Optical properties of electron irradiation induced defects in InP

The optical properties of deep hole traps H₄ and H₅ in p type and of the deep electron trap E₁₁ in n type InP, introduced by electron irradiation, have been studied using deep level optical spectroscopy. Comparison of the optical threshold with the thermal activation energy of H₅ level shows that it is highly relaxed with a Frank-Condon shift d_Fc = 0.45 eV. The electron level E₁₁ is weakly relaxed and its optical cross section σ ⁰ is well accounted for by transitions to the Γ_6c minimum. The optical absorption σ_p⁰ associated to level H₄ shows two successive onsets at hν = 0.5 and hν = 1.2 eV which can be attributed to hole transitions to the Γ_7–8 and to the L_4–5 valence band extrema, respectively. The deduced Frank-Condon shift, d_Fc = 0.23 eV, agrees with the measured difference of 40 meV between its apparent activation energy E_a and its thermal activation energy E_T.     

Synchrotron radiation from relativistic electrons in intense magnetic fields

The synchrotron radiation spectrum is calculated for relativistic electrons in the case where no restriction is placed on the strength of the magnetic field. It is shown that in intense fields H? H₀ = m²c³/e₀? =4.41 · 10¹³ G a major contribution to the total radiation intensity comes from transitions to the ground state and also to weakly excited levels. In particular, the contribution from transitions to the ground state (final electron energy E' =mc²) for electrons of initial energy E = 10 MeV in a field H = 2H₀ is 14% of the contribution from transitions to highly excited states (E'?mc²).     

The ground state of two-dimensional electrons in a nonuniform magnetic field

An exact solution to the Schrödinger equation for the ground state of two-dimensional Pauli electrons in a nonuniform transverse magnetic field H is presented for two cases. In the first case, the field H depends on a single variable, H = H(y), while in the second case, the field is axially symmetric, H = H(ρ), ρ²=x ²+y ². The electron density distributions n = n(y) and n = n(ρ) that correspond to a completely filled lower level are found. For quasiuniform fields of fixed sign, the functions n(y) and n(ρ) are locally related to the magnetic field: n(y) = H(y)/?₀ and n(ρ) = H(ρ)/?₀, where ?₀ = hc/|e| is a magnetic flux quantum. Magnetic fields are considered that are periodic, singular, and bounded in the plane xy. Finite electron objects in a nonuniform magnetic field are analyzed.     

Electronic photodissociation spectra of the Arn-C4H2 (n=1-4) weakly bound cationic complexes

Electronic spectra of a series of weakly bound clusters consisting of argon (Ar_n, n=1-4) bound to the butadiyne cation, C₄H₂⁺, have been recorded in the visible range from 440 to 520 nm by photodissociation. The C₄H₂⁺ fragment signal was recorded as a function of the laser wavelength during excitation of the A←X electronic transition. The observed transitions were assigned to the band origin of the cationic complexes and to vibronic bands involving excitation of the ν₃ and ν₇ vibrational modes of the C₄H₂⁺ moiety, as well as combination bands of these modes. Comparison of the photodissociation spectra of the various clusters reveals a small blue shift, 25 cm⁻¹ of the band maxima relative to the corresponding transitions reported from gas phase spectra of the bare C₄H₂⁺ cation. The magnitude of the blue shift of each band increases with successive Ar solvation up to n=3. Furthermore, each band becomes increasingly broadened towards the red with the addition of Ar atoms due to an increasing number of unresolved transitions involving excited intermolecular modes.     

High-precision frequency measurements of the ν1 + ν3 combination band of C2H2 in the 1.5 μm region

A pair of 1.5 μm semiconductor laser frequency standards have been developed for optical telecommunications use, stabilised to transitions of ¹²C₂H₂ and ¹³C₂H₂, using cavity-enhanced Doppler-free saturation absorption spectroscopy. The absolute frequencies of 41 lines of the ν₁ + ν₃ band of ¹²C₂H₂, covering the spectral region 1520-1545 nm, have been measured by use of a passive optical frequency comb generator, referenced to ¹³C₂H₂ transitions of known frequency. The mean experimental uncertainties (coverage factor k = 1) of the frequency values are 3.0 kHz (type A) and 10 kHz (type B). Improved values of the band origin ν₀, rotational constants B′ and B″, and centrifugal distortion coefficients D′, D″, H′, and H″ are presented.     

