Javascript must be enabled to continue!
Spectral, Electrochemical, and Solar Cell Studies of Peripheral Modified Carboxy Zinc Porphyrins
View through CrossRef
Six peripherally meso-modified Zn (II) porphyrin sensitizer dyes are designed and their J-V performance in dye sensitized solar cell (DSSC) evaluated. Electron-donating groups including phenothiazine, carbazole and pyrene are used to modify the porphyrin macrocycle at the meso-carbon position(s). To compare the effect of donor substitution on the performance of the cells in terms of short circuit current (Jsc), light harvesting efficiency (LHE) and power conversion efficiency (η), two sets of sensitizers with different degrees of substitution are synthesized. One set of dyes (mono-substituted) have one electron donor at trans-position to the acceptor, while the second set (tri-substituted) dyes have three of the same type electron donor groups at 5, 10 and 15 meso-carbon positions making all the six dyes push-pull type sensitizers incorporating 4'-carboxyphenyl as an electron-acceptor/anchor group. Different spectroscopic and electrochemical methods are used to study the photophysical and electrochemical properties of the dyes, while the photovoltaic performance of their cells under 1.5 A.M is studied using solar simulator. Meso-substitution of Zinc (II) porphyrin with these small donor molecules is shown to improve the light harvesting character of the Zinc (II) porphyrin macrocycle in the UV-Vis absorption while at same time improving its fluorescence quantum yield, excited-state life time and electron donating potential. All these factors combined make these meso-modified dyes better sensitizers with suitable Δ0 Δ0, and much improved power conversion efficiencies (PCE) compared to unsubstituted Zn (II) porphyrin. In particular, as a result of the peripheral modification, a doubling in efficiency in the mono- substituted series (RA-200-Zn; η=^M 4.2%, Jsc= -13.13 mA cm-2, Voc=0.54 ) and tripling in the tri-substituted series ( tri-phenothiazine Zn (II) Porphyrin; η= 7.3%, Jsc= -18.15 mA cm-2, Voc= 0.55 ) compared to unsubstituted Zn (II) porphyrin (η= 2.11%, Jsc= -5.7 mA cm-2, Voc= 0.53 V) has been accomplished.
Title: Spectral, Electrochemical, and Solar Cell Studies of Peripheral Modified Carboxy Zinc Porphyrins
Description:
Six peripherally meso-modified Zn (II) porphyrin sensitizer dyes are designed and their J-V performance in dye sensitized solar cell (DSSC) evaluated.
Electron-donating groups including phenothiazine, carbazole and pyrene are used to modify the porphyrin macrocycle at the meso-carbon position(s).
To compare the effect of donor substitution on the performance of the cells in terms of short circuit current (Jsc), light harvesting efficiency (LHE) and power conversion efficiency (η), two sets of sensitizers with different degrees of substitution are synthesized.
One set of dyes (mono-substituted) have one electron donor at trans-position to the acceptor, while the second set (tri-substituted) dyes have three of the same type electron donor groups at 5, 10 and 15 meso-carbon positions making all the six dyes push-pull type sensitizers incorporating 4'-carboxyphenyl as an electron-acceptor/anchor group.
Different spectroscopic and electrochemical methods are used to study the photophysical and electrochemical properties of the dyes, while the photovoltaic performance of their cells under 1.
5 A.
M is studied using solar simulator.
Meso-substitution of Zinc (II) porphyrin with these small donor molecules is shown to improve the light harvesting character of the Zinc (II) porphyrin macrocycle in the UV-Vis absorption while at same time improving its fluorescence quantum yield, excited-state life time and electron donating potential.
All these factors combined make these meso-modified dyes better sensitizers with suitable Δ0 Δ0, and much improved power conversion efficiencies (PCE) compared to unsubstituted Zn (II) porphyrin.
In particular, as a result of the peripheral modification, a doubling in efficiency in the mono- substituted series (RA-200-Zn; η=^M 4.
2%, Jsc= -13.
13 mA cm-2, Voc=0.
54 ) and tripling in the tri-substituted series ( tri-phenothiazine Zn (II) Porphyrin; η= 7.
3%, Jsc= -18.
15 mA cm-2, Voc= 0.
55 ) compared to unsubstituted Zn (II) porphyrin (η= 2.
11%, Jsc= -5.
7 mA cm-2, Voc= 0.
53 V) has been accomplished.
Related Results
Complex Collision Tumors: A Systematic Review
Complex Collision Tumors: A Systematic Review
Abstract
Introduction: A collision tumor consists of two distinct neoplastic components located within the same organ, separated by stromal tissue, without histological intermixing...
A New Method for Calculating Zinc Content and Determining Appropriate Zinc Levels in Foods
A New Method for Calculating Zinc Content and Determining Appropriate Zinc Levels in Foods
Calculating the zinc content per 100 kcal, 100 g or 100 mL, or the reference amount customarily consumed (RACC) of food shows the zinc content of some foods inappropriately. So, ma...
Frequency of Common Chromosomal Abnormalities in Patients with Idiopathic Acquired Aplastic Anemia
Frequency of Common Chromosomal Abnormalities in Patients with Idiopathic Acquired Aplastic Anemia
Objective: To determine the frequency of common chromosomal aberrations in local population idiopathic determine the frequency of common chromosomal aberrations in local population...
Porphyrins and Expanded Porphyrins as Receptors
Porphyrins and Expanded Porphyrins as Receptors
AbstractThis chapter summarizes recent efforts to use porphyrins and expanded porphyrins as receptors. These unique macrocycles bear resemblance to naturally occurring tetrapyrroli...
Solar Trackers Using Six-Bar Linkages
Solar Trackers Using Six-Bar Linkages
Abstract
A solar panel faces the sun or has the solar ray normal to its face to enhance power reaping. A fixed solar panel can only meet this condition at one moment...
Biodisponibilidad del zinc
Biodisponibilidad del zinc
La deficiencia marginal de zinc (déficit sub-clínico de zinc) ha sido reconocida como una condición muy prevalente en diferentes regiones del mundo. La absorción intestinal de zinc...
Employing Metadynamics to Predict the Membrane Partitioning of Carboxy-2H-Azirine Natural Products
Employing Metadynamics to Predict the Membrane Partitioning of Carboxy-2H-Azirine Natural Products
Natural products have diverse chemical structures and biological activities which often serve as sources of new therapeutic agents. Those containing a carboxy-2H-azirine moiety are...
3rd international Biometals webinars
3rd international Biometals webinars
Introduction to the 3rd Biometals webinars and tribute to Pierre CornelisWelcome to the 3rd international webinars series. For those who don't already know, these webinars have bee...

