Role of MW-ECR hydrogen plasma on dopant deactivation and open-circuit voltage in crystalline silicon solar cells

Plasma hydrogenation is an efficient method to passivate intergrain and intragrain defects of polycrystalline silicon (pc-Si) solar cells. The hydrogenation experiments were carried out in hydrogen plasma generated in an electron cyclotron resonance system controlling different operating parameters such as microwave power (P _MW), process time (t _H) and hydrogenation temperature (T _H) for a fixed hydrogen flux of 30 sccm. The hydrogenation of n⁺pp⁺ pc-Si solar cells resulted in an improvement in the open-circuit voltage. The improvement was correlated with the dopant deactivation due to the formation of boron–hydrogen bonding. This was demonstrated from the changes in the doping level after hydrogenation of n⁺p diode structures made using single crystalline silicon as a reference material. It was found that deactivation of boron was more pronounced at high microwave plasma power, in good agreement with the high open-circuit voltage values obtained on pc-Si mesa cells. On the other hand, the effect of longer hydrogenation time and higher temperature resulted in a decrease of boron deactivation, while an increase in V _oc with a tendency of saturation at high T _H was observed. Reasons for such behavior were thoroughly explained.     

Losses through bremsstrahlung in relativistic and ultra-relativistic region of electron temperatures of plasma

The losses through bremsstrahlung in a sufficiently diluted hydrogen plasma (plasma with infinitely large Debye-Hückel radius) are calculated for the relativistic (kT?mc ²) and ultra-relativistic (kT?mc ²) region of electron temperatures. (m is the rest mass of the electron). In the ultra-relativistic temperature region the amount of energyI ^tot emitted by 1 cm³ of plasma per sec as a result of electron-ion and electron-electron collisions is given by

$$I^{tot} = 3 \cdot 39 \times 10^{ - 29} \frac{{n^2 }}{\mu }[1 \cdot 86 + E_1 (\mu )]Wattcm^{ - 3} $$     

On the mechanisms of formation of excited hydrogen atoms in a decaying helium-hydrogen plasma

We spectroscopically studied the population of the excited hydrogen atomic states with the principal quantum numbers n=3 and 4 in a decaying plasma produced by a pulsed discharge in a mixture of helium (p=40.4 Torr) with a small amount of hydrogen ([H₂]≈10¹² cm^?3). Experiments on recording the response of the spectral line intensities to a short-duration electron temperature perturbation revealed the contribution of electron-ion recombination to the population of the H*(n=3) states in the early afterglow. The ions produced by collisions of hydrogen molecules with metastable He(2³ S ₁) atoms, whose density decreases relatively rapidly with time in the decaying plasma, were assumed to be involved in this process. No population of the H*(n=4) atomic levels due to electron-ion recombination was found. Our experimental results are consistent with the conclusions of previous studies that excitation transfer during collisions of metastable helium molecules with hydrogen molecules plays a major role in the population of the excited hydrogen atomic states both with n=3 and with n=4 during most of the afterglow.     

NQR application to the study of hydrogen dynamics in hydrogen-bonded molecular dimers

The temperature dependences of ¹H NMR as well as ³⁵Cl NQR spin-lattice relaxation times T ₁ were investigated in order to study the hydrogen transfer dynamics in carboxylic acid dimers in 3,5-dichloro- and 2,6-dichlorobenzoic acids. The asymmetry energy A/ k _B and the activation energy V/ k _B for the hydrogen transfer were estimated to be 240 K and 900 K, and 840 K and 2500 K, respectively, for these compounds. In spite of a large asymmetric potential the quantum nature of hydrogen transfer is recognized in the slope of the temperature dependence of T ₁ on the low-temperature side of the T ₁ minimum. The NQR T ₁ measurements was revealed to be a good probe for the hydrogen transfer dynamics.     

Plasma-volume generation of H<Superscript>−</Superscript> ions in a low-voltage xenon-hydrogen discharge. II

A low-voltage xenon-hydrogen discharge is considered theoretically at an interelectrode distance of L = 1 cm and cathode emission current densities of j _s = 2–20 A/cm². Basic parameters of the discharge plasma, in particular, the total hydrogen and xenon densities, are optimized to attain the maximum possible density of negative hydrogen ions \(N_{H^ - } (L)\) at the plasma-anode boundary. The distributions of the plasma parameters over the discharge gap are calculated for optimized regimes. According to calculations, at intermediate cathode emission current densities (j _s ≈ 5–10 A/cm²) in optimized discharge regimes, the density of negative hydrogen ions in the anode region of the plasma is \(N_{H^ - } (L)\) ≈ (1.5–2.5) × 10¹² cm^?3 and the total plasma pressure is p ₀ = 0.5–0.6 Torr.     

