异氰酸分子NH(a1Δ)+CO(X1Σ+)通道在193nm的离子成像光解动力学研究

The photodissociation dynamics of isocyanic acid (HNCO) has been studied by the timesliced velocity map ion imaging technique at 193 nm. The NH(a¹Δ) products were measured via (2+1) resonance enhanced multiphoton ionization. Images have been accumulated for the NH(a¹Δ) rotational states in the ground and vibrational excited state (v=0 and 1). The center-of-mass translational energy distribution derived from the NH(a¹Δ) images implies that the CO vibrational distributions are inverted for most of the measured ¹NH(v|j) internal states. The anisotropic product angular distribution observed indicates a rapid dissociation process for the N-C bond cleavage. A bimodal rotational state distribution of CO(v) has been observed, this result implies that isocyanic acid dissociates in the S₁ state in two different pathways.     

二氧化碳分子离子经由Ã2Πu1/2电子态振动能级共振的光解动力学：一项时间切片离子速度成像技术研究

We report on the photodissociation dynamics of CO₂⁺ via its òΠ_u,1/2 state using the scheme of [1+1] photon excitation that is intermediated by the mode-selected òΠ_u,1/2( u1,u2,0) vibronic states. Photodissociation fragment exciation spectrum and images of photofragment CO⁺ have been measured to obtain reaction dynamics parameters such as the available energy and the average translational energy. Combining with the potential energy functions of CO₂⁺, the dissociation mechanism of CO₂⁺ is discussed. The conformational variation of CO₂⁺ from linear to bent on the photodissociation dynamics of CO₂⁺ is verified.     

Feshbach resonances in an ultracold mixture of 87Rb and 40K

We report the experimental preparations of the absolute ground states of ⁸⁷Rb and ⁴⁰K atoms (| F=1, m_F=1,〉+ |F=9/2, m_F=-9/2,〉) by means of the radio-frequency and microwave adiabatic rapid passages, and the observation of magnetic Feshbach resonances in an ultracold mixture of bosonic ⁸⁷Rb and fermionic ⁴⁰K atoms between 0 T and 6.0 × 10^-2 T, including 7 homonuclear and 4 heteronuclear Feshbach resonances. The resonances are identified by the abrupt trap loss of atoms induced by the strong inelastic three-body collisions. These Feshbach resonances should enable the experimental control of interspecies interactions.     

Investigations of spectroscopic parameters and molecular constants for X1Σg+, w3Δu, and W1Δu electronic states of P2 molecule

The potential energy curves (PECs) of three low-lying electronic states (X¹Σ_g⁺, w³Δ_u, and W¹Δ_u)of P₂ molecule are investigated using the full valence complete active space self-consistent field (CASSCF) method followed by the highly accurate valence internally contracted multireference configuration interaction (MRCI) approach in conjunction with the correlation-consistent basis set in the valence range. The PECs of the electronic states involved are modified by the Davidson correction and extrapolated to the complete basis set (CBS) limit. With these PECs, the spectroscopic parameters of the three electronic states are determined and compared in detail with the experimental data. The comparison shows that excellent agreement exists between the present results and the available experimental data. The complete vibrational states are computed for the w³Δ_u, and W¹Δ_u electronic states when the rotational quantum number J equals zero and the vibrational level G(v), the inertial rotation constant B_v, and the centrifugal distortion constant D_v of the first 30 vibrational states are reported, which accord well with the experimental data. The present results show that the two-point extrapolation scheme can obviously improve the quality of spectroscopic parameters and molecular constants.     

