195 research outputs found
Methods for Encouraging Economic Diversity in Academically Rigorous Courses
In International Baccalaureate (IB) classes at Thomas Jefferson High School, the economic status of students in honors classes does not reflect that of the school as a whole. The author sought ways to bring more students from impoverished backgrounds into rigorous courses. In this school, there is a strong coincidence between etlmic minority status and socioeconomic status. The author believed that in addressing the economic issue the ethnicity issue would also be addressed. This is a practical issue as well as a pedagogical one, because the school\u27s scores on state-wide standardized tests are lower for economically disadvantaged students than for the overall student body. Research is available on helping students from impoverished backgrounds to achieve in school. This project compiled a body of research that will help teachers at Thomas Jefferson to address the needs of economically disadvantaged students
Investigation of Tension-Compression Fatigue Behavior of a Unidirectional Metal Matrix Composite at Elevated Temperature
This study investigated the fatigue behavior in a unidirectional metal matrix composite under tension-compression loading conditions. Stress-strain responses, modulus and strain trends were monitored to characterize damage. Fractography and microscopy were used to characterize failure modes. Fatigue life curves were plotted base on different parameters such as stress and strain. Tension-compression fatigue life was shorter than the obtained under tension-tension fatigue cycling. Creep, observed in tension-tension. fatigue cycling, and the effects of the compressive load on the plastic zone around the crack tip explain shorter life under tension-compression fatigue loading
Theory of photoinduced charge transfer in weakly coupled donor-acceptor conjugated polymers: application to an MEH-PPV:CN-PPV pair
In a pair of coupled donor-acceptor conjugated polymer chains, it is possible
for an exciton photoexcited on either polymer to decay into a hole in the donor
polymer's valence band and an electron in the conduction band of the acceptor
polymer. We calculate the corresponding exciton decay rate and its dependence
on inter-polymer distance. For a pair of derivatives of poly(phenylene
vinylene), PPV, specifically poly[2-methoxy, 5-(2-ethyl-hexyloxy)-1, 4
PPV], MEH-PPV, and poly(2,5-hexyloxy -phenylene cyanovinylene), CN-PPV, at a
separation of 6 \AA the characteristic decay time is 2.2 ps, whereas at 4 \AA
it is fs.Comment: 9 pages, RevTeX, 4 PS files, to be published in a special issue of
Chem. Phy
Effect of interchain coupling on conducting polymer luminescence: excimers in derivatives of poly(phenylene vinylene)
Optical excitation of a chain in a polymer film may result in formation of an
excimer, a superposition of on-chain excitons and charge-transfer excitons on
the originally excited chain and a neighboring chain. The excimer emission is
red-shifted compared to that of an on-chain exciton by an amount depending on
the interchain coupling . Setting up the excimer wavefunction and
calculating the red shift, we determine average values, referred to a
monomer, of 0.52 eV and 0.16 eV for poly(2,5-hexyloxy -phenylene
cyanovinylene), CN-PPV, and poly[2-methoxy, 5-(2'-ethyl-hexyloxy)-1, 4
p-phenylene vinylene], MEH-PPV, respectively, and use them to determine the
effect of interchain distance on the emission.Comment: 10 pages, RevTeX, 1 PS figure, replaced version of cond-mat/9707095,
accepted for publication in Phys. Rev. B, Rapid Communicatio
The low-lying excitations of polydiacetylene
The Pariser-Parr-Pople Hamiltonian is used to calculate and identify the
nature of the low-lying vertical transition energies of polydiacetylene. The
model is solved using the density matrix renormalisation group method for a
fixed acetylenic geometry for chains of up to 102 atoms. The non-linear optical
properties of polydiacetylene are considered, which are determined by the
third-order susceptibility. The experimental 1Bu data of Giesa and Schultz are
used as the geometric model for the calculation. For short chains, the
calculated E(1Bu) agrees with the experimental value, within solvation effects
(ca. 0.3 eV). The charge gap is used to characterise bound and unbound states.
The nBu is above the charge gap and hence a continuum state; the 1Bu, 2Ag and
mAg are not and hence are bound excitons. For large chain lengths, the nBu
tends towards the charge gap as expected, strongly suggesting that the nBu is
the conduction band edge. The conduction band edge for PDA is agreed in the
literature to be ca. 3.0 eV. Accounting for the strong polarisation effects of
the medium and polaron formation gives our calculated E(nBu) ca. 3.6 eV, with
an exciton binding energy of ca. 1.0 eV. The 2Ag state is found to be above the
1Bu, which does not agree with relaxed transition experimental data. However,
this could be resolved by including explicit lattice relaxation in the Pariser-
Parr-Pople-Peierls model. Particle-hole separation data further suggest that
the 1Bu, 2Ag and mAg are bound excitons, and that the nBu is an unbound
exciton.Comment: LaTeX, 23 pages, 4 postscript tables and 8 postscript figure
Theory of excited state absorptions in phenylene-based -conjugated polymers
Within a rigid-band correlated electron model for oligomers of
poly-(paraphenylene) (PPP) and poly-(paraphenylenevinylene) (PPV), we show that
there exist two fundamentally different classes of two-photon A states in
these systems to which photoinduced absorption (PA) can occur. At relatively
lower energies there occur A states which are superpositions of one
electron - one hole (1e--1h) and two electron -- two hole (2e--2h) excitations,
that are both comprised of the highest delocalized valence band and the lowest
delocalized conduction band states only. The dominant PA is to one specific
member of this class of states (the mA). In addition to the above class of
A states, PA can also occur to a higher energy kA state whose 2e--2h
component is {\em different} and has significant contributions from excitations
involving both delocalized and localized bands. Our calculated scaled energies
of the mA and the kA agree reasonably well to the experimentally
observed low and high energy PAs in PPV. The calculated relative intensities of
the two PAs are also in qualitative agreement with experiment. In the case of
ladder-type PPP and its oligomers, we predict from our theoretical work a new
intense PA at an energy considerably lower than the region where PA have been
observed currently. Based on earlier work that showed that efficient
charge--carrier generation occurs upon excitation to odd--parity states that
involve both delocalized and localized bands, we speculate that it is the
characteristic electronic nature of the kA that leads to charge generation
subsequent to excitation to this state, as found experimentally.Comment: Revtex4 style, 2 figures inserted in the text, three tables, 10 page
Exciton bimolecular annihilation dynamics in supramolecular nanostructures of conjugated oligomers
We present femtosecond transient absorption measurements on -conjugated
supramolecular assemblies in a high pump fluence regime.
