Isotope effect in electron capture by protons into the 2S-state of hydrogen

We have investigated the isotope effect for electron capture into the 2S-state of hydrogen in close collisions for the processes H⁺ in H₂ and H⁺ in D₂. The differential cross sections and transition probabilities P_2S obtained for capture into H(2S) as a function of energy at a fixed angle of θ = 1° exhibit distinctive features, but no apparent isotope effects are detected.     

Absolute coverage measurements of deuterium on Ni (110)

The absolute coverage of deuterium adsorbed on Ni(110) at temperatures below 170 K to the formation of a (1 × 2) LEED pattern has been determined by nuclear microanalysis (NMA). The result, θ_D = 0.96 ± 0.08, is consistent with a saturation coverage of one full monolayer. Heating the crystal above ～ 190 K is shown to result in a gradual loss of deuterium from the system, accompanied by streaking of the LEED pattern, with complete desorption above ～ 340 K. The low-temperature (2 × 1)-D phase was found to correspond to θ_D = 0.64 ± 0.05 monolayers. The results are expected to be valid also for the equivalent phases obtained by hydrogen adsorption.     

Ordered oxygen overlayers on Cr(100) observed by leed and photoemission

Chemisorbed oxygen atoms on Cr(100) induce strong O(2p) derived surface resonances which are studied by angle resolved photoemission. Well ordered structures are observed after annealing (300°C). In the submonolayer range (θ_O < 1) a study of the symmetry and dispersion of the O(2p) derived features shows the two-dimensional Bloch character associated with either a c(2 × 2)-O surface at low coverages (θ_O?0.25) or a (1 × 1)-O structure at high coverages (θ_O?0.9). When combined with LEED observations and work function data this study indicates that both structures coexist around θ_O = 0.5 and chemisorbed oxygen is probably incorporated into the fourfold hollow sites. At θ_O > 1, the onset of oxidation is clearly shown in the valence band and core level spectra and the data support the existence of a thin spinel-like oxide layer.     

EFFECT OF ATOMIC HYDROGEN ON THE ACETYLENE-ADSORBED Si(100)(2×1) SURFACE AT ROOM TEMPERATURE

High resolution electron energy loss spectroscopy, low energy electron diffraction and quadrupole maas spectrometer (QMS) have been employed to study the effect of atomic hydrogen on the acetylene-saturated pre-adsorbed Si(100)(2×1) surface and the surface phase transition at room temperature. It is evident that the atomic hydrogen has a strong effect on the adsorbed C₂H₂ and the underlying surface structure of Si. The experimental results show that CH and CH₂ radicals co-exist on the Si surface after the dosing of atomic hydrogen; meanwhile, the surface structure changes from Si(100)(2×1) to a dominant of (1×1). These results indicate that the atomic hydrogen can open C=C double bonds and change them into C-C single bonds, transfer the adsorbed C₂H₂ to C₂H_x(x = 3,4) and break the underlying Si-Si dimer, but it cannot break the C-C bond intensively. The QMS results show that some C₄ species axe formed during the dosing of atomic hydrogen. It may be the result of atomic hydrogen abstraction from C₂H_x which leads to carbon catenation between two adjacent C-C directs. The C₄ species formed are stable on Si(100) surfaces up to 1100 K, and can be regarded as the potential host of diamond nucleation.     

Hydrogen-induced reconstruction of the W(100) surface,studied by surface core level spectroscopy

We report W(4?) surface core level shifts which yield new information on the energetics of the W(100) (1 × 1) → C(2 × 2)H phase transition. At small hydrogen coverages we find two co-existing surface core levels from atoms on normal lattice sites and from atoms in reconstructed domains. These surface levels are shifted to smaller binding energy (toward E_F) by 0.35 eV and 0.13 eV relative to the bulk level, respectively. The most stable configuration is obtained at a fractional coverage θ_H ? 0.2, at which all surface atoms are shown to be paired with neighboring atoms in the surface plane.     

