Ammonium ion-promoted electrochemical production of synthetic gas from water and carbon dioxide on a fluorine-doped tin oxide electrode.

In this study, highly transparent conducting fluorine-doped tin oxide (FTO) electrodes were fabricated using the horizontal ultrasonic spray pyrolysis deposition. In order to improve their transparent conducting performances, we carried out oxygen activation by adjusting the ratio of O2/(O2+N2) in the carrier gas (0%, 20%, and 50%) used during the deposition process. The oxygen activation on the FTO electrodes accelerated the substitution concentration of F (FO•) into the oxygen sites in the FTO electrode while the oxygen vacancy (VO••) concentration was reduced. In addition, due to growth of pyramid-shaped crystallites with (200) preferred orientations, this oxygen activation caused the formation of a uniform surface structure. As a result, compared to others, the FTO electrode prepared at 50% O2 showed excellent electrical and optical properties (sheet resistance of ∼4.0 ± 0.14 Ω/□, optical transmittance of ∼85.3%, and figure of merit of ∼5.09 ± 0.19 × 10-2 Ω-1). This led to a superb photoconversion efficiency (∼7.03 ± 0.20%) as a result of the improved short-circuit current density. The photovoltaic performance improvement can be defined by the decreased sheet resistance of FTO used as a transparent conducting electrode in dye-sensitized solar cells (DSSCs), which is due to the combined effect of the high carrier concentration by the improved FO• concentration on the FTO electrodes and the fasted Hall mobility by the formation of a uniform FTO surface structure and distortion relaxation on the FTO lattices resulting from the reduced VO••• concentration.

Electrochemistry behavior of endogenous thiols on fluorine doped tin oxide electrodes

Sandwich photoelectrochemical biosensing of concanavalin A based on CdS/AuNPs/NiO Z-scheme heterojunction and lectin-sugar binding

This work shows the formation of a heterojunction between tin (II) sulfide (SnS) and electrochemically reduced graphene oxide (ERGO), carried out through two electrochemical steps. In the first step, graphene oxide (GO) was electrochemically reduced on a fluorine‐doped tin oxide (FTO) electrode. In the second step, the ERGO/FTO substrate was used as an electrode for the electrodeposition of SnS. In this study, each electrodeposited material (ERGO, SnS and SnS/ERGO heterojunction) was analyzed and characterized using different techniques, which confirmed the SnS/ERGO heterojunction formation. By employing electrochemical impedance spectroscopy (EIS) and linear sweep photovoltammetry measurements, it was confirmed that SnS deposited in both, bare FTO and ERGO, is a p‐type semiconductor. Furthermore, an improvement of the photocatalytic properties of the SnS/ERGO photocathode in comparison with the SnS film was observed. This effect is related to the ERGO interlayer between the SnS film and the FTO electrode, and the structural and morphology modification of the SnS film onto ERGO.

Metal particles were electrodeposited on a variety of conducting substrates, and their electrocatalytic activity toward H2O oxidation to O2 and H(+) reduction to H2 was evaluated. Co, Ni, Cu, Pd, Ag, and Pt were all electrodeposited on fluorine-doped tin oxide (FTO) electrodes. Particularly active were Pd and Pt for H(+) reduction and Co and Ag for H2O oxidation. When cycled reductively in 0.1 M HClO4, FTO electrodes derivatized with Pt and Pd reached current densities for hydrogen evolution of 18.3 and 13.2 mA/cm(2), respectively, at -0.6 V vs normal hydrogen electrode (NHE). FTO electrodes with electrodeposited Co or Ag were cycled oxidatively in H2O buffered to pH 7 with phosphate buffer. Current densities of 10.5 and 8.70 mA/cm(2), respectively, were reached at +1.8 V vs NHE with H2O oxidation onsets at +1.3 and +1.4 V, respectively. The impacts on catalytic stability and performance of electrodeposited metals in/on an electrically conductive polymer support were also investigated. Films of poly-[Fe(vbpy)3](PF6)2 (vbpy is 4-methyl-4'-vinyl-2,2'-bipyridine) were generated on FTO by reductive electropolymerization. Significant improvements to the long-term stability of electrodeposited Ag and Pt particles were observed in the poly-[Fe(vbpy)3](PF6)2 support. Films of poly-[M(vbpy)3](PF6)2 with M = Co(II) or Cu(II) were also prepared and evaluated as electrocatalysts for H2O oxidation. Films containing Co(II) reached current densities of 6.0 mA/cm(2) at +1.8 V vs NHE in H2O.