Oligo(\emph{p}-phenylenevinylene) monofunctionalized with
ureido-\emph{s}-triazine (MOPV) self-assembles into chiral stacks in dodecane
solution below 75C at a concentration of M. We
observe exciton bimolecular annihilation in MOPV stacks at high excitation
fluence, indicated by the fluence-dependent decay of B-exciton
spectral signatures, and by the sub-linear fluence dependence of time- and
wavelength-integrated photoluminescence (PL) intensity. These two
characteristics are much less pronounced in MOPV solution where the phase
equilibrium is shifted significantly away from supramolecular assembly,
slightly below the transition temperature. A mesoscopic rate-equation model is
applied to extract the bimolecular annihilation rate constant from the
excitation fluence dependence of transient absorption and PL signals. The
results demonstrate that the bimolecular annihilation rate is very high with a
square-root dependence in time. The exciton annihilation results from a
combination of fast exciton diffusion and resonance energy transfer. The
supramolecular nanostructures studied here have electronic properties that are
intermediate between molecular aggregates and polymeric semiconductors
Recent advances in solid-state organic lasers
Organic solid-state lasers are reviewed, with a special emphasis on works
published during the last decade. Referring originally to dyes in solid-state
polymeric matrices, organic lasers also include the rich family of organic
semiconductors, paced by the rapid development of organic light emitting
diodes. Organic lasers are broadly tunable coherent sources are potentially
compact, convenient and manufactured at low-costs. In this review, we describe
the basic photophysics of the materials used as gain media in organic lasers
with a specific look at the distinctive feature of dyes and semiconductors. We
also outline the laser architectures used in state-of-the-art organic lasers
and the performances of these devices with regard to output power, lifetime,
and beam quality. A survey of the recent trends in the field is given,
highlighting the latest developments in terms of wavelength coverage,
wavelength agility, efficiency and compactness, or towards integrated low-cost
sources, with a special focus on the great challenges remaining for achieving
direct electrical pumping. Finally, we discuss the very recent demonstration of
new kinds of organic lasers based on polaritons or surface plasmons, which open
new and very promising routes in the field of organic nanophotonics
The nature of singlet exciton fission in carotenoid aggregates.
Singlet exciton fission allows the fast and efficient generation of two spin triplet states from one photoexcited singlet. It has the potential to improve organic photovoltaics, enabling efficient coupling to the blue to ultraviolet region of the solar spectrum to capture the energy generally lost as waste heat. However, many questions remain about the underlying fission mechanism. The relation between intermolecular geometry and singlet fission rate and yield is poorly understood and remains one of the most significant barriers to the design of new singlet fission sensitizers. Here we explore the structure-property relationship and examine the mechanism of singlet fission in aggregates of astaxanthin, a small polyene. We isolate five distinct supramolecular structures of astaxanthin generated through self-assembly in solution. Each is capable of undergoing intermolecular singlet fission, with rates of triplet generation and annihilation that can be correlated with intermolecular coupling strength. In contrast with the conventional model of singlet fission in linear molecules, we demonstrate that no intermediate states are involved in the triplet formation: instead, singlet fission occurs directly from the initial 1B(u) photoexcited state on ultrafast time scales. This result demands a re-evaluation of current theories of polyene photophysics and highlights the robustness of carotenoid singlet fission.This work was supported by the EPSRC (UK) (EP/G060738/
1), the European Community (LASERLAB-EUROPE, grant
agreement no. 284464, EC’s Seventh Framework Programme;
and Marie-Curie ITN-SUPERIOR, PITN-GA-2009-238177),
and the Winton Programme for the Physics of Sustainability.
G.C. acknowledges support by the European Research Council
Advanced Grant STRATUS (ERC-2011-AdG No. 291198).
J.C. acknowledges support by the Royal Society Dorothy
Hodgkin Fellowship and The University of Sheffield’s Vice-
Chancellor’s Fellowship scheme.This is the final published version. It was first made available by ACS at http://pubs.acs.org/doi/abs/10.1021/jacs.5b01130
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