Francis D’Souza

ORCID: 0000-0003-3815-8949
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About
Contact & Profiles
Research Areas
  • Porphyrin and Phthalocyanine Chemistry
  • Fullerene Chemistry and Applications
  • Photochemistry and Electron Transfer Studies
  • Luminescence and Fluorescent Materials
  • Molecular Junctions and Nanostructures
  • X-ray Diffraction in Crystallography
  • Crystallization and Solubility Studies
  • Molecular Sensors and Ion Detection
  • Carbon Nanotubes in Composites
  • Synthesis and Properties of Aromatic Compounds
  • Conducting polymers and applications
  • Graphene research and applications
  • Electrochemical sensors and biosensors
  • Electrochemical Analysis and Applications
  • Photosynthetic Processes and Mechanisms
  • Organic Electronics and Photovoltaics
  • Analytical Chemistry and Sensors
  • Analytical chemistry methods development
  • Metal-Catalyzed Oxygenation Mechanisms
  • Advanced Photocatalysis Techniques
  • TiO2 Photocatalysis and Solar Cells
  • Electrocatalysts for Energy Conversion
  • Photochromic and Fluorescence Chemistry
  • Perovskite Materials and Applications
  • Ammonia Synthesis and Nitrogen Reduction

University of North Texas
2016-2025

Extreme Light Infrastructure - Nuclear Physics
2025

Wichita State University
2005-2020

Circle (United States)
2020

National Institute for Materials Science
2006-2018

Emirates Aviation University
2015

Osaka University
1999-2013

Kafrelsheikh University
2013

Tohoku University
2001-2010

Polish Academy of Sciences
1998-2010

Since the three-dimensional electron-accepting fullerene has been found to be an excellent building block for self-assembled supramolecular systems, we have investigated photoinduced electron transfer processes in systems with porphyrins and phthalocyanines as donors mimic natural photosynthesis. We successfully formed dyads triads via metal–ligand coordination, crown-ether inclusion, ion pairing, hydrogen-bonding, or π–π stacking interactions. Although single mode of binding gives usually...

10.1039/b905753f article EN Chemical Communications 2009-01-01

Molecular water-oxidation catalysts can deactivate by side reactions or decompose to secondary materials over time due the harsh, oxidizing conditions required drive oxygen evolution. Distinguishing electrode surface-bound heterogeneous (such as iridium oxide) from homogeneous molecular is often difficult. Using an electrochemical quartz crystal nanobalance (EQCN), we report a method for probing electrodeposition of metal oxide precursors. previously reported [Cp*Ir(H(2)O)(3)](2+) complex,...

10.1021/ja2004522 article EN Journal of the American Chemical Society 2011-06-15

Abstract The electrochemical behavior of fullerene and derivatives are reviewed with special reference to their catalytic sensor applications. Recent work on carbon nanotubes, used as catalyst supports in heterogeneous catalysis development is also presented. An overview recent progress the area electrochemistry included. Several cases electrocatalytic dehalogenation alkyl halides, assisted by electrode charge transfer fullerenes, discussed. Research electrocatalysis biomolecules, such...

10.1002/elan.200390094 article EN Electroanalysis 2003-06-01

The first example of a working model the photosynthetic antenna-reaction center complex, constructed via self-assembled supramolecular methodology, is reported. For this, triad assembled by axially coordinating imidazole-appended fulleropyrrolidine to zinc covalently linked porphyrin−boron dipyrrin dyad. Selective excitation boron moiety in dipyrrin−zinc porphyrin dyad resulted efficient energy transfer (kENTsinglet = 9.2 × 109 s-1; ΦENTsinglet 0.83) creating singlet excited porphyrin. Upon...

10.1021/ja030647u article EN Journal of the American Chemical Society 2004-06-01

Spectroscopic, redox, and photochemical behavior of self-assembled donor−acceptor dyads formed by axial coordination zinc tetraphenylporphyrin, (TPP)Zn, fulleropyrrolidine bearing either pyridine or imidazole coordinating ligands were investigated. The UV−vis, 1H NMR, ESI-mass spectral studies, as well computational revealed supramolecular 1:1 dyad formation between the electron donor [(TPP)Zn] acceptor, entities. determined constant K values followed order o-pyridyl ≪ m-pyridyl ≃ p-pyridyl...

10.1021/jp013165i article EN The Journal of Physical Chemistry A 2002-03-08

The first example of covalently linked free-base corrole-fullerene dyads is reported. In the newly synthesized dyads, free-energy calculations performed by employing redox and singlet excited-state energy in both polar nonpolar solvents suggested possibility electron transfer from excited state corrole to fullerene entity. Accordingly, steady-state time-resolved emission studies revealed efficient fluorescence quenching entity dyads. Further involving femtosecond laser flash photolysis...

10.1021/ja804665y article EN Journal of the American Chemical Society 2008-10-07

By employing well-defined self-assembly methods, a biomimetic bacterial photosynthetic reaction center complex has been constructed, and photoinduced electron transfer originating in this supramolecular donor−acceptor conjugate investigated. The model of the "special pair" donor, cofacial zinc phthalocyanine dimer, was formed via potassium ion induced dimerization 4,5,4′,5′,4′′, 5′′,4′′′,5′′′-zinc tetrakis(1,4,7,10,13-pentaoxatridecamethylene)phthalocyanine. dimer subsequently self-assembled...

