scholarly journals The Stark effect for mercury

The Stark effect in the mercury spectrum has already received some attention. The first observations were made by Wendt and Wetzel, who used a canal-ray method. They reported small displacements in the diffuse series groups 2 3 P i — n 3 D i , n = 4, 5, 6, and in the sharp series line 2 3 P 1 —4 3 S. Ritter investigated the effect, using a Lo Surdo source, and noted small displacements toward the red in the lines 2 3 P 0 —5 3 D 1 , 2 3 P 1 —6 3 D 2 in the fields up to 26,000 volts per centimetre. Using an absorption method, Terenin detected a definite effect in the diffuse series triplets 2 3 P i — 3 3 D i . A far more extensive and valuable investigation of the effect for mercury was made by Hansen, Takamine and Werner at the Institute for Theoretical Physics, Copenhagen. A fine column of mercury in a quartz tube served as the cathode of a discharge tube. The light immediately above the mercury surface was analysed with a Hilger E 2 spectrograph. Observations were limited mainly to the diffuse series triplets 2 3 P i — n 3 D i , and the associated combination lines which appeared even in low electric fields. For values of n lower than five no definite Stark effect was observed, but in the higher members of the three series the 3 D lines were displaced to the red by an amount which increased with increasing term number. Grouped about the 3 D lines new combination lines of the types 3 P— 3 F, 3 P— 3 G, etc., were photographed and interpreted on the Bohr theory. In these mercury line groups, the restriction regard­ing the change in the azimuthal quantum number (∆ k = ± 1) is removed by low external fields, hence the new lines may be traced to a point very near their zero field position. No analysis of the patterns formed by individual lines could be attempted, however, since the electric fields which were established in the source were too weak to permit the necessary resolutions.

1974 ◽  
Vol 29 (11) ◽  
pp. 1558-1571
Author(s):  
H.-J. Rehm

Paraelectric resonance spectra of beryl crystals are observed in the X-band region between 5 and 20 kV/cm under the condition that the external electric field F[101̅0]. Additional dielectric measurements show, that the paraelectric centres are the monomeric water molecules in the beryl cavities. For water dipoles in beryl only two orientations of the molecular a-axis relative to the crystal C6-axis are possible, and only those with their a-axis parallel to the C6-axis contribute to the paraelectric resonance effect. The electric moment vector µ of these latter molecules may rotate in the (0001)-crystal plane, i. e. around their own a-axis, and has a value of (1.9 ± 0.2) D. A theoretical description of paraelectric resonance is presented for a simplified model: the electric dipoles have 6 equivalent equilibrium positions along the [101̅0]-directions, tunnel effect and external electric fields remove the site degeneracy and we observe a molecular Stark splitting. We calculate a value of (2.0 ± 0.4) GHz for the zero-field splitting in the one-parameter Hamiltonian model.


1999 ◽  
Vol 4 (S1) ◽  
pp. 357-362
Author(s):  
C. Wetzel ◽  
T. Takeuchi ◽  
H. Amano ◽  
I. Akasaki

Identification of the electronic band structure in AlInGaN heterostructures is the key issue in high performance light emitter and switching devices. In device-typical GaInN/GaN multiple quantum well samples in a large set of variable composition a clear correspondence of transitions in photo- and electroreflection, as well as photoluminescence is found. The effective band offset across the GaN/GaInN/GaN piezoelectric heterointerface is identified and electric fields from 0.23 - 0.90 MV/cm are directly derived. In the bias voltage dependence a level splitting within the well is observed accompanied by the quantum confined Stark effect. We furthermore find direct correspondence of luminescence bands with reflectance features. This indicates the dominating role of piezoelectric fields in the bandstructure of such typical strained layers.


1973 ◽  
Vol 51 (5) ◽  
pp. 641-649 ◽  
Author(s):  
Maurice G. Robinson ◽  
Gordon R. Freeman

X-Radiolysis ion yields were measured at electric fields between 1 and 60 kV/cm in argon at 87 °K, krypton at 148 °K, and xenon at 183 °K. The results were analyzed according to a theoretical model to obtain the total ion yields Gtot,the free ion yields at zero field strength Gfi0 and the most probable penetration ranges b of the secondary electrons in the liquids. The respective values were: Ar, 7.3, 2.9, 1330 Å; Kr, 13.0, 5.8, 880 Å; Xe, 13.7, 7.0, 720 Å. The total ionization yields in these substances are greater in the liquid than in the gas phase, probably due to smaller ionization potentials in the condensed phase (polarization energy effect). Field dependent electron mobilities are also reported.


1970 ◽  
Vol 25 (5) ◽  
pp. 608-611
Author(s):  
P. Zimmermann

Observing the change of the Hanle effect under the influence of a homogeneous electric field E the Stark effect of the (5p1/25d5/2)j=2-state in Sn I was studied. Due to the tensorial part β Jz2E2 in the Hamiltonian of the second order Stark effect the signal of the zero field crossing (M ∓ 2, M′ = 0 β ≷ 0 ) is shifted to the magnetic field H with gJμBH=2 | β | E2. From these shifts for different electric field strengths the value of the Stark parameter|β| = 0.21(2) MHz/(kV/cm)2 · gJ/1.13was deduced. A theoretical value of ß using Coulomb wave functions is discussed.