High sensitivity ICLAS of H2O in the region of the second decade (11 520-12 810 cm)

The high resolution absorption spectrum of the H₂¹⁸O isotopologue of water has been recorded by Intracavity Laser Absorption Spectroscopy (ICLAS) with a sensitivity on the order of α_min ∼ 10⁻⁹ cm⁻¹. The 11 520-12 810 cm⁻¹ spectral region corresponding to the 3ν + δ decade of vibrational states, was explored with an ICLAS spectrometer based on a Ti:Sapphire laser. It allowed detecting transitions with an intensity down to 10⁻²⁷ cm/molecule which is about 100 times lower than the weaker line intensities available in the literature, in particular in the HITRAN database.The rovibrational assignment was performed on the basis of the results of variational calculations and allowed for assigning 3659 lines to the H₂¹⁶O, H₂¹⁸O, H₂¹⁷O, HD¹⁶O and HD¹⁸O species, leaving only 1.7% unassigned transitions. A line list including 1712 transitions of H₂¹⁸O has been generated and assigned leading to the determination of 692 rovibrational energy levels belonging to a total of 16 vibrational states, 386 being newly observed. A deviation on the order of 25% has been evidenced for the average intensity values given by HITRAN and the results of variational calculations. Ninety two transitions of the HD¹⁸O isotopologue could also be assigned and the corresponding upper rovibrational levels are given.     

Pressure-induced H2 opacity in the 5-μm region

The H₂ opacity arising from the pure-rotational hexadecapole-induced U₀(J) transitions occurring during H₂H₂ and H₂He collisions, and from the hexadecapole-induced U₀(J) + S₀(J′) and the quadrupole-induced S₀(J) + S₀(J′) transitions in H₂He collisions, has been calculated. The U₀(J) and S₀(J) + S₀(J′) contributions from H₂H₂ collisions are important H₂ opacities in the frequency range from 700–3000 cm^?1 for temperatures appropriate to the outer planets. It is concluded that this opacity is needed in addition to the opacity from the extrapolation of the 0-0 and 1-0 H₂H₂ collisionally induced bands to interpret the spectrum at 5 μm for the outer planets.     

Influence of ultrashort laser pulse duration on the X-ray emission spectrum of plasma produced in cluster target

Line emission spectrum of a laser plasma produced in an argon cluster jet target was measured on the n ¹ P1?1¹ S ₀ (n=5–9) transitions of the helium-like Ar XVII ion for a pulse duration varying from 45 fs to 1.1 ps and a constant fluence of ～10⁵ J/cm². The independent modeling of the relative intensities of the transitions from the n=5,..., 10 levels, as well as of the 2¹ P ₁? 1² S ₀ and 2³ P ₁?1² S ₀ lines and dielectronic satellites indicates that the electron temperature is anomalously low and that the electron density in emitting plasma increases with shortening the laser pulse. The excitation from the ground state by a small fraction of hot electrons is expected to be the main channel of populating the Ar XVII levels.     

The heat capacity of the layer compounds (CH3CH2CH2NH3)2MnCl4 and (CH3CH2CH2NH3)2CdCl4 from 10 K TO 300 K

