565 research outputs found
Recent advances in the formation of phase inversion membranes made from amorphous or semi-crystalline polymers
Structural characteristics in membranes formed by diffusion induced phase separation processes are discussed. Established theories on membrane formation from ternary systems can be extended to describe the effects of high or low molecular weight additives. A mechanism for the formation of nodular structures in the top layer of ultrafiltration membranes is presented. In the last part structures arising from polymer crystallization during immersion precipitation are discussed
Impact of Alkyl Chain Length on the Formation of Regular- and Reverse-Graded Quasi-2D Perovskite Thin Films
Crystallization of low-dimensional perovskites is a complex process that leads to multidimensional films comprising two-dimensional (2D), quasi-2D, and three-dimensional (3D) phases. Most quasi-2D perovskite films possess a regular gradient with 2D phases located at the bottom of the film and 3D phases at the top. Recently, multiple studies have reported reverse-graded perovskite films, where the location of the 2D and 3D structures is inverted. The underlying reasons for such a peculiar phase distribution are unclear. While crystallization of regular-graded quasi-2D perovskites has been described as starting with 3D phases from the liquid-air interface, the film formation of reverse-graded films has not been investigated yet. Here, we examine the impact of the alkyl chain length on the formation of regular- and reverse-graded perovskites using n-alkylammonium ions. We find that long alkyl chains reverse the phase distribution gradient. By combining photoluminescence spectroscopy with in situ optical absorption measurements, we demonstrate that crystallization starts at the liquid-N2 interface, though as 3D phases for short-chain n-alkylammonium ions and as quasi-2D phases for long chains. We link this behavior to enhanced van der Waals interactions between long-chain n-alkylammonium ions in polar solvents and their tendency to accumulate at the liquid-N2 interface, creating a concentration gradient along the film thickness.</p
Quadruple junction polymer solar cells with four complementary absorber layers
A monolithic two‐terminal solution‐processed quadruple junction polymer solar cell in an n–i–p (inverted) configuration with four complementary polymer:fullerene active bulk‐heterojunction layers is presented. The subcells possess different optical bandgaps ranging from 1.90 to 1.13 eV. Optical modeling using the transfer matrix formalism enables prediction of the fraction of absorbed photons from sunlight in each subcell and determine the optimal combination of layer thicknesses. The quadruple junction cell features an open‐circuit voltage of 2.45 V and has a power conversion efficiency of 7.6%, only slightly less than the modeled value of 8.2%. The external quantum efficiency spectrum, determined with appropriate light and voltage bias conditions, exhibits in general an excellent agreement with modeled spectrum. The device performance is presently limited by bimolecular recombination, which prevents using thick photoactive layers that could absorb light more efficiently
Photovoltaic performance of an ultrasmall band gap polymer
A conjugated polymer (PBTTQ) that consists of alternating electron-rich bithiophene and electron-deficient thiadiazoloquinoxaline units was synthesized via Yamamoto polymerization with Ni(cod)(2) and provides a band gap of 0.94 eV. This represents one of the smallest band gaps obtained for a soluble conjugated polymer. When applied in a bulk heterojunction solar cell together with [84]PCBM as the electron acceptor, the polymer affords a response up to 1.3 mu m
Spatial modeling of the 3D morphology of hybrid polymer-ZnO solar cells, based on electron tomography data
A spatial stochastic model is developed which describes the 3D nanomorphology
of composite materials, being blends of two different (organic and inorganic)
solid phases. Such materials are used, for example, in photoactive layers of
hybrid polymer zinc oxide solar cells. The model is based on ideas from
stochastic geometry and spatial statistics. Its parameters are fitted to image
data gained by electron tomography (ET), where adaptive thresholding and
stochastic segmentation have been used to represent morphological features of
the considered ET data by unions of overlapping spheres. Their midpoints are
modeled by a stack of 2D point processes with a suitably chosen correlation
structure, whereas a moving-average procedure is used to add the radii of
spheres. The model is validated by comparing physically relevant
characteristics of real and simulated data, like the efficiency of exciton
quenching, which is important for the generation of charges and their transport
toward the electrodes.Comment: Published in at http://dx.doi.org/10.1214/11-AOAS468 the Annals of
Applied Statistics (http://www.imstat.org/aoas/) by the Institute of
Mathematical Statistics (http://www.imstat.org
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
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