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  • AIP Publishing  (48)
  • Asia - CrossAsia  (48)
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  • AIP Publishing  (48)
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  • Asia - CrossAsia  (48)
  • 1
    Online Resource
    Online Resource
    AIP Publishing ; 2016
    In:  Chinese Journal of Chemical Physics Vol. 29, No. 1 ( 2016-02-27), p. 10-20
    In: Chinese Journal of Chemical Physics, AIP Publishing, Vol. 29, No. 1 ( 2016-02-27), p. 10-20
    Abstract: The reaction of laser-ablated vanadium, niobium and tantalum atoms with hydrogen sulfide has been investigated using matrix isolation FTIR and theoretical calculations. The metal atoms inserted into the H−S bond of H2S to form the HMSH molecules (M=V, Nb, Ta), which rearranged to H2MS molecules on annealing for Nb and Ta. The HMSH molecule can also further react with another H2S to form the H2M(SH)2 molecules. These new molecules were identified on the basis of the D2S and H234S isotopic substitutions. DFT (B3LYP and BPW91) theoretical calculations are used to predict energies, geometries, and vibrational frequencies for these novel metal dihydrido complexes and molecules. Reaction mechanism for formation of group V dihydrido complex was investigated by DFT internal reaction coordinate calculations. The dissociation of HVSH gave VS+H2 on broad band irradiation and reverse reaction happened on annealing. Based on B3LYP calculation releasing hydrogen from HVSH is endothermic only by 13.5 kcal/mol with lower energy barrier of 16.9 kcal/mol.
    Type of Medium: Online Resource
    ISSN: 1674-0068 , 2327-2244
    Language: English
    Publisher: AIP Publishing
    Publication Date: 2016
    detail.hit.zdb_id: 2381472-X
    SSG: 6,25
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  • 2
    Online Resource
    Online Resource
    AIP Publishing ; 2017
    In:  Chinese Journal of Chemical Physics Vol. 30, No. 6 ( 2017-12-27), p. 678-684
    In: Chinese Journal of Chemical Physics, AIP Publishing, Vol. 30, No. 6 ( 2017-12-27), p. 678-684
    Abstract: Laser ablated boron atoms have been reacted with hydrogen sulfide and the reaction products condensed with argon at 4 K, which gave BS2, BS2−, HSBS, and HBS molecules. Reagent isotopic substitution (H2S, H234S, D2S, 10B, 11B) and variation of boron and hydrogen sulfide concentrations have been used to identify the major products. Both BS2− and BS2 were identified as linear molecules with no significant difference in the structure parameters, but the B–S anti-symmetric stretching vibration of BS2 is significantly lower than that of BS2−, which is ascribed to pseudo Jahn-Teller effect. Theoretical calculation was employed to have an insight into the interaction nature of the bonds in the corresponding products.
    Type of Medium: Online Resource
    ISSN: 1674-0068 , 2327-2244
    Language: English
    Publisher: AIP Publishing
    Publication Date: 2017
    detail.hit.zdb_id: 2381472-X
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  • 3
    Online Resource
    Online Resource
    AIP Publishing ; 2023
    In:  Chinese Journal of Chemical Physics Vol. 36, No. 3 ( 2023-06-01), p. 259-264
    In: Chinese Journal of Chemical Physics, AIP Publishing, Vol. 36, No. 3 ( 2023-06-01), p. 259-264
    Abstract: A narrow-pulsed and velocity-controlled molecular beam system is constructed by using a high-speed chopper and a temperature adjustable pulsed valve. The duration of the hydrogen molecular beam pulse is reduced to approximately 6.3 µs and characterized using resonance-enhanced multiphoton ionization (REMPI) at a distance of ~193 mm downstream from the nozzle. To precisely determine the velocity of the hydrogen molecules, a pump-probe technique combining stimulated Raman pumping and REMPI is employed at a fixed distance (193 mm) with nanosecond lasers. By adjusting the temperature of the pulsed valve, the velocity of the hydrogen beam varies continuously from 1290 m/s to 3550 m/s. The system exhibits potential for multiple applications in the field of chemical reaction dynamics, including its potential to integrate with ion traps and surface scattering experiments.
    Type of Medium: Online Resource
    ISSN: 1674-0068 , 2327-2244
    Language: English
    Publisher: AIP Publishing
    Publication Date: 2023
    detail.hit.zdb_id: 2381472-X
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  • 4
    Online Resource
    Online Resource
    AIP Publishing ; 2022
    In:  Chinese Journal of Chemical Physics Vol. 35, No. 5 ( 2022-10-01), p. 774-782
    In: Chinese Journal of Chemical Physics, AIP Publishing, Vol. 35, No. 5 ( 2022-10-01), p. 774-782
    Abstract: Dimension-controllable supramolecular organic frameworks (SOFs) with aggregation-enhanced fluorescence are hierarchically fabricated through the host-guest interactions of cucurbit[8]uril (CB[8] ) and coumarin-modified tetraphenylethylene derivatives (TPEC). The three-dimensional layered SOFs could be constructed from the further stacking of two-dimensional mono-layered structures via simply regulating the self-assembly conditions including the culturing time and concentration. Upon light irradiation under the wavelength of 365 nm, the photodimerization of coumarin moieties occurred, which resulted in the transformation of the resultant TPECn/CB[8]4n two-dimensional SOFs into robust covalently-connected 2D polymers with molecular thickness. Interestingly, the supramolecular system of TPECn/CB[8] 4n exhibited intriguing multicolor fluorescence emission from yellow to blue in the time range of 0−24 h at 365 nm irradiation, possessing potential applicability for photochromic fluorescence ink.
