Highly efficient, near-infrared electrophosphorescence from a Pt-metalloporphyrin complex.
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Biomedical subjects
Stephen R Forrest
Publications and source records attributed to Stephen R Forrest.
Intermediate-band solar cells employing quantum dots embedded in an energy fence barrier.
Power efficiencies>60% have been predicted for idealized quantum dot (QD) intermediate band solar cells. This goal has not yet been realized, due in part to nonidealities that result in charge trapping followed by recombination of photocarriers in the QDs, and the lack of an optimal materials combination. To eliminate charge trapping, a p+-i-n+ cell employing QDs buried within a high band gap barrier layer is proposed and analyzed. The maximum solar power conversion efficiency under AM1.5 spectral radiation of an example GaAs-based photovoltaic cell employing 10-20 layers of InAs QDs surrounded by AlxGa1-xAs barriers in the junction built-in depletion region can be as high as 45%. Higher efficiencies are anticipated for InP-based cells. This represents a significant improvement over GaAs homojunction cells with maximum efficiencies of <25%.
Electric Power Supplies↗
Enhanced open-circuit voltage in subphthalocyanine/C60 organic photovoltaic cells.
A double-heterostructure boron subphthalocyanine chloride (SubPc)/C60 thin-film photovoltaic cell exhibits a more than doubled Voc compared to a conventional copper phthalocyanine (CuPc)/C60 cell under 1 sun AM1.5G simulated illumination. The lower oxidation potential of SubPc results in an increase in the energy difference between the lowest unoccupied molecular orbital of the acceptor-like material and the highest occupied molecular orbital of the donor-like material (referred to as the interface gap, Ig) by 400 meV. We attribute the significant increase in Voc to this increase in Ig.
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Management of singlet and triplet excitons for efficient white organic light-emitting devices.
Lighting accounts for approximately 22 per cent of the electricity consumed in buildings in the United States, with 40 per cent of that amount consumed by inefficient (approximately 15 lm W(-1)) incandescent lamps. This has generated increased interest in the use of white electroluminescent organic light-emitting devices, owing to their potential for significantly improved efficiency over incandescent sources combined with low-cost, high-throughput manufacturability. The most impressive characteristics of such devices reported to date have been achieved in all-phosphor-doped devices, which have the potential for 100 per cent internal quantum efficiency: the phosphorescent molecules harness the triplet excitons that constitute three-quarters of the bound electron-hole pairs that form during charge injection, and which (unlike the remaining singlet excitons) would otherwise recombine non-radiatively. Here we introduce a different device concept that exploits a blue fluorescent molecule in exchange for a phosphorescent dopant, in combination with green and red phosphor dopants, to yield high power efficiency and stable colour balance, while maintaining the potential for unity internal quantum efficiency. Two distinct modes of energy transfer within this device serve to channel nearly all of the triplet energy to the phosphorescent dopants, retaining the singlet energy exclusively on the blue fluorescent dopant. Additionally, eliminating the exchange energy loss to the blue fluorophore allows for roughly 20 per cent increased power efficiency compared to a fully phosphorescent device. Our device challenges incandescent sources by exhibiting total external quantum and power efficiencies that peak at 18.7 +/- 0.5 per cent and 37.6 +/- 0.6 lm W(-1), respectively, decreasing to 18.4 +/- 0.5 per cent and 23.8 +/- 0.5 lm W(-1) at a high luminance of 500 cd m(-2).
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Blue and near-UV phosphorescence from iridium complexes with cyclometalated pyrazolyl or N-heterocyclic carbene ligands.
Two approaches are reported to achieve efficient blue to near-UV emission from triscyclometalated iridium(III) materials related to the previously reported complex, fac-Ir(ppz)(3) (ppz = 1-phenylpyrazolyl-N,C(2)'). The first involves replacement of the phenyl group of the ppz ligand with a 9,9-dimethyl-2-fluorenyl group, i.e., fac-tris(1-[(9,9-dimethyl-2-fluorenyl)]pyrazolyl-N,C(2)')iridium(III), abbreviated as fac-Ir(flz)(3). Crystallographic analysis reveals that both fac-Ir(flz)(3) and fac-Ir(ppz)(3) have a similar coordination environment around the Ir center. The absorption and emission spectra of fac-Ir(flz)(3) are red shifted from those of fac-Ir(ppz)(3). The fac-Ir(flz)(3) complex gives blue photoluminescence (PL) with a high efficiency (lambda(max) = 480 nm, phi(PL) = 0.38) at room temperature. The lifetime and quantum efficiency were used to determine the radiative and nonradiative rates (1.0 x 10(4) and 2.0 x 10(4) s(-1), respectively). The second approach utilizes N-heterocyclic carbene (NHC) ligands to form triscyclometalated Ir complexes. Complexes with two different NHC ligands, i.e., iridium tris(1-phenyl-3-methylimidazolin-2-ylidene-C,C(2)'), abbreviated as Ir(pmi)(3), and iridium tris(1-phenyl-3-methylbenzimidazolin-2-ylidene-C,C(2)'), abbreviated as Ir(pmb)(3), were both isolated as facial and meridianal isomers. Comparison of the crystallographic structures of the fac- and mer-isomers of Ir(pmb)(3) with the corresponding Ir(ppz)(3) isomers indicates that the imidazolyl-carbene ligand has a stronger trans influence than pyrazolyl and, thus, imparts a greater ligand field strength. Both fac-Ir(pmi)(3) and fac-Ir(pmb)(3) complexes display strong metal-to-ligand-charge-transfer absorption transitions in the UV (lambda = 270-350 nm) and phosphoresce in the near-UV region (E(0)(-)(0) = 380 nm) at room temperature with phi(PL) values of 0.02 and 0.04, respectively. The radiative decay rates for fac-Ir(pmi)(3) and fac-Ir(pmb)(3) (5 x 10(4) s(-1) and 18 x 10(4) s(-1), respectively) are somewhat higher than that of fac-Ir(flz)(3), but the nonradiative rates are two orders of magnitude faster (i.e., (2-4) x 10(6) s(-1)).
