In this work, bipolar electrochemistry (BPE) is used as a dual wireless tool to generate and to activate a thermoresponsive electrochemiluminescent (ECL) Janus object. For the first time, BPE allows regioselective growth of a poly(N-isopropylacrylamide) (pNIPAM) hydrogel film on one side of a carbon fiber. It is achieved thanks to the local reduction of persulfate ions, which initiate radical polymerization of NIPAM. By controlling the electric field and the time of the bipolar electrochemical reactions, we are able to control the length and the thickness of the deposit. The resulting pNIPAM film is found to be swollen in water at room temperature and collapsed when heated above 32 °C. We further incorporated a covalently attached ruthenium complex luminophore, Ru(bpy), in the hydrogel film. In the second time, BPE is used to activate remotely the electrogenerated chemiluminescence (ECL) of the Ru(bpy) moieties in the film. We take advantage of the film responsiveness to amplify the ECL signal. Upon collapse of the film, the ECL signal, which is sensitive to the distance between adjacent Ru(bpy) centers, is strongly amplified. It is therefore shown that BPE is a versatile tool to generate highly sophisticated materials based on responsive polymers, which could lead to sensitive sensors.
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http://dx.doi.org/10.1021/acs.langmuir.6b03040 | DOI Listing |
Anal Chem
December 2024
National Centre for Sensor Research, School of Chemical Sciences, Dublin City University, Dublin 9 D09 V209, Ireland.
Wirefree, or bipolar electrochemistry, is advancing key fields, including (nano)materials, human health, and energy. Central to these applications is an understanding of the potential distribution induced in the bipolar electrode, BPE. Here, the impact of the electric field distribution is reported for the wirefree deposition of the conducting polymer, poly(3,4-ethylenedioxythiophene), PEDOT, in the absence of deliberately added electrolytes.
View Article and Find Full Text PDFChem Sci
December 2024
University Bordeaux, CNRS, Bordeaux INP, ISM UMR 5255 33607 Pessac France
Electrochemiluminescence (ECL) has emerged as a valuable tool for understanding multiphasic and compartmentalized systems, which have crucial wide-ranging applications across diverse fields. However, ECL reactions are limited to the vicinity of the electrode surface due to spatial constraints of electron transfer and the short lifetime of radical species, making ECL emission in bulk multiphasic solution challenging. To address this limitation, we propose a novel bipolar electrochemistry (BPE) approach for wireless dual-color ECL emission at the water/organic (w/o) interface.
View Article and Find Full Text PDFMikrochim Acta
November 2024
Center of Excellence in Electrochemistry, School of Chemistry, College of Science, University of Tehran, Tehran, Iran.
ACS Appl Mater Interfaces
October 2024
Department of Energy Conversion and Storage, Technical University of Denmark, Elektrovej, Building 375, Lyngby 2800, Denmark.
Bipolar membranes (BPMs) enable the operation of electrochemical reactors with electrode compartments in different chemical environments or pH. The transport properties at the microscopic scale are dictated by the composition and morphology of the interfacial junctions as well as the specific chemistry of the ion-exchange layers that support the current of protons and hydroxide ions. This work elucidates the relation between water-dissociation efficiency and the physicochemical properties of the individual ion-exchange membrane layers in the poly(styrene--poly(ethylene--butylene)--polystyrene) (SEBS)-based BPM.
View Article and Find Full Text PDFNat Commun
September 2024
Department of Chemical Engineering, Delft University of Technology; 9 van der Maasweg, Delft, 2629HZ, the Netherlands.
Bipolar membranes in electrochemical CO conversion cells enable different reaction environments in the CO-reduction and O-evolution compartments. Under ideal conditions, water-splitting in the bipolar membrane allows for platinum-group-metal-free anode materials and high CO utilizations. In practice, however, even minor unwanted ion crossover limits stability to short time periods.
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