Electron Transport during the 1999 August 20 Flare Inferred from Microwave and Hard X‐Ray Observations

2002 ◽  
Vol 572 (1) ◽  
pp. 609-625 ◽  
Author(s):  
Jeongwoo Lee ◽  
Dale E. Gary ◽  
Jiong Qiu ◽  
Peter T. Gallagher
Keyword(s):  
1991 ◽  
Vol 46 (1-2) ◽  
pp. 93-98 ◽  
Author(s):  
Helen G. McFadden ◽  
Donald C. Craig ◽  
John L. Huppatz ◽  
John N. Phillips

Abstract X-ray crystallographic data for the highly potent cyanoacrylate photosynthetic electron transport inhibitor, (Z)-ethoxyethyl 3-(4-chlorobenzylamino)-2-cyano-4-methylpent-2-enoate, are presented. This compound has a particularly high affinity for the photosystem II (PS II) herbicide receptor with a p I50 value of 9.5 (in the Hill reaction under uncoupled condi­tions with a chlorophyll concentration of 0.1 μg/ml). Data regarding the structure of small li­gands, such as this potent cyanoacrylate, which bind to the site with high affinity may be used to provide the basis for modelling studies of PS II/herbicide complexes. The X-ray data presented confirm the Z-stereochemistry of active cyanoacrylates and demonstrate the pres­ence of a planar core stabilized by an intramolecular hydrogen bond between the ester car­bonyl oxygen and a benzylamino hydrogen atom. In order to assess the importance of the benzylamino -NH -group in this type of cyanoacrylate, analogues containing a methylene group in its place were synthesized and found to be 100-and 1000-fold less active as Hill inhibitors.


Coatings ◽  
2020 ◽  
Vol 10 (3) ◽  
pp. 237
Author(s):  
Chih-Hung Tsai ◽  
Chia-Ming Lin ◽  
Cheng-Hao Kuei

In this study, four organic solvents including 1,2-dichlorobenzene (DCB), chlorobenzene (CB), methylbenzene (MB), and chloroform (CF) were used as solvents in the [6,6]-phenyl-C61-butyric acid methyl ester (PCBM) electron transport layer (ETL) of perovskite solar cells (PSCs). This study observed the effects of various solvents on the surface morphology of the ETL by using an optical microscope (OM) and scanning electron microscope (SEM). The surface roughness, crystal structure, and surface element bonding of the ETL were observed using an atomic force microscope (AFM), X-ray diffractometer (XRD), and X-ray photoelectron spectroscope (XPS), respectively. The absorption spectrum of the perovskite layer was explored using an ultraviolet-visible (UV-Vis) spectrometer. The characteristics of the PSC device were analyzed in terms of its current density–voltage (J–V) curve, external quantum efficiency (EQE), and electrochemical impedance spectroscopy (EIS) measurements. The results showed that DCB is a solvent with a high boiling point, low vapor pressure, and high dielectric constant, and using DCB as the solvent for ETL, the uniformity, coverage, and surface roughness of the ETL showed better properties. The power conversion efficiency of the PSC in which DCB was used as the solvent achieved a value of 11.07%, which was higher than that of the PSCs in which other solvents were used.


2017 ◽  
Vol 473 (3) ◽  
pp. 3211-3222 ◽  
Author(s):  
Jian-Fu Zhang ◽  
Zhi-Ren Li ◽  
Fu-Yuan Xiang ◽  
Ju-Fu Lu

1985 ◽  
Vol 38 (9) ◽  
pp. 1293 ◽  
Author(s):  
SJ Cochran ◽  
FP Larkins

The surfaces of lithium-and chromium-doped nickel oxide and of nickel oxide supported on alumina have been examined by X-ray photoelectron spectroscopy. The concentration of the nickel(III) species increased for the lithium-doped oxide and decreased for the chromium-doped oxide relative to the undoped oxide. The effects of doping were manifested most clearly however by the amount of oxygen-containing species adsorbed on the oxide surface rather than by variations in the nickel(III) peak intensity. Lithium-doped oxides were also shown to reduce more readily than undoped or chromium-doped oxides in the presence of carbon-containing impurities. The rate of reduction is influenced by the activation energy for electron transport which is related to the availability of the nickel(III) species. Supported oxides showed significant surface enhancement of nickel(II) as well as an absence of the nickel(III) species. The nickel(II) species in the supported oxide was not easily reduced to nickel(0).


2008 ◽  
Vol 42 (6) ◽  
pp. 669-674 ◽  
Author(s):  
T. B. Popova ◽  
L. A. Bakaleĭnikov ◽  
M. V. Zamoryanskaya ◽  
E. Yu. Flegontova

2004 ◽  
Author(s):  
Stefano Del Sordo ◽  
M. Strazzeri ◽  
Gaetano Agnetta ◽  
B. Biondo ◽  
Filippo Celi ◽  
...  

2020 ◽  
Vol 27 (2) ◽  
pp. 023302 ◽  
Author(s):  
M. Dozières ◽  
S. Hansen ◽  
P. Forestier-Colleoni ◽  
C. McGuffey ◽  
D. Kawahito ◽  
...  

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