John Forgie - Academia.edu (original) (raw)
Papers by John Forgie
Inorganica Chimica Acta, 2010
... Katherine D. Trotter a , Michelle K. Taylor a , John C. Forgie a , John Reglinski a , Corresp... more ... Katherine D. Trotter a , Michelle K. Taylor a , John C. Forgie a , John Reglinski a , Corresponding Author Contact Information , E-mail The Corresponding Author , Leonard EA Berlouis a , Alan R. Kennedy a , Corinne M. Spickett b and Rebecca J. Sowden b. ...
Micro & Nano Letters, 2009
ABSTRACT A resistive micro-sensor for humidity sensing based on a conductive polymer material tha... more ABSTRACT A resistive micro-sensor for humidity sensing based on a conductive polymer material that is deposited electrochemically is presented. The resistor is formed by filling a narrow air gap (12 mum) between two conductor pads with conductive poly(3,4-ethylenedioxythiophene) (PEDOT) polymer, and the resistance of the polymer micro-resistor thus formed is measured to be 41 Omega at a temperature of 20degC. The conductor pads are prepared with a thick layer (20 mum) of nickel using a multi-user microelectromechanical systems (MEMS) process. The area of the entire sensor is around 100 times 200 mum, making it very compact. The humidity sensor has been characterised within a sealed chamber where the relative humidity is controlled by different saturated salt solutions at a constant temperature of 20degC. The resistance of the sensor varies from 37 to 62 Omega from 22 to 99.9% of relative humidity at room temperature.
Macromolecules, 2009
2 )] were performed in solution and in the solid states as Langmuir-Blodgett (LB) films. The type... more 2 )] were performed in solution and in the solid states as Langmuir-Blodgett (LB) films. The type of the central metal of the complexes slightly altered the potentials of the electron transfer reactions. Redox peaks shifted toward the negative potentials as a function of the decreasing metal ion size. All complexes gave three reduction and one oxidation reactions with in the whole potential window of the electrolyte system. Due to the π-π interaction of phthalocyanine rings around the lanthanide metal ions the complexes were easily reduced at even positive potentials. Assignments of the redox processes, spectra and color of the electrogenerated species of the complexes were determined with in-situ spectroelectrochemical, and in-situ electrocolorimetric measurements. Various colors recorded during the electron transfer reactions well reflected electrochromic characters of the complexes. For practical usage, LB thin films of the complexes were easily coated on the ITO electrodes and investigated as electrochromic materials. All complexes displayed three distinctive color alternatives as green, orange, and red for their different redox states. Electrochromic measurements indicated that the nature of the metal ions in the phthalocyanine cavity alters the basic electrochromic parameters of the complexes. LB films of DyPc 2 and LuPc 2 were especially found as ideal neutral and anodic coloring electrochromic materials with their short response times, and high optical and coulombic stabilities.
Inorganica Chimica Acta, 2009
... Katherine D. Trotter a , John Reglinski a , Corresponding Author Contact Information , E-mail... more ... Katherine D. Trotter a , John Reglinski a , Corresponding Author Contact Information , E-mail The Corresponding Author , Keith Robertson a , John C. Forgie a , John A. Parkinson a , Alan R. Kennedy a , David R. Armstrong a , Rebecca J. Sowden b and Corinne M. Spickett b. ...
Macromolecular Rapid Communications, 2008
Macromolecules, 2009
2 )] were performed in solution and in the solid states as Langmuir-Blodgett (LB) films. The type... more 2 )] were performed in solution and in the solid states as Langmuir-Blodgett (LB) films. The type of the central metal of the complexes slightly altered the potentials of the electron transfer reactions. Redox peaks shifted toward the negative potentials as a function of the decreasing metal ion size. All complexes gave three reduction and one oxidation reactions with in the whole potential window of the electrolyte system. Due to the π-π interaction of phthalocyanine rings around the lanthanide metal ions the complexes were easily reduced at even positive potentials. Assignments of the redox processes, spectra and color of the electrogenerated species of the complexes were determined with in-situ spectroelectrochemical, and in-situ electrocolorimetric measurements. Various colors recorded during the electron transfer reactions well reflected electrochromic characters of the complexes. For practical usage, LB thin films of the complexes were easily coated on the ITO electrodes and investigated as electrochromic materials. All complexes displayed three distinctive color alternatives as green, orange, and red for their different redox states. Electrochromic measurements indicated that the nature of the metal ions in the phthalocyanine cavity alters the basic electrochromic parameters of the complexes. LB films of DyPc 2 and LuPc 2 were especially found as ideal neutral and anodic coloring electrochromic materials with their short response times, and high optical and coulombic stabilities.
Chemistry of Materials, 2009
... A Panchromatic Boradiazaindacene (BODIPY) Sensitizer for Dye-Sensitized Solar Cells. Sule Ert... more ... A Panchromatic Boradiazaindacene (BODIPY) Sensitizer for Dye-Sensitized Solar Cells. Sule Erten-Ela, M. Deniz Yilmaz, Burcak Icli, Yavuz Dede, Siddik Icli and Engin U. Akkaya. Organic Letters 2008 10 (15), pp 3299–3302. ...