10.1021/ja903467w article EN Journal of the American Chemical Society 2009-06-08

The occurrence of photoinduced electron transfer in donor−acceptor self-assembled zinc naphthalocyanine (ZnNc) or porphyrin (ZnP) single-wall carbon nanotube (SWNT) nanohybrids has been demonstrated. were constructed by solubilizing nanotubes π−π stacking pyrene functionalized to bear an imidazole moiety, ImPy-SWNT. Through the use ligand soluble ImPy-SWNT, donor ZnNc and ZnP entities axially coordinated yield ZnNc−ImPy-SWNT ZnP−ImPy-SWNT nanohybrids. thus obtained fully characterized using...

10.1021/jp0704416 article EN The Journal of Physical Chemistry C 2007-04-20

Anion binding has emerged as an attractive strategy to construct supramolecular electron donor-acceptor complexes. In recent years, the level of sophistication in design these systems advanced point where it is possible create ensembles that mimic key aspects photoinduced electron-transfer events operative photosynthetic reaction centre. Although anion a reversible process, kinetic studies on and dissociation processes, well back reactions complexes formed by binding, have revealed transfer...

10.1039/c2cc32848h article EN Chemical Communications 2012-01-01

We have constructed supramolecular solar cells composed of a series porphyrin–peptide oligomers [porphyrin functionalized α-polypeptides, P(H2P)n or P(ZnP)n (n = 1, 2, 4, 8, 16)], and fullerenes assembled on nanostructured SnO2 electrode using an electrophoretic deposition method. Remarkable enhancement in the photoelectrochemical performance as well broader photoresponse visible near-infrared regions is seen with increasing number porphyrin units α-polypeptide structures. Formation clusters...

10.1039/b706678c article EN Journal of Materials Chemistry 2007-01-01

This review article highlights the recent progress made in design and study of self-assembled supramolecular architectures based on tetrapyrrole macrocycles as donors, fullerene carbon nanotubes electron acceptors for energy transfer applications solution. The remarkable features utilized biomimetic organization principles viz., hydrogen bonding, π–π stacking, metal-mediated complexation, electrostatic attraction governing stability geometry nanohybrids, their significance controlling...

10.1039/b717502g article EN Journal of Materials Chemistry 2008-01-01

A 'molecular clip' featuring a near-IR emitting fluorophore, BF(2)-chelated tetraarylazadipyrromethane (aza-BODIPY) covalently linked to two porphyrins (MP, M = 2H or Zn) has been newly synthesized host three-dimensional electron acceptor fullerene via 'two-point' metal-ligand axial coordination. Efficient singlet-singlet excitation transfer from (1)ZnP* aza-BODIPY was witnessed in the dyad and triad nonpolar less polar solvents, such as toluene o-dichlorobenzene, however, additional...

10.1021/ja209718g article EN Journal of the American Chemical Society 2011-11-24

Single-wall carbon nanotube (SWNT)-based supramolecular nanoarchitectures constructed using photosensitizing donor and acceptor molecules reveal efficient photoinduced charge separation, thus carrying out the role of functional materials desired for light-energy-harvesting photovoltaic cells development novel photocatalysts. Various self-assembly strategies based on SWNT−pyrene π−π interaction are developed in a search double-decker SWNT-based nanohybrids revealing better photochemical,...

10.1021/jz1009407 article EN The Journal of Physical Chemistry Letters 2010-08-16

The effect of the orientation porphyrin sensitizer onto TiO2 surface on performance dye-sensitized solar cells (DSSCs) is reported. Free-base and zinc porphyrins bearing a carboxyl anchoring group at para, meta, or ortho positions one meso-phenyl rings were synthesized for application in Grätzel-type photoelectrochemical cells. remainder was substituted with alkyl chains different length to visualize any aggregation effects. Absorption fluorescence studies performed characterize observe...

10.1021/am401201q article EN ACS Applied Materials & Interfaces 2013-05-06

Water into oxygen: Mono-iridium complexes (see picture; L=PO3H2 or COOH) were immobilized on an indium tin oxide (ITO) surface to form a molecular electrocatalytic water oxidation assembly that mimics photosystem II in producing oxygen with high turnover numbers (TONs). The catalyst shows TONs for O2 higher than 210 000 and frequencies 6.7 s−1 during electrochemical catalytic splitting.

10.1002/anie.201203560 article EN Angewandte Chemie International Edition 2012-08-22

Effect of positioning the cyanoacrylic acid anchoring group on ring periphery phenothiazine dye performance dye-sensitized solar cells (DSSCs) is reported. Two types dyes, one having substitution C-3 aromatic (Type 1) and another through N-terminal 2), have been synthesized for this purpose. Absorption fluorescence studies performed to visualize effect pattern spectral coverage electrochemical monitor tuning redox levels. B3LYP/6-31G* are frontier orbital location their significance in...

10.1021/am3014407 article EN ACS Applied Materials & Interfaces 2012-10-08
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