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Low through channel loss wavelength multiplexer using multiple transmission volume Bragg gratings.
We describe a wavelength multiplexer design that employs multiple transmission volume Bragg gratings written in the same region of a photosensitive glass having a through channel loss of < 0.5 dB. A two-channel multiplexer for wavelengths of lambda = 1310 and 1550 nm is demonstrated to test our design methods and assumptions. Agreement between simulation and experiment is within 0.2 dB at the peak diffraction efficiency. Grating apodization is used to reduce the interchannel cross talk from (13.5 +/- 0.5) to (41.5 +/- 8.5) dB, with an experimental through channel loss of (0.6 +/- 0.2) dB. Effects of angular dispersion on diffraction efficiency and grating spectral shape due to the finite diameter of the incident reading beam are also analyzed.
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The path to ubiquitous and low-cost organic electronic appliances on plastic.
Organic electronics are beginning to make significant inroads into the commercial world, and if the field continues to progress at its current, rapid pace, electronics based on organic thin-film materials will soon become a mainstay of our technological existence. Already products based on active thin-film organic devices are in the market place, most notably the displays of several mobile electronic appliances. Yet the future holds even greater promise for this technology, with an entirely new generation of ultralow-cost, lightweight and even flexible electronic devices in the offing, which will perform functions traditionally accomplished using much more expensive components based on conventional semiconductor materials such as silicon.
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Nonreciprocity of counterpropagating signals in a monolithically integrated Sagnac interferometer.
We demonstrate nonlinearly induced nonreciprocity of counterpropagating waves in a monolithically integrated Sagnac interferometer that employs a semiconductor optical amplifier as the nonlinear element. We show that the dependence of the linewidth enhancement factor on charge injection can influence the third-order nonlinearity in the semiconductor gain medium to a surprisingly large degree. This effect is utilized to control the phases of the counterpropagating signals in the interferometer. A theoretical model is used to explain the experimental observations. We show that these effects have significant practical implications by demonstrating an all-optical controlled-NOT gate.
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A polymer/semiconductor write-once read-many-times memory.
Organic devices promise to revolutionize the extent of, and access to, electronics by providing extremely inexpensive, lightweight and capable ubiquitous components that are printed onto plastic, glass or metal foils. One key component of an electronic circuit that has thus far received surprisingly little attention is an organic electronic memory. Here we report an architecture for a write-once read-many-times (WORM) memory, based on the hybrid integration of an electrochromic polymer with a thin-film silicon diode deposited onto a flexible metal foil substrate. WORM memories are desirable for ultralow-cost permanent storage of digital images, eliminating the need for slow, bulky and expensive mechanical drives used in conventional magnetic and optical memories. Our results indicate that the hybrid organic/inorganic memory device is a reliable means for achieving rapid, large-scale archival data storage. The WORM memory pixel exploits a mechanism of current-controlled, thermally activated un-doping of a two-component electrochromic conducting polymer.
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Efficient bulk heterojunction photovoltaic cells using small-molecular-weight organic thin films.
The power conversion efficiency of small-molecular-weight and polymer organic photovoltaic cells has increased steadily over the past decade. This progress is chiefly attributable to the introduction of the donor-acceptor heterojunction that functions as a dissociation site for the strongly bound photogenerated excitons. Further progress was realized in polymer devices through use of blends of the donor and acceptor materials: phase separation during spin-coating leads to a bulk heterojunction that removes the exciton diffusion bottleneck by creating an interpenetrating network of the donor and acceptor materials. The realization of bulk heterojunctions using mixtures of vacuum-deposited small-molecular-weight materials has, on the other hand, posed elusive: phase separation induced by elevating the substrate temperature inevitably leads to a significant roughening of the film surface and to short-circuited devices. Here, we demonstrate that the use of a metal cap to confine the organic materials during annealing prevents the formation of a rough surface morphology while allowing for the formation of an interpenetrating donor-acceptor network. This method results in a power conversion efficiency 50 per cent higher than the best values reported for comparable bilayer devices, suggesting that this strained annealing process could allow for the formation of low-cost and high-efficiency thin film organic solar cells based on vacuum-deposited small-molecular-weight organic materials.
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