Electrolyte tuning in dye-sensitized solar cells with N-heterocyclic carbene (NHC) iron(II) sensitizers

• Mariia Karpacheva,
• Catherine E. Housecroft and
• Edwin C. Constable

Beilstein J. Nanotechnol. 2018, 9, 3069–3078, doi:10.3762/bjnano.9.285

• achieved giving η in the range of 0.47 to 0.57% which represents 7.8 to 9.3% relative to an N719 reference DSC set at 100%. Electrochemical impedance spectroscopy has been used to understand the role of the MBI additive in the electrolytes. Keywords: dye-sensitized solar cell; electrolyte; nanoparticles

• mV (no TBP) to 541 mV (0.5 M TBP). However, this gain is not sufficient to enhance the global efficiency which drops from 0.51% to 0.26% (Table 4). The trends are reproduced for duplicate DSCs (Table S2, Supporting Information File 1). Electrochemical impedance spectroscopy (EIS) Electrochemical

• impedance spectroscopy (EIS) is an important technique for the investigation of interfaces in DSCs [49][50]. Fitting of the Nyquist and Bode plots, which are used to describe the EIS results, leads to parameters including the recombination resistance (Rrec), electron/hole transport resistance (Rtr), charge

Impact of the anodization time on the photocatalytic activity of TiO₂ nanotubes

• Jesús A. Díaz-Real,
• Geyla C. Dubed-Bandomo,
• Juan Galindo-de-la-Rosa,
• Luis G. Arriaga,
• Janet Ledesma-García and
• Nicolas Alonso-Vante

Beilstein J. Nanotechnol. 2018, 9, 2628–2643, doi:10.3762/bjnano.9.244

• hypothesis of a doping effect originating from an extended anodization time (Figure S3a, Supporting Information File 1). As it was stated in previous sections, a relation between the capacitive processes seems to be associated with the length of the TNTs. Consequently, electrochemical impedance spectroscopy

Correlative electrochemical strain and scanning electron microscopy for local characterization of the solid state electrolyte Li_1.3Al_0.3Ti_1.7(PO₄)₃

• Nino Schön,
• Deniz Cihan Gunduz,
• Shicheng Yu,
• Hermann Tempel,
• Roland Schierholz and
• Florian Hausen

Beilstein J. Nanotechnol. 2018, 9, 1564–1572, doi:10.3762/bjnano.9.148

• improvement of solid state electrolytes such as LATP is a better understanding of interfacial and ion transport properties on relevant length scales in the nanometer to micrometer range. Using common techniques, such as electrochemical impedance spectroscopy, only global information can be obtained. In this

• grain boundaries with an overall conductivity of 0.2 mS cm−1 [11] and has therefore attracted much research within the last decade [12][13][14][15]. In classical electrochemical impedance spectroscopy (EIS), the ionic conductivity is measured through the entire sample and over the full electrode contact

Ag₂WO₄ nanorods decorated with AgI nanoparticles: Novel and efficient visible-light-driven photocatalysts for the degradation of water pollutants

• Shijie Li,
• Shiwei Hu,
• Wei Jiang,
• Yanping Liu,
• Yu Liu,
• Yingtang Zhou,
• Liuye Mo and
• Jianshe Liu

Beilstein J. Nanotechnol. 2018, 9, 1308–1316, doi:10.3762/bjnano.9.123

• RhB in the presence of 0.3AgI/Ag2WO4. (a) The cycled photocatalytic degradation of RhB over 0.3AgI/Ag2WO4; (b) XRD patterns of the fresh and used 0.3AgI/Ag2WO4. Active-species trapping tests over 0.3AgI/Ag2WO4. Electrochemical impedance spectroscopy (EIS) Nyquist plots of AgI and 0.3AgI/Ag2WO4

• impedance spectroscopy (EIS) measurement was applied to study the charge transport and separation [49]. A smaller arc radius commonly signifies a higher charge transport rate. As displayed in Figure 10, the arc radius of 0.3AgI/Ag2WO4 is smaller than that of AgI, suggesting that 0.3AgI/Ag2WO4 holds a higher

