Electrochemistry of Conjugated Polymers and Electrochemical Applications

MRS Bulletin ◽  
1997 ◽  
Vol 22 (6) ◽  
pp. 24-30 ◽  
Author(s):  
Alan G. MacDiarmid ◽  
Weigong Zheng

The discovery in 1977–78 that trans-polyacetylene — (CH)x, the prototype conducting polymer (Figure 1)—could be chemically p-doped (partly oxidized) or n-doped (partly reduced) with a concomitant increase of its conductivity through the semiconducting to the metallic regime introduced new concepts of considerable theoretical and possible technological importance to condensed matter science. In 1979 it was discovered that p- or n-doping of trans-(CH)x could be accomplished electrochemically and that these processes were electrochemically reversible. Polyacetylene is the simplest example of a conjugated polymer, a polymer in which the “backbone” atoms are joined alternately by single and double bonds. All conducting polymers, “synthetic metals,” are conjugated polymers, at least in their doped forms. Other conducting polymers, including for example, poly(paraphenylene), polypyrrole, polythiophene, and polyaniline, have since been examined as electrochemically active materials. These findings have stimulated much industrial and academic interest in the electro-chemistry of conducting polymers and their possible technological applications in for example, energy storage, electrochromic displays, electrochemical drug-delivery systems, electromechanical devices, and light-emitting devices.This article will show the relationship between the doping of a conjugated polymer, the reduction potential of the polymer, and the role of “dopant” ions. These interrelationships have frequently caused considerable confusion in understanding electrochemical doping. Electrochemical synthesis of conjugated polymers and the role of cyclic voltammetry in elucidating the mechanism of electrochemical redox processes involving conjugated organic polymers will also be discussed. This article will also summarize a few selected applications involving electro-chemical properties of conjugated polymers. The coverage is intended to beexemplary rather than exhaustive. Furthermore since the electrochemistry of (CH), the “prototype” conducting polymer, has been extensively studied and comprises a relatively simple, reversible electrochemical system, it will be used to exemplify the basic concepts involved. These basic concepts can then be applied with appropriate modification as necessary to the electrochemistry of other conjugated polymers. Polyaniline will then be used to illustrate a more complex conjugated polymer electrochemical system.

2021 ◽  
pp. 81-101
Author(s):  
Christopher O. Oriakhi

Chemical Bonding I: Basic Concepts examines general ideas of chemical bonding between atoms and ions and how this bonding affects the chemical properties of the elements. An overview of Lewis symbols, Lewis structures and the octet rule is presented including the role of valence electrons in ionic and covalent bonding. The energy changes that accompany ionic bond formation are also discussed with emphasis on lattice energy. The chapter covers guidelines and general procedures for writing Lewis structures or electron dot formulas for molecular compounds and polyatomic ions. The concepts and applications of resonance, formal charge and exceptions to the octet rules are presented, along with coverage of the relationship between bond polarity and electronegativity.


Electronics ◽  
2021 ◽  
Vol 10 (18) ◽  
pp. 2283
Author(s):  
Sooyong Lee ◽  
Hwajeong Kim ◽  
Youngkyoo Kim

Here, we report the hole injection role of p-type conjugated polymer layer in phosphorescent organic light-emitting devices (OLEDs). Poly(3-hexylthiophene) (P3HT) nanolayers (thickness = ~1 nm thick), which were subjected to thermal annealing at 140 °C by varying annealing time, were inserted between indium tin oxide (ITO) anodes and hole transport layers (N,N′-bis(naphthalen-1-yl)-N,N′-bis(phenyl)-benzidine, NPB). The 1 nm-thick P3HT layers showed very weak absorption in the visible light range of 500~650 nm. The device results disclosed that the presence of P3HT layers were just able to improve the charge injection of OLEDs leading to an enhanced luminance irrespective of thermal annealing condition. The highest luminance and efficiency were achieved for the OLEDs with the P3HT layers annealed at 140 °C for 10 min. Further annealing for 30 min resulted in turn-down of device performances. The emission color was almost unchanged by the presence of P3HT layers even though the color coordinates were marginally fluctuated according to the annealing time. The present result delivers the possibility to use p-type conjugated polymers (i.e., P3HT) as a hole injection layer in OLEDs.


2020 ◽  
Vol 8 (4) ◽  
pp. 592-606 ◽  
Author(s):  
Thais Fedatto Abelha ◽  
Cécile A. Dreiss ◽  
Mark A. Green ◽  
Lea Ann Dailey

In this review, the role of conjugated polymer nanoparticles (CPNs) in emerging bioimaging techniques is described.


