Pulsed-periodic UV emitter tunable near the main absorption maximum of a DNA molecule

The spectral characteristics of a pulsed-periodic lamp with three dielectric barriers are presented for the range 220–250 nm. As the active media of the lamp, krypton (Kr)-sulfur hexafluoride (SF₆) and krypton-carbon tetrachloride (CCl₄) mixtures are tested. The use of Kr-SF₆ and Kr-CCl₄ binary mixtures in two noncommunicating volumes is shown to be more effective than the use of a Kr-SF₆-CCl₄ ternary mixture with the same amount of Kr, SF₆, and CCl₄ constituents. The emission spectrum of the lamp near the maxima of the KrF(X-B) 248-nm and KrCl(X-B) 222-nm bands can be controlled by varying the partial pressures of halogen carriers and krypton.     

Mercury-free emitter pumped by a krypton fluoride molecule pulse-periodic barrier discharge

The characteristics of a pulsed-periodic short-barrier-discharge emitter operating at wavelength λ = 248 nm KrF(X-B) are investigated. The operating mixtures of the UV lamp are low-aggressive krypton-sulfur hexafluoride (SF6) mixtures at a total pressure in the range 1–50 kPa and a SF₆ partial pressure of 0.1–0.4 kPa. The spectral characteristics of the plasma are studied, and the 248 nm KrF(X-B) band luminosity is optimized in terms of the operating mixture composition, pump voltage, and pulse repetition rate. The mean power of UV emission from the lateral surface of the cylindrical lamp is estimated.     

Emission characteristics of pulse-periodic barrier-discharge plasma in a mixture of krypton with argon and liquid freon vapor

Radiation of a nanosecond barrier discharge in a mixture of krypton, argon, and carbon-tetrachloride vapor is studied in the spectral range of 150–300 nm. The plasma radiation spectra and the dependences of the intensities of the 258 nm Cl₂(D′ → A′), 222 nm KrCl(B → X), and 175 nm ArCl(B → X) bands on the partial pressure of liquid freon vapor, argon, and krypton, as well as on the discharge excitation conditions, are studied. The optimal compositions of gas mixtures for creating a broadband UV-VUV emitter based on the band system of argon chloride, krypton chloride, and chlorine molecule are determined.     

Multiwave Low‐Pressure Excimer Radiator

The excitation conditions and characteristics of a longitudinal glow discharge in a short tube of small diameter in Kr/Cl₂ and Ar/Kr/Cl₂ mixtures are investigated. It is shown that this discharge is a multiwave radiation source on systems of the 199/222/258 and 175/199/222/258 nm bands. Optimization of the pressure and composition of working mixtures most applicable for obtaining the approximately equal intensity of the ArCl(B X), KrCl(D, B X), and Cl₂(DA) radiation bands is carried out in the discharge investigated. A multiwave UVVUV radiation source is of interest for use in photometry, microelectronics, photochemistry, and medicine.     

An emission spectrum of InCl+

A spectrum, found in the 360- to 420-nm region following hollow-cathode excitation of InCl₃/In/He mixtures has been attributed to the InCl⁺ ion. Sixteen bands have been classified for the system which has been identified through rotational analysis to be B²Σ-X²Σ, consistent with photoelectron observations by Berkowitz and Dehmer. A second, very much weaker set of bands has been observed between 320 and 335 nm under the same experimental conditions. These latter bands constitute either a new system of InCl or a second InCl⁺ system.     

Kr-KCl exciplex lamp

A new source of UV radiation (excilamp) based on Kr-KCl vapor-gas mixture excited by a longitudinal high-voltage pulsed-periodic discharge is created. The emission spectrum and time characteristic of the discharge radiation are studied. The B → X transition in the KrCl* excimer molecule (λ = 222 nm) is found to dominate in the radiation spectrum of the source. The dependence of the pulse output power of the lamp on various factors is investigated, and the mechanism of B state formation in the excimer molecule is discussed.     