• −) scavenger) or ammonium oxalate (a hole radical (h+) scavenger) was introduced, the degradation rate of RhB was severely depressed. That is, •O2−, •OH, and h+ were generated in the 0.3AgI/Ag2WO4 mediated degradation system, but •O2− and h+ played a more crucial role in RhB degradation. Electrochemical

Cyclodextrin inhibits zinc corrosion by destabilizing point defect formation in the oxide layer

• Abdulrahman Altin,
• Maciej Krzywiecki,
• Adnan Sarfraz,
• Cigdem Toparli,
• Claudius Laska,
• Philipp Kerger,
• Aleksandar Zeradjanin,
• Karl J. J. Mayrhofer,
• Michael Rohwerder and
• Andreas Erbe

Beilstein J. Nanotechnol. 2018, 9, 936–944, doi:10.3762/bjnano.9.86

• . This work uses electrochemical impedance spectroscopy to show the cyclic oligosaccharide β-cyclodextrin (β-CD) to inhibit corrosion of zinc in 0.1M chloride with an inhibition efficiency of up to 85%. Only a monomolecular adsorption layer of β-CD is present on the surface of the oxide covered metal

• inhibitors [8][12][13]. Metallic zinc is industrially used for cathodic protection of steel [15]. In this work, the inhibition of zinc corrosion by β-CD was investigated electrochemically. Inhibition efficiencies were determined by electrochemical impedance spectroscopy (EIS). After exposure to chloride

Synthesis and characterization of electrospun molybdenum dioxide–carbon nanofibers as sulfur matrix additives for rechargeable lithium–sulfur battery applications

• Ruiyuan Zhuang,
• Shanshan Yao,
• Maoxiang Jing,
• Xiangqian Shen,
• Jun Xiang,
• Tianbao Li,
• Kesong Xiao and
• Shibiao Qin

Beilstein J. Nanotechnol. 2018, 9, 262–270, doi:10.3762/bjnano.9.28

• electrodes were evaluated by cyclic voltammetry (CV), galvanostatic charge–discharge and electrochemical impedance spectroscopy (EIS). The electrochemical characteristics of the cells with S/MoO2–CNF cathodes and pure sulfur cathodes were examined by CV in the voltage range of 1.7–3.0 V at the scanning rate

• effect of the MoO2–CNF matrix material calcined at different temperatures on the electrochemical performance of the sulfur cathode. Compared to the CV technique, the diffusion coefficients under equilibrium conditions can be expressed by electrochemical impedance spectroscopy (EIS). Additionally, the

• temperatures with S/composite cathodes and pure sulfur cathode at 0.25 mA cm−2. (a) Electrochemical impedance spectroscopy of MoO2–CNFs calcined at different temperatures with sulfur cathodes and a pure sulfur cathode. (b) The dependence of Z’ (Zre) on the reciprocal square root of the frequency ω−1/2 in the

Facile synthesis of silver/silver thiocyanate (Ag@AgSCN) plasmonic nanostructures with enhanced photocatalytic performance

• Xinfu Zhao,
• Dairong Chen,
• Abdul Qayum,
• Bo Chen and
• Xiuling Jiao

Beilstein J. Nanotechnol. 2017, 8, 2781–2789, doi:10.3762/bjnano.8.277

• source. N2 adsorption–desorption isotherms were determined by using a Quadrasorb SI apparatus to obtain the Brunauer–Emmett–Teller (BET) surface area. Electrochemical impedance spectroscopy (EIS) was recorded on a CHI660A electrochemical workstation (CH Instrument Company, Shanghai, China

One-step chemical vapor deposition synthesis and supercapacitor performance of nitrogen-doped porous carbon–carbon nanotube hybrids

• Egor V. Lobiak,
• Lyubov G. Bulusheva,
• Ekaterina O. Fedorovskaya,
• Yury V. Shubin,
• Pavel E. Plyusnin,
• Pierre Lonchambon,
• Boris V. Senkovskiy,
• Zinfer R. Ismagilov,
• Emmanuel Flahaut and
• Alexander V. Okotrub

