Informacja

Drogi użytkowniku, aplikacja do prawidłowego działania wymaga obsługi JavaScript. Proszę włącz obsługę JavaScript w Twojej przeglądarce.

Wyszukujesz frazę "Daniel, M." wg kryterium: Autor


Wyświetlanie 1-2 z 2
Tytuł:
Raman Spectra of In$\text{}_{0.30}$Se$\text{}_{0.70}$ Amorphous Films
Autorzy:
Weszka, J.
Daniel, Ph.
Burian, A. M.
Powiązania:
https://bibliotekanauki.pl/articles/2014453.pdf
Data publikacji:
2000-11
Wydawca:
Polska Akademia Nauk. Instytut Fizyki PAN
Tematy:
71.55.Jv
63.50.+x
Opis:
Amorphous films of In$\text{}_{0.30}$Se$\text{}_{0.70}$ alloy thermally evaporated from one source onto borosilicate glass substrates were studied by Raman scattering at 300K and 10K. The Raman scattering spectra excited with 488 and 457.9nm laser lines were recorded in a quasi-rectangular geometry with the use of a single channel spectrometer. All the Raman scattering spectra reveal a continuum spreading from the Rayleigh line up to about 250cm$\text{}^{-1}$ and rather featureless background due to second-order processes beyond it. The room temperature spectra show a strong feature at about 143cm$\text{}^{-1}$ that is lacking in the spectra taken at 10K and, instead, a weak band at about 125cm$\text{}^{-1}$ is observed. The Raman scattering spectra recorded at both temperatures appear to be dependent on the excitation line within the 40-50cm$\text{}^{-1}$ range. The feature at about 143cm$\text{}^{-1}$ is attributed to Se chain modes while a weaker band at about 125cm$\text{}^{-1}$ observed at low temperature is due to Se$\text{}_{8}$ ring molecules. The dynamics of the In$\text{}_{0.30}$ Se$\text{}_{0.70}$ films is treated in terms of a continuous random network composed of rather strongly interconnected InSe$\text{}_{4}$ tetrahedral clusters.
Źródło:
Acta Physica Polonica A; 2000, 98, 5; 619-623
0587-4246
1898-794X
Pojawia się w:
Acta Physica Polonica A
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Intramolecular and Lattice Dynamics in V$\text{}_{6-n}^{IV}$V$\text{}_{n}\text{}^{V}$ O$\text{}_{7}$(OCH$\text{}_{3}$)$\text{}_{12}$ Crystal
Autorzy:
Yablokov, Yu. V.
Augustyniak-Jabłokow, M. A.
Borshch, S.
Daniel, C.
Hartl, H.
Powiązania:
https://bibliotekanauki.pl/articles/2043556.pdf
Data publikacji:
2005-08
Wydawca:
Polska Akademia Nauk. Instytut Fizyki PAN
Tematy:
76.30.Fc
36.40.Cg
Opis:
Multi-nuclear mixed-valence clusters V$\text{}_{4}^{IV}$V$\text{}_{2}^{V}$O$\text{}_{7}$(OCH$\text{}_{3}$)$\text{}_{12}$ were studied by X-band EPR in the temperature range 4.2-300 K. An isotropic exchange interactions between four V$\text{}^{IV}$ ions with individual spin S$\text{}_{i}$=1/2 determine the energy levels structure of the compound with the total spin states S=0, 1, and 2, which are doubled and split due to the extra electron transfer. The spin-Hamiltonian approach was used for the analysis of the temperature dependences of the EPR spectra parameters and the cluster dynamics. Two types of the electron transfer are assumed: the single jump transfer leading to the splitting of the total spin states by intervals comparable in magnitude with the exchange parameter J≈100-150 cm$\text{}^{-1}$ and the double jump one resulting in dynamics. The dependence of the transition ratesν$\text{}_{tr}$ on the energy of the total spin states was observed. In particular, in the range 300-220 K theν$\text{}_{tr}$ ≈0.7×10$\text{}^{10}$ cm$\text{}^{-1}$ and below 180 K the ν$\text{}_{tr}$≈1×10$\text{}^{10}$ cm$\text{}^{-1}$ was estimated. The g-factors of the spin states were shown to depend on the values of the intermediate spins. A phase transition in the T-range 210-180 K leading to the change in the initial V$\text{}^{IV}$ ions localization was discovered.
Źródło:
Acta Physica Polonica A; 2005, 108, 2; 271-281
0587-4246
1898-794X
Pojawia się w:
Acta Physica Polonica A
Dostawca treści:
Biblioteka Nauki
Artykuł
    Wyświetlanie 1-2 z 2

    Ta witryna wykorzystuje pliki cookies do przechowywania informacji na Twoim komputerze. Pliki cookies stosujemy w celu świadczenia usług na najwyższym poziomie, w tym w sposób dostosowany do indywidualnych potrzeb. Korzystanie z witryny bez zmiany ustawień dotyczących cookies oznacza, że będą one zamieszczane w Twoim komputerze. W każdym momencie możesz dokonać zmiany ustawień dotyczących cookies