Oxidation of ethylene on Pd(100); bonding of ethylene and scavenging of dehydrogenation fragments by surface oxygen

The adsorption and reaction of C₂H₄ on oxygen covered Pd(100) was studied with high resolution electron energy loss spectroscopy (EELS) and temperature programmed reaction spectroscopy (TPRS). The clean Pd(100) surface at 300 K was exposed to O₂ to produce atomic oxygen in the p(2×2) structure for coverages between 0.05 and 0.25. The EELS and TPRS measurements were conducted following saturation coverage of the oxygen covered surface by C₂H₄ at 80 K. Both the di-σ- and π-bonded forms of C₂H₄ were stable on the surface for θ_O less than 0.25. The π-bonded form desorbed without reaction between 100 and 300 K, but the di-σ-bonded form underwent dehydrogenation above 250 K. The C₂H₄ dehydrogenation products were reactive towards atomic oxygen and produced H₂, H₂O, CO, CO₂, and adsorbed C. Oxygen preadsorption inhibited C₂H₄ Oxidation by limiting the formation of di-σ-bonded C₂H₄, and the fully developed p(2×2)O overlayer, corresponding to θ_O = 0.25, was sufficient to block completely the reaction of ethylene. The extent of reaction decreased in a 2:1 ratio to the increase in oxygen coverage, and indicated that oxygen islands blocked C₂H₄ dissociation. Only the π-bonded form of C₂H₄ was stable on the surface for θ_O greater than 0.25; the saturation coverage of π-bonded C₂H₄ of 0.25 was the same as for clean Pd(100).     

The ground state of molecular hydrogen

The v = 0?0 quadrupole spectrum of H₂ has been recorded using a 0.005-cm^?1 resolution Fourier transform spectrometer. The rotational lines S(1) through S(5) are observable in the spectra, in the region 587 to 1447 cm^?1. The spectral position for S(0) was also obtained from its v = 1-0 ground-state combination difference. The high accuracy of the H₂ measurements has permitted a determination of four rotational constants. These are (in cm^?1) B₀ = 59.33455(6); D₀ = 0.045682(4); H₀ = 4.854(12) × 10^?5; L₀ = ?5.41(12) × 10^?8. The hydrogen line positions will facilitate studies of structure and dynamics in astrophysical objects exhibiting infrared H₂ spectra. The absolute accuracy of frequency calibration over wide spectral ranges was verified using 10-μm CO₂ and 3.39-μm CH₄ laser frequencies. Standard frequencies for 5-μm CO were found to be high by 12 MHz (3.9 × 10^?4 cm^?1).     

High-precision evaluation of the magnetic moment of the helion

NMR spectra of samples containing a mixture of hydrogen deuteride HD with pressure of about 80 atm and helium-3 with partial pressure of about 1 atm are analyzed. The ratio of the resonance frequencies of the nuclei, F(³He)/F(H₂), is determined to be 0.761786594(2), which is equal to the magnetic moment of the helion (bound in a helium atom) in the units of the magnetic moment of a proton (bound in molecular hydrogen). The uncertainty of two digits in the last place corresponds to a relative error of ??[F(³He)/F(H₂)] = 2.6 × 10^?9. The use of the known calculated data on the shielding of nuclei in the helium-3 atom (??(³He) = 59924(2) × 10^?9) and on the shielding of protons in hydrogen (??(H₂) = 26288(2) × 10^?9) yields a value of ??(³He)/?? _p = ?0.761812217(3) for the free magnetic moment of the helion in the units of the proton magnetic moment.     

Chemisorption of CO on the unreconstructed Pt(100) surface

The chemisorption of CO on the clean, unreconstructed Pt(100)-1 × 1 surface was investigated by LEED and XPS. Three LEED patterns, c(2 × 2), (√2 × 3√2) R45° and c(4 × 2), were observed with increasing CO exposure and structure models corresponding to these LEED patterns were proposed. The absolute coverage of CO was determined by combining the O(1s) XPS data with coverage information derived from LEED. The maximum CO coverage thus obtained was θ = 0.75 and the initial sticking coefficient was determined to be s₀ = 0.6. This coverage calibration can also be utilized for other oxygen containing molecules by comparing the corresponding O(1s)it peak intensities.     

