Stable doping of indacenodithieno[3,2-]thiophene (IDTT) structures enables easy color tuning and significant improvement in the charge storage capacity of electrochromic polymers, making use of their full potential as electrochromic supercapacitors and in other emerging hybrid applications. Here, the IDTT structure is copolymerized with four different donor-acceptor-donor (DAD) units, with subtle changes in their electron-donating and electron-withdrawing characters, so as to obtain four different donor-acceptor copolymers. The polymers attain important form factor requirements for electrochromic supercapacitors: desired switching between achromatic black and transparent states (*** 45.9, -3.1, -4.2/86.7, -2.2, and -2.7 for PIDTT-TBT), high optical contrast (72% for PIDTT-TBzT), and excellent electrochemical redox stability (I/I 1.0 for PIDTT-EBE). Poly[indacenodithieno[3,2-]thiophene-2,8-diyl--4,7-bis(2,3-dihydrothieno[3,4-][1,4]dioxin-5-yl)-2-(2-hexyldecyl)-2-benzo[][1,2,3]triazole-7,7'-diyl] (PIDTT-EBzE) stands out as delivering simultaneously a high contrast (69%) and doping level (>100%) and specific capacitance (260 F g). This work introduces IDTT-based polymers as bifunctional electro-optical materials for potential use in color-tailored, color-indicating, and self-regulating smart energy systems.

Download full-text PDF

Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7872426PMC
http://dx.doi.org/10.1021/acs.macromol.0c02212DOI Listing

Publication Analysis

Top Keywords

donor-acceptor copolymers
8
electrochromic supercapacitors
8
highly stable
4
stable indacenodithieno[32-]thiophene-based
4
indacenodithieno[32-]thiophene-based donor-acceptor
4
copolymers hybrid
4
electrochromic
4
hybrid electrochromic
4
electrochromic energy
4
energy storage
4

Similar Publications

Conjugated donor-acceptor (D-A) copolymers are widely used in optoelectronic devices due to their influence on the resulting properties. This study focuses on the synthesis and characterization of the conjugated D-A copolymer constructed with fluorene and di-2-thienyl-2,1,3-benzothiadiazole units, resulting in Poly[2,7-(9,9-dioctyl-fluorene)-alt-5,5-(4,7-di(2-thienyl)-2,1,3-benzothiadiazole)] (PFDTBT). The synthesis associated with reaction times of 48 and 24 h, the latter incorporating the phase-transfer catalyst Aliquat 336, was investigated.

View Article and Find Full Text PDF

Naphthalenediimide (NDI)-based donor-acceptor co-polymers with tunable electronic, optical, mechanical, and transport properties have shown immense potential as n-type conducting polymers in organic (opto)electronics. During the operation, the polymers undergo reduction at different charged states, which alters their (opto)electronic properties mainly due to the formation of the quasiparticles, polaron/bipolaron. The theoretical study based on quantum mechanical calculations can provide us with a detailed understanding of their (opto)electronic properties, which is missing to a great extent.

View Article and Find Full Text PDF

Core-Shell PLGA Nanoparticles: In Vitro Evaluation of System Integrity.

Biomolecules

December 2024

Faculty of Chemical and Pharmaceutical Technologies and Biomedical Preparations, D. Mendeleev University of Chemical Technology of Russia, Miusskaya pl. 9, Moscow 125047, Russia.

The objective of this study was to compare the properties of core-shell nanoparticles with a PLGA core and shells composed of different types of polymers, focusing on their structural integrity. The core PLGA nanoparticles were prepared either through a high-pressure homogenization-solvent evaporation technique or nanoprecipitation, using poloxamer 188 (P188), a copolymer of divinyl ether with maleic anhydride (DIVEMA), and human serum albumin (HSA) as the shell-forming polymers. The shells were formed through adsorption, interfacial embedding, or conjugation.

View Article and Find Full Text PDF

Strong Anionic Fluorene Donor-Acceptor Copolyelectrolytes from Protected Hydrophobic Precursors.

Macromol Rapid Commun

January 2025

Polymer Science, Zernike Institute for Advanced Materials, University of Groningen, Nijenborgh 3, Groningen, 9747 AG, The Netherlands.

Conjugated polyelectrolytes (CPEs), materials that are defined by a -conjugated backbone and charged ionic functional groups, are frequently prepared through direct polymerization of charged monomer species in aqueous media. This route is, however, often accompanied by labor-intensive work-up procedures, low yields, and ultimately results in materials that are difficult to characterize. To overcome these inconveniences, in this work protection chemistry is applied on sulfonate-functionalized fluorene monomers that are polymerized under standard Suzuki polycondensation conditions to obtain protected donor-acceptor copolymers.

View Article and Find Full Text PDF

The intermolecular host-guest complexation of head-to-tail monomers consisting of cleft-shaped bisporphyrin and trinitrofluorenone units connected by a chiral binaphthyl linker was employed to construct helically twisted supramolecular polymers. Results from 1H NMR, diffusion-ordered NMR spectroscopy, and viscometry experiments revealed that the supramolecular polymerization of these monomers follows a ring-chain competition mechanism. The introduction of bulky substituents at the linker significantly suppressed the formation of macrocyclic oligomers, whereas smaller alkyl chains facilitated the formation of the cyclic form.

View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!