Beilstein J. Nanotechnol. 2017, 8, 2669–2679, doi:10.3762/bjnano.8.267

• concentration of incorporated nitrogen. The hybrid materials were tested as electrodes in a 1M H2SO4 electrolyte and the best performance was found for a nitrogen-enriched material produced using the Fe/Mo catalyst. From the electrochemical impedance spectroscopy data, it was concluded that the nitrogen doping

• reduces the resistance at the carbon surface/electrolyte interface and the nanotubes permeating the porous carbon provide fast charge transport in the cell. Keywords: bimetallic catalyst; electrochemical impedance spectroscopy; N-doped carbon; porous carbon–carbon nanotube hybrid; supercapacitor

• composition of the obtained CNx hybrids were correlated with the data of cyclic voltammetry (CV) and electrochemical impedance spectroscopy (EIS) measurements in 1 M H2SO4 electrolyte. Experimental Synthesis Catalysts were prepared using polyoxomolybdate clusters of the ε-Keggin-type structure Mo12O28(μ2-OH

Enhanced photoelectrochemical water splitting performance using morphology-controlled BiVO₄ with W doping

• Xin Zhao and
• Zhong Chen

Beilstein J. Nanotechnol. 2017, 8, 2640–2647, doi:10.3762/bjnano.8.264

• photocurrents with hole scavenger was measured in a 0.5 M Na2SO4 aqueous solution with 0.1 M Na2SO3. Electrochemical impedance spectroscopy (EIS) measurements were carried out under illumination of an AM 1.5G solar simulator in a 0.5 M Na2SO4 electrolyte at the applied potential of 1.23 V vs RHE using a PCI4

Bi-layer sandwich film for antibacterial catheters

• Gerhard Franz,
• Florian Schamberger,
• Hamideh Heidari Zare,
• Sara Felicitas Bröskamp and
• Dieter Jocham

Beilstein J. Nanotechnol. 2017, 8, 1982–2001, doi:10.3762/bjnano.8.199

• ions were expected to move slowly in the porous membrane, the measurement cycle was repeated every 5 min. Applying electrochemical impedance spectroscopy, the areal capacitance of layers of PPX-C is measured and ε is calculated with Equation 3. The striking increase below a thickness of 350 nm is

Freestanding graphene/MnO₂ cathodes for Li-ion batteries

• Şeyma Özcan,
• Aslıhan Güler,
• Tugrul Cetinkaya,
• Mehmet O. Guler and
• Hatem Akbulut

Beilstein J. Nanotechnol. 2017, 8, 1932–1938, doi:10.3762/bjnano.8.193

• specific capacity of the freestanding graphene/MnO2 cathodes was calculated depending on the active mass of the graphene/MnO2 composite (about 20 mg) on Al foil. The resistance of the electrodes was evaluated via electrochemical impedance spectroscopy (EIS) using a Nyquist curve in the frequency range 1000

• the cell, electrochemical impedance spectroscopy (EIS) measurements were performed and results are shown in Figure 5. The width of the Nyquist curves indicates the charge transfer resistance (Rct) of the graphene/α-MnO2, graphene/β-MnO2 and graphene/γ-MnO2 cathodes [30]. As seen from Figure 5, the

Oxidative stabilization of polyacrylonitrile nanofibers and carbon nanofibers containing graphene oxide (GO): a spectroscopic and electrochemical study

• İlknur Gergin,
• Ezgi Ismar and
• A. Sezai Sarac

Beilstein J. Nanotechnol. 2017, 8, 1616–1628, doi:10.3762/bjnano.8.161

• analyzer, and thermal studies are conducted by using thermogravimetric analysis. Electrochemical impedance spectroscopy, and cyclic voltammetry are used to investigate capacitive behavior of the products. The proposed equivalent circuit model was consistent with charge-transfer processes taking place at

• (CV) and electrochemical impedance spectroscopy (EIS). Electrochemical measurements were performed by using potentiostat 2263 Electrochemical Analyser (Princeton Applied Research, Tennessee, USA). EIS data were simulated with the electrical equivalent circuit by ZSimpWin V.3.10 analysis program