Anomalous coverage behavior of the CsAg distance on CsAg(110)

The position of Cs on the (1 × 2) missing row reconstructed Ag(110) surface was determined by X-ray diffraction for two different Cs-coverages: θ_Cs = 0.2 and θ_Cs = 0.3. The Cs was found to be adsorbed in incommensurate chains in the troughs of the missing row with an average adsorption height of 1.7 Å (θ_Cs = 0.2) and 1.4 Å (θ_Cs = 0.3) above the topmost Ag layer. The apparent contradiction to the classical picture of alkali adsorption, which expects an increase of the Cs adsorption height with coverage, might be partly resolved by introducing a fraction of commensurately adsorbed Cs at θ_Cs = 0.2.     

Phase diagram of oxygen on Ni(100)

We have studied the coverage-temperature phase diagram of chemisorbed oxygen on Ni(100) with LEED and AES. We find that the oxygen p(2 × 2) structure undergoes a nearly reversible order- disorder phase transition for coverages between 0.15 and 0.30 monolayer (T_c ≈ 560 K for θ = 0.25). For these coverages, it is also found that the chemisorbed oxygen begins dissolving into the bulk nickel as the overlayer disorders. A reversible order-disorder transition is not seen for the oxygen c(2 × 2) structure, but there is evidence that bulk dissolution here also occurs coincident with the overlayer disordering.     

Quark masses and cabibbo angles

A simple symmetric pattern of Higgs fields in an SU (2)_L × SU (2)_R × U (1) gauge model with six quarks yields: tan²θ_c = m_d/m_s and θ_c = 15° in good agreement with experiment. A eight-quark extension of the model leads to successful determination of the three Cabibbo-like angles connecting the first six quarks and to the prediction m_t ～ 9.3 m_c ～ 14 GeV.     

Chemisorption of H2 on W(100): Absolute sticking probability,coverage, and electron stimulated desorption

Measurements of both the absolute sticking probability near normal incidence and the coverage of H₂ adsorbed on W(100) at ~ 300K have been made using a precision gas dosing system; a known fraction of the molecules entering the vacuum chamber struck the sample crystal before reaching a mass spectrometer detector. The initial sticking probability S₀ for H₂/W(100) is 0.51 ± 0.03; the hydrogen coverage extrapolated to S = 0 is 2.0 × 10¹⁵ atoms cm^?2. The initial sticking probability S₀ for D₂/W(100) is 0.57 ± 0.03; the isotope effect for sticking probability is smaller than previously reported. Electron stimulated desorption (ESD) studies reveal that the low coverage β₂ hydrogen state on W(100) yields H⁺ ions upon bombardment by 100 eV electrons; the ion desorption cross section is ~ 1.8 × 10^?23 cm². The H⁺ ion cross section at saturation hydrogen coverage when the β₁ state is fully populated is ? 10^?25 cm². An isotope effect in electron stimulated desorption of H⁺ and D⁺ has been found. The H⁺ ion yield is ? 100 × greater than the D⁺ ion yield, in agreement with theory.     

The temperature dependence of the angular variation of,and the critical point exponent for the EPR linewidth in the two-dimensional canted antiferromagnetic (C2H5NH3)2MnBr4: Evidence for a structural phase transition

The angular variation of the EPR linewidths in single crystals of (C₂H₅NH₃)₂MnBr₄ has been measured as a function of temperature. The angular dependence is well characterized by δH(θ) = a + b(3 cos²θ ? 1) + c(3 cos²θ ? 1)². The temperature dependence of the expansion coefficients is reported, and the effect of critical point fluctuations near the Néel temperature as well as a linear temperature dependence at high temperature are observed. A sharp decrease in linewidths at 160°K is attributed to a structural phase transition. The Néel temperature is determined to be 46°K (± 1°) from linewidth measurements of a powder sample. The linewidths diverge exponentially near the Néel temperature with a critical point exponent of 1.5.     