The heat capacity of the layer compounds tetrachlorobis (n-propylammonium) manganese II and tetrachlorobis (n-propylammonium) cadmium II, (CH₃CH₂CH₂NH₃)₂MnCl₄ and (CH₃CH₂CH₂NH₃)₂CdCl₄ respectively, has been measured over the temperature range 10 K ?T ? 300 K.Two known structural phase transitions were observed for the Mn compound in this temperature region: at T = 112.8 ± 0.1 K (ΔH_t= 586 ± 2 J mol^?1; ΔS_t = 5.47 ± 0.02 J K^?1mol^?1) and at T =164.3 ± (ΔH_t = 496 ± 7 J mol^?1; ΔS_t =3.29 ± 0.05 J K^?1mol^?1). The lower transition is known to be from a monoclinic structure to a tetragonal structure, while the upper is from the tetragonal phase to an orthorhombic one. From comparison with the results for the corresponding methyl Mn compound it is deduced that the lower transition primarily involves changes in H-bonding while the upper transition involves motion in the propyl chain.A new structural phase transition was observed in the Cd compound at T= 105.5 ± 0.1 K (ΔH_t= 1472.3 ± 0.1 J mol^?1; ΔS_t = 13.956 ± 0.001 J K^?1mol^?1), in addition to two transitions that have been observed previously by other techniques. The higher of these transitions(T = 178.7 ± 0.3 K; ΔH_t = 982 ± 4 J mol^?1 ΔS_t = 6.16 ± 0.02 J K^? mol^?1) is known to be between two orthorhombic structures, while the structural changes at the lower transition (T= 156.8 ± 0.2 K; ΔH_t = 598 ± 5 J mol^?1, ΔS_t = 3.85 ± 0.03 J K^?1 mol^?1) and at the new transition are not known. It is proposed that these two transitions correspond respectively to the tetragonal to orthorhombic and monoclinic to tetragonal transitions in the propyl Mn compounds.In addition to the structural phase transitions (CH₃CH₂CH₂NH₃)₂MnCl₄ magnetically orders at t? 130 K. The magnetic contribution to the heat capacity is deduced from the heat capacity of the corresponding diamagnetic Cd compound and is of the form expected for a quasi 2-dimensional Heisenberg antiferromagnet.     

Fourier transform microwave spectroscopy of the reactive intermediate monoiodosilylene,HSiI and DSiI

The pure rotational spectra of three silicon isotopologues of HSiI and two isotopologues of DSiI have been recorded by pulsed-jet Fourier transform microwave (FTMW) spectroscopy. Neon was passed over dry ice cooled H₃SiI or D₃SiI and introduced into the pulsed valve of the FTMW spectrometer. The monoiodosilylenes HSiI and DSiI were produced in situ with a 1000 V DC-discharge nozzle. Only a-type transitions occur in monoiodosilylene from 6 to 26 GHz. We observe K_a = 0 a-type transitions for H²⁸SiI, H²⁹SiI, H³⁰SiI, and D²⁹SiI, and both K_a = 0 and 1 a-type transitions for D²⁸SiI. Rotational constants, centrifugal distortion constants, iodine nuclear quadrupole coupling constants, and nuclear spin–molecular rotation constants were measured.     

Enhanced luminescence of Ca3B2O6:Dy phosphors by Na-codoping for LED applications

The Ca_2.95−yDy_0.05B₂O₆:yNa⁺ (0≤y≤0.20) phosphors were synthesized at 1100 °C in air by the solid-state reaction route. The as-synthesized phosphors were characterized by X-ray powder diffraction (XRD), scanning electron microscopy (SEM), photoluminescence excitation (PLE), photoluminescence (PL) spectra and thermoluminescence (TL) spectra. The PLE spectra show the excitation peaks from 300 to 400 nm due to the 4f-4f transitions of Dy³⁺. This mercury-free excitation is useful for solid-state lighting and light-emitting diodes (LEDs). The emission of Dy³⁺ ions on 350 nm excitation was observed at 480 nm (blue) due to the ⁴F_9/2→⁶H_15/2 transitions, 575 nm (yellow) due to ⁴F_9/2→⁶H_13/2 transitions and 660 nm (red) due to weak ⁴F_9/2→⁶H_11/2 emissions. The PL results from the investigated Ca_2.95−yDy_0.05B₂O₆:yNa⁺ phosphors show that Dy³⁺ emissions increase with the increase of the Na⁺ codoping ions. The integral intensity of yellow to blue (Y/B) can be tuned by controlling Na⁺ content. By the simulation of white light, the optimal CIE value (0.328, 0.334) can be achieved when the content of Na⁺-codoping ions is y=0.2. The results imply that the Ca_2.95−yDy_0.05B₂O₆:yNa⁺ phosphors could be potentially used as white LEDs.     