Macromolecular Rapid Communications, 2009
Scheme 1. Reagents and conditions: (i) KOH, DMSO, 190 8C, overnight; (ii) DCC, CF 3 COOH, chlorof... more Scheme 1. Reagents and conditions: (i) KOH, DMSO, 190 8C, overnight; (ii) DCC, CF 3 COOH, chloroform, RT, 3 d; (iii) Pd(PPh 3 ) 4 , DMF, mW, 160 8C, 1 h; (iv) anodic polymerisation into thin films on ITO.
Journal of Materials Chemistry, 2010
Three new diindenodithienothiophene (DITT) based materials were synthesised and their electrochem... more Three new diindenodithienothiophene (DITT) based materials were synthesised and their electrochemical properties investigated. The HOMO-LUMO gaps were observed to be 3.33, 3.48 and 2.81 eV, respectively. Cyclic voltammetry results indicate increased stability for the alkylated derivatives. The dioxide exhibits strong photoluminescence, giving a photoluminescence quantum yield of 0.72 in solution and 0.14 in the solid state. Hole mobility measurements were carried out on the non-alkylated derivative and the corresponding values were $10 À4 cm 2 V À1 s À1 .
Polymer, 2010
Cross-linked polymers based on 2,3,5,6-tetra-substituted pyrrolo[3,4-c]pyrrole-1,4(2H,5H)-dione (... more Cross-linked polymers based on 2,3,5,6-tetra-substituted pyrrolo[3,4-c]pyrrole-1,4(2H,5H)-dione (DPP): Synthesis, optical and electronic properties a b s t r a c t A series of 2,3,5,6-tetra-substituted pyrrolo[3,4-c]pyrrole-1,4(2H,5H)-dione (DPP) derivatives carrying thienyl-, 3,4-ethylenedioxy-thienyl-(EDOT-) and 3,4-ethylenedithiathienyl-(EDTT-) substituent groups have been synthesized and electrochemically polymerized. The polymers were investigated using UV/vis absorption spectroscopy and cyclic voltammetry. It was found that the growth of the polymers proceeded as random coupling of the thiophene groups in the 2-,3-,5-, and 6-positions of the DPP chromophore. In the cross-linked polymers, conjugated sequences were only built through coupling of thiophene groups in 3,6-positions, and separated by non-conjugated sequences through coupling with thiophene units in other positions of the DPP core.
Inorganica Chimica Acta, 2010
... Katherine D. Trotter a , Michelle K. Taylor a , John C. Forgie a , John Reglinski a , Corresp... more ... Katherine D. Trotter a , Michelle K. Taylor a , John C. Forgie a , John Reglinski a , Corresponding Author Contact Information , E-mail The Corresponding Author , Leonard EA Berlouis a , Alan R. Kennedy a , Corinne M. Spickett b and Rebecca J. Sowden b. ...
Micro & Nano Letters, 2009
ABSTRACT A resistive micro-sensor for humidity sensing based on a conductive polymer material tha... more ABSTRACT A resistive micro-sensor for humidity sensing based on a conductive polymer material that is deposited electrochemically is presented. The resistor is formed by filling a narrow air gap (12 mum) between two conductor pads with conductive poly(3,4-ethylenedioxythiophene) (PEDOT) polymer, and the resistance of the polymer micro-resistor thus formed is measured to be 41 Omega at a temperature of 20degC. The conductor pads are prepared with a thick layer (20 mum) of nickel using a multi-user microelectromechanical systems (MEMS) process. The area of the entire sensor is around 100 times 200 mum, making it very compact. The humidity sensor has been characterised within a sealed chamber where the relative humidity is controlled by different saturated salt solutions at a constant temperature of 20degC. The resistance of the sensor varies from 37 to 62 Omega from 22 to 99.9% of relative humidity at room temperature.
Macromolecules, 2009
2 )] were performed in solution and in the solid states as Langmuir-Blodgett (LB) films. The type... more 2 )] were performed in solution and in the solid states as Langmuir-Blodgett (LB) films. The type of the central metal of the complexes slightly altered the potentials of the electron transfer reactions. Redox peaks shifted toward the negative potentials as a function of the decreasing metal ion size. All complexes gave three reduction and one oxidation reactions with in the whole potential window of the electrolyte system. Due to the π-π interaction of phthalocyanine rings around the lanthanide metal ions the complexes were easily reduced at even positive potentials. Assignments of the redox processes, spectra and color of the electrogenerated species of the complexes were determined with in-situ spectroelectrochemical, and in-situ electrocolorimetric measurements. Various colors recorded during the electron transfer reactions well reflected electrochromic characters of the complexes. For practical usage, LB thin films of the complexes were easily coated on the ITO electrodes and investigated as electrochromic materials. All complexes displayed three distinctive color alternatives as green, orange, and red for their different redox states. Electrochromic measurements indicated that the nature of the metal ions in the phthalocyanine cavity alters the basic electrochromic parameters of the complexes. LB films of DyPc 2 and LuPc 2 were especially found as ideal neutral and anodic coloring electrochromic materials with their short response times, and high optical and coulombic stabilities.
