@article{FridmanWollenbergerBogdanovskayaetal.2000, author = {Fridman, Vadim and Wollenberger, Ursula and Bogdanovskaya, V. A. and Lisdat, Fred and Ruzgas, T. and Lindgren, A. and Gorton, Lo and Scheller, Frieder W.}, title = {Electrochemical investigation of cellobiose oxidation by cellobiose dehydrogenase in the presence of cytochrome c as mediator}, year = {2000}, language = {en} } @article{ToetzkeCermakNadezhdinaetal.2017, author = {T{\"o}tzke, Christian and Cermak, Jan and Nadezhdina, Nadezhda and Tributsch, Helmut}, title = {Electrochemical in-situ studies of solar mediated oxygen transport and turnover dynamics in a tree trunk of Tilia cordata}, series = {iForest - Biogeosciences and Forestry}, volume = {10}, journal = {iForest - Biogeosciences and Forestry}, number = {2}, publisher = {SISEF - The Italian Society of Silviculture and Forest Ecology}, address = {Potenza}, issn = {1971-7458}, doi = {10.3832/ifor1681-010}, pages = {355 -- 361}, year = {2017}, abstract = {Platinum electrodes were implanted into the xylem of a lime tree (Tilia cordata) stem and solar- induced electrochemical potential differences of up to 120 mV were measured during the vegetative period and up to 30 mV in winter. The time dependent curves were found to be delayed with respect to solar radiation, sap flow activity, temperature and vapor pressure deficit. A general equation for the potential difference was derived and simplified by analyzing the effect of temperature and tensile strength. The potential determining influence of oxygen concentration on the respective location of the platinum electrode was identified as the principal phenomenon measured. A systematic analysis and investigation of the observed periodic oxygen concentration signals promises new information on sap flow, oxygen diffusion through tree tissues and on oxygen consumption related to the energy turnover in tree tissues.}, language = {en} } @article{TurhanSaracGencturketal.2012, author = {Turhan, Metehan C. and Sarac, A. Sezai and Gencturk, Asli and Gilsing, Hans-Detlev and Faltz, Heike and Schulz, Burkhard}, title = {Electrochemical impedance characterization and potential dependence of poly[3,4-(2,2-dibutylpropylenedioxy)thiophene] nanostructures on single carbon fiber microelectrode}, series = {Synthetic metals : the journal of electronic polymers and electronic molecular materials}, volume = {162}, journal = {Synthetic metals : the journal of electronic polymers and electronic molecular materials}, number = {5-6}, publisher = {Elsevier}, address = {Lausanne}, issn = {0379-6779}, doi = {10.1016/j.synthmet.2012.01.012}, pages = {511 -- 515}, year = {2012}, abstract = {The electropolymerization of 3,4-(2,2-dibutylpropylenedioxy)thiophene (ProDOT-Bu-2) onto single carbon fiber microelectrode (SCFME) was conducted in acetonitrile (ACN) containing sodium perchlorate (NaClO4) as electrolyte and investigated by cyclic voltammetry (CV). The nanostructured films of poly[3,4-(2,2-dibutyl-propyleneclioxy)thiophene] (PProDOT-Bu-2) which were depositing showed complete reversible redox behavior in monomer-free electrolyte solution. The capacitive behavior of the films was investigated by electrochemical impedance spectroscopy (EIS) at applied potentials from 0.1 V to 1.3 V. The analysis by equivalent circuit modeling revealed an applied potential around 0.4V to be most suitable for the system PProDOT-Bu-2/SCFME as a double layer supercapacitor component inducing a double layer capacitance C-d, value of 62 mFcm(-2).}, language = {en} } @article{HoefsHuelagueBennetetal.2021, author = {H{\"o}fs, Soraya and Huelague, Deniz and Bennet, Francesca and Carl, Peter and Flemig, Sabine and Schmid, Thomas and Schenk, Jorg A. and Hodoroaba, Vasile-Dan and Schneider, Rudolf J.