Photoinduzierte Stoßprozesse metastabiler Wasserstoffatome mit H2 im Energiebereich von 0,05 — 0,47 eV

1969 ◽  
Vol 24 (4) ◽  
pp. 587-596 ◽  
Author(s):  
F. J. Comes ◽  
U. Wenning

Abstract Molecular hydrogen was excited by selective absorption of ultraviolet radiation of appropriate wavelength into the vibrational levels ν′ 3, 4, and 5 of the electronic D (1IIu)-state. For the radiation bandwidth chosen the molecule was only formed in the rotational levels J = 1 and 2 of the R-branch. The excited molecules decay by predissociation into two hydrogen atoms of translational energy which is equal to one half of the difference between the excitation and dissociation energies. One of the atoms is formed in its first excited state. The formation of the excited species can be proven by its fluorescence (Lymanα-radiation). As a result the measurements show, that the excited atoms are all in the metastable 2S-state and not in the short-lived 2P -state. Without electric fields these metastable atom s loose their excitation energy in collisions with the surrounding hydrogen molecules. One part (a) follows an induced transition to the electronic ground state by the emission of Lyα-radiation (1216 Å), the other part (b) is transformed to products or undergoes an energy transfer process without emitting Lyα-radiation. If a quenching field is applied spontaneous emission will compete with collisional deactivation, which allows the deactivation cross sections to be calculated. These cross sections are between 50 and 100 Å2 (a) and about 50 Å2 in case (b). In case (a) the collision cross section increases with the velocity of the particles whereas in case (b) a constant value was found.

In view of the extremely important results obtained by Sir E. Rutherford and others from a study of the scattering of α -rays, it seemed worth while to investigate the scattering of particles moving with smaller velocities such as occur in the positive rays. The most interesting, because the simplest, are the rays of positively charged hydrogen atoms, which presumably consist simply of a nuclear particle, or proton. The experiments described in this paper were made in some cases with these rays, in others with the positively charged hydrogen molecules, systems consisting of two protons and one electron. The scattering medium was in all cases hydrogen gas. This was chosen largely for convenience, as the experimental arrangement is considerably simplified if the same gas is used to produce the rays and to scatter them, and also because, with the exception of helium, the molecule of hydrogen is the simplest known, and there seemed more hope of obtaining results which could be given a definite theoretical interpretation. The general scheme of experiment was to produce the rays in a discharge tube, analyse them by magnetic and electric fields in the ordinary way, cut off all except those of the kind required by a slotted diaphragm, pass the remainder through a chamber containing the scattering gas, and receive them in a Faraday cylinder arranged behind a slit of variable width. The experiment consisted in finding how the charge received by the Faraday cylinder varied with the width of the slit, when this was made wider than the geometrical “shadow” of the slot in the diaphragm. Any rays lying outside this “shadow” must have been scattered.


The second-order differential equation which expresses the equilibrium condition of an electron swarm in a uniform electric field in a gas, the electrons suffering both elastic and inelastic collisions with the gas molecules, is solved by the Jeffreys or W.K.B. method of approximation. The distribution function F(ε) of electrons of energy ε is obtained immediately in a general form involving the elastic and inelastic collision cross-sections and without any restriction on the range of E/p (electric strength/gas pressure) save that introduced in the original differential equation. In almost all applications the approximation is likely to be of high accuracy, and easy to use. Several of the earlier derivations of F(ε) are obtained as special cases. Using the function F(ε) an attempt is made to relate the Townsend ionization coefficient a to the properties of the gas in a more general manner than hitherto, using realistic functions for the collision cross-section. It is finally expressed by the equation α/ p = A exp ( — Bp/E ) in which A and B are functions involving the properties of the gas and the ratio E/p . The important coefficient B is directly related to the form and magnitude of the total inelastic cross-section below the ionization potential and can be evaluated for a particular gas once the cross-section is known experimentally. The present theory shows clearly the influence of E/p on both A and B, a matter which has not been satisfactorily discussed previously. The theory is illustrated by calculations of F (ε) and a/p for hydrogen over a range of E/p from 10 to 1000. The agreement between the calculated results and recent reliable observations of α/ p is surprisingly good considering the nature of the calculations and the wide range of E/p .


1992 ◽  
Vol 45 (3) ◽  
pp. 365 ◽  
Author(s):  
H Tagashira

Some recent studies of electron swarms in gases under the action of an electric field are introduced. The studies include a new type of continuity equation for electrons having a form in which the partial derivative of the electron density with respect to position and to time are interchanged, a method to deduce the time-of-flight and arrival-time-spectrum swarm parameters based on a Fourier-transformed Boltzmann equation, an examination of the correspondence between experimental and theoretical electron drift velocities, and an automatic technique to deduce the electron-gas molecule collision cross section from electron drift velocity data. We also briefly introduce a method for the deduction of electron collision cross sections with gas molecules having vibrational excitation cross sections greater than the elastic momentum transfer cross section by using a gas mixture technique, an integral type of method for solution of the Boltzmann equation with salient numerical stability, a quantitative analysis of the effect of Penning ionisation, and the behaviour of electron swarms under radio frequency electric fields.