OCS在217 nm的光解动力学研究

The S(¹D₂)+CO(X¹Σ⁺) product channel from photodissociation of OCS at 217 nm has been measured using the DC slice velocity map imaging (VMI) technique in combination with resonance enhanced multiphoton ionization (REMPI). Two diflerent REMPI intermediate states (¹F₃ and ¹P₁) and several pump-probe laser polarization geometries are used to detect the angular momentum polarization of the photofragmented S(¹D₂). The molecular- frame polarization parameters, as well as the laboratory-frame anisotropy parameters, for individual rotational states of co-fragment CO, are determined using two diflerent full quantum theories. The measured total kinetic energy release spectrum from photodissociation of OCS indicates two dissociation channels, corresponding to the fast and slow recoiling velocities of S(¹D₂), respectively. The slow channel is concluded to originate from an initial photoexcitation to the A(¹A'') state, followed by a non-adiabatic transition to the ground state. The fast channel is found to follow a coherent excitation to A(¹A'') and B(¹A'') states, where contributions of the two states are almost equal at 217 nm. The determined alignment and anisotropy parameters further indicate that the slow channel follows an incoherent excitation, while the fast channel follows a coherent excitation to A(¹A'') and B(¹A'') states with a phase di erence of π/2.     

1-戊基的紫外光解动力学

The ultraviolet (UV) photodissociation of jet-cooled 1-pentyl radical is investigated in the wavelength region of 236-254 nm using the high-n Rydberg-atom time-of-flight (HRTOF) technique. The H-atom photofragment yield spectrum of the 1-pentyl radical shows a broad UV absorption feature peaking near 245 nm, similar to the 2p_z→3s absorption bands of ethyl and n-propyl. The center-of-mass translational energy distribution, P(E_T), of the H+C₅H₁₀ product channel is bimodal, with a slow peak at~5 kcal/mol and a fast peak at~50 kcal/mol. The fraction of the average translational energy release in the total available energy, 〈f_T〉, is 0.30, with those of the slow and fast components being 0.13 and 0.58, respectively. The slow component has an isotropic product angular distribution, while the fast component is anisotropic with an anisotropy parameter~0.4. The bimodal translational energy and angular distributions of the H+C₅H₁₀ products indicate two H-atom elimination channels in the photodissociation of 1-pentyl:(i) a direct, prompt dissociation from the electronic excited state and/or the repulsive part of the ground electronic state potential energy surface; and (ii) a unimolecular dissociation of internally hot radical in the ground electronic state after internal conversion from the electronic excited state.     

1,3,4-噁二唑环金属配体的磷光型铱阳离子配合物:溶剂相关的激发态动力学研究

To elucidate the nature of low-lying triplet states and the effect of ligand modifications on the excited-state properties of functional cationic iridium complexes,the solventdependent excited-state dynamics of two phosphorescent cationic iridium (III) complexes,namely[Ir (dph-oxd)₂(bpy)]PF₆(1) and[Ir (dph-oxd)₂(pzpy)]PF₆(2),were investigated by femtosecond and nanosecond transient absorption spectroscopy.Upon photoexcitation to the metal-to-ligand charge-transfer (MLCT) states,the excited-state dynamics shows a rapid process (τ=0.7-3 ps) for the formation of solvent stabilized ³MLCT states,which significantly depends on the solvent polarity for both 1 and 2.Sequentially,a relatively slow process assigned to the vibrational cooling/geometrical relaxation and a long-lived phosphorescent emissive state is identified.Due to the different excited-state electronic structures regulated by ancillary ligands,the solvation-induced stabilization of the ³MLCT state in 1 is faster than that in 2.The present results provide a better sight of excited-state relaxation dynamics of ligand-related iridium (III) complexes and solvation effects on triplet manifolds.     

boldmath B3Σu-–X3Σg- transition in selenium dimer: ab initio multireference configuration interaction calculations

Theoretical investigation of low-lying electronic states and B³Σ_u^-–X³Σ_g^- transition properties of selenium dimer using size-extensivity singly and doubly excitation multireference configuration interaction theory with nonrelativistic all-electron basis set and relativistic effective core potential plus its split valence basis set is presented in this paper. The spectroscopic constants of ten low-lying Λ-S bound states have been obtained and compared with experiments. Spin-orbit calculations for coupling between B³Σ_u^- sates and repulsive ¹Π_u, ⁵Π_u states have been made to interpret the predissociation mechanisms of the B³Σ_u^- state. The lifetimes of B³Σ_u^- (v=0～6) have been calculated with scalar relativistic effects included or excluded, respectively, and reasonably agree with experimental values.     

