2012
DOI: 10.1016/j.matchemphys.2012.01.126
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Embedding and electropolymerization of terthiophene derivatives in porous n-type silicon

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Cited by 13 publications
(11 citation statements)
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“…New components for optoelectronics have been elaborated by incorporating π‐ conjugated monomers into mesoporous silicon matrices. Through hydrogen bonding interactions, supramolecular architectures can be achieved within the pores as already observed with a diacetylenic monomer bearing carboxylic end groups, as well as with a terthiophene carboxylic acid: (2,2′:5′‐2″‐terthiophene‐3′‐acetic acid) (3‐TTAA) . Moreover, the subsequent in situ electrochemical polymerization of the 3‐TTAA monomer molecules embedded in the porous silicon matrix leads to organization of conjugated macromolecules within the pores .…”
Section: Introductionmentioning
confidence: 89%
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“…New components for optoelectronics have been elaborated by incorporating π‐ conjugated monomers into mesoporous silicon matrices. Through hydrogen bonding interactions, supramolecular architectures can be achieved within the pores as already observed with a diacetylenic monomer bearing carboxylic end groups, as well as with a terthiophene carboxylic acid: (2,2′:5′‐2″‐terthiophene‐3′‐acetic acid) (3‐TTAA) . Moreover, the subsequent in situ electrochemical polymerization of the 3‐TTAA monomer molecules embedded in the porous silicon matrix leads to organization of conjugated macromolecules within the pores .…”
Section: Introductionmentioning
confidence: 89%
“…Through hydrogen bonding interactions, supramolecular architectures can be achieved within the pores as already observed with a diacetylenic monomer bearing carboxylic end groups, as well as with a terthiophene carboxylic acid: (2,2′:5′‐2″‐terthiophene‐3′‐acetic acid) (3‐TTAA) . Moreover, the subsequent in situ electrochemical polymerization of the 3‐TTAA monomer molecules embedded in the porous silicon matrix leads to organization of conjugated macromolecules within the pores . Hydrogen bonding assemblies are also involved in the synthesis of some molecular imprinted polymers (MIPs), which find numerous applications such as in the domain of analytical chemistry .…”
Section: Introductionmentioning
confidence: 93%
“…Another important advantage to be considered for justifying the use of oligothiophene instead of the monomer, is the significant redox potential decreases required for the electropolymerization. 31 Deposits obtained on Pt«(SiO 2 ) n and Pt electrodes were initially evaluated by their electrochemical response in solutions containing solely the supporting electrolyte. In this case obtainment of stable and reproducible profiles, as a way to prevent over-oxidation of the polymeric material, was searched for, behavior also observed and reported by other authors.…”
Section: ¹1mentioning
confidence: 99%
“…As Badeva et al pointed out, 31 it must be kept in mind that success of pore filling with the polymeric material is an important factor for the efficient obtention of materials. However, no many reports exist that give evidence concerning the level of pore filling, such as parameters for determining how many cycles of polymerization are needed to homogeneously "fill" the pores forming the template; consequently a study comparing the profile of deposit growth performing one to five polymerization cycles was accomplished.…”
Section: ¹1mentioning
confidence: 99%
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