Adsorption and reaction of bromine with Ag(110)

The adsorption and reaction of Br₂ with Ag(110) was studied with Auger electron spectroscopy, LEED, work function measurements and thermal desorption spectroscopy in the temperature range of 130–1000 K. Depending on Br coverage and crystal temperature, four different adsorption and reaction states could be detected. For fractional monolayer coverages, chemisorbed Br(ad) is found to be the most stable species. This adsorption state saturates for θ(Br) ? 0.75. In the chemisorption stage, two LEED patterns, a p(2 × 1) with θ(Br) ? 0.5 and a c(4 × 2) with θ(Br) ? 0.75, were observed. For higher Br₂ exposures and T = 130 K a layer-by-layer growth of AgBr is detected. At higher temperature, T > 190 K, there is evidence for a transformation from a 2D growth mechanism of AgBr into a 3D agglomeration of larger AgBr cluster. Molecularly adsorbed.     

The clean thermally induced W {001} (1 × 1) → (√2 × √2) R 45° surface structure transition and its crystallography

A (√2 × √2)R45° surface structure on W {001} produced only by cooling below ~370 K, first reported by Yonehara and Schmidt, has been investigated by LEED, AES, work function change, characteristic loss and low energy Auger fine structure measurements. No significant changes at any energy up to 520 eV occur in the standard Auger spectrum upon cooling to 220 K for as long as 30 min after a flash to >2 500 K. The work function of the (√2 × √2) R45° at 210 K is 20 ± 10 mV below that of the (1 × 1) surface, and a sensitive feature in the fine structure of the N₇VV AES transition shows approximately 60% attenuation. Unlike for H₂ adsorption, the “surface plasmon” loss peak exhibits little if any measurable attenuation and no measurable shift in energy as the crystal cools to form the (√2 × √2)R45°. The rate of intensity buildup in the $\text{1}\text{2}$-order LEED beams is strictly temperature dependent, and significant differences exist between the $\text{1}\text{2}$-order LEED spectra produced by cooling and those produced by H₂ adsorption. Only 2-fold symmetry was observed in the LEED beam intensities at exactly normal incidence, rather than 4-fold as expected for statistically equal numbers of rotationally equivalent domains. The LEED I-V spectra for 24 fractional order beams and 12 integral order beams, taken over large energy ranges at normal incidence, clearly establish that the beam intensities display 2 mm point group symmetry, and hence a preference of one domain orientation over the other. No beam broadening or splitting effects were apparent, implying only incoherent scattering from the various domains. The half-order beam spectra (±h/2, ±h/2) are identical in relative intensity to the (±h/2, ±h/2) spectra but different in absolute intensity by a constant factor, which can be explained only by domains with p2mg space group symmetry rather than just p2mm. Adsorption of H₂ onto the cooled (√2 × √2)R45° structure restores the 4-fold symmetry in the LEED beam intensities at normal incidence, giving a c(2 × 2) hydrogen structure, the same as when adsorbing H₂ onto the above room temperature (1 × 1) crystal. This strongly supports the observed p2mg symmetry as being a true property of the cooled (√2 × √2)R45° surface structure. These results show that the (1 × 1) → (√2 × √2) R45° transition produced by cooling is a transition involving displacement of surface W atoms, and that it apparently can be characterized as an order-order, second degree, homogeneous nucleation process, which is strongly prohibited by the presence of impurities or defects.     