• the low-temperature carbonization process with increasing elimination of other elements (N,H,O) [38][48]. Electrochemical impedance measurements of oxidized PAN nanofibers Electrochemical properties of oxidized PAN nanofibers were analyzed by using electrochemical impedance spectroscopy (EIS). EIS

Fabrication of hierarchically porous TiO₂ nanofibers by microemulsion electrospinning and their application as anode material for lithium-ion batteries

• Jin Zhang,
• Yibing Cai,
• Xuebin Hou,
• Xiaofei Song,
• Pengfei Lv,
• Huimin Zhou and
• Qufu Wei

Beilstein J. Nanotechnol. 2017, 8, 1297–1306, doi:10.3762/bjnano.8.131

• capability, which stemmed mostly from the hierarchically porous structure and the large specific surface area. Electrochemical impedance spectroscopy (EIS) was carried out on the electrode of sample A2 and solid TiO2 nanofibers. Nyquist impedance plots obtained for sample A2 and solid TiO2 nanofibers in a

High photocatalytic activity of Fe₂O₃/TiO₂ nanocomposites prepared by photodeposition for degradation of 2,4-dichlorophenoxyacetic acid

• Shu Chin Lee,
• Hendrik O. Lintang and
• Leny Yuliati

Beilstein J. Nanotechnol. 2017, 8, 915–926, doi:10.3762/bjnano.8.93

• clarified using electrochemical impedance spectroscopy (EIS). Figure 5 shows the Nyquist plots of the unmodified TiO2 (NT) and Fe2O3(0.5)/TiO2 (PD) samples. The arc radius of the Nyquist plot reflects the impedance of the interface layer arising at the electrode surface. The smaller the arc radius the

First examples of organosilica-based ionogels: synthesis and electrochemical behavior

• Andreas Taubert,
• Ruben Löbbicke,
• Barbara Kirchner and
• Fabrice Leroux

Beilstein J. Nanotechnol. 2017, 8, 736–751, doi:10.3762/bjnano.8.77

• -act X-ray detector. Prior to measurements the samples were coated with a 100 nm carbon layer using a POLARON CC7650 Carbon Coater. Electrochemical impedance spectroscopy (EIS). For EIS the dry IGs were contacted with a graphite paper layer and sandwiched between platinum electrodes. The graphite paper

• water possibly present in the IL was removed. Moreover, DSC traces obtained from third and fourth heating cycles are identical to those shown in Figure 11, thus confirming this assumption. Electrochemical impedance spectroscopy (EIS) was used to evaluate the electrical behavior of the IGs. Figure 12

Carbon nanotube-wrapped Fe₂O₃ anode with improved performance for lithium-ion batteries

• Guoliang Gao,
• Yan Jin,
• Qun Zeng,
• Deyu Wang and
• Cai Shen

Beilstein J. Nanotechnol. 2017, 8, 649–656, doi:10.3762/bjnano.8.69

• rate of 0.05 mV·s−1. Electrochemical impedance spectroscopy was carried out at a frequency range 10 mHz to 1 MHz with an AC amplitude of 10 mV. Both CV and EIS measurements were carried out on an electrochemical workstation (Ametek 1470E) Results and Discussion Figure 1a shows XRD spectra of Fe2O3/COOH

• oxygen levels of less than 0.1 ppm. The assembled cells were kept at room temperature for 12 h before electrochemical performance test Electrochemical performance of the assembled cells were then tested by galvanostatic charge/discharge measurements, cyclic voltammetry (CV) and electrochemical impedance

• spectroscopy (EIS). Charge/discharge tests of the assembled cells were carried out using a commercial battery test system (LAND model, CT2001A) at a constant current in the potential range of 0.01–3.00 V (vs Li/Li+). The cyclic voltammetry measurements were conducted in the same potential window at a scanning

A novel electrochemical nanobiosensor for the ultrasensitive and specific detection of femtomolar-level gastric cancer biomarker miRNA-106a