X-ray detected magnetic resonance at the Fe K-edge in YIG: Forced precession of magnetically polarized orbital components

X-ray detected magnetic resonance (XDMR) has been measured for the first time on exciting the Fe K-edge in a high-quality yttrium iron garnet film epitaxially grown on a gadolinium gallium garnet substrate. This challenging experiment required resonant pumping of yttrium iron garnet at high microwave power, i.e., in the foldover regime. X-ray magnetic circular dichroism (XMCD) was used to probe the change in the longitudinal component of the magnetization M _Z induced by the precession of magnetic moments located at the iron sites. Since XMCD at the Fe K-edge refers mostly to the equilibrium contribution of magnetically polarized 4p orbital components, XDMR at the Fe K-edge should reflect the precessional dynamics of the latter orbital moments. From the measured precession angle, we show that there is no dynamical quenching of the polarized orbital components at the iron sites in yttrium iron garnet.     

Investigation of the D(<Superscript>3</Superscript>He, <Emphasis Type="Italic">p</Emphasis>)<Superscript>4</Superscript>He Reaction in the Astrophysical Energy Region of 18–30 keV

The D(³He, p)⁴He reaction is first investigated in a solid target of deuterated zirconium (ZrD) in the ³He⁺ ion energy range E_He = 18–30 (E = 7.2?12.0keV keV in the center-of-mass system) with a step of 2 keV. The electron screening potential U_e = (617.8 ± 154.7) eV and the D(³He, p)⁴He reaction enhancement factors are experimentally determined in the given energy range. The measured electron screening potential is six times higher than in gaseous targets. This can be due to the ZrD lattice effects, which have not been studied either theoretically or experimentally so far. The D(³He, p)⁴He reaction has been investigated at the pulsed plasma Hall accelerator (Tomsk).     

Intrinsic and Zn-, Ce-, Tb-, Er-, Sm-, and Eu-Activated photoluminescence of pseudoamorphous GaN and InGaN thin films

Thin films of pseudoamorphous GaN (a-nc-GaN), as well as of its alloys with indium, In_xGa_1−x N (x=0.04, 0.16), were prepared by magnetron sputtering of a metallic target in the plasma of a reactive nitrogen and argon mixture. The a-nc-GaN films were codoped by the Zn acceptor impurity and a set of rare-earth metal (REM) dopants, namely, Ce, Tb, Er, Sm, and Eu. Photoluminescence (PL) spectra excited by a nitrogen laser with wavelength λ=337 nm at room temperature and 77 K were measured for all compositions and a set of impurities. It was shown that the high-energy PL edge of the pseudoamorphous (a-nc) GaN matrix lies at the same energy as that of the crystalline (epitaxial) c-GaN. As in c-GaN, the Zn acceptor impurity stimulates blue luminescence; however, the PL spectrum is substantially more diffuse, with practically no temperature quenching of the PL present. Indium doping in an amount of 16 at. % results in strong PL with a diffuse peak at 2.1–2.2 eV; the PL of the alloy exhibits temperature quenching as high as a factor of three to four in the interval 77–300 K. The decay time of the PL response increases up to 50 μs. RE impurities enter the amorphous GaN host as trivalent ions and produce narrow-band (except Ce) high-intensity spectra, thus indicating both a high solubility of RE impurities in a-nc-GaN and the generation of an effective crystal field (by the GaN anion sublattice) whose local symmetry makes the intracenter f-f transitions partly allowed. __________ Translated from Fizika Tverdogo Tela, Vol. 45, No. 3, 2003, pp. 395–402. Original Russian Text Copyright ? 2003 by Andreev.     

Effect of Nitrogenation and Hydrogenation on the Magnetic Properties and Structure of the Sm<Subscript>2</Subscript>Fe<Subscript>17</Subscript> Alloy: Analysis of XMCD Data

Changes in the local magnetic and structural properties of Sm₂Fe₁₇ alloys at nitrogenation and hydrogenation of samples have been studied by the X-ray magnetic circular dichroism (XMCD) technique at the Fe K absorption edge and Sm L₃ absorption edge using synchrotron radiation. The results have been discussed in comparison with X-ray diffraction data and macroscopic vibration magnetometry measurements. The observed changes in XMCD spectra indicate a noticeable effect of nitrogenation on the local magnetic properties of sublattices of both iron and samarium, whereas hydrogenation of samples makes a small effect. The mentioned effects have been analyzed and discussed in terms of the effect of nitrogen (N) and hydrogen (H) interstitial atoms on Sm 5d and Fe 4p electronic states. The effect of nitrogenation is larger than the effect of hydrogenation because the volume expansion of the crystal lattice of initial Sm₂Fe₁₇ in the case of nitrogenation is larger than that in the case of hydrogenation. The studied local magnetization curves for samarium and iron sublattices in magnetic fields up to 17 T also indicate a strong increase in the magnetocrystalline anisotropy at nitrogenation.     

