Enhancing ElectrochromicStability of Triphenylamine-BasedPolymers via Monomer Ratio Optimization

In the pursuit of high-performance organic electrochromic (OEC) materials that transition from transparent to deep colors, we design and synthesize a series of copolymerstermed MeT<sub>m</sub>PhF<sub>n</sub>composed of TPA and fluorene with triethylene glycol and ester groups incorporated. This is achieved through gradient tuning of monomer ratios via Suzuki copolymerization. Five of these polymers exhibit excellent film-forming properties, and their electrochromic devices demonstrate remarkable pale blue-to-reddish brown switching behavior. Notably, benefiting from the suitable continuity and moderate porosity of MeT<sub>0.5</sub>PhF<sub>0.5</sub> film, the electrochromic device based on MeT<sub>0.5</sub>PhF<sub>0.5</sub> showcases rapid reversible switching times of 2.5 s for coloring and 1.3 s for bleaching, highlighting its exceptional responsiveness. This device achieves the highest contrast of 58.7% at 465 nm, paired with impressive cycling stability, retaining 93.7% of its initial contrast ratio after 1440 cycles, and exhibits a high coloration efficiency of 619 cm<sup>2</sup> C<sup>–1</sup>. This study presents an effective approach for designing and synthesizing high-performance electrochromic copolymers that effectively transition from colorless to vibrant hues, paving the way for advanced applications in smart windows and display technologies.

Publication Details

Journal
Figshare
Published
2025-03-28
DOI
https://doi.org/10.1021/acsami.4c22689.s001
Primary Topic
Wheat and Barley Genetics and Pathology
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Enhancing ElectrochromicStability of Triphenylamine-BasedPolymers via Monomer Ratio Optimization

Figshare
Wheat and Barley Genetics and Pathology
article

Enhancing ElectrochromicStability of Triphenylamine-BasedPolymers via Monomer Ratio Optimization

article en

Abstract

In the pursuit of high-performance organic electrochromic (OEC) materials that transition from transparent to deep colors, we design and synthesize a series of copolymerstermed MeT<sub>m</sub>PhF<sub>n</sub>composed of TPA and fluorene with triethylene glycol and ester groups incorporated. This is achieved through gradient tuning of monomer ratios via Suzuki copolymerization. Five of these polymers exhibit excellent film-forming properties, and their electrochromic devices demonstrate remarkable pale blue-to-reddish brown switching behavior. Notably, benefiting from the suitable continuity and moderate porosity of MeT<sub>0.5</sub>PhF<sub>0.5</sub> film, the electrochromic device based on MeT<sub>0.5</sub>PhF<sub>0.5</sub> showcases rapid reversible switching times of 2.5 s for coloring and 1.3 s for bleaching, highlighting its exceptional responsiveness. This device achieves the highest contrast of 58.7% at 465 nm, paired with impressive cycling stability, retaining 93.7% of its initial contrast ratio after 1440 cycles, and exhibits a high coloration efficiency of 619 cm<sup>2</sup> C<sup>–1</sup>. This study presents an effective approach for designing and synthesizing high-performance electrochromic copolymers that effectively transition from colorless to vibrant hues, paving the way for advanced applications in smart windows and display technologies.

Figshare
Openalex Percentile: Top 42%
Wheat and Barley Genetics and Pathology
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.

Enhancing ElectrochromicStability of Triphenylamine-BasedPolymers via Monomer Ratio Optimization · Figshare (2025) | TGRS Research Map | TGRS