1998 ◽  
Vol 537 ◽  
Author(s):  
C. Wetzel ◽  
T. Takeuchi ◽  
H. Amano ◽  
I. Akasaki

AbstractIdentification of the electronic band structure in AlInGaN heterostructures is the key issue in high performance light emitter and switching devices. In device-typical GaInN/GaN multiple quantum well samples in a large set of variable composition a clear correspondence of transitions in photo- and electroreflection, as well as photoluminescence is found. The effective band offset across the GaN/GaInN/GaN piezoelectric heterointerface is identified and electric fields from 0.23 - 0.90 MV/cm are directly derived. In the bias voltage dependence a level splitting within the well is observed accompanied by the quantum confined Stark effect. We furthermore find direct correspondence of luminescence bands with reflectance features. This indicates the dominating role of piezoelectric fields in the bandstructure of such typical strained layers.


2014 ◽  
Vol 70 (a1) ◽  
pp. C674-C674
Author(s):  
Sajesh Thomas ◽  
Rebecca Fuller ◽  
Alexandre Sobolev ◽  
Philip Schauer ◽  
Simon Grabowsky ◽  
...  

The effect of an electric field on the vibrational spectra, the Vibrational Stark Effect (VSE), has been utilized extensively to probe the local electric field in the active sites of enzymes [1, 2]. For this reason, the electric field and consequent polarization effects induced by a supramolecular host system upon its guest molecules attain special interest due to the implications for various biological processes. Although the host-guest chemistry of crown ether complexes and clathrates is of fundamental importance in supramolecular chemistry, many of these multicomponent systems have yet to be explored in detail using modern techniques [3]. In this direction, the electrostatic features associated with the host-guest interactions in the inclusion complexes of halogenated acetonitriles and formamide with 18-crown-6 host molecules have been analyzed in terms of their experimental charge density distribution. The charge density models provide estimates of the molecular dipole moment enhancements which correlate with the simulated values of dipole moments under electric field. The accurate electron density mapping using the multipole formalism also enable the estimation of the electric field experienced by the guest molecules. The electric field vectors thus obtained were utilized to estimate the vibrational stark effect in the nitrile (-C≡N) and carbonyl (C=O) stretching frequencies of the guest molecules via quantum chemical calculations in gas phase. The results of these calculations indicate remarkable elongation of C≡N and C=O bonds due to the electric fields. The electronic polarization in these covalent bonds induced by the field manifests as notable red shifts in their characteristic vibrational frequencies. These results derived from the charge densities are further supported by FT-IR experiments and thus establish the significance of a phenomenon that could be termed as the "supramolecular Stark effect" in crystal environment.


1966 ◽  
Vol 21 (11) ◽  
pp. 1920-1930
Author(s):  
H. D. Beckey ◽  
H. Knöppel

The kinetics of unimolecular decomposition of organic ions in the presence of electric fields up to 108 V/cm is discussed. The results are deduced from the mass spectra obtained by field ionization of organic molecules. The time interval between formation and decomposition of the ions can be derived from the shape of the mass lines. It is shown that field induced decomposition can occur at a minimum time of about 3 · 10–14 sec after field ionization. The optimum time resolution with these experiments, 10–12 sec, is given by the resolving power of the mass spectrometer.The results can be interpreted in terms of five different mechanisms :1. Field induced dissociation. Excitation of the molecular ion to a state above the dissociation limit is possible at high enough fields. Spontaneous dissociation within one vibrational period will then be possible because the excitation energy is contained in the reaction coordinate.2. Field induced dissociation by tunneling of radicals through the potential barrier. This may occur after excitation of the molecular ion to a state lying in an interval between the dissociation limit and about half a vibrational energy quantum below this, provided the field strength is high enough. The maximum observable life time of ions resulting from this process is about 6·10–12 sec.3. Field induced dissociation, delayed by re-orientation of the molecular ion. Certain orientations of the molecular ion are favoured with respect to field dissociation. The maximum re-orientation time for a favourable position is of the order 3·10–12 sec.4. Field induced statistical dissociation. This is due to fluctuation of energy within the ion, as in the case of common reaction kinetics, but with lowering of the dissociation limit by the field. The time intervall for these processes lies between about 10–13 and 10–11 sec.5. Statistical decomposition in the space of low or zero field strength. This process is due to energy fluctuation within the molecular ion excited to a state above the dissociation limit, lowered only by a minute amount by the weak field. The range of life times is about 10–11 to 10–8 sec. Processes of the same type, occurring at zero field strength within about 10–8 and 10–6 sec, are called — as usually — “metastable” processes.The processes described here are derived mainly from the FI mass spectra of paraffins, alcohols, ethers and ketones. Dissociation is hindered, in some cases, by high electric fields.


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