TY  - JOUR
A1  - Fandrich, Artur
A1  - Buller, Jens
A1  - Memczak, Henry
A1  - Stoecklein, W.
A1  - Hinrichs, K.
A1  - Wischerhoff, E.
A1  - Schulz, B.
A1  - Laschewsky, André
A1  - Lisdat, Fred
T1  - Responsive Polymer-Electrode Interface-Study of its Thermo- and pH-Sensitivity and the Influence of Peptide Coupling
JF  - Electrochimica acta : the journal of the International Society of Electrochemistry (ISE)
N2  - This study introduces a thermally responsive, polymer-based electrode system. The key component is a surface-attached, temperature-responsive poly(oligoethylene glycol) methacrylate (poly(OEGMA)) type polymer bearing photoreactive benzophenone and carboxy groups containing side chains. The responsive behavior of the polymer in aqueous media has been investigated by turbidimetry measurements. Polymer films are formed on gold substrates by means of the photoreactive 2(dicyclohexylphosphino)benzophenone (DPBP) through photocrosslinking. The electrochemical behavior of the resulting polymer-substrate interface has been investigated in buffered [Fe(CN)6](3-)/[Fe (CN)6](4-)solutions at room temperature and under temperature variation by cyclic voltammetry (CV). The CV experiments show that with increasing temperature structural changes of the polymer layer occur, which alter the output of the electrochemical measurement. Repeated heating/cooling cycles analyzed by CV measurements and pH changes analyzed by quartz crystal microbalance with dissipation monitoring (QCM-D) reveal the reversible nature of the restructuring process. The immobilized films are further modified by covalent coupling of two small biomolecules - a hydrophobic peptide and a more hydrophilic one. These attached components influence the hydrophobicity of the layer in a different way the resulting change of the temperature-caused behavior has been studied by CV indicating a different state of the polymer after coupling of the hydrophobic peptide.
KW  - Stimuli-responsive materials
KW  - electroanalysis
KW  - modified electrode
KW  - bioreceptors
KW  - peptides
KW  - surface modification
KW  - cyclic voltammetry
KW  - IR ellipsometry
KW  - quartz crystal microbalance
Y1  - 2017
U6  - https://doi.org/10.1016/j.electacta.2017.01.080
SN  - 0013-4686
SN  - 1873-3859
VL  - 229
SP  - 325
EP  - 333
PB  - Elsevier
CY  - Oxford
ER  - 
TY  - JOUR
A1  - Lange, Ilja
A1  - Reiter, Sina
A1  - Paetzel, Michael
A1  - Zykov, Anton
A1  - Nefedov, Alexei
A1  - Hildebrandt, Jana
A1  - Hecht, Stefan
A1  - Kowarik, Stefan
A1  - Woell, Christof
A1  - Heimel, Georg
A1  - Neher, Dieter
T1  - Tuning the work function of polar zinc oxide surfaces using modified phosphonic acid self-assembled monolayers
JF  - Advanced functional materials
N2  - Zinc oxide (ZnO) is regarded as a promising alternative material for transparent conductive electrodes in optoelectronic devices. However, ZnO suffers from poor chemical stability. ZnO also has a moderate work function (WF), which results in substantial charge injection barriers into common (organic) semiconductors that constitute the active layer in a device. Controlling and tuning the ZnO WF is therefore necessary but challenging. Here, a variety of phosphonic acid based self-assembled monolayers (SAMs) deposited on ZnO surfaces are investigated. It is demonstrated that they allow the tuning the WF over a wide range of more than 1.5 eV, thus enabling the use of ZnO as both the hole-injecting and electron-injecting contact. The modified ZnO surfaces are characterized using a number of complementary techniques, demonstrating that the preparation protocol yields dense, well-defined molecular monolayers.
KW  - ZnO
KW  - self-assembled monolayers
KW  - phosphonic acid
KW  - surface modification
KW  - electrodes
Y1  - 2014
U6  - https://doi.org/10.1002/adfm.201401493
SN  - 1616-301X
SN  - 1616-3028
VL  - 24
IS  - 44
SP  - 7014
EP  - 7024
PB  - Wiley-VCH
CY  - Weinheim
ER  -