Synthesis,structure, and properties of BIFENBVOX

Solid solutions Bi₄V_2-x Fe _x/2Nb _x/2O_11-δ (х?=?0.05–1.0) and Bi₄V_2-х-y Fe _x Nb _y O_11–δ (with fixed x or y?=?0.2 and variable х or y?=?0.2–0.5 with step 0.1) were synthesized by the standard ceramic technology in the temperature range 773–1113 K and by mechanochemical activation method using Bi₂O₃, V₂O₅ Fe₂O₃, and Nb₂O₅ oxides as initial compounds. The formation of solid solutions was studied. Ranges of stability and temperature values of phase transitions for different polymorphous modifications were defined using dylatometric and thermo gravimetric studies. The morphology and the local chemical composition of the ceramic samples were studied. Samples with concentration of dopants x?>?0.3 contain two phases; both major and impurity phases are solid solutions of the BIFENBVOX type although the dopants atoms distribution between them is random. The thermal expansion coefficients (TEC) were measured. The electrical conductivity of ceramic samples was investigated in a wide range of temperatures. The highest conductivity values among the studied solid solutions are observed for the sample with a small amount of dopants x?=?0.25.     

Theory of the muonic hydrogen-muonic deuterium isotope shift

Corrections of the α³, α⁴, and α⁵ orders are calculated for the Lamb shift of the 1S and 2S energy levels of muonic hydrogen μp and muonic deuterium μd. The nuclear structure effects are taken into account in terms of the charge radii of the proton r _p and deuteron r _d for one-photon interaction, as well as in terms of the electromagnetic form factors of the proton and deuteron for the case of one-loop amplitudes. The μd-μp isotope shift for the 1S-2S splitting is found to be equal to 101003.3495 meV, which can be treated as a reliable estimate when conducting the corresponding experiment with an accuracy of 10^?6. The fine-structure intervals E(1S)-8E(2S) in muonic hydrogen and muonic deuteron are calculated.     

Tests of discrete symmetries with the neutral kaon system at the KLOE and KLOE-2 experiments

The KLOE-2 experiment continues and extends the program of its predecessor KLOE in the field of discrete symmetry tests with the K meson system, among other studies which comprise light meson spectroscopy, dark matter searches and γγ physics. Together, KLOE and KLOE-2 have recorded the largest sample (almost 8 fb^??1) of e⁺e^? collisions at the energy equal to ? meson mass, amounting to 2.4 × 10¹⁰ of produced ? mesons. We report on the latest results and ongoing analyses of KLOE and KLOE-2 concerning discrete symmetry tests and measurements of symmetry-violating observables. A measurement of the CPT violation sensitive asymmetry in semileptonic decays of K˙S with 1.7 fb^??1 of KLOE data will be presented, which improves the sensitivity w.r.t. previous measurements about twice. Moreover, status of direct tests of T and CPT in transitions of neutral kaons performed with the ? →K˙SK˙L → πeν, 3π⁰(2π) processes will be reported, followed by the search of the CP-violating decay K˙S → 3π⁰ using the data recently acquired by KLOE-2.     

Zur Erniedrigung des Sättigungsmoments von Nickel durch chemisorbierten Wasserstoff

The decrease of the magnetic saturation moment of superparamagnetic nickel particles of 30 Å radius by hydrogenation was investigated, and proved to be?=0.72 Bohr magnetons per hydrogen atom chemisorbed. This is the same amount that has been reported byDietz andSelwood for 64 Å particles. From this the conclusion may be drawn that most probably the effect does not depend on particle size. Interpreting the result in Pauling’s model of the covalent bond, one may conclude the Ni-H-chemisorption bond to have about 14% ionic character. This seems reasonable in view of the difference in electronegativity between hydrogen and nickel surface, but one of the assumptions of the model seems to be not safely fulfilled as will be discussed. On the other hand one may conceive chemisorption to be the first step towards formation of nickel hydride at the particle surface. Doing so, the comparison of the found result for? with recent experiments on thick nickel films electrolytically loaded with hydrogen yields a satisfactory result.     

