Silver nanoparticles doped on titanium oxide (TiO2) were produced by laser-liquid interaction of silver nitrate (AgNO3) in isopropanol. Characteristics of Ag/TiO2 (Ag doped TiO2) nanoparticles produced by the methods presented in this article were investigated by XRD, TEM, SEM, EDX, and UV-Vis. From the UV-Vis measurements, the absorption of visible light of the Ag/TiO2 photocatalysts was improved (additional absorption at longer wavelength in visible light region) obviously. The photocatalytic efficiency of Ag/TiO2 was tested by the degradation of methylene blue (MB) in aqueous solution. A maximum of 82.3% MB degradation is achieved by 2.0 wt% Ag/TiO2 photocatalyst under 2 h illumination with a halogen lamp.
The dissociation energy of the ground state of NaH was determined by analyzing the observed near dissociation rovibrational levels. These levels were reached by stimulated emission pumping and fluorescence depletion spectroscopy. A total of 114 rovibrational levels in the ranges 9
Vibrational levels (v = 6-42) of the NaH C Σ state including the inner and outer wells and the near-dissociation region were observed by pulsed optical-optical double resonance fluorescence depletion spectroscopy. The absolute vibrational quantum number is identified by comparing the vibrational energy difference of this experiment with the ab initio calculations. The outer well with v up to 34 is analyzed using the Dunham expansion and a Rydberg-Klein-Rees (RKR) potential energy curve is constructed. A hybrid double-well potential combined with the RKR potential, the ab initio calculation, and a long-range potential is able to describe the whole NaH C Σ state including the higher vibrational levels (v = 35-42). The dissociation energy of the NaH C Σ state is determined to be D(C) = 6595.10 ± 5 cm and then the dissociation energy of the NaH ground state D(X) = 15 807.87 ± 5 cm can be derived.
The 2 1Π state of NaH has been observed up to the last bound vibrational level using pulsed optical-optical double resonance fluorescence depletion spectroscopy. A total of 20 rovibrational energy levels (v = 2–4 and J = 1–9) were assigned to this electronic state by means of comparing the successive rovibrational spectra to the eigenvalues of the ab initio potential energy curve. The decrease of background fluorescence near the atomic asymptotic limit Na(3d) + H(1s) is an indication of reaching the dissociation limit of the NaH 2 1Π state. Unobserved rovibrational levels (v = 0 and 1) are due to poor Franck-Condon overlap of 2 1Π ← A 1Σ+ transition within the accessible rovibrational levels of intermediate A 1Σ+ state of this work.
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