Diode laser line strength measurements of the (ν4 + ν5)0 band of 12C2H2

A diode laser spectrometer that was operated in sweep integration mode was used to measure individual line strengths for 17 R-branch transitions of the (ν₄ + ν₅)⁰ combination band of ¹²C₂H₂ at 7.4 μm. Analysis of these results gives a band strength S_v = 64.4 ± 2.0 cm^?2 atm^?1 at 296 K. Line-broadening parameters for several of these transitions were determined by using both N₂ and He as broadening gases.     

Coexistence of ferro- and antiferromagnetism and phase transitions in itinerant electron systems

It is shown from a general point of view that the coexistence of ferro- and antiferromagnetism with a symmetry-breaking is possible in certain itinerant electron systems where the wave vector dependent susceptibility χ_q⁰ without the electron-electron interaction has two peaks at q = 0 and q = Q, the antiferromagnetic vector. The conditions for the coexistence and the possible phase diagrams in the H-T plane and the nature of phase transitions are discussed.     

Electron and nuclear magnetic resonances associated with magnetoelectric and antiferroelectric interactions in the exchange-noncollinear (“square”) chiral antiferromagnet Nd<Subscript>2</Subscript>CuO<Subscript>4</Subscript> and their behavior in chiral phase transitions

Experiments with the tetragonal antiferromagnet Nd₂CuO₄ in the temperature range 1.5 K < T < T _N = 245 K show that the magnetic moments of Cu²⁺ possess an exchange-noncollinear magnetic structure of the “square” type, which has the form of an exchange doublet whose components exhibit different chiralities (Γ₄ and Γ₅ phases). Between these phases, consecutive phase transitions Γ₄ ? Γ₅ ? Γ₄ with a change in chirality take place at temperatures T₁ = 30 K and T₂ = 70 K. The electron and nuclear magnetic resonances (natural frequencies and susceptibilities) associated with excitation of magnons (due to the magnetoelectric and antiferroelectric interactions) by an ac electric field E(t), as well as a variable magnetic field H(t) applied in the case of a constant electric field E⁰, are calculated. It is predicted that nuclear magnetic resonance is excited by an ac electric field at frequencies determined by hyperfine fields of the sublattices. The change in the resonance frequencies upon the above chiral phase transitions are analyzed (being first-order phase transitions, these transitions possess a number of features associated with the chirality of the magnetic structures).     

Ion-electron coincidence study of the thermal He(23S) + H2 Penning reaction

A new Penning-electron-Penning-ion coincidence method is described. It is applied to the study of the thermal reaction of He(2³S) with H₂. The main results reported are separate electron energy spectra that are coincident with the three different ions formed: HeH₂⁺, HeH⁺ and H₂⁺. Based on these results it is shown that the Penning reaction of the He(2³S)/H ₂ system proceeds in two well-separated steps: (i) ionization at distances R (HeH₂) ? 6a₀ in which H₂⁺ (v) is formed in different vibrational states; and (ii) reactive collision of H₂⁺ (v) with He. For the second step the variation of the branching ratios with vibrational quantum numbers v = 0 to v = 10 is derived, and it is shown that these branching ratios may be regarded as relative vibrational-energy-dependent cross-sections for the collision of H₂⁺ (v) with He at an average relative kinetic energy of ～20 meV.     

Variable temperature EPR spectra of Copper (II) ions in kainite crystals

X-band electron paramagnetic resonance (EPR) studies on divalent copper ions embedded in KMgClSO₄·3H₂O single crystals have been performed at low temperature (123 K). The angular variation of the EPR spectra reveals the presence of two Cu²⁺ sites, which have different orientations. The spin-Hamiltonian parameters of this six-coordinated cupric ion have been evaluated from the EPR spectra at 123 K. The forbidden lines due to Δm_I=±1 transitions are observed in between allowed transitions. The temperature variation EPR studies have also been performed both for a single crystal and a polycrystalline sample. The ground state wavefunction of Cu²⁺ ions has been estimated and is found to be an admixture of d_3z²−r² and d_x²−y². The temperature variation of the EPR spectra reveals that Cu²⁺ ions exhibit dynamic Jahn-Teller effect. From the polycrystalline EPR data, the temperature dependent magnetic susceptibilities are evaluated and discussed.     