Overview on neutrinos and the Daya Bay experiment

Neutrinos are elementary particles in the Standard Model. Neutrino oscillation is a quantum mechanical phenomenon beyond the Standard Model. Neutrino oscillation can be described by two independent mass-squared differences Δm ₂₁ ² , Δm ₃₁ ² (or Δm ₃₂ ² ) and a 3 × 3 unitary matrix, containing three mixing angles θ ₁₂, θ ₂₃, θ ₁₃, and one charge-parity (CP) phase. θ ₁₂ is about 34° and determined by solar neutrino experiments and the reactor neutrino experiment KamLAND. θ ₂₃ is about 45° and determined by atmospheric neutrino experiments and accelerator neutrino experiments. θ ₁₃ can be measured by either accelerator or reactor neutrino experiments. On Mar. 8, 2012, the Daya Bay Reactor Neutrino Experiment reported the first observation of non-zero θ ₁₃ with 5.2 standard deviations. In June, with 2.5× previous data, Daya Bay improved the measurement of sin²2θ ₁₃ = 0.089 ± 0.010(stat) ± 0.005(syst).     

Structure of ZnZrF<Subscript>6</Subscript> · <Emphasis Type="Italic">n</Emphasis>H<Subscript>2</Subscript>O (<Emphasis Type="Italic">n</Emphasis> = 6–2) and ZnZrF<Subscript>6</Subscript> crystallohydrates according to vibrational spectroscopy data

Fluoridezirconate crystallohydrates ZnZrF₆ · nH₂O (n = 6–2) and anhydrous ZnZrF₆ are investigated by vibrational spectroscopy and thermography. The influence of the hydrate number on the structure of the cationic and anionic sublattices of the crystallohydrates is studied. The changes in the strength of HOH···F and HOH···O hydrogen bonds of coordinated and outer-sphere water molecules occurring with variations in the hydrate number are determined by changes in the IR spectra. The IR spectra of ZnZrF₆ · nH₂O (n =6, 4) compounds, which have isolated complex anions [ZrF₆]^2– in their structure, revealed a band with two peaks in the range of 3470–3430 cm^–1, which corresponds to stretching vibrations of coordinated water molecules. The spectra of ZnZrF₆ · nH₂O (n = 5, 3, 2, 1) crystallohydrates with a polymeric structure show a high-frequency shift of this band, which corresponds to weakening of hydrogen bonds. The vibrations of crystallization water molecules involved in the network of strong O–H···F and O–H···O hydrogen bonds manifest themselves in the spectra of ZnZrF₆ · nH₂O (n =5, 3) crystallohydrates by broad structureless bands in the region of stretching, bending, and libration vibrations.     

Adsorption of carbon monoxide,oxygen, hydrogen,nitrogen, ethylene and benzene on an iridium (110) surface; Correlation with other iridium crystal faces

The interaction of CO, O₂, H₂, N₂, C₂H₄ and C₆H₆ with an Ir(110) surface has been studied using LEED, Auger electron spectroscopy and flash desorption mass spectroscopy. Adsorption of oxygen at 30°C produces a (1× 2) structure, while a c(2 × 2) structure is formed at 400°C. Two peaks have been detected in the thermal desorption spectrum of oxygen following adsorption at 30°C. The heat of adsorption of hydrogen is slightly higher on Ir(110) than on Ir(111). Adsorption of carbon monoxide at 30°C produces a (2 × 1) surface structure. The main CO desorption peak is found around 230, while two other desorption peaks are observed around 340 and 160°C. At exposures between 250 and 500°C carbon monoxide adsorption yields a c(2 × 2) structure and a desorption peak around 600°C. Carbon monoxide is adsorbed on an Ir(110) surface partly covered with oxygen or carbon in a new binding state with a significantly higher desorption temperature than on the clean surface. Adsorption of nitrogen could not be detected on either clean or on carbon covered Ir(110) surfaces. The hydrocarbon molecules do not form ordered surface structures on Ir(110). The thermal desorption spectra obtained after adsorption of C₆H₆ or C₂H₄ are similar to those reported previously for Ir(111) consisting mostly of hydrogen. Heating the (110) surface above 700°C in the presence of C₆H₆ or C₂H₄ results in the formation of an ordered carbonaceous overlayer with (1 × 1) structure. The results are compared with those obtained previously on the Ir(111) and Ir(755) or stepped [6(111) × (100)] surfaces. The CO adsorption results are discussed in relation to data on similar surfaces of other Group VIII metals.