Water splitting is a helpful way of converting renewable electricity into fuel. The oxygen evolution reaction (OER) is a slow reaction that provides low-cost electrons for water reduction reactions. Thus, finding an efficient, low-cost, stable, and environmentally friendly OER catalyst is critical for water splitting. Here, sodium cobalticarborane (1) is introduced as a promising precatalyst for forming an OER cobalt-based catalyst. The cobalt-based catalyst was characterized by several methods and is suggested to be Co(III) (hydr)oxide. Using fluorine-doped tin oxide, glassy carbon, platinum, and gold electrodes, the OER activity of the cobalt-based precatalyst was investigated. The overpotential for the onset of OER in the presence of 1 is 315 mV using fluorine-doped tin oxide electrodes. The onsets of OERs in the presence of 1 using gold, platinum, and glassy carbon electrodes in KOH solutions (1.0 M) turned out to be 275, 284, and 330 mV, respectively. The nanoparticles on the gold electrodes exhibit significant OER activity with a Tafel slope of 63.8 mV/decade and an overpotential at 541 mV for 50 mA/cm2. In the case of the glassy carbon electrodes, a Tafel slope of 109.9 mV/decade and an overpotential of 548 mV for 10 mA/cm2 is recorded for the catalyst. This paper outlines an interesting approach to synthesize cobalt oxide for OER through a slow decomposition of a precatalyst.

Organic–inorganic halide two-dimensional (2D) layered perovskites have been demonstrated to have better environmental stability than conventional three-dimensional perovskites. In this study, we investigate the fabrication of electron transport layer (ETL)-free Ruddlesden–Popper 2D perovskite solar cells (PSCs) by tuning the work function of a fluorine-doped tin oxide (FTO) electrode. With the deposition of polyethylenimine (PEIE) onto its surface, the work function of the FTO electrode could be raised from −4.72 to −4.08 eV, which is more suitable for electron extraction from the perovskite absorber. Using this technique, the ETL-free 2D PSCs exhibited an excellent power conversion efficiency (PCE) of 12.7% (on average), which is substantially higher than that of PSCs fabricated on a pristine FTO electrode (9.6%). Compared with the PSCs using TiO2, the ETL-free PSCs could be fabricated under a low processing temperature of 100 °C with excellent long-term stability. After 15 days, the FTO/PEIE-based ETL-free PSCs showed a PCE degradation of 16%, which is significantly lower than that of the TiO2-based case (29%). The best-performing PSC using a FTO/PEIE cathode showed a high PCE of 13.0%, with a small hysteresis degree of 2.3%.

A novel application of fluorine‐doped tin oxide (FTO) electrodes is reported in the present work. To this end, the captopril electrochemical oxidation mechanism on FTO electrodes at various pH and its determination in pharmaceutical preparations was investigated. Captopril oxidation on FTO proceeds at pH between 2.0 and 4.0. The study revealed that interferences for captopril determination in pharmaceutical samples was totally suppressed using these electrode materials. Voltammetric survey showed an anodic peak at about 0.375 V (Ag|AgCl) for captopril oxidation, that takes place through an EC process at pH interval 2.0–4.0. The investigation demonstrated that captopril oxidation occurs through protonated species and these electroactive species interact by adsorption on FTO electrodes, with a large heterogeneous rate constant and a mechanism involving 1H+/1e− in the global reaction. Moreover, a captopril sensor based upon FTO electrodes, with a linear range miliMolar, is proposed. These electrodes are promising candidates for the efficient electrochemical determination of captopril in pharmaceutical preparations.

