for the first time over a wide pressure range (0-14 GPa) using a diamond anvil cell. The frequency range explored (200-1100 cm(-1)) and the very good quality of the data allowed us to carefully analyze the pressure evolution of the phonon modes of the MnO(6) octahedra. The results show an abrupt transition at approximately 7.5 GPa with an evident deviation from the linear trend of the frequency of the Jahn-Teller phonon versus the applied pressure, accompanied by a strong phonon broadening. This behavior disagrees with the predicted insulator to metal transition and, on the contrary, indicates the occurrence of a new unpredicted phase in the very high pressure regime.
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