2012 ◽  
Vol 2012 ◽  
pp. 1-7 ◽  
Author(s):  
Rapiphun Janmanee ◽  
Sopis Chuekachang ◽  
Saengrawee Sriwichai ◽  
Akira Baba ◽  
Sukon Phanichphant

In recent years, conducting polymers have emerged as one of the most promising transducers for both chemical, sensors and biosensors owing to their unique electrical, electrochemical and optical properties that can be used to convert chemical information or biointeractions into electrical or optical signals, which can easily be detected by modern techniques. Different approaches to the application of conducting polymers in chemo- or biosensing applications have been extensively studied. In order to enhance the application of conducting polymers into the area of biosensors, one approach is to introduce functional groups, including carboxylic acid, amine, sulfonate, or thiol groups, into the conducting polymer chain and to form a so-called “self-doped” or by doping with negatively charged polyelectrolytes. The functional conducting polymers have been successfully utilized to immobilize enzymes for construction of biosensors. Recently, the combination of SPR and electrochemical, known as electrochemical-surface plasmon resonance (EC-SPR), spectroscopy, has been used for in situ investigation of optical and electrical properties of conducting polymer films. Moreover, EC-SPR spectroscopy has been applied for monitoring the interaction between biomolecules and electropolymerized conjugated polymer films in biosensor and immunosensor applications. In this paper, recent development and applications on EC-SPR in biosensors will be reviewed.


Author(s):  
E.M. Waddell ◽  
J.N. Chapman ◽  
R.P. Ferrier

Dekkers and de Lang (1977) have discussed a practical method of realising differential phase contrast in a STEM. The method involves taking the difference signal from two semi-circular detectors placed symmetrically about the optic axis and subtending the same angle (2α) at the specimen as that of the cone of illumination. Such a system, or an obvious generalisation of it, namely a quadrant detector, has the characteristic of responding to the gradient of the phase of the specimen transmittance. In this paper we shall compare the performance of this type of system with that of a first moment detector (Waddell et al.1977).For a first moment detector the response function R(k) is of the form R(k) = ck where c is a constant, k is a position vector in the detector plane and the vector nature of R(k)indicates that two signals are produced. This type of system would produce an image signal given bywhere the specimen transmittance is given by a (r) exp (iϕ (r), r is a position vector in object space, ro the position of the probe, ⊛ represents a convolution integral and it has been assumed that we have a coherent probe, with a complex disturbance of the form b(r-ro) exp (iζ (r-ro)). Thus the image signal for a pure phase object imaged in a STEM using a first moment detector is b2 ⊛ ▽ø. Note that this puts no restrictions on the magnitude of the variation of the phase function, but does assume an infinite detector.


Author(s):  
J. Fink

Conducting polymers comprises a new class of materials achieving electrical conductivities which rival those of the best metals. The parent compounds (conjugated polymers) are quasi-one-dimensional semiconductors. These polymers can be doped by electron acceptors or electron donors. The prototype of these materials is polyacetylene (PA). There are various other conjugated polymers such as polyparaphenylene, polyphenylenevinylene, polypoyrrole or polythiophene. The doped systems, i.e. the conducting polymers, have intersting potential technological applications such as replacement of conventional metals in electronic shielding and antistatic equipment, rechargable batteries, and flexible light emitting diodes.Although these systems have been investigated almost 20 years, the electronic structure of the doped metallic systems is not clear and even the reason for the gap in undoped semiconducting systems is under discussion.


The authors' methodic for assessing the role of chemical and physic-chemical factors during the structure formation of gypsum stone is presented in the article. The methodic is also makes it possible to reveal the synergistic effect and to determine the ranges of variation of controls factors that ensure maximum values of such effect. The effect of a micro-sized modifier based on zinc hydro-silicates on the structure formation of building gypsum is analyzed and corresponding dependencies are found. It is shown that effects of influence of modifier on the properties of gypsum compositions are determined by chemical properties of modifier. Among the mentioned properties are sorption characteristics (which depend on the amount of silicic acid and its state) and physicochemical properties - the ability to act as a substrate during crystal formation. The proposed method can also be extended to other binding substances and materials. This article contributes to the understanding of the processes that occur during the structure formation of composites, which will make it possible to control the structure formation in the future, obtaining materials with a given set of properties.


2020 ◽  
Author(s):  
Tulin Okbinoglu ◽  
Pierre Kennepohl

Molecules containing sulfur-nitrogen bonds, like sulfonamides, have long been of interest due to their many uses and chemical properties. Understanding the factors that cause sulfonamide reactivity is important, yet their continues to be controversy regarding the relevance of S-N π bonding in describing these species. In this paper, we use sulfur K-edge x-ray absorption spectroscopy (XAS) in conjunction with density functional theory (DFT) to explore the role of S<sub>3p</sub> contributions to π-bonding in sulfonamides, sulfinamides and sulfenamides. We explore the nature of electron distribution of the sulfur atom and its nearest neighbors and extend the scope to explore the effects on rotational barriers along the sulfur-nitrogen axis. The experimental XAS data together with TD-DFT calculations confirm that sulfonamides, and the other sulfinated amides in this series, have essentially no S-N π bonding involving S<sub>3p</sub> contributions and that electron repulsion and is the dominant force that affect rotational barriers.


2016 ◽  
Vol 4 (2) ◽  
pp. 1
Author(s):  
KUMAR RAJIV ◽  
SHARMA SHUCHI ◽  
DHIMAN NARESH ◽  
PATHAK DINESH ◽  
◽  
...  

1997 ◽  
Author(s):  
Y. Z. Wang ◽  
D. D. Gebler ◽  
D. K. Fu ◽  
T. M. Swager ◽  
A. J. Epstein

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