502 research outputs found
Designing Ultraflexible Perovskite X-Ray Detectors through Interface Engineering
X-ray detectors play a pivotal role in development and advancement of humankind, from far-reaching impact in medicine to furthering the ability to observe distant objects in outer space. While other electronics show the ability to adapt to flexible and lightweight formats, state-of-the-art X-ray detectors rely on materials requiring bulky and fragile configurations, severely limiting their applications. Lead halide perovskites is one of the most rapidly advancing novel materials with success in the field of semiconductor devices. Here, an ultraflexible, lightweight, and highly conformable passively operated thin film perovskite X-ray detector with a sensitivity as high as 9.3 ± 0.5 µC Gy−1 cm−2 at 0 V and a remarkably low limit of detection of 0.58 ± 0.05 μGy s−1 is presented. Various electron and hole transporting layers accessing their individual impact on the detector performance are evaluated. Moreover, it is shown that this ultrathin form-factor allows for fabrication of devices detecting X-rays equivalently from front and back side
Plasmon-assisted direction-and polarization-sensitive organic thin-film detector
Utilizing Bragg surface plasmon polaritons (SPPs) on metal nanostructures for the use in optical devices has been intensively investigated in recent years. Here, we demonstrate the integration of nanostructured metal electrodes into an ITO-free thin film bulk heterojunction organic solar cell, by direct fabrication on a nanoimprinted substrate. The nanostructured device shows interesting optical and electrical behavior, depending on angle and polarization of incidence and the side of excitation. Remarkably, for incidence through the top electrode, a dependency on linear polarization and angle of incidence can be observed. We show that these peculiar characteristics can be attributed to the excitation of dispersive and non-dispersive Bragg SPPs on the metal–dielectric interface on the top electrode and compare it with incidence through the bottom electrode. Furthermore, the optical and electrical response can be controlled by the organic photoactive material, the nanostructures, the materials used for the electrodes and the epoxy encapsulation. Our device can be used as a detector, which generates a direct electrical readout and therefore enables the measuring of the angle of incidence of up to 60\ub0 or the linear polarization state of light, in a spectral region, which is determined by the active material. Our results could furthermore lead to novel organic Bragg SPP-based sensor for a number of applications
Semiconducting Monolayer Materials as a Tunable Platform for Excitonic Solar Cells
The recent advent of two-dimensional monolayer materials with tunable
optoelectronic properties and high carrier mobility offers renewed
opportunities for efficient, ultra-thin excitonic solar cells alternative to
those based on conjugated polymer and small molecule donors. Using
first-principles density functional theory and many-body calculations, we
demonstrate that monolayers of hexagonal BN and graphene (CBN) combined with
commonly used acceptors such as PCBM fullerene or semiconducting carbon
nanotubes can provide excitonic solar cells with tunable absorber gap,
donor-acceptor interface band alignment, and power conversion efficiency, as
well as novel device architectures. For the case of CBN-PCBM devices, we
predict the limit of power conversion efficiencies to be in the 10 - 20% range
depending on the CBN monolayer structure. Our results demonstrate the
possibility of using monolayer materials in tunable, efficient, polymer-free
thin-film solar cells in which unexplored exciton and carrier transport regimes
are at play.Comment: 7 pages, 5 figure
Triplet Exciton Generation in Bulk-Heterojunction Solar Cells based on Endohedral Fullerenes
Organic bulk-heterojunctions (BHJ) and solar cells containing the trimetallic
nitride endohedral fullerene 1-[3-(2-ethyl)hexoxy
carbonyl]propyl-1-phenyl-Lu3N@C80 (Lu3N@C80-PCBEH) show an open circuit voltage
(VOC) 0.3 V higher than similar devices with [6,6]-phenyl-C[61]-butyric acid
methyl ester (PC61BM). To fully exploit the potential of this acceptor molecule
with respect to the power conversion efficiency (PCE) of solar cells, the short
circuit current (JSC) should be improved to become competitive with the state
of the art solar cells. Here, we address factors influencing the JSC in blends
containing the high voltage absorber Lu3N@C80-PCBEH in view of both
photogeneration but also transport and extraction of charge carriers. We apply
optical, charge carrier extraction, morphology, and spin-sensitive techniques.
In blends containing Lu3N@C80-PCBEH, we found 2 times weaker photoluminescence
quenching, remainders of interchain excitons, and, most remarkably, triplet
excitons formed on the polymer chain, which were absent in the reference
P3HT:PC61BM blends. We show that electron back transfer to the triplet state
along with the lower exciton dissociation yield due to intramolecular charge
transfer in Lu3N@C80-PCBEH are responsible for the reduced photocurrent
Annotated bibliography of research in the teaching of English
The committee reviews important research works in the teaching of English that have been published in the last year. Committee members include Richard Beach, Martha Bigelow, Martine Braaksma, Deborah Dillon, Jessie Dockter, Lee Galda, Lori Helman, Tanja Janssen, Karen Jorgensen, Richa Kapoor, Lauren Liang, Bic Ngo, David O’Brien, Mistilina Sato, and Cassie Scharber
Nanocarbon-Based photovoltaics
Carbon materials are excellent candidates for photovoltaic solar cells: they
are Earth-abundant, possess high optical absorption, and superior thermal and
photostability. Here we report on solar cells with active layers made solely of
carbon nanomaterials that present the same advantages of conjugated
polymer-based solar cells - namely solution processable, potentially flexible,
and chemically tunable - but with significantly increased photostability and
the possibility to revert photodegradation. The device active layer composition
is optimized using ab-initio density functional theory calculations to predict
type-II band alignment and Schottky barrier formation. The best device
fabricated is composed of PC70BM fullerene, semiconducting single-walled carbon
nanotubes and reduced graphene oxide. It achieves a power conversion efficiency
of 1.3% - a record for solar cells based on carbon as the active material - and
shows significantly improved lifetime than a polymer-based device. We calculate
efficiency limits of up to 13% for the devices fabricated in this work,
comparable to those predicted for polymer solar cells. There is great promise
for improving carbon-based solar cells considering the novelty of this type of
device, the superior photostability, and the availability of a large number of
carbon materials with yet untapped potential for photovoltaics. Our results
indicate a new strategy for efficient carbon-based, solution-processable, thin
film, photostable solar cells
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