Inorganica Chimica Acta, 2009
... Katherine D. Trotter a , John Reglinski a , Corresponding Author Contact Information , E-mail... more ... Katherine D. Trotter a , John Reglinski a , Corresponding Author Contact Information , E-mail The Corresponding Author , Keith Robertson a , John C. Forgie a , John A. Parkinson a , Alan R. Kennedy a , David R. Armstrong a , Rebecca J. Sowden b and Corinne M. Spickett b. ...
Macromolecular Rapid Communications, 2008
Macromolecules, 2009
2 )] were performed in solution and in the solid states as Langmuir-Blodgett (LB) films. The type... more 2 )] were performed in solution and in the solid states as Langmuir-Blodgett (LB) films. The type of the central metal of the complexes slightly altered the potentials of the electron transfer reactions. Redox peaks shifted toward the negative potentials as a function of the decreasing metal ion size. All complexes gave three reduction and one oxidation reactions with in the whole potential window of the electrolyte system. Due to the π-π interaction of phthalocyanine rings around the lanthanide metal ions the complexes were easily reduced at even positive potentials. Assignments of the redox processes, spectra and color of the electrogenerated species of the complexes were determined with in-situ spectroelectrochemical, and in-situ electrocolorimetric measurements. Various colors recorded during the electron transfer reactions well reflected electrochromic characters of the complexes. For practical usage, LB thin films of the complexes were easily coated on the ITO electrodes and investigated as electrochromic materials. All complexes displayed three distinctive color alternatives as green, orange, and red for their different redox states. Electrochromic measurements indicated that the nature of the metal ions in the phthalocyanine cavity alters the basic electrochromic parameters of the complexes. LB films of DyPc 2 and LuPc 2 were especially found as ideal neutral and anodic coloring electrochromic materials with their short response times, and high optical and coulombic stabilities.
Chemistry of Materials, 2009
... A Panchromatic Boradiazaindacene (BODIPY) Sensitizer for Dye-Sensitized Solar Cells. Sule Ert... more ... A Panchromatic Boradiazaindacene (BODIPY) Sensitizer for Dye-Sensitized Solar Cells. Sule Erten-Ela, M. Deniz Yilmaz, Burcak Icli, Yavuz Dede, Siddik Icli and Engin U. Akkaya. Organic Letters 2008 10 (15), pp 3299–3302. ...
Macromolecular Rapid Communications, 2009
Scheme 1. Reagents and conditions: (i) KOH, DMSO, 190 8C, overnight; (ii) DCC, CF 3 COOH, chlorof... more Scheme 1. Reagents and conditions: (i) KOH, DMSO, 190 8C, overnight; (ii) DCC, CF 3 COOH, chloroform, RT, 3 d; (iii) Pd(PPh 3 ) 4 , DMF, mW, 160 8C, 1 h; (iv) anodic polymerisation into thin films on ITO.
Journal of Materials Chemistry, 2010
Three new diindenodithienothiophene (DITT) based materials were synthesised and their electrochem... more Three new diindenodithienothiophene (DITT) based materials were synthesised and their electrochemical properties investigated. The HOMO-LUMO gaps were observed to be 3.33, 3.48 and 2.81 eV, respectively. Cyclic voltammetry results indicate increased stability for the alkylated derivatives. The dioxide exhibits strong photoluminescence, giving a photoluminescence quantum yield of 0.72 in solution and 0.14 in the solid state. Hole mobility measurements were carried out on the non-alkylated derivative and the corresponding values were $10 À4 cm 2 V À1 s À1 .
Polymer, 2010
Cross-linked polymers based on 2,3,5,6-tetra-substituted pyrrolo[3,4-c]pyrrole-1,4(2H,5H)-dione (... more Cross-linked polymers based on 2,3,5,6-tetra-substituted pyrrolo[3,4-c]pyrrole-1,4(2H,5H)-dione (DPP): Synthesis, optical and electronic properties a b s t r a c t A series of 2,3,5,6-tetra-substituted pyrrolo[3,4-c]pyrrole-1,4(2H,5H)-dione (DPP) derivatives carrying thienyl-, 3,4-ethylenedioxy-thienyl-(EDOT-) and 3,4-ethylenedithiathienyl-(EDTT-) substituent groups have been synthesized and electrochemically polymerized. The polymers were investigated using UV/vis absorption spectroscopy and cyclic voltammetry. It was found that the growth of the polymers proceeded as random coupling of the thiophene groups in the 2-,3-,5-, and 6-positions of the DPP chromophore. In the cross-linked polymers, conjugated sequences were only built through coupling of thiophene groups in 3,6-positions, and separated by non-conjugated sequences through coupling with thiophene units in other positions of the DPP core.