}, title = {Electrochemical immunomagnetic Ochratoxin A sensing}, series = {ChemElectroChem}, volume = {8}, journal = {ChemElectroChem}, number = {13}, publisher = {Wiley-VCH}, address = {Weinheim}, issn = {2196-0216}, doi = {10.1002/celc.202100446}, pages = {2597 -- 2606}, year = {2021}, abstract = {Electrochemical methods offer great promise in meeting the demand for user-friendly on-site devices for monitoring important parameters. The food industry often runs own lab procedures, for example, for mycotoxin analysis, but it is a major goal to simplify analysis, linking analytical methods with smart technologies. Enzyme-linked immunosorbent assays, with photometric detection of 3,3',5,5'-tetramethylbenzidine (TMB), form a good basis for sensitive detection. To provide a straightforward approach for the miniaturization of the detection step, we have studied the pitfalls of the electrochemical TMB detection. By cyclic voltammetry it was found that the TMB electrochemistry is strongly dependent on the pH and the electrode material. A stable electrode response to TMB could be achieved at pH 1 on gold electrodes. We created a smartphone-based, electrochemical, immunomagnetic assay for the detection of ochratoxin A in real samples, providing a solid basis for sensing of further analytes.}, language = {en} } @article{WarsinkeBenkertScheller2000, author = {Warsinke, Axel and Benkert, Alexander and Scheller, Frieder W.}, title = {Electrochemical immunoassays}, year = {2000}, language = {en} } @article{QinHeilSchmidtetal.2019, author = {Qin, Qing and Heil, T. and Schmidt, J. and Schmallegger, Max and Gescheidt, Georg and Antonietti, Markus and Oschatz, Martin}, title = {Electrochemical Fixation of Nitrogen and Its Coupling with Biomass Valorization with a Strongly Adsorbing and Defect Optimized Boron-Carbon-Nitrogen Catalyst}, series = {ACS Applied Energy Materials}, volume = {2}, journal = {ACS Applied Energy Materials}, number = {11}, publisher = {American Chemical Society}, address = {Washington}, issn = {2574-0962}, doi = {10.1021/acsaem.9b01852}, pages = {8359 -- 8365}, year = {2019}, abstract = {The electrochemical conversion of low-cost precursors into high-value chemicals using renewably generated electricity is a promising approach to build up an environmentally friendly energy cycle, including a storage element. The large-scale implementation of such process can, however, only be realized by the design of cost-effective electrocatalysts with high efficiency and highest stability. Here, we report the synthesis of N and B codoped porous carbons. The constructed B-N motives combine abundant unpaired electrons and frustrated Lewis pairs (FLPs). They result in desirable performance for electrochemical N-2 reduction reaction (NRR) and electrooxidation of 5-hydroxymethylfurfural (HMF) in the absence of any metal cocatalyst. A maximum Faradaic efficiency of 15.2\% with a stable NH3 production rate of 21.3 mu g h(-1) mg(-1) is obtained in NRR. Besides, 2,5-furandicarboxylic acid (FDCA) is first obtained by using non-metalbased electrocatalysts at a conversion of 71\% and with yield of 57\%. Gas adsorption experiments elucidate the relationship between the structure and the ability of the catalysts to activate the substrate molecules. This work opens up deep insights for the rational design of non-metal-based catalysts for potential electrocatalytic applications and the possible enhancement of their activity by the introduction of FLPs and point defects at grain boundaries.}, language = {en} } @article{DechtriratGajovicEichelmannWojciketal.2014, author = {Dechtrirat, Decha and Gajovic-Eichelmann, Nenad and Wojcik, Felix and Hartmann, Laura and Bier, Frank Fabian and Scheller, Frieder W.}, title = {Electrochemical displacement sensor based on ferrocene boronic acid tracer and immobilized glycan for saccharide binding proteins and E. coli}, series = {Biosensors and bioelectronics : the principal international journal devoted to research, design development and application of biosensors and bioelectronics}, volume = {58}, journal = {Biosensors and bioelectronics : the principal international journal devoted to research, design development and application of biosensors and bioelectronics}, publisher = {Elsevier}, address = {Oxford}, issn = {0956-5663}, doi = {10.1016/j.bios.2014.02.028}, pages = {1 -- 8}, year = {2014}, abstract = {Pathogens such as viruses and bacteria use their envelope proteins and their adhesin lectins to recognize the glycan residues presented on the cell surface of the target tissues. This principle of recognition is used in a new electrochemical displacement sensor for the protein concanavalin A (ConA). A gold electrode was first modified with a self-assembled monolayer of a thiolated