Role of Ga-doping in ironben gallium alloy clusters

The structural and magnetic properties of Fe_n-mGa_m (n=3～6, m=0～2; n=13, m=0～3) alloy clusters have been studied using density functional theory. The substitutional doping is favourable for small clusters with up to six atoms at low Ga concentration and substitutional Ga atoms in 13-atom clusters prefer surface sites. The Ga-doping generally could reduce the energetic stability but enhance the electronic stability of Fe clusters, along with a decrease of the local magnetic moments of Fe atoms around Ga dopants. These findings provide a microscopic insight into Fe-Ga alloys which are well-known magnetostriction materials.     

活化气氛对钼基合成醇催化剂的结构和性能的影响

Activated carbon supported Mo-based catalysts were prepared and reduced under different activation atmospheres, including pure H₂, syngas (H₂/CO=2/1), and pure CO. The catalysts structures were characterized by X-ray diffraction, X-ray absorption fine structure, and in situ diffuse reflectance infrared Fourier transform spectroscopy. The catalytic performance for the higher alcohol synthesis from syngas was tested. The pure H₂ treatment showed a high reduction capacity. The presence of a large amount of metallic Co⁰. and low valence state Mo^φ+ (0<φ<2) on the surface suggested a super activity for the CO dissociation and hydrogenation, which promoted hydrocarbons formation and reduced the alcohol selectivity. In contrast, the pure CO-reduced catalyst had a low reduction degree. The Mo and Co species at the catalyst mainly existed in the form of Mo⁴⁺ and Co²⁺. The syngas-reduced catalyst showed the highest activity and selectivity for the higher alcohols synthesis. We suggest that the syngas treatment had an appropriate reduction capacity that is between those of pure H₂ and pure CO and led to the coexistence of multivalent Co species as well as the enrichment of Mo^δ+ on the catalyst''s surface. The synergistic effects between these active species provided a better cooperativity and equilibrium between the CO dissociation, hydrogenation and CO insertion and thus contributed beneficially to the formation of higher alcohols.     

Theoretical analysis and simulation of conjugate heights for dual-conjugate AO system in lidar

A multi-conjugate adaptive optics （MCAO） can offer a possibility of widening field of view （FOV） characterized by the isoplanatic angle, and the choose of conjugate height becomes a basic problem for MCAO, which influences the size of iosplanatic angle. Considering the application of lidar, the isoplanatic angle＇s expressions of two deformable mirrors （DMs） MCAO for uplink and downlink are deduced. The effects of conjugate heights for dual-conjugate AO are thoughtfully discussed, and the isoplanatic angles are further analyzed. The results show that the isopanatic angle varies with the conjugate height and reaches the maximum as the conjugate height is at the optimal altitude. Moreover, the optimal conjugate height changes with the propagation distance.     

Quick single-photon detector with many avalanche photo diodes working on the time division

Due to the limit of response speed of the present single-photon detector, the code rate is still too low to come into practical use for the present quantum key distribution (QKD) system.A new idea is put up to design a quick single-photon detector.This quick single-photon detector is composed of a multi-port optic-fiber splitter and many avalanche photo diodes (APDs).Au of the ports with APDs work on the time division and cooperate with a logic discriminating and deciding unit driven by the clock signal.The operation frequency lies on the number N of ports, and can reach N times of the conventional single-photon detector.The single-photon prompt detection can come true for high repetition-rate pulses.The applying of this detector will largely raise the code rate of the QKD, and boost the commercial use.     

Characterization of PolyA and PolyC mismatches by Raman spectroscopy

A.C mismatches are studied by Raman spectral characterization of PolyA, PolyC, and their equimolar complex in solution of 0.14 mol/L Na ,pH7.0.Experimental results show that A·C mismatches occur to be A/B (mainly A) conformers, and unlike Watson-Crick base pairing, this kind of mismatches is stabilized by only one hydrogen bond involving cytosine N4H2 and adenine N7.The formation of A·C complex makes the base stacking interactions much stronger, and conformation of the backbone more ordered, which leads to obvious Raman hypochromic effect with some shifts in corresponding bands.     