• Maryam Daneshpour,
• Kobra Omidfar and
• Hossein Ghanbarian

Beilstein J. Nanotechnol. 2016, 7, 2023–2036, doi:10.3762/bjnano.7.193

• miRNA were confirmed by electrochemical impedance spectroscopy (EIS) and cyclic voltammetry (CV) methods. Differential pulse voltammetry (DPV) was used for quantitative evaluation of miR-106a via recording the reduction peak current of gold nanoparticles. The electrochemical signal had a linear

• attractive targets for the construction of electrochemical nanobiosensors [8][21][28]. There are numerous studies on fabricating electrochemical nanobiosensors for the detection of label-free or labeled miRNA. Although biosensors based on electrochemical impedance spectroscopy (EIS) offered a label-free

Layered composites of PEDOT/PSS/nanoparticles and PEDOT/PSS/phthalocyanines as electron mediators for sensors and biosensors

• Celia García-Hernández,
• Cristina García-Cabezón,
• Fernando Martín-Pedrosa,
• José Antonio De Saja and
• María Luz Rodríguez-Méndez

Beilstein J. Nanotechnol. 2016, 7, 1948–1959, doi:10.3762/bjnano.7.186

• with PEDOT/PSS/LuPc2 electrodes where a strong decrease in the oxidation peak voltage was not observed [33]. The electrocatalytic properties of the layered composite PEDOT/PSS/EM electrodes were further investigated using electrochemical impedance spectroscopy (EIS). At −0.5 V, a RMS sine wave was

• unbound enzyme and stored at 4 °C. Characterization of the sensors Scanning electron microscopy (SEM) (FEI, QUANTA 200F) was used to record the images of the electrode surfaces. A square resistance was measured using a four-point tester (HAAMEG, HM 8040-2). Electrochemical impedance spectroscopy (EIS

Reconstitution of the membrane protein OmpF into biomimetic block copolymer–phospholipid hybrid membranes

• Matthias Bieligmeyer,
• Franjo Artukovic,
• Stephan Nussberger,
• Thomas Hirth,
• Thomas Schiestel and
• Michaela Müller

Beilstein J. Nanotechnol. 2016, 7, 881–892, doi:10.3762/bjnano.7.80

• capacitance measurements. Electrochemical impedance spectroscopy Electrochemical impedance spectroscopy of PIPEO, PIPEO/DPhPC and DPhPC membranes was performed using a Zahner IM6 electrochemical workstation equipped with HighZ-Probes (Zahner-Elektrik, Kronach, Germany), respectively. The HighZ-Probes were

Gold nanoparticles covalently assembled onto vesicle structures as possible biosensing platform

• M. Fátima Barroso,
• M. Alejandra Luna,
• Juan S. Flores Tabares,
• Cristina Delerue-Matos,
• N. Mariano Correa,
• Fernando Moyano and
• Patricia G. Molina

Beilstein J. Nanotechnol. 2016, 7, 655–663, doi:10.3762/bjnano.7.58

• electrochemical impedance spectroscopy or square wave voltammetry [22][23]. It is known that antibodies can be immobilized onto AuNPs without losing their biological properties [24][25]. Thus, the covalent immobilization of vesicles decorated with AuNPs on a gold surface could increase the amount of immobilized

Mismatch detection in DNA monolayers by atomic force microscopy and electrochemical impedance spectroscopy

• Maryse D. Nkoua Ngavouka,
• Pietro Capaldo,
• Elena Ambrosetti,
• Giacinto Scoles,
• Loredana Casalis and
• Pietro Parisse

Beilstein J. Nanotechnol. 2016, 7, 220–227, doi:10.3762/bjnano.7.20

• mismatches. The second strategy exploits the change in capacitance at the interface between an ssDNA-functionalized gold electrode and the solution due to the hybridization process in a miniaturized electrochemical cell. Through electrochemical impedance spectroscopy measurements on extended ssDNA self

