Despite the recent progress toward the synthesis of monodisperse semiconducting nanocrystals, it remains a challenge to prepare quantum dot structures with a precise number of atoms. Here, we report synthesis, crystal structure, and optical properties of a family of cadmium sulfide nanocrystal superlattices assembled through single-sized semiconducting clusters. Clusters of various sizes have been made. The largest cluster determined from single-crystal analysis has a total of 138 metal-chalcogen sites. It is the largest known single-sized II-VI quantum dot and is also the first one with more than 100 metal-chalcogen sites. X-ray powder diffraction (XRD) and optical absorption studies indicate the presence of even larger single-sized quantum dots (>200 metal-chalcogen sites). These clusters consist of cubic zinc blende-type core and hexagonal wurtzite-type corners and can exist in up to five isomeric forms that differ only in the position of the hexagonal-cubic interface.

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Since their discovery, carbon nanotubes (CNTs) have been considered to be promising candidates for polymer-based solar cells, but their functional incorporation and utilization in such devices have been limited due to processing bottlenecks. Here, we demonstrate the realization of controlled placement of a single-walled CNT (SWNT) monolayer network at four different positions in polymer-fullerene bulk-heterojunction (BHJ) solar cells. SWNTs were deposited by dip-coating from a hydrophilic suspension, and a very brief, largely nondestructive argon plasma treatment of the active layer was utilized for incorporation of a SWNT layer within or above it. We demonstrate that SWNTs on the hole-collection side of the active layer lead to an increase in power conversion efficiency (PCE) of the photovoltaic devices from 4 to 4.9% (under AM 1.5 G, 1.3 suns illumination). This is the highest reported PCE for polymer-based solar cells incorporating CNTs, upon consideration of expected scaling of device parameters for 1 sun illumination. We also observe that SWNTs deposited on the top of the active layer lead to major electro-optical changes in the device functionality, including an increased fluorescence lifetime of poly-3-hexylthiophene (P3HT).

Spinal cord injury (SCI) is a devastating neurological disease without effective treatment. To generate a comprehensive view of the mechanisms involved in SCI pathology, we applied RNA-Sequencing (RNA-Seq) technology to characterize the temporal changes in global gene expression after contusive SCI in mice. We sequenced tissue samples from acute and subacute phases (2 days and 7 days after injury) and systematically characterized the transcriptomes with the goal of identifying pathways and genes critical in SCI pathology. The top enriched functional categories include “inflammation response,” “neurological disease,” “cell death and survival” and “nervous system development.” The top enriched pathways include LXR/RXR Activation and Atherosclerosis Signaling, etc. Furthermore, we developed a systems-based analysis framework in order to identify key determinants in the global gene networks of the acute and sub-acute phases. Some candidate genes that we identified have been shown to play important roles in SCI, which demonstrates the validity of our approach. There are also many genes whose functions in SCI have not been well studied and can be further investigated by future experiments. We have also incorporated pharmacogenomic information into our analyses. Among the genes identified, the ones with existing drug information can be readily tested in SCI animal models. Therefore, in this study we have described an example of how global gene profiling can be translated to identifying genes of interest for functional tests in the future and generating new hypotheses. Additionally, the RNA-Seq enables splicing isoform identification and the estimation of expression levels, thus providing useful information for increasing the specificity of drug design and reducing potential side effect. In summary, these results provide a valuable reference data resource for a better understanding of the SCI process in the acute and sub-acute phases.

Chalcogenide II-VI nanoclusters are usually prepared as isolated clusters and have defied numerous efforts to join them into covalent open-framework architecture with conventional templating methods such as protonated amines or inorganic cations commonly used to direct the formation of porous frameworks. Herein, we report the first templated synthesis of II-VI covalent superlattices from large II-VI tetrahedral clusters (i.e., [Cd32S14(SPh)38]2-). Our method takes advantage of low charge density of metal-chelate dyes that is a unique match with three-dimensional II-VI semiconductor frameworks in charge density, surface hydrophilicity-hydrophobicity, and spatial organization. In addition, metal-chelate dyes also serve to tune the optical properties of resulting dye semiconductor composite materials.

BackgroundSpinal cord injury (SCI) results in fatal damage and currently has no effective treatment. The pathological mechanisms of SCI remain unclear. In this study, genome-wide transcriptional profiling of spinal cord samples from injured rats at different time points after SCI was performed by RNA-Sequencing (RNA-Seq). The transcriptomes were systematically characterized to identify the critical genes and pathways that are involved in SCI pathology.ResultsRNA-Seq results were obtained from total RNA harvested from the spinal cords of sham control rats and rats in the acute, subacute, and chronic phases of SCI (1 day, 6 days and 28 days after injury, respectively; n = 3 in every group). Compared with the sham-control group, the number of differentially expressed genes was 1797 in the acute phase (1223 upregulated and 574 downregulated), 6590 in the subacute phase (3460 upregulated and 3130 downregulated), and 3499 in the chronic phase (1866 upregulated and 1633 downregulated), with an adjusted P-value <0.05 by DESeq. Gene ontology (GO) enrichment analysis showed that differentially expressed genes were most enriched in immune response, MHC protein complex, antigen processing and presentation, translation-related genes, structural constituent of ribosome, ion gated channel activity, small GTPase mediated signal transduction and cytokine and/or chemokine activity. Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway analysis showed that the most enriched pathways included ribosome, antigen processing and presentation, retrograde endocannabinoid signaling, axon guidance, dopaminergic synapses, glutamatergic synapses, GABAergic synapses, TNF, HIF-1, Toll-like receptor, NF-kappa B, NOD-like receptor, cAMP, calcium, oxytocin, Rap1, B cell receptor and chemokine signaling pathway.ConclusionsThis study has not only characterized changes in global gene expression through various stages of SCI progression in rats, but has also systematically identified the critical genes and signaling pathways in SCI pathology. These results will expand our understanding of the complex molecular mechanisms involved in SCI and provide a foundation for future studies of spinal cord tissue damage and repair.The sequence data from this study have been deposited into Sequence Read Archive (http://www.ncbi.nlm.nih.gov/sra; accession number PRJNA318311).Electronic supplementary materialThe online version of this article (doi:10.1186/s12864-017-3532-x) contains supplementary material, which is available to authorized users.

Even though different approaches have been developed to achieve various 1D assemblies of nanocrystals, few studies have been done on the assembly of crystallographically well-defined chalcogenide nanoclusters. Here, by using bifunctional organic ligands as the directional linker, a series of one-dimensional assemblies of semiconducting chalcogenide nanoclusters have been prepared and characterized. The synthetic method allows for the preparation of differently sized tetrahedral nanoclusters that are joined together with organic linkers of different length and rigidity. Multiple linking modes between nanoclusters and organic ligands are revealed in four different assemblies that also exhibit size-dependent optical properties.

We report a microfluidic fluorescence activated cell-sorting (μFACS) device that employs traveling surface acoustic waves (TSAW) to sort cells at rates comparable to conventional jet-in-air FACS machines, with high purity and viability.