0000000000131738
AUTHOR
Richard T. Williams
Luminescence and ultraviolet excitation spectroscopy of SrI2 and SrI2:Eu2+
Abstract We report measurements of luminescence and its ultraviolet excitation spectra in SrI2 and SrI2:Eu2+ at temperatures of 10 and 300 K. Attention is focused on determining the exciton energy and its temperature shift from features of the excitation spectra and limits placed by absorption spectroscopy on a 120 μm thin crystal, on observation of a broadened Eu emission band attributed to trace Eu associated with oxygen in nominally undoped crystals, and on adding observations concerning the 3.4 eV band at low temperature attributed by Pustovarov et al. to the self-trapped exciton.
Model of scanning force microscopy on ionic surfaces.
We present a theoretical model of the scanning force microscope using an atomistic simulation technique for the interaction between a crystalline sample and a tip nanoasperity combined with a semi- empirical treatment of the mesoscopic van der Waals attraction between tip and surface, and the macroscopic parameter of cantilever deflection. For the nanoasperity at the end of the tip, we used a neutral and a protonated (MgO${)}_{32}$ cube, which model a hard tip made of oxide material. Static calculations based on total-energy minimization were used to determine the surface and tip geometries and total energy as a function of tip position. Scan lines of the perfect (001) surfaces of NaCl and …
Time‐resolved absorption and luminescence following electron‐hole pair creation in ZnO
We report transient absorption induced by electron-hole excitation in undoped ZnO. A laser pump/continuum probe method covers 2–300 ps, and an electron pulse with lamp transmission covers 8–300 ns. The broad absorption spectrum increases monotonically with wavelength from 900 to 1600 nm. Following a reasonable hypothesis that the free-carrier-like induced infrared absorption is proportional to the total number of free carriers, excitons, and shallow-trapped carriers in the sample, these data allow setting an upper limit on the quantum efficiency of a specified lifetime component of luminescence. For the undoped commercial ZnO studied in this report, the quantum efficiency of room temperatur…
Subpicosecond Laser Spectroscopy of Blue-Light-Induced Absorption in KNbO3 and LiNbO3
Pulses of 427-nm light from am amplified Ti:sapphire frequency-doubled laser are absorbed in two-photon band-gap excitations of KNbO3 and LiNbO3. Induced absorption spectra measured in the visible and recently extended in the infrared have been recorded as a function of delay from 0 to 250 ps after two-photon blue excitation. Samples include stoichiometric as well as congruent LiNbO3. Comparison is made to transient absorption in the nanosecond and longer time range induced by electron pulses of~10 ns width and 270 keV energy. Parts of the absorption can be attributed to bound and free polarons, including the intrinsic electron polaron.
Experimental and theoretical studies of polaron optical properties in KNbO3 perovskite
Time-resolved absorption and luminescence spectra have been measured in KNbO3 perovskite crystals after pulsed band-gap excitation by 200 fs laser pulses and 10 ns electron pulses. Quantum chemical calculations using the large unit cell periodic model support the interpretation of the observed transient absorption bands at 0.8 and 1.1 eV as the self-trapped electron polarons and bound hole polarons, respectively. The activation energy for the 2.2 eV green luminescence quenching is 0.05 eV. We suggest that the short lifetime (,15 ns) of the luminescence at RT is caused by the radiative recombination of nearest electron and hole polarons. q 2003 Elsevier Ltd. All rights reserved.
Photoluminescence excitation spectroscopy in boron nitride nanotubes compared to microcrystalline h‐BN and c‐BN
Photoluminescence spectra and photoluminescence excitation spectra have been measured on samples of hexagonal boron nitride microcrystalline powder, cubic boron nitride single crystal, and boron nitride nanotubes (mixture of single-walled and multi-walled with some h-BN precursor). The reason for studying these 3 samples in a comparative fashion is that nanotube BN, while based on a rolled hexagonal-BN (sp2-bonded) sheet, is expected to take on more sp3 bond-character reminiscent of cubic-BN as the curvature becomes tighter. With some simplicity of statement, this study was planned to view spectroscopy of nanotube BN with respect to its two limiting cases of bond character, all measured in …
Exciton luminescence of boron nitride nanotubes and nano-arches
We report photoluminescence (PL) and PL-excitation spectroscopy of BN nanotubes (nt-BN) mixed with some residual hexagonal crystalline (h-BN) starting material, and of pure h-BN microcrystalline powder. The nanotube phase exhibits a broad-band PL near 380 nm, in agreement with a published report of cathodoluminescence from a sample comprising >90% nanotubes. This emission is almost 3 eV lower in energy than unrelaxed exciton states found in recent all-electron theories of nt-BN and h-BN and about 1.4 eV lower than the lowest (perturbed dark?) exciton seen in absorption of nt-BN. This may suggest that excitons in nt-BN vibrationally relax to self-trapped states before emitting, a path found …
Transient absorption of polarons in KNbO3
Abstract Transient absorption spectra have been measured in a number of undoped KNbO 3 crystals following two kinds of electronic excitation: two-photon absorption of 200 fs laser pulses and 10 ns pulsed electron beam. A band peaking at 0.8 eV and broad, poorly resolved absorption in the range 1.3–3.3 eV were observed. Based on similarity to the 1 eV band in LiNbO 3 previously identified as the intrinsic electron polaron (electron self-localized on niobium in the regular lattice site), we suggest that the transient absorption band at 0.8 eV in KNbO 3 is also associated with the intrinsic electron polaron.