Radiation of the Plasma of a Transverse Discharge in a Helium–Krypton–Elegas Mixture

We carried out a spectroscopic investigation of the degradation of the active medium of a pulsed-periodic KrF emitter based on a He/Kr/SF₆ mixture (P = 10–150 kPa) with pumping by a transverse volumetric discharge. The plasma radiation spectra in the range 200–620 nm at different stages of degradation of the working mixture and the dynamics of the radiation of inert gases as well as of the products of decomposition of SF₆ molecules in the plasma are studied. It is shown that since the number of discharge pulses is 10⁴, rather effective formation of excited sulfur molecules is observed which decompose with emission in the spectral range 260–550 nm. This can be employed for developing a wideband lamp based on the system of KrF(B–X; D–X), S₂(B–X), and S₂(f–a) bands.     

Laser spectroscopy of the B[21.68]8-X8, B′[21.65]8-X8 and C[22.3]7-X27 transitions of holmium monofluoride

The spectrum of holmium monofluoride (HoF) in the blue (420-480 nm) region has been studied using laser-induced fluorescence. Previous work [J. Phys. B 7 (1974) L234] had assigned several bands in this region to the B8-X8 transition. By obtaining wavelength selected laser excitation spectra at high resolution and rotationally analyzing seven bands in this region, we have shown that not all the bands previously assigned to the B8-X8 system belong to the same electronic transition and have identified three separate transitions which we have labelled B8-X8, B′8-X8, and C7-X₂7. Preliminary low resolution dispersed fluorescence spectra have shown several excited states at energies greater than 4000 cm⁻¹ above the ground state and, though not all could be assigned, ligand field theory calculations are consistent with assigning them to the first excited spin-orbit component of the Ho⁺(4f¹⁰6s²)F⁻ ground state configuration or to the first excited configuration, Ho⁺(4f¹¹6s)F⁻. The results of the dispersed fluorescence experiments also tentatively place the X₂7 state at ∼70 cm⁻¹ above the ground X7 state.     

New spectroscopic studies of the Comet-Tail (AΠi-XΣ) system of the CO molecule

In the electronic emission spectrum of the ¹²C¹⁶O⁺ molecule, 11 bands of the Comet-Tail (A²Π_i-X²Σ⁺) system have been recorded and analyzed. Spin splitting in most of the observed lines of the 0-2, 1-0, 2-0, 2-1, 3-0, 4-0, 4-2, 6-0, 7-0, 7-1, and 8-1 bands, comprising nearly 3400 lines, has been recorded under high resolution by conventional spectroscopy. The rotational analysis of bands has been performed by nonlinear least-squares procedures and by means of effective Hamiltonians of Brown et al. and the rovibronic structure parameters have been obtained. The data of bands of the A-X system and earlier analyzed bands of the B-X and B-A systems have been merged together. As a result of this global fit, the state of information about the energy structure has been significantly enlarged for the A state and enlarged and improved for the X state. Also RKR potential curves for both states and Franck-Condon factors as well as r-centroids of the Comet-Tail system of CO⁺ have been calculated.     

Emission of cyan upon excitation of nitrogen,air, and N<Subscript>2</Subscript>-CH<Subscript>4</Subscript> mixture by discharge pulses in an inhomogeneous electric field

We have studied spectral and amplitude-time characteristics of the emission by nitrogen, air, and the N₂-CH₄ mixture upon excitation by nanosecond and microsecond high-voltage discharge pulses in an inhomogeneous electric field in the pressure range of 0.01–3 atm. In the pulsed and pulse-periodic discharge regimes, we have observed emission bands of the violet system of cyan, the transition B ²Σ⁺ → X ²Σ⁺, which were comparable in intensity with bands of the (2⁺) system of nitrogen. We show that, in the pulsed regime, the highest intensity of the violet system of cyan is observed in the N₂-CH₄ mixture. We show that, in the pulse-periodic discharge in nitrogen with a small amount of a carbon-containing admixture, upon contracting the discharge, the efficiencies of formation and emission of the violet system of cyan considerably increase. We confirm that admixtures of oxygen to nitrogen lead to suppression of the emission of the violet system of cyan molecules.     

Spectroscopic studies of the sulphur afterglow

The afterglow emission spectrum of sulphur and argon mixture is found to consist of (a) the main band system of S₂(B³Σ^-_u?X³Σ^-_g) in the region 3200–6600 Å and (b) the atomic spectrum of argon in the 7500–9000 Å region. Although B?X bands of S₂ obtained by ordinary excitation extends from 2829 to 7100 Å, the lower wavelength limit of these bands from the afterglow is only 3200Å. It is proposed that the S₂ molecules are formed in the B³Σ^-_u state through inverse predissociation when two S atoms approach each other along the potential curve of the predissociating electronic state 1_u.     