    Type of Medium: Online Resource
    ISSN: 1674-0068 , 2327-2244
    Language: English
    Publisher: AIP Publishing
    Publication Date: 2022
    detail.hit.zdb_id: 2381472-X
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  • 5
    Online Resource
    Online Resource
    AIP Publishing ; 2019
    In:  Chinese Journal of Chemical Physics Vol. 32, No. 4 ( 2019-08-01), p. 431-436
    In: Chinese Journal of Chemical Physics, AIP Publishing, Vol. 32, No. 4 ( 2019-08-01), p. 431-436
    Abstract: As a clean and renewable future energy source, hydrogen fuel can be produced via solar water splitting. Two-dimensional (2D) black phosphorene (black-P) can harvest visible light due to the desirable band gap, which promises it as a metal-free photocatalyst. However, black-P can be only used to produce hydrogen since the oxidation potential of water locates lower than the position of the valence band maximum. To improve the photocatalytic performance of black-P, here, using black-P and blue phosphorene (blue-P) monolayers, we propose a 2D van der Waals (vdW) heterojunction. Theoretical results, including the band structures, density of states, Bader charge population, charge density difference, and optical absorption spectra, clearly reveal that the visible light absorption ability is obviously improved, and the band edge alignment of the proposed vdW heterojunction displays a typical type-II feature to effectively separate the photogenerated carriers. At the same time, the built-in interfacial electric field prevents the electron-hole recombination. These predictions suggest that the examined phosphorene-based vdW heterojunction is an efficient photocatalyst for solar water splitting.
    Type of Medium: Online Resource
    ISSN: 1674-0068 , 2327-2244
    Language: English
    Publisher: AIP Publishing
    Publication Date: 2019
    detail.hit.zdb_id: 2381472-X
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  • 6
    Online Resource
    Online Resource
    AIP Publishing ; 2007
    In:  Chinese Journal of Chemical Physics Vol. 20, No. 4 ( 2007-08-01), p. 388-394
    In: Chinese Journal of Chemical Physics, AIP Publishing, Vol. 20, No. 4 ( 2007-08-01), p. 388-394
    Abstract: The photodissociation of isocyanic acid (HNCO) on the first excited singlet state following the excitation at 210 nm was investigated with an ion velocity slice imaging technique by probing the CO fragment. It was found from the (2+1) resonance-enhanced multi-photon ionization (REMPI) spectrum that the CO fragments are rotationally hot with population up to Jmax=50. The velocity imagings of the CO fragments at JCO=30 and 35 indicate that formation of NH(a1)+CO(X1+, v=0) is the predominant dissociation channel at 210 nm. From analysis of the CO fragment translational energy distributions, the NH(a1) fragment was observed to be rotationally cold, about half of the available energy was partitioned into the translational motion of fragments after dissociation, and the NH(a1)+CO(X1+) dissociation threshold was determined at 4273830 cm1. From analysis of the CO fragment angular distributions, the dissociation anisotropy parameter was found to be negative, and increasing with the rotational quantum number of the NH fragment, i.e., from -0.75 at JNH=2-4 to -0.17 at JNH=11. Impulsive direct and vertical dissociation process of HNCO on the singlet state at 210 nm was confirmed experimentally. A classical impact dissociation model was employed to explain the dependence of the value on the rotational excitation of the NH fragment.
    Type of Medium: Online Resource
    ISSN: 1674-0068 , 2327-2244
    Language: English
    Publisher: AIP Publishing
    Publication Date: 2007
    detail.hit.zdb_id: 2381472-X
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  • 7
    Online Resource
    Online Resource
    AIP Publishing ; 2020
    In:  Chinese Journal of Chemical Physics Vol. 33, No. 2 ( 2020-04-01), p. 239-242
    In: Chinese Journal of Chemical Physics, AIP Publishing, Vol. 33, No. 2 ( 2020-04-01), p. 239-242
    Abstract: The reaction dynamics of yttrium atoms with sulfur dioxide molecules at a high collision energy of 36 kcal/mol was studied using time-sliced velocity map ion imaging, crossed molecular beam and laser-ablation method. The product YO was detected via multiphoton ionization at various wavelengths in the region of 482–615 nm. The slice images of YO show a broad velocity distribution and forward-backward peaking angular distribution. The forward scattering signal is stronger than its backward distribution. This indicates that the reaction proceeds via an intermediate complex and the lifetime of the intermediate state is less than one rotational period. The formation of complex suggests that electron transfer occurs in the oxidation reaction.
