Simple Formula for the Ionization Rate of Rydberg States in Static Electric Fields

1982 ◽  
Vol 49 (12) ◽  
pp. 867-870 ◽  
Author(s):  
J. A. C. Gallas ◽  
H. Walther ◽  
E. Werner
1996 ◽  
Vol 51 (12) ◽  
pp. 1236-1246
Author(s):  
A. Held ◽  
L. Ya. Baranov ◽  
H. L. Selzle ◽  
E. W. Schlag

Abstract ZEKE states are highly stabilized Rydberg states which exist below each ionic eigenstate of a molecular system even high up into the continuum. The stability and neutrality of these states is the basis on which the high resolution ZEKE technique for the study of molecular ions is built upon. A new mechanism is proposed for the production of ZEKE states from optically accessible, relatively short lived Rydberg states. The mechanism is based on experimental results for a range of fields and ion concentrations. The experiments were performed with pulsed and static electric fields of different magnitudes at various ion concentrations.


1998 ◽  
Vol 18 (1-2) ◽  
pp. 13-33 ◽  
Author(s):  
A. Held ◽  
E. W. Schlag

ZEro Kinetic Energy (ZEKE) spectroscopy relies on electrons produced through delayed field ionization of the narrow band of high-n Rydberg states which exist just below the ionization limit of each ionic eigenstate. Using the unique properties of these weakly bound, stable, high-n Rydberg states (ZEKE states) below the ionization limit rather than the unbound states above the limit, as in PES, leads to an improvement in resolution of more than two orders of magnitude. Several different types of ZEKE experiments, each designed to probe the formation and stability of these states, are presented here. These experiments were performed with pulsed and static electric fields of different magnitude and duration at different ion concentrations. The results indicate an enhanced ZEKE state decay with increasing electric field strengths and an enhanced formation and stabilization with increasing ion concentrations. A strong interplay between field strength and ion concentration ZEKE state formation is demonstrated. The strong influence of electric fields and ion concentrations on the physical properties of the ZEKE state, above and below the classical ionization threshold, is also demonstrated through late time (tens of microseconds) decay rate measurements.


1991 ◽  
Vol 1 (8) ◽  
pp. 875-897 ◽  
Author(s):  
P. F. Brevet ◽  
Ch. Bordas ◽  
M. Broyer ◽  
G. Jalbert ◽  
P. Labastie

2021 ◽  
Vol 9 ◽  
Author(s):  
Long Zhang ◽  
Xiaohua Yang ◽  
Shun Li ◽  
JianMing Zhang

Oriented external electric fields are now emerging as “smart effectors” of chemical changes. The key challenges in experimentally studying electrostatic catalysis are (i) controlling the orientation of fields along the reaction axis and (ii) finely adjusting the magnitudes of electrostatic stimuli. Surface models provide a versatile platform for addressing the direction of electric fields with respect to reactants and balancing the trade-off between the solubility of charged species and the intensity of electric fields. In this mini-review, we present the recent advances that have been investigated of the electrostatic effect on the chemical reaction on the monolayer-functionalized silicon surfaces. We mainly focus on elucidating the mediator/catalysis role of static electric fields induced from either solid/liquid electric double layers at electrode/electrolyte interfaces or space charges in the semiconductors, indicating the electrostatic aspects is of great significance in the semiconductor electrochemistry, redox electroactivity, and chemical bonding. Herein, the functionalization of silicon surfaces allows scientists to explore electrostatic catalysis from nanoscale to mesoscale; most importantly, it provides glimpses of the wide-ranging potentials of oriented electric fields for switching on/off the macroscale synthetic organic electrochemistry and living radical polymerization.


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