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Title: Hydrophobic effects in surface-confined decaalkylferrocene redox polymers

Journal Article · · Langmuir; (United States)
DOI:https://doi.org/10.1021/la00031a043· OSTI ID:5713399
;  [1]
  1. Massachusetts Inst. of Technology, Cambridge, MA (United States)

Surface-confined redox-active polymers formed from a decaalkylferrocene derivative containing two trialkoxysilylbutyl groups, 1, are durable, pinhole-free electroactive films in nonaqueous solvents (E[degrees][prime] = [minus]0.09 V vs SCE). n-Si electrodes can be derivatized with 1 to give photoelectrodes that, when illuminated with light of energy greater than the band gap, cause the photooxidation of 1 with a photovoltage of 0.45 V. Electrodes derivated with 1 show pronounced solvent effects upon switching from nonaqueous to aqueous electrolyte; in aqueous media current associated with oxidation of the polymers decreases significantly. Contact angle measurements of H[sub 2]O on films of 1 approach 90[degrees], showing that decalkylferrocene polymer/solution interfaces are hydrophobic. In contrast, by covalently binding a cyanopropyl group into the decaalkylferrocene film using (3-cyanopropy) triethoxylsilane, the electrode response in aqueous media was similar to that in nonaqueous media. However, the contact angle of H[sub 2]O is not significantly lower than for films of 1, suggesting that the nitrile groups act to support ion transport within the film. 18 refs., 5 figs., 1 tab.

OSTI ID:
5713399
Journal Information:
Langmuir; (United States), Vol. 9:7; ISSN 0743-7463
Country of Publication:
United States
Language:
English