scholarly journals The role of the atmospheric electric field in the dust‐lifting process

2016 ◽  
Vol 43 (10) ◽  
pp. 5501-5508 ◽  
Author(s):  
F. Esposito ◽  
R. Molinaro ◽  
C. I. Popa ◽  
C. Molfese ◽  
F. Cozzolino ◽  
...  
1998 ◽  
Vol 168 (5) ◽  
pp. 582 ◽  
Author(s):  
S.A. Pulinets ◽  
V.V. Khegai ◽  
K.A. Boyarchuk ◽  
A.M. Lomonosov

Catalysts ◽  
2021 ◽  
Vol 11 (2) ◽  
pp. 271
Author(s):  
Nisa Ulumuddin ◽  
Fanglin Che ◽  
Jung-Il Yang ◽  
Su Ha ◽  
Jean-Sabin McEwen

Despite its high thermodynamic stability, the presence of a negative electric field is known to facilitate the activation of CO2 through electrostatic effects. To utilize electric fields for a reverse water gas shift reaction, it is critical to elucidate the role of an electric field on a catalyst surface toward activating a CO2 molecule. We conduct a first-principles study to gain an atomic and electronic description of adsorbed CO2 on YSZ (111) surfaces when external electric fields of +1 V/Å, 0 V/Å, and −1 V/Å are applied. We find that the application of an external electric field generally destabilizes oxide bonds, where the direction of the field affects the location of the most favorable oxygen vacancy. The direction of the field also drastically impacts how CO2 adsorbs on the surface. CO2 is bound by physisorption when a +1 V/Å field is applied, a similar interaction as to how it is adsorbed in the absence of a field. This interaction changes to chemisorption when the surface is exposed to a −1 V/Å field value, resulting in the formation of a CO3− complex. The strong interaction is reflected through a direct charge transfer and an orbital splitting within the Olatticep-states. While CO2 remains physisorbed when a +1 V/Å field value is applied, our total density of states analysis indicates that a positive field pulls the charge away from the adsorbate, resulting in a shift of its bonding and antibonding peaks to higher energies, allowing a stronger interaction with YSZ (111). Ultimately, the effect of an electric field toward CO2 adsorption is not negligible, and there is potential in utilizing electric fields to favor the thermodynamics of CO2 reduction on heterogeneous catalysts.


2015 ◽  
Vol 646 ◽  
pp. 012013 ◽  
Author(s):  
H G Silva ◽  
J C Matthews ◽  
R Conceição ◽  
M D Wright ◽  
S N Pereira ◽  
...  

2021 ◽  
Vol 23 (35) ◽  
pp. 19647-19658
Author(s):  
Demeter Tzeli ◽  
Ioannis D. Petsalakis ◽  
Giannoula Theodorakopoulos ◽  
Faiz-Ur Rahman ◽  
Yang Yu ◽  
...  

Significant 1H upfield chemical shifts of the guests in the capsules are consequences of polarizability of chalcogens, electric field effects and peripheral chains. The effects of the electric field and of magnetic field are of equal importance.


2013 ◽  
Vol 31 (2) ◽  
pp. 251-261 ◽  
Author(s):  
J. De Keyser ◽  
M. Echim

Abstract. Strong localized high-altitude auroral electric fields, such as those observed by Cluster, are often associated with magnetospheric interfaces. The type of high-altitude electric field profile (monopolar, bipolar, or more complicated) depends on the properties of the plasmas on either side of the interface, as well as on the total electric potential difference across the structure. The present paper explores the role of this cross-field electric potential difference in the situation where the interface is a tangential discontinuity. A self-consistent Vlasov description is used to determine the equilibrium configuration for different values of the transverse potential difference. A major observation is that there exist limits to the potential difference, beyond which no equilibrium configuration of the interface can be sustained. It is further demonstrated how the plasma densities and temperatures affect the type of electric field profile in the transition, with monopolar electric fields appearing primarily when the temperature contrast is large. These findings strongly support the observed association of monopolar fields with the plasma sheet boundary. The role of shear flow tangent to the interface is also examined.


1989 ◽  
Vol 161 (5-6) ◽  
pp. 574-580 ◽  
Author(s):  
X.X. Tang ◽  
A. Manthiram ◽  
J.B. Goodenough

Sign in / Sign up

Export Citation Format

Share Document