2014
DOI: 10.1016/j.jelechem.2014.06.036
|View full text |Cite
|
Sign up to set email alerts
|

Synthesis and characterization of electrochromic [Ru(terpy)2 selenophene]-based polymer film

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
2
1

Citation Types

3
5
0

Year Published

2016
2016
2024
2024

Publication Types

Select...
7
1

Relationship

1
7

Authors

Journals

citations
Cited by 20 publications
(10 citation statements)
references
References 24 publications
3
5
0
Order By: Relevance
“…Electrochemical studies of iron and ruthenium complexes of L on ITO-30 film (Fe–L/ITO-30 and Ru–L/ITO-30) show good reversibility at all scan rates from 1 to 200 mV/s. The E 1/2 determined at 50 mV/s for Fe–L/ITO and Ru–L/ITO are equal to 0.49 and 0.54 V (vs Fc/Fc + ), respectively, which is consistent with previously reported values for similar complexes in solution , and on a solid support …”
Section: Resultssupporting
confidence: 91%
See 1 more Smart Citation
“…Electrochemical studies of iron and ruthenium complexes of L on ITO-30 film (Fe–L/ITO-30 and Ru–L/ITO-30) show good reversibility at all scan rates from 1 to 200 mV/s. The E 1/2 determined at 50 mV/s for Fe–L/ITO and Ru–L/ITO are equal to 0.49 and 0.54 V (vs Fc/Fc + ), respectively, which is consistent with previously reported values for similar complexes in solution , and on a solid support …”
Section: Resultssupporting
confidence: 91%
“…Electrochemical studies of iron and ruthenium complexes of L on ITO-30 film (Fe−L/ITO-30 and Ru−L/ITO-30) show good reversibility at all scan rates from 1 to 200 mV/s. The E 1/2 determined at 50 mV/s for Fe− L/ITO and Ru−L/ITO are equal to 0.49 and 0.54 V (vs Fc/ Fc + ), respectively, which is consistent with previously reported values for similar complexes in solution 25,26 and on a solid support. 27 The durability of both Fe−L/ITO and Ru−L/ITO materials is very good and the peak current just insignificantly decreases after 400 cycles compared to the 50 cycle durability test (Figure 2).…”
Section: ■ Results and Discussionsupporting
confidence: 91%
“…As expected, introduction of an aliphatic chain onto the thiophene ring subsequently lowered the melting point of the product (98-99 • C) when compared to other non-functionalized chalcogenophene-substituted terpyridine molecule [20][21][22][23]. This phenomenon is also observed in an hexylthiophene-functionalized 2,2 :2 ,2"-terpyridine [11] (Table 1).…”
Section: Resultssupporting
confidence: 71%
“…Besides the successful integration of terpy into soft materials and polymers, incorporation of this functional component into solid supports is an important step for the creation of materials for molecular electronics and photonics [22], electrochromic materials [23], and solar cells. Terpy motifs have been anchored onto a large number of solid supports resulting in functional materials with enhanced stability and excellent light absorption properties [18,[23][24][25][26][27][28][29].…”
Section: Introductionmentioning
confidence: 99%
“…Terpy motifs have been anchored onto a large number of solid supports resulting in functional materials with enhanced stability and excellent light absorption properties [18,[23][24][25][26][27][28][29]. Nishihara et al have achieved long range electron transport for molecular electric wires by assembling bis(terpyridine) metal complexes on gold surfaces.…”
Section: Introductionmentioning
confidence: 99%