• microRNAs or in genomic DNA. Keywords: atomic force microscopy; DNA monolayers; electrochemical impedance spectroscopy; hybridization; mismatches; Introduction Most current technologies for genotyping and sequencing are based on DNA hybridization, exploiting the high grade of selectivity due to the unique

• cell. In a previous work we demonstrated the ability to follow the hybridization of perfectly matched sequences in real time through electrochemical impedance spectroscopy (EIS) measurements on extended ssDNA self-assembled monolayers (SAMs) [27]. Here we successfully tested EIS for the detection of

Synthesis and applications of carbon nanomaterials for energy generation and storage

• Marco Notarianni,
• Jinzhang Liu,
• Kristy Vernon and
• Nunzio Motta

Beilstein J. Nanotechnol. 2016, 7, 149–196, doi:10.3762/bjnano.7.17

Electrochemical behavior of polypyrrol/AuNP composites deposited by different electrochemical methods: sensing properties towards catechol

• Celia García-Hernández,
• Cristina García-Cabezón,
• Cristina Medina-Plaza,
• Fernando Martín-Pedrosa,
• Yolanda Blanco,
• José Antonio de Saja and
• María Luz Rodríguez-Méndez

Beilstein J. Nanotechnol. 2015, 6, 2052–2061, doi:10.3762/bjnano.6.209

• incorporated in the Ppy films was higher when using CP than that when using CA. In turn, using cogeneration, the amount of nanoparticles incorporated was higher than using trapping. Electrochemical impedance spectroscopy Electrochemical impedance spectroscopy (EIS) can provide information about the

• . Electrochemical impedance spectroscopy (EIS) characterization EIS was performed in a 0.1 mol/L KCl solution with a frequency range from 105 to 0.1 Hz and a signal amplitude of 10 mV, at a working potential of 0.0 V. Tests of the voltammetric sensors The Ppy and Ppy/AuNPs films were used as working electrodes in

Optimized design of a nanostructured SPCE-based multipurpose biosensing platform formed by ferrocene-tethered electrochemically-deposited cauliflower-shaped gold nanoparticles

• Wicem Argoubi,
• Maroua Saadaoui,
• Sami Ben Aoun and
• Noureddine Raouafi

Beilstein J. Nanotechnol. 2015, 6, 1840–1852, doi:10.3762/bjnano.6.187

• and concentration of the ferrocene derivatives have been studied using cyclic voltammetry (CV), electrochemical impedance spectroscopy (EIS) and scanning electron microscopy (SEM). Selectivity and specificity tests have been also performed in the presence of potentially interfering substances to

• competitive proteins using a panel of electrochemical techniques such as cyclic voltammetry (CV), differential pulse voltammetry (DPV) and electrochemical impedance spectroscopy (EIS). Application of the two platforms for the detection of hIgG and H2O2 respectively in human serum and in honey are presented

• is ideal to obtain a nanostructured surface with high density of well-dispersed nanoparticles and a surface of about 7.8 × 10−3 cm2 corresponding to a 1 mm diameter bulk gold electrode. Study by electrochemical impedance spectroscopy Gold is a more conductive material than carbon, so the

Surface engineering of nanoporous substrate for solid oxide fuel cells with atomic layer-deposited electrolyte

• Sanghoon Ji,
• Waqas Hassan Tanveer,
• Wonjong Yu,
• Sungmin Kang,
• Gu Young Cho,
• Sung Han Kim,
• Jihwan An and
• Suk Won Cha

Beilstein J. Nanotechnol. 2015, 6, 1805–1810, doi:10.3762/bjnano.6.184

• via impedance spectroscopy To investigate the effects of BEC thickness on the individual resistances, electrochemical impedance spectroscopy (EIS) data were obtained for the Cell-A and Cell-B. Before comparing the EIS data for two kinds of cells, the EIS curves obtained under different direct current

• (left side) and 320 (right side) nm-thick BECs; (B) transmission electron microscopic image for 80 nm pore AAO supported 320 nm-thick BEC. Tafel plots, measured at 500 °C, for the Cell-A and Cell-B. Electrochemical impedance spectroscopy analysis results, measured at 500 °C, at bias voltage of 0.1 V for