Electric field driven fractal growth in polymer electrolyte composites: Experimental evidence of theoretical simulations

2012 ◽  
Vol 376 (47-48) ◽  
pp. 3604-3608 ◽  
Author(s):  
Anit Dawar ◽  
Amita Chandra
2017 ◽  
Vol 204 ◽  
pp. 159-172 ◽  
Author(s):  
Brandon E. Hirsch ◽  
Kevin P. McDonald ◽  
Steven L. Tait ◽  
Amar H. Flood

The interaction and mobility of ions in complex systems are fundamental to processes throughout chemistry, biology, and physics. However, nanoscale characterization of ion stability and migration remains poorly understood. Here, we examine ion movements to and from physisorbed molecular receptors at solution–graphite interfaces by developing a theoretical model alongside experimental scanning tunneling microscopy (STM) results. The model includes van der Waals forces and electrostatic interactions originating from the surface, tip, and physisorbed receptors, as well as a tip–surface electric field arising from the STM bias voltage (Vb). Our model reveals how both the electric field and tip–surface distance, dtip, can influence anion stability at the receptor binding sites on the surface or at the STM tip, as well as the size of the barrier for anion transitions between those locations. These predictions agree well with prior and new STM results from the interactions of anions with aryl-triazole receptors that order into functional monolayers on graphite. Scanning produces clear resolution at large magnitude negative surface biases (−0.8 V) while resolution degrades at small negative surface biases (−0.4 V). The loss in resolution arises from frequent tip retractions assigned to anion migration within the tip–surface tunneling region. This experimental evidence in combination with support from the model demonstrates a local voltage gating of anions with the STM tip inside physisorbed receptors. This generalized model and experimental evidence may help to provide a basis to understand the nanoscale details of related chemical transformations and their underlying thermodynamic and kinetic preferences.


2020 ◽  
Vol 192 ◽  
pp. 108753
Author(s):  
Jiyan Liu ◽  
Wei Fang ◽  
Shuyu Gao ◽  
Yuwei Chen ◽  
Shaoyun Chen ◽  
...  

1996 ◽  
Vol 23 (16) ◽  
pp. 2137-2140 ◽  
Author(s):  
T. A. Blix ◽  
E. V. Thrane ◽  
S. Kirkwood ◽  
Y. S. Dimant ◽  
R. N. Sudan

1992 ◽  
Vol 258 ◽  
Author(s):  
P.V. Santos ◽  
N.M. Johnson ◽  
R.A. Street

ABSTRACTWe provide experimental evidence for the fact that hydrogen diffusion in hydroge-nated amorphous silicon is controlled by the concentration of electronic carriers. It is experimentally demonstrated that the hydrogen diffusion coefficient (a) is enhanced if the carrier population is increased by illumination and (b) is strongly suppressed if carriers are extracted from the diffusion region by the application of an electric field.


1991 ◽  
Vol 6 (8) ◽  
pp. 1680-1684 ◽  
Author(s):  
T. Carrière ◽  
C. Ortiz ◽  
G. Fuchs

This work presents the first experimental evidence of the formation of a fractal network of crystalline clusters in the first stage of the amorphous-crystal transformation. Although this transformation has been extensively studied, such an intermediate stage between amorphous and crystalline phases has never been experimentally revealed before. This fractal network was obtained by laser irradiation of an amorphous Te–Se–Br alloy. The irradiation conditions have been determined in order to be in a regime of limited diffusion, which is the basis of fractal formation. Moreover, the fractal dimension has been determined to be 1.55, which corresponds to the theoretical value obtained for fractal growth by a process of cluster-cluster aggregation with some structural readjustment.


2000 ◽  
Vol 62 (5) ◽  
pp. R5927-R5930 ◽  
Author(s):  
F. Pisani ◽  
A. Bernardinello ◽  
D. Batani ◽  
A. Antonicci ◽  
E. Martinolli ◽  
...  

1996 ◽  
Vol 10 (23n24) ◽  
pp. 2925-2932 ◽  
Author(s):  
REX C. KANU ◽  
MONTGOMERY T. SHAW

Chaining of micron-sized polarizable particles in ER fluids is generally accepted to be responsible for the liquid-to-solid transitions on the application of an external electric field. It has been hypothesized that the strength of the particle-particle interactions solely determines the rheological properties of ER fluids. In our work, the particle’s structure has been used to control interactions; for example, we have developed systems featuring rodlike particles. With such particles it should be possible to enhance the dielectric interaction of the particles as well as their mechanical interaction. The main goal of our effort has been to distinguish between these two mechanisms through measurements of the dielectric properties in conjunction with the rheological responses. Based on the experimental evidence thus far gathered, we can state that most, but not all, of the rheological effects are explainable in terms of the dielectric changes in the fluid.


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