Long-Range π-Conjugation in Phenothiazine-containing Donor-Acceptor Dyes for Application in Dye-Sensitized Solar Cells.

Four organic donor-π-bridge-acceptor dyes containing phenothiazine as a spacer and cyanoacrylic acid as an acceptor were synthesized and tested as sensitizers in dye-sensitized solar cells (DSCs). The influence of iodide- and cobalt-based redox electrolytes on the photovoltaic device performance was investigated. In these new dyes, systematic π-conjugation was extended by inserting one or two phenothiazine moieties and investigated within the context of the resulting photoinduced charge-transfer properties. A detailed investigation, including transient absorption spectroscopy and quantum chemical methods, provided important information on the role of extended π-conjugation on the photophysical properties and photovoltaic device performance. Overall, the results showed that the extension of π-conjugation by one phenothiazine unit resulted in the best device performance owing to reduced recombination rates, whereas extension by two phenothiazine units reduced dye adsorption on TiO2 probably owing to the increase in molecular size. The performance of the dyes in DSCs was found to be a complex interaction between dye structure and size.

Voltammetric bioassay of caffeine using sensor implant.

In this article, we examined the performance of the voltammetric assay of caffeine using DNA immobilized onto a carbon nanotube paste electrode (DPE) and compared it with that of an ordinary carbon nanotube paste electrode (PE). Under optimal conditions, the working ranges for caffeine were from 0.1 to 12 mg l(-1) (for DPE) and 30-230 mg l(-1) (for PE). Detection limits (DLs) of 0.068 mg l(-1) (3.50 x 10(-7) M) DPE and 9.94 mg l(-1) (5.12 x 10(-5) M) PE were obtained and the relative standard deviation at the caffeine concentration of 5.0 mg l(-1) was 0.064% (n = 15) DPE under optimum conditions. The sensor could be implanted in a leaf skin or animal brain cell, which can then be interfaced with an electrochemical workstation. It can be used in real-time in vivo caffeine analysis in a live cell or leaf skin.

High-performance quasi-solid-state dye-sensitized solar cell based on an electrospun PVdF-HFP membrane electrolyte.

An electrospun membrane was prepared from a 16 wt % solution of poly(vinylidenefluoride- co-hexafluoropropylene) (PVdF-HFP) in a mixture of acetone/ N, N-dimethylacetamide (7:3 wt %) at an applied voltage of 12 kV. It was then activated by immersing it in 0.6 M 1-hexyl-2,3-dimethylimidazolium iodide, 0.1 M LiI, 0.05 M I 2, and 0.5 M 4- tert-butylpyridine in ethylene carbonate/propylene carbonate (1:1 wt %) to obtain the corresponding membrane electrolyte with an ionic conductivity of 10 (-5) S cm (-1) at 25 degrees C. On the basis of this electrospun membrane electrolyte, quasi-solid-state dye-sensitized solar cells were fabricated, which showed an open-circuit voltage ( V oc) of 0.76 V, a fill factor of 0.62, and a short-circuit current density ( J sc) of 15.57 mA cm (-2) at an incident light intensity of 100 mW cm (-2). This yields a light-to-electricity conversion efficiency of 7.3%. Moreover, this cell possessed better long-term stability than that fabricated with conventional liquid electrolyte.

Electrochemical detection of ascorbic acid (vitamin C) using a glassy carbon electrode.

A method for the detection of ascorbic acid (AA) was developed using square wave anodic stripping voltammetric (SWASV) analysis with a glassy carbon electrode (GCE). The results indicated a sensitive oxidation peak current of AA on the GCE. A linear curve was obtained within a concentration range of 1-130.0 microg/L with a preconcentration time of 270 s. The relative standard deviation of 30.0 microg/L observed was 0.1016% (n = 12) under optimum conditions. The low detection limit (S/N) was pegged at 0.30 microg/L. Results showed that the method developed can be used to assay biological and pharmaceutical samples, and food samples, as well as other materials requiring AA analyses.