Spectral characteristics of a barrier discharge in cadmium dihalide vapor-inert gas mixtures

Spectral characteristics of a barrier-discharge plasma produced in atmospheric-pressure mixtures of cadmium diiodide and cadmium dibromide vapors with neon, krypton, and xenon at a repetition rate of sine voltage pulses up to 130 kHz are studied. The emission from the discharge is studied within the spectral range 200–900 nm with a resolution of 0.05 nm. Emission of exciplex molecules CdI(B → X) and CdBr(C, B → X), and cadmium and inert gas atoms is revealed, as well as emission of exciplex molecules XeI(B → X, A) and XeBr(B → X, A) in xenon-containing mixtures. The emission of xenon halides prevails in the spectra at a mixture temperature up to 200°C. With a further temperature increase, the emission of cadmium halides becomes dominating. It is ascertained that the most intense emissions of CdI(B → X) and CdI₂/CdBr₂/Xe/Kr and CdBr(B → X) molecules are observed, respectively, in CdI₂/CdBr₂/Xe/Kr and CdI₂/CdBr₂/Xe mixtures. The cadmium dihalide-inert gas mixtures are of interest for the use as a radiating gas in a multiwavelength and broadband excilamp emitting in the UV and visible spectral ranges.     

The B3Π(0+) → X1Σ+ emission spectrum of 79BrF and 81BrF in the range 6250–8700 Å: Rotational analysis of bands in the v′ = 0, 1, 2, 3, 4 progressions,and merged molecular constants for the X1Σ+ and B3Π(0+) states

Sixteen emission bands of the B³Π(0⁺) → X¹Σ⁺ systems of ⁷⁹BrF and ⁸¹BrF have been analyzed rotationally. Measured line frequencies are fitted by least-squares to determine the rotational constants and origin for each band. The least-squares results for 0 ≤ v′ ≤ 4 and 4 ≤ v″ ≤ 12 are merged with constants from previously reported B ← X absorption and X-state microwave data. RKR potentials for the two states and Franck-Condon factors and r-centroids for the BrF (B-X) system are reported.     

High resolution Fourier transform spectrum of GaCl

The electronic emission spectrum of the A³Π₀-X¹Σ⁺ and B³Π₁-X¹Σ⁺ transitions of Gallium monochloride molecule (⁶⁹GaCl) has been recorded on BOMEM DA8 Fourier transform spectrometer at an apodized resolution of 0.035 cm⁻¹. The rotational structure of the 0-0, 1-0, 2-1, and 3-2, bands belonging to A-X and 0-0, 0-1, 1-2, and 0-2 bands belonging to B-X transitions has been analyzed and equilibrium rotational constants for the X¹Σ⁺ and A³Π₀ states have been obtained. For the first time we are able to determine the Λ-doubling constants in the v = 0 and 1 levels of the B³Π₁ state.     

Analysis of the Comet-Tail (AΠi-XΣ) Bands of CO

In the electronic emission spectrum of the isotopic carbon monoxide ion ¹³C¹⁶O⁺ molecule, seven bands of the comet-tail (A²Π_i-X²Σ⁺) system have been recorded and analyzed. The spin splitting in most observed lines of the bands 1-0, 2-0, 3-0, 4-0, 5-0, 2-1, and 7-1 comprising over 1900 lines has been recorded under high resolution by using conventional spectroscopy. The rotational analysis of bands has been performed by nonlinear least-squares procedures and by means of effective Hamiltonians of Brown et al., the rovibronic structure parameters have been obtained. As a result of multistaged and merged analysis of the currently obtained bands of the A-X system and of the bands of the B-X system obtained earlier the state of information about the energy structure has been significantly enlarged for the A state and enlarged and improved for the X state. Also RKR potential curves have been calculated for both states and Franck-Condon factors as well as r-centroids of the comet-tail system of ¹³C¹⁶O⁺.     

