2 research outputs found

    Average and Local Structural Origins of the Optical Properties of the Nitride Phosphor La<sub>3–<i>x</i></sub>Ce<sub><i>x</i></sub>Si<sub>6</sub>N<sub>11</sub> (0 < <i>x</i> ≤ 3)

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    Structural intricacies of the orange-red nitride phosphor system La<sub>3–<i>x</i></sub>Ce<sub><i>x</i></sub>Si<sub>6</sub>N<sub>11</sub> (0 < <i>x</i> ≤ 3) have been elucidated using a combination of state-of-the art tools, in order to understand the origins of the exceptional optical properties of this important solid-state lighting material. In addition, the optical properties of the end-member (<i>x</i> = 3) compound, Ce<sub>3</sub>Si<sub>6</sub>N<sub>11</sub>, are described for the first time. A combination of synchrotron powder X-ray diffraction and neutron scattering is employed to establish site preferences and the rigid nature of the structure, which is characterized by a high Debye temperature. The high Debye temperature is also corroborated from ab initio electronic structure calculations. Solid-state <sup>29</sup>Si nuclear magnetic resonance, including paramagnetic shifts of <sup>29</sup>Si spectra, are employed in conjunction with low-temperature electron spin resonance studies to probes of the local environments of Ce ions. Detailed wavelength-, time-, and temperature-dependent luminescence properties of the solid solution are presented. Temperature-dependent quantum yield measurements demonstrate the remarkable thermal robustness of luminescence of La<sub>2.82</sub>Ce<sub>0.18</sub>Si<sub>6</sub>N<sub>11</sub>, which shows little sign of thermal quenching, even at temperatures as high as 500 K. This robustness is attributed to the highly rigid lattice. Luminescence decay measurements indicate very short decay times (close to 40 ns). The fast decay is suggested to prevent strong self-quenching of luminescence, allowing even the end-member compound Ce<sub>3</sub>Si<sub>6</sub>N<sub>11</sub> to display bright luminescence

    Rapid Microwave Preparation of Thermoelectric TiNiSn and TiCoSb Half-Heusler Compounds

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    The 18-electron ternary intermetallic systems TiNiSn and TiCoSb are promising for applications as high-temperature thermoelectrics and comprise earth-abundant, and relatively nontoxic elements. Heusler and half-Heusler compounds are usually prepared by conventional solid state methods involving arc-melting and annealing at high temperatures for an extended period of time. Here, we report an energy-saving preparation route using a domestic microwave oven, reducing the reaction time significantly from more than a week to one minute. A microwave susceptor material rapidly heats the elemental starting materials inside an evacuated quartz tube resulting in near single phase compounds. The initial preparation is followed by a densification step involving hot-pressing, which reduces the amount of secondary phases, as verified by synchrotron X-ray diffraction, leading to the desired half-Heusler compounds, demonstrating that hot-pressing should be treated as part of the preparative process. For TiNiSn, high thermoelectric power factors of 2 mW/mK<sup>2</sup> at temperatures in the 700 to 800 K range, and <i>zT</i> values of around 0.4 are found, with the microwave-prepared sample displaying somewhat superior properties to conventionally prepared half-Heuslers due to lower thermal conductivity. The TiCoSb sample shows a lower thermoelectric figure of merit when prepared using microwave methods because of a metallic second phase
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