mannose/OEG conjugate and a ferrocene boroxol derivative was pre-assembled as reporter molecule onto the mannose surface. The novel tracer molecule based on a 2-hydroxymethyl phenyl boronic acid derivative binds even at neutral pH to the saccharides which could expand the application towards biological samples (i.e., urine and feces). Upon the binding of ConA, the tracer was displaced and washed away from the sensor surface leading to a decrease in the electrochemical signal. Using square wave voltammetry (SWV), the concentration of ConA in the sample solution could be determined in the dynamic concentration range established from 38 nmol L-1 to 5.76 mu mol L-1 with a reproducible detection limit of 1 mu g mL(-1) (38 nmol L-1) based on the signal-to-noise ratio (S/N=3) with fast response of 15 min. The new reporter molecule showed a reduced non-specific displacement by BSA and ribonuclease A. The sensor was also successfully transferred to the first proof of principle for the detection of Escherichia coli exhibiting a detection limit of approximately 6 x 102 cells/mL Specificity of the displacement by target protein ConA and E. coli was demonstrated since the control proteins (i.e., BSA and RNaseA) and the control E. coli strain, which lack of type 1 fimbriae, were ineffective. (C) 2014 Elsevier B.V. All rights reserved.}, language = {en} } @article{ChenStoeckleinSchelleretal.2003, author = {Chen, Jian and St{\"o}cklein, Walter F. M. and Scheller, Frieder W. and Wollenberger, Ursula}, title = {Electrochemical determination of human hemoglobin by using ferrocene carboxylic acid modified carbon powder microelectrode}, year = {2003}, language = {en} } @article{FandrichBullerWischerhoffetal.2012, author = {Fandrich, Artur and Buller, Jens and Wischerhoff, Erik and Laschewsky, Andr{\´e} and Lisdat, Fred}, title = {Electrochemical detection of the thermally induced phase transition of a thin stimuli-responsive polymer film}, series = {ChemPhysChem : a European journal of chemical physics and physical chemistry}, volume = {13}, journal = {ChemPhysChem : a European journal of chemical physics and physical chemistry}, number = {8}, publisher = {Wiley-VCH}, address = {Weinheim}, issn = {1439-4235}, doi = {10.1002/cphc.201100924}, pages = {2020 -- 2023}, year = {2012}, language = {en} } @article{FandrichBullerSchaeferetal.2015, author = {Fandrich, Artur and Buller, Jens and Sch{\"a}fer, Daniel and Wischerhoff, Erik and Laschewsky, Andr{\´e} and Lisdat, Fred}, title = {Electrochemical characterization of a responsive macromolecular interface on gold}, series = {Physica status solidi : A, Applications and materials science}, volume = {212}, journal = {Physica status solidi : A, Applications and materials science}, number = {6}, publisher = {Wiley-VCH}, address = {Weinheim}, issn = {1862-6300}, doi = {10.1002/pssa.201431698}, pages = {1359 -- 1367}, year = {2015}, abstract = {This study reports on the investigation of a thermoresponsive polymer as a thin film on electrodes and the influence of coupling a peptide and an antibody to the film. The utilized polymer from the class of poly(oligoethylene glycol)-methacrylate polymers (poly(OEGMA)) with carboxy functions containing side chains was synthesized and properly characterized in aqueous solutions. The dependence of the cloud point on the pH of the surrounding media is discussed. The responsive polymer was immobilized on gold electrodes as shown by electrochemical, quartz crystal microbalance (QCM), and atomic force microscopy (AFM) techniques. The temperature dependent behavior of the polymer covalently grafted to gold substrates is investigated using cyclic voltammetry (CV) in ferro-/ferricyanide solution. Significant changes in the slope of the temperature-dependence of the voltammetric peak current and the peak separation values clearly indicate the thermally induced conformational change on the surface. Finally, a biorecognition reaction between a short FLAG peptide (N-Asp-Tyr-Lys-Asp-Asp-Asp-Asp-Lys-C) covalently immobilized on the polymer interface and the corresponding IgG antibody was performed. The study shows that the responsiveness of the electrode is retained after peptide coupling and antibody binding, although the response is diminished.}, language = {en} }