The electronic spectrum of bismuth monofluoride: An 0+ ← X10+ band system at 3838 Å

Emission bands of BiF (in the region of 3800 Å), formerly designated as belonging to the B-X₁0⁺ and A₃-X₁0⁺ transitions, have been photographed and rotationally analyzed under high resolution. These bands have been found to belong to an 0⁺ ← X0⁺ system. Extensive rotational and vibrational perturbations have been observed and the nature of the perturbing state is discussed.     

Laser spectroscopy of the B[17.7]8-X8 and C[19.3]9-X8 transitions of holmium monochloride

Several new transitions of holmium monochloride (HoCl) have been studied at high resolution using laser excitation spectroscopy. Two main transitions, B[17.7]8-X8 and C[19.3]9-X8 have been observed and five bands, 0-0, 0-1, 1-0, 1-1, and 2-1 of the B-X transition and three bands, 0-0, 0-1, and 0-3 of the C-X transition have been obtained at high resolution and rotationally analyzed. Among several low lying states observed in dispersed fluorescence was a strong transition from the C state to a state ∼2140 cm⁻¹ above the ground state. Excitation spectra of this transition have shown that there are apparently two states, ∼6 cm⁻¹ apart. Comparison with ligand field theory calculations are consistent with assigning these states to the excited low lying Ho⁺(4f¹¹6s)Cl⁻ configuration. Several other low lying electronic states have been observed in dispersed fluorescence spectra. Although their assignments could not be established, their energies suggest that they are from the Ho⁺(4f¹⁰6s²)Cl⁻ or Ho⁺(4f¹¹6s)Cl⁻ configurations. Rotational constants have been obtained for the B[17.7]8 and C[19.3]9 states and have been used to speculate on the possible electron configurations for these states.     

The first negative (BΣ→XΣ) system of CO: excitation of higher vibrational levels

Six bands of the B²Σ⁺→X²Σ⁺ system in the ¹²C¹⁶O⁺ molecule were photographed by conventional spectroscopic techniques under high resolution. The 4-7 band was reinvestigated and the 4-6, 4-8, 5-8, 5-9, and 6-10 bands were recorded and analysed for the first time. The rovibronic structure parameters of the individual bands were obtained from their wavenumber data via a non-linear least-squares procedure fit. The effective Hamiltonians of Brown with direct matrix elements given by Amiot et al. [J. Mol. Spectrosc. 87 (1981) 196] have been used. By means of a merge calculations molecular constants B_v, D_v, and γ_v for B²Σ⁺ (v=4-6) and for the X²Σ⁺ (v=6-10) states and six bands origins ν_v^′-v″ of all the six analysed bands were computed for the B→X system.     

Multiwave excimer lamps using XeF/XeCl/KrF/KrCl molecules

Results are presented of an investigation of the spectral and temporal characteristics of an electricdischarge excimer lamp emitting simultaneously on the 351 nm XeF, 308 nm XeCl, 249 nm KrF, and 222 nm KrCl transitions. The He/Kr/Xe/SF₆/HCl working mixtures were excited in a transverse discharge with ultraviolet spark preionization at a total pressure of 25–100 kPa. In order to obtain the same brightness the concentration ratio [Kr]/[Xe] for the excimer molecular transitions was 8/0.8 kPa, and that for the halogen-containing molecules was [SF₆]/[HCl][=[0.06–0.12]/[0.08–0.16] kPa. The duration of the radiation pulses for the excimer molecular transitions at atmospheric pressure was 100–200 ns and when the total mixture pressure was reduced to 250 kPa, this was doubled or trebled. The service life of the spontaneous radiation for B-X transitions in excimer molecules was 10⁵ pulses. Zh. Tekh. Fiz. 68, 64–67 (December 1998)     

The Fourier Transform Emission Spectrum of BΠ1-XΣ Band-System of InCl

The emission spectrum of the B³Π₁-X¹Σ⁺ band-system of the InCl molecule has been recorded on a Fourier transform spectrometer at an apodized resolution of 0.025 cm⁻¹. The rotational structure of 1-0, 2-1, 0-0, 0-1, 1-2, 0-2, and 1-3 bands belonging to the B³Π₁-X¹Σ⁺ transition of In³⁵Cl has been analyzed and accurate equilibrium rotational constants of the B³Π₁ state, have been obtained. Precise Λ-doubling constants of the B³Π₁ state (v=0, 1, and 2) are also reported for the first time.