High-temperature dynamic behavior in bulk liquid water: A molecular dynamics simulation study using the OPC and TIP4P-Ew potentials

Classical molecular dynamics simulations were performed to study the high-temperature (above 300 K) dynamic behavior of bulk water, specifically the behavior of the diffusion coefficient, hydrogen bond, and nearest-neighbor lifetimes. Two water potentials were compared: the recently proposed “globally optimal” point charge (OPC) model and the well-known TIP4P-Ew model. By considering the Arrhenius plots of the computed inverse diffusion coefficient and rotational relaxation constants, a crossover from Vogel–Fulcher–Tammann behavior to a linear trend with increasing temperature was detected at T* ≈ 309 and T* ≈ 285 K for the OPC and TIP4P-Ew models, respectively. Experimentally, the crossover point was previously observed at T* ± 315–5 K. We also verified that for the coefficient of thermal expansion α _P (T, P), the isobaric α _P (T) curves cross at about the same T* as in the experiment. The lifetimes of water hydrogen bonds and of the nearest neighbors were evaluated and were found to cross near T*, where the lifetimes are about 1 ps. For T < T*, hydrogen bonds persist longer than nearest neighbors, suggesting that the hydrogen bonding network dominates the water structure at T < T*, whereas for T > T*, water behaves more like a simple liquid. The fact that T* falls within the biologically relevant temperature range is a strong motivation for further analysis of the phenomenon and its possible consequences for biomolecular systems.     

Eigenschaften der Lösungen der nichtlinearisierten Ginsburg-Landau-Gleichungen in Zylindersymmetrie

Solutions of the nonlinear Ginzburg-Landau equations in cylindrical symmetry have been computed for a type I superconductor. From these solutions the behaviour of a circular cylinder of infinite length in a magnetic field parallel to its axis has been deduced. For a series of values of the magnetic field solutions are given in two cases. The first case was calculated with the assumption of no fluxoid frozen in (fluxoid quantum number n=0), whereas in the second case a vortex with fluxoid quantum numbern=1 was assumed on the axis of the cylinder. For both series of solutions investigation of the thermodynamic stability was carried out. This and further thermodynamic considerations led to the result that in a gedankenexperiment the transition from the normal to the superconducting state and vice versa can be performed in a reversible manner. The expulsion of the magnetic field from the sample during the reversible transition to the superconducting state (Meissner-Effect) is also described by the solutions. Further results are the existence of a supercooled state down to a magnetic fieldH _c2=κ√2H_cb and of a superheated state up to a fieldH _c1>H _cb. The value ofH _c1 depends on the radius of the cylinder. If a condensation to the superconducting state takes place at a fieldH ₀ whereH _c2<H ₀<H _cb, condensation withn=0 seems to be preferred in comparison to that withn=1.     

Nuclear-structure corrections to the energy spectra of ordinary and muonic deuterium

One-loop nuclear-structure-induced corrections of order (Zα)⁵ to the Lamb shift and to the hyperfine structure of deuterium are calculated. The contribution of deuteron-structure effects to the (ep)-(ed) and (μp)-(μd) isotopic shifts for the 1S–2S splitting is obtained with the aid of modern experimental data on the electromagnetic form factors for the deuteron. A comparison with the analogous contributions to the Lamb shift for ordinary and muonic hydrogen shows that the relative contribution of corrections associated with the nuclear structure increases as we go over from the hydrogen to the deuterium atom owing to the growth of the nuclear size.     

Hydrogen solubility in amorphous Mg<Subscript>0.6</Subscript>SiO<Subscript>2.6</Subscript> at high pressure

The solubility of hydrogen in amorphous Mg_0.6SiO_2.6 at a temperature of 250°C and pressures up to 75 kbar is studied using a quenching technique. The molar ratio H₂/formula unit is found to nonlinearly increase with pressure from x = 0.12 at P = 10 kbar to x = 0.303 at P = 75 kbar. An investigation of the quenched samples by Raman spectroscopy demonstrated that hydrogen dissolves in amorphous Mg_0.6SiO_2.6 in the form of H₂ molecules. X-ray diffraction and Raman studies showed that the hydrogenation of the samples is likely to be accompanied by a phase transition in the amorphous lattice of Mg_0.6SiO_2.6 at P ≈ 52.5 kbar to a denser amorphous modification.     

Anisotropy of the magnetoresistive properties of granular high-temperature superconductors resulting from magnetic flux compression in the intergrain medium

To elucidate the origin of the well-known anisotropy of the magnetoresistive properties of granular high-temperature superconductors (HTSs), which is related to the mutual orientation of magnetic field H and transport current j, we investigate the hysteretic dependences of magnetoresistance R(H) of the yttrium HTS sample at the perpendicular (H ⊥ j) and parallel (H || j) configurations. The hysteretic R(H) dependences are analyzed using the concept of the effective field in the intergrain boundaries through which superconducting current carriers tunnel. The effective degree of magnetic flux compression in the intergrain medium at the perpendicular configuration was found to be twice as much as at the parallel one. This approach explains well the anisotropy of the magnetoresistive properties of granular HTSs, which was previously reported by many authors, and the temperature dependences of the resistance in the resistive transition region.