1992 ◽  
Vol 168 (1) ◽  
pp. 145-150 ◽  
Author(s):  
Teiichiro Ogawa ◽  
Satoru Ihara ◽  
Nobuaki Yonekura ◽  
To-oru Yasuda ◽  
Keiji Nakashima

1990 ◽  
Vol 17 (2) ◽  
pp. 101-107 ◽  
Author(s):  
G. Vassilev ◽  
F. Perales ◽  
Ch. Miniatura ◽  
J. Robert ◽  
J. Reinhardt ◽  
...  

1993 ◽  
Vol 32 (Part 1, No. 7) ◽  
pp. 3296-3299 ◽  
Author(s):  
Nobuaki Yonekura ◽  
Toshiyuki Tsuboi ◽  
Hideaki Tomura ◽  
Keiji Nakashima ◽  
Junichi Kurawaki ◽  
...  

2021 ◽  
Vol 11 (8) ◽  
pp. 3317
Author(s):  
C.S. Quintans ◽  
Denis Andrienko ◽  
Katrin F. Domke ◽  
Daniel Aravena ◽  
Sangho Koo ◽  
...  

External electric fields (EEFs) have proven to be very efficient in catalysing chemical reactions, even those inaccessible via wet-chemical synthesis. At the single-molecule level, oriented EEFs have been successfully used to promote in situ single-molecule reactions in the absence of chemical catalysts. Here, we elucidate the effect of an EEFs on the structure and conductance of a molecular junction. Employing scanning tunnelling microscopy break junction (STM-BJ) experiments, we form and electrically characterize single-molecule junctions of two tetramethyl carotene isomers. Two discrete conductance signatures show up more prominently at low and high applied voltages which are univocally ascribed to the trans and cis isomers of the carotenoid, respectively. The difference in conductance between both cis-/trans- isomers is in concordance with previous predictions considering π-quantum interference due to the presence of a single gauche defect in the trans isomer. Electronic structure calculations suggest that the electric field polarizes the molecule and mixes the excited states. The mixed states have a (spectroscopically) allowed transition and, therefore, can both promote the cis-isomerization of the molecule and participate in electron transport. Our work opens new routes for the in situ control of isomerisation reactions in single-molecule contacts.


2008 ◽  
Vol 23 (27n30) ◽  
pp. 2512-2515 ◽  
Author(s):  
HIDEKO NAGAHIRO ◽  
DAISUKE JIDO ◽  
SATORU HIRENZAKI

We investigate the properties of η-nucleus interaction by postulating the N*(1535) dominance for η-N system. We evaluate the N*(1535) properties in the nuclear medium using two kinds of chiral models, and find that these two models provide qualitatively different η-nucleus optical potentials reflecting the quite distinct properties of N*(1535) in these chiral models. Especially, in the chiral doublet model, we can expect to have the level crossing between η and N*(1535)-hole which is expected to provide the characteristic features for the optical potential and the formation spectra. We find also that the difference of these models can be seen in the formation cross sections of the η mesic nuclei with (π+, p ) reaction expected to be performed at J-PARC project.


2007 ◽  
Vol 131-133 ◽  
pp. 425-430 ◽  
Author(s):  
Anis M. Saad ◽  
Oleg Velichko ◽  
Yu P. Shaman ◽  
Adam Barcz ◽  
Andrzej Misiuk ◽  
...  

The silicon substrates were hydrogenated at approximately room temperature and hydrogen concentration profiles vs. depth have been measured by SIMS. Czochralski grown (CZ) wafers, both n- and p-type conductivity, were used in the experiments under consideration. For analysis of hydrogen transport processes and quasichemical reactions the model of hydrogen atoms diffusion and quasichemical reactions is proposed and the set of equations is obtained. The developed model takes into account the formation of bound hydrogen in the near surface region, hydrogen transport as a result of diffusion of hydrogen molecules 2 H , diffusion of metastable complexes * 2 H and diffusion of nonequilibrium hydrogen atoms. Interaction of 2 H with oxygen atoms and formation of immobile complexes “oxygen atom - hydrogen molecule” (O - H2 ) is also taken into account to explain the hydrogen concentration profiles in the substrates of n-type conductivity. The computer simulation based on the proposed equations has shown a good agreement of the calculated hydrogen profiles with the experimental data and has allowed receiving a value of the hydrogen molecules diffusivity at room temperature.


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