    Type of Medium: Online Resource
    ISSN: 1674-0068 , 2327-2244
    Language: English
    Publisher: AIP Publishing
    Publication Date: 2020
    detail.hit.zdb_id: 2381472-X
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  • 8
    Online Resource
    Online Resource
    AIP Publishing ; 2009
    In:  Chinese Journal of Chemical Physics Vol. 22, No. 1 ( 2009-02-01), p. 41-45
    In: Chinese Journal of Chemical Physics, AIP Publishing, Vol. 22, No. 1 ( 2009-02-01), p. 41-45
    Abstract: Liquid mixtures of water and deuterium oxide as the liquid phase, were used to match the density of charged colloidal particles. Kossel diffraction method was used to detect the crystal structures. The experiments under the density-matched (g = 0) and unmatched (g = 1) conditions are compared to examine the influence of gravity on the crystal structures formed by self-assembly of 110 nm (in diameter) polystyrene microspheres. The result shows that the gravity tends to make the lattice constants of colloidal crystals smaller at lower positions, which indicates that the effect of gravity should be taken into account in the study of the colloidal crystals.
    Type of Medium: Online Resource
    ISSN: 1674-0068 , 2327-2244
    Language: English
    Publisher: AIP Publishing
    Publication Date: 2009
    detail.hit.zdb_id: 2381472-X
    SSG: 6,25
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  • 9
    Online Resource
    Online Resource
    AIP Publishing ; 2015
    In:  Chinese Journal of Chemical Physics Vol. 28, No. 5 ( 2015-10-27), p. 617-622
    In: Chinese Journal of Chemical Physics, AIP Publishing, Vol. 28, No. 5 ( 2015-10-27), p. 617-622
    Abstract: Vertically aligned multi-walled carbon nanotube arrays grown on quartz substrate are obtained by co-pyrolysis of xylene and ferrocene at 850 °C in a tube furnace. Raman spectroscopy and high resolution transmission electron microscopy measurements show that the single-walled carbon nanotubes are only present on top of vertically aligned multi-walled carbon nanotube arrays. It has been revealed that isolated single-walled carbon nanotubes are only present in those floating catalyst generated materials. It thus suggests that the single-walled carbon nanotubes here are also generated by floating catalyst. Vertically aligned carbon nanotube arrays on the quartz substrate have shown good orientation and good graphitization. Meanwhile, to investigate the growth mechanism, two bi-layers carbon nanotube films with different thickness have been synthesized and analyzed by Raman spectroscopy. The results show that the two-layer vertically aligned carbon nanotube films grow “bottom-up”. There are distinguished Raman scattering signals for the second layer itself, surface of the first layer, interface between the first and second layer, side wall and bottom surface. It indicates that the obtained carbon nanotubes follow the base-growth mechanism, and the single-walled carbon nanotubes grow from their base at the growth beginning when iron catalyst particles have small size. Those carbon nanotubes with few walls (typically & lt;5 walls) have similar properties, which also agree with the base-growth mechanism.
    Type of Medium: Online Resource
    ISSN: 1674-0068 , 2327-2244
    Language: English
    Publisher: AIP Publishing
    Publication Date: 2015
    detail.hit.zdb_id: 2381472-X
    SSG: 6,25
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  • 10
    Online Resource
    Online Resource
    AIP Publishing ; 2018
    In:  Chinese Journal of Chemical Physics Vol. 31, No. 6 ( 2018-12-01), p. 767-771
    In: Chinese Journal of Chemical Physics, AIP Publishing, Vol. 31, No. 6 ( 2018-12-01), p. 767-771
    Abstract: We present atomic-resolution images of TiSe2, MoTe2 and TaS2 single crystals in liquid condition using our home-built scanning tunneling microscopy (STM). By facilely cleaving of single crystals in liquid, we were able to keep the fresh surface not oxidized within a few hours. Using the high-stable home-built STM, we have obtained atomic resolution images of TiSe2 accompanied with the single atom defects as well as the triangle defects in solution for the first time. Besides, the superstructure of MoTe2 and hexagonal charge-density wave domain structure in nearly commensurate phase of TaS2 were also obtained at room temperature (295 K). Our results provide a more efficient method in investigating the lively surface of transition metal dichalcogenides. Besides, the high stable liquid-phase STM will support the further investigations in liquid-phase catalysis or electrochemistry.
    Type of Medium: Online Resource
    ISSN: 1674-0068 , 2327-2244
    Language: English
    Publisher: AIP Publishing
    Publication Date: 2018
    detail.hit.zdb_id: 2381472-X
    SSG: 6,25
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