10,690 research outputs found
Broadband enhancement of light harvesting in luminescent solar concentrator
Luminescent solar concentrator (LSC) can absorb large-area incident sunlight,
then emit luminescence with high quantum efficiency, which finally be collected
by a small photovoltaic (PV) system. The light-harvesting area of the PV system
is much smaller than that of the LSC system, potentially improving the
efficiency and reducing the cost of solar cells. Here, based on Fermi-golden
rule, we present a theoretical description of the luminescent process in
nanoscale LSCs where the conventional ray-optics model is no longer applicable.
As an example calculated with this new model, we demonstrate that a slot
waveguide consisting of a nanometer-sized low-index slot region sandwiched by
two high-index regions provides a broadband enhancement of light harvesting by
the luminescent centers in the slot region. This is because the slot waveguide
can (1) greatly enhance the spontaneous emission due to the Purcell effect, (2)
dramatically increase the effective absorption cross-section of luminescent
centers, and (3) strongly improve the quantum efficiency of luminescent
centers. It is found that about 80% solar photons can be ultimately converted
to waveguide-coupled luminescent photons even for a low luminescent quantum
efficiency of 0.5. This LSC is potential to construct a tandem structure which
can absorb nearly full-spectrum solar photons, and also may be of special
interest for building integrated nano-PV applications
A Novel Data Association Algorithm for Unequal Length Fluctuant Sequence
AbstractThere are quantities of such sensors as radar, ESM, navigator in aerospace areas and the sequence data is the most ordinary data in sensor domain. How to mine the information of these data has attracted a great interest in data mining. But sequence data is easily interfered and produces some fluctuant points. When dealing with these sequences, traditional sequence similarity measurement such as Euclidean distance arises large error, especially for unequal length fluctuant sequence. A novel average weight 1-norm unequal length fluctuant sequence similarity measurement algorithm based on dynamic time warping (DTW) is proposed to solve this problem. It constructs an absolute distance matrix based on DTW firstly, then weight average weight 1-norm and modify it with modifying factor to measure the distance of unequal length fluctuant sequence. It solves the fluctuation sensitivity of maximum distance measurement algorithm. Finally transform distance to similarity as the index of the association, associate the sequence data according to the maximum similarity association rule. Simulation results show the effectiveness of the proposed algorithm when associating unequal length fluctuant sequence, association rate is above 70% and simulate the effect of variation of the sequence length, fluctuant rate and processing time to the proposed algorithm
Interaction of Human Papillomavirus (Hpv) Type-16 Capsid Proteins with Hpv Dna Requires An Intact L2 N-Terminal Sequence
Encapsidation of papillomavirus DNA involves DNA-protein and protein-protein interactions. We sought to define the role of each human papillomavirus (HPV) capsid protein in HPV DNA encapsidation. HPV16 major (L1) and minor (L2) capsid proteins purified from recombinant vaccinia virus-infected cells were compared for their ability to bind nucleic acids. L2 protein, but not L1 protein, could bind HPV DNA. To map the DNA-binding region of L2, a series of truncated or point-mutated L2 protein open reading frames were used to show that only the N terminal of L2 was required for L2-DNA binding. This interaction depends critically on charged amino acids (Lys or Arg) in the first 12 amino acids of the N terminal of the protein. Several techniques were used to show that L2 interaction with DNA did not require specific DNA sequences. We propose that HPV L2 protein may play a major role in papillomavirus capsid assembly by introducing HPV DNA to the virus particles formed by the self assembly of the L1 major structural protein
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