Improvement of four-wave mixing-based wavelength conversion efficiency in dispersion shifted fiber by 40-GHz clock pumping

40-GHz clock modulated signal as a pump to improve the efficiency of four-wave mixing (FWM)-based wavelength conversion in a 26.5-km dispersion shifted fiber (DSF) is investigated. The experimental results demonstrate that the conjugated FWM component has higher intensity with the clock pumping than that with the continuous-wave (CW) light pumping. The improvement of FWM-based wavelength conversion efficiency is negligible when the pump power is less than Brillouin threshold. But when the pump power is greater than Brillouin threshold, the improvement becomes significant and increases with the increment of pump power. The improvement can increase up to 9 dB if pump power reaches 17 dBm.     

Multi-pulse operation of a Kerr-lens mode-locked femtosecond laser

Our experimental results show that the presence of a proper amount of negative group velocity dispersion is essential to multi-pulse operation of a Kerr-lens mode-locked femtosecond laser. We demonstrate that the pulse separations and the number of pulses contained within a cavity round trip are strongly dependent on the initial perturbations. The results allow us to get a better understanding on the influences of the convoluted self-phase modulation and intra-cavity dispersions on the stable multi-pulse oscillation in a Kerr-lens mode-locked femtosecond laser.     

Propagation of Helmholtz-Gauss beams in weak turbulent atmosphere

Based on the Rytov approximation of light propagation in weak turbulent atmosphere,the closed-form expressions of field and average irradiance of each one of the four fundamental families of Helmholtz-Gauss (HzG)beams:cosine-Gauss beams,stationary Mathieu-Gauss beams,stationary parabolic-Gauss beams,and Bessel-Gauss beams,which are propagating in weak turbulent atmosphere,are obtained.The results show that the field and average irradiance can be written as the product of four factors:complex amplitude depending on the z-coordinate only,a Ganssian beam.a factor of complex phase perturbation induced by atmospheric turbulence,and a complex scaled version of the transverse shape of the non-diffracting beam.The effect of weak atmospheric turbulence on irradiance distribution of the HzG beam can be ignored.     

An effective method for reducing speckle noise in digital holography

An effective method for reducing the speckle noise in digital holography is proposed in this paper.Different from the methods based on classical filtering technique,it utilizes the multiple holograms which are generated by rotating the illuminating light continuously.The intensity images reconstructed by a series of holograms generated by rotating the illuminating light possess different speckle patterns.Hence by properly averaging the reconstructed intensity fields,the speckle noises can be reduced greatly.Experimental results show that the proposed method is simple and effective to reduce speckle noise in digital holography.     

Influence of purity of HfO2 on reflectance of ultraviolet multilayer

The impurities in two kinds of HfO2 materials and in their corresponding single layer thin films were determined through glow discharge mass spectrum technology and secondary ion mass spectrometry(SIMS) equipment respectively.It was found that ZrO2 was the main impurity in the two kinds of HfO2 either in the original HfO2 materials or in the electron beam deposited films.In addition,the difference of Zr content in the two kinds of HfO2 single laver films was much laxger than that of the other impurities such as Ti and Fe.which showed that it was just ZrO2 that made the difference between the optical performance of the film products including the two kinds of HfO2.With these two kinds of HfO2 and the same kind of SiO2.we deposited HfO2/SiO2 multilayer reflective coatings at the wavelength of 266 nm.Experimental results showed that the reflectances of these two mirrors were about 99.85% and 99.15% respectively,which agreed well with the designed results what were based on the optical constants obtained from the corresponding single layer thin films.     

Speech enhancement by array crosstalk resistant ANC and spectrum subtraction

Microphone array-based speech enhancement has great importance for speech communications and speech recognition. To reduce the aperture of the microphone array and to increase the effect of the speech enhancement will greatly broaden the application areas of the microphone array. An array crosstalk resistant adaptive noise cancellation method is therefore presented. And then an improved spectral subtraction algorithm is further cascaded to obtain better enhancement results. Theoretic analysis and experiments indicate that the proposed scheme needs only a very small microphone array while it simultaneously achieves a higher SNR improvement. Besides, the proposed scheme can be used in many noisy environments and is easy for real-time implementation.