High sensitivity ICLAS of H2O in the 12,580-13,550 cm transparency window

High-sensitivity Intracavity Laser Absorption Spectroscopy (ICLAS) is used to measure the high resolution absorption spectrum of H₂¹⁸O between 12,580 and 13,550 cm⁻¹. This spectral region covers the 3v+δ polyad of very weak absorption. Four isotopologues of water (H₂¹⁸O, H₂¹⁶O, H₂¹⁷O, HD¹⁸O) are found to contribute to the observed spectrum. Spectrum analysis is performed with the aid of variational calculations and allowed for assigning 1126 lines belonging to H₂¹⁸O, while only 160 H₂¹⁸O lines are included in the HITRAN-2008 database. Altogether, 823 accurate energy levels of H₂¹⁸O are determined from transitions attributed to 26 upper vibrational states, 438 of them being reported for the first time. New information includes energy levels of four newly observed vibrational states of H₂¹⁸O: (2 4 0), (1 4 1), (0 4 2) and (2 3 1) at 13,167.718, 13,212.678, 13,403.71 and 15,073.975 cm⁻¹, respectively. H₂¹⁸O transitions involving highly excited bending states like (1 6 0), (0 6 1), (0 7 1), (1 7 0), (0 9 0) and even (0 10 0) have been identified as a result of an intensity borrowing from stronger bands via high-order resonance interactions. Thirty-six new energy levels of H₂¹⁷O, present with a 2% relative concentration in our sample, could be determined. The rotational structure of the (0 2 3) state of HD¹⁸O at 13,245.497 cm⁻¹ is also reported for the first time.     

The electronic absorption spectra of [(CH3)3NH] MnCl3.2H2O single crystals

The electronic absorption spectra of [(CH₃)₃NH] MnCl₃.2H₂O single crystals are reported in the 15,000–45,000 cm^-1 region. In addition to the normally studied sextet → quartet transitions, special attention has been paid to the sextet → doublet transitions. Crystal field parameters evaluated (including the Trees' correction factor) to fit the observed spectra are B = 800, C = 2900, Dq = 680, and α = 76 cm^-1.     

Low-uncertainty H2O line intensities for the 930-nm region

We measured room-temperature H₂O spectra of the 3ν polyad within the wave number range 10 603 cm⁻¹ to 10 852 cm⁻¹ using frequency-stabilized cavity ring-down spectroscopy. More than 70 transitions, divisible into two groups based on their relative intensities (strong and weak) were investigated. For the 23 lines comprising the set of strong transitions, the water vapor sample was prepared as a dilute mixture in a steady flow of N₂ carrier gas, and the measurement of the water vapor sample number density was linked to primary methods of humidity generation. For these strong transitions, the measured line intensities were within 1% of previous measurements. The line intensity measurements of the weaker H₂O transitions, were made on samples of static pure water vapor, and these results were systematically greater than previous measurements by approximately 20%.     

Microwave spectrum of 2-chloropyridine

The microwave spectrum of 2-chloropyridine, C₅H₄NCl, has been studied in the frequency range from 26.5–40.0 GHz. The spectrum is characterized by strong parallel type transitions of a near-prolate asymmetric top. The assigned transitions have been used to evaluate the ground state rotational constants of the two chlorine isotopes. The rotational constants are (in MHz): A = 5872.52, B = 1637.83, C = 1280.48 for the ³⁵Cl isotopic species and A = 5872.16, B = 1591.76, C = 1252.17 for the ³⁷Cl isotopic species. The small inertial defect indicates the molecule is planar. In addition an excited vibrational state of C₅H₄N³⁵Cl has been observed and analyzed. The chlorine quadrupolar coupling constants were determined for the ground state and are: χ_aa = ?71.9 MHz for ³⁵Cl and χ_aa = ?54.9 MHz for ³⁷Cl. By assuming the pyridine ring structure the CCl bond length is found to be 1.72 Å.