Electrochemical oxidation of chlorpromazine, characterisation of products by mass spectroscopy and determination in pharmaceutical samples

The effective glass frit composition used to absorb laser energy and to seal commercial dye-sensitized solar cell panel substrates has been previously developed using V₂O 5 -TeO₂-based glass with 10 wt% β-eucryptite as a CTE controlling filler. The optimum sealing conditions are provided using a 3 mm beam, a laser power of 40 watt, a scan speed of 300 mm/s, and 200 irradiation cycles. In this study, the feasibility of the developed glass frit is investigated in terms of the sealing strength and chemical durability against the commercial iodide/triiodide electrolyte solution and fluorine-doped tin oxide (FTO) electrode in order to increase the solar cell lifetime. The sealing strength of the laser-sealed V₂O 5 -TeO₂-based glass frit is 20.5 ± 1.7 MPa, which is higher than those of thermally sealed glass frit and other reported glass frit. Furthermore, the developed glass frit is chemically stable against electrolyte solutions. The glass frit constituents are not leached out from the glass after soaking in the electrolyte solution for up to three months. During the laser sealing, the glass frit does not react with the FTO electrode; thus, the resistivity of the FTO electrode beneath the laser-sealed area remains the same.

Influence of the major pilA transcriptional regulator in electrochemical responses of Geobacter sulfureducens PilR-deficient mutant biofilm formed on FTO electrodes

Modification of fluorine-doped tin oxide surface: Optimization of the electrochemical grafting of diazonium salt

Surface-engineered vertically-aligned ZnO nanorod for sensitive non-enzymatic electrochemical monitoring of cholesterol

This research demonstrated the development of a simple, cost-effective, and label-free immunosensor for the detection of α-synuclein (α-Syn) based on a cystamine (CYS) self-assembled monolayer (SAM) decorated fluorine-doped tin oxide (FTO) electrode. CYS-SAM was formed onto the FTO electrode by the adsorption of CYS molecules through the head sulfur groups. The free amine (–NH2) groups at the tail of the CYS-SAM enabled the immobilization of anti-α-Syn-antibody, which concurrently allowed the formation of immunocomplex by covalent bonding with α-Syn-antigen. The variation of the concentrations of the attached α-Syn at the immunosensor probe induced the alternation of the current and the charge transfer resistance (Rct) for the redox response of [Fe(CN)6]3−/4−, which displayed a linear dynamic range from 10 to 1000 ng/mL with a low detection limit (S/N = 3) of ca. 3.62 and 1.13 ng/mL in differential pulse voltammetry (DPV) and electrochemical impedance spectra (EIS) measurements, respectively. The immunosensor displayed good reproducibility, anti-interference ability, and good recoveries of α-Syn detection in diluted human serum samples. The proposed immunosensor is a promising platform to detect α-Syn for the early diagnose of Parkinson’s disease, which can be extended for the determination of other biologically important biomarkers.

We present evidence of the generation of radical ion formation during the oxidation of iodide on a fluorine doped tin oxide (FTO) electrode in acetonitrile. The cyclic voltammograms for the oxidation of iodide and triiodide on FTO are significantly different as in the case of the oxidation of Pt electrode. These differences are assigned to kinetic differences on the FTO surface that require significant over potentials to drive the oxidation of iodide and triiodide. We propose that at the highly positive potentials the iodine radical intermediate, I·, becomes thermodynamically stable at FTO. The radical nature of the intermediate was verified by the formation of radicals of the usual traps of 5,5-dimethyl-1-pyrroline N-oxide (DMPO) and 2,2,5,5 tetramethyl-1-pyrroline N-oxide (TMPO) when these were added to an electrolyzed solution. Irradiation of an iodine solution causes the homolytic cleavage of I2 and yields the same radical intermediate with TMPO as in the electrolysis experiment. Similar results were obtained from the electrolysis of bromide solutions upon addition of TMPO. Short term electrolysis (< 1 h) gives triiodide as a final product while long-term electrolysis (> 17 h) yields additional byproducts. Byproducts were determined to be organoiodines by gas chromatography-mass spectrometry (GC-MS). Overall, our results are consistent with iodine atoms reacting with the electrolyte during electrolysis at the FTO electrode and with a sequential two-electron transfer process.