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Christopher B. Murray

Bio: Christopher B. Murray is an academic researcher from University of Pennsylvania. The author has contributed to research in topics: Nanocrystal & Quantum dot. The author has an hindex of 88, co-authored 336 publications receiving 54410 citations. Previous affiliations of Christopher B. Murray include Universal Display Corporation & Lawrence Berkeley National Laboratory.


Papers
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Journal ArticleDOI
TL;DR: In this paper, the formation of coaxial PbSe/PbS core−shell heterostructures and observed Stranski−Krastanov growth regime of PbS shell on pbSe nanowires at low reaction temperature (150 °C) that switched to layer-by-layer epitaxial growth above 180 °C.
Abstract: The oriented attachment of PbSe nanocrystals results in single-crystalline colloidal PbSe nanowires. The addition of different surfactants allows tailoring nanowire morphology, choosing between straight, zigzag, helical, and branched nanowires. In this work, we studied the formation of coaxial PbSe/PbS core−shell heterostructures and observed Stranski−Krastanov growth regime of PbS shell on PbSe nanowires at low reaction temperature (150 °C) that switched to layer-by-layer epitaxial growth above 180 °C. The protection of PbSe nanowires with a PbS shell substantially improves the nanowire stability against oxidation. We also developed a technique for controllable decoration of colloidal PbSe nanowires with Au nanoparticles and found that the morphology of nanowire template had a strong effect on nucleation and growth of gold nanoparticles.

119 citations

Journal ArticleDOI
05 Mar 2013-ACS Nano
TL;DR: The shape-controlled synthesis of tripodal and triangular gadolinium oxide (Gd2O3) nanoplates is reported, showing that the morphology transforms from an initial tripodal shape to a triangular shape with increasing reaction time or elevated temperatures.
Abstract: Here, we report the shape-controlled synthesis of tripodal and triangular gadolinium oxide (Gd2O3) nanoplates. In the presence of lithium ions, the shape of the nanocrystals is readily controlled by tailoring reaction parameters such as temperature and time. We observe that the morphology transforms from an initial tripodal shape to a triangular shape with increasing reaction time or elevated temperatures. Highly uniform Gd2O3 nanoplates are self-assembled into nanofibril-like liquid-crystalline superlattices with long-range orientational and positional order. In addition, shape-directed self-assemblies are investigated by tailoring the aspect ratio of the arms of the Gd2O3 nanoplates. Due to a strong paramagnetic response, Gd2O3 nanocrystals are excellent candidates for MRI contrast agents and also can be doped with rare-earth ions to form nanophosphors, pointing to their potential in multimodal imaging. In this work, we investigate the MR relaxometry at high magnetic fields (9.4 and 14.1 T) and the opti...

119 citations

Journal ArticleDOI
10 Jan 2014-ACS Nano
TL;DR: It is demonstrated that nanocrystal-based nanoimprinting can be employed to pattern multilayered subwavelength nanostructures, such as three-dimensional VO2 nanopillar arrays, that exhibit plasmonic dipolar responses tunable with a temperature change.
Abstract: We demonstrate thermally switchable VO2 metamaterials fabricated using solution-processable colloidal nanocrystals (NCs). Vanadium oxide (VOx) NCs are synthesized through a nonhydrolytic reaction and deposited from stable colloidal dispersions to form NC thin films. Rapid thermal annealing transforms the VOx NC thin films into monoclinic, nanocrystalline VO2 thin films that show a sharp, reversible metal–insulator phase transition. Introduction of precise concentrations of tungsten dopings into the colloidal VOx NCs enables the still sharp phase transition of the VO2 thin films to be tuned to lower temperatures as the doping level increases. We fabricate “smart”, differentially doped, multilayered VO2 films to program the phase and therefore the metal–insulator behavior of constituent vertically structured layers with temperature. With increasing temperature, we tailored the optical response of multilayered films in the near-IR and IR regions from that of a strong light absorber, in a metal–insulator stru...

117 citations

Journal ArticleDOI
TL;DR: It is demonstrated that, in addition to the use of common cation dopants, the incorporation of fluorine into the lattice as an anion dopant can further increase the free-carrier concentration within individual NCs; this supports the cooperative effects of mixed cation-anion doping in shifting the LSPR to higher energies.
Abstract: We present a generalized cation–anion codoping methodology for the synthesis of monodisperse, doped metal-oxide nanocrystals (NCs) that exhibit near-infrared localized surface plasmon resonance (LSPR) with the highest reported quality factors. We demonstrate that, in addition to the use of common cation dopants, the incorporation of fluorine into the lattice as an anion dopant can further increase the free-carrier concentration within individual NCs; this supports the cooperative effects of mixed cation–anion doping in shifting the LSPR to higher energies. As a result, this method allows the LSPR of doped metal-oxide NCs to become tunable across a significantly broader wavelength range (1.5–3.3 μm), circumventing the prior limitations on the highest possible LSPR energies associated with single-element doping for a given oxide host. The strategy of cation–anion codoping can offer new possibilities for the chemical design of doped semiconductor and metal-oxide NCs with tailored LSPR characteristics.

115 citations

Journal ArticleDOI
TL;DR: In this paper, carbon-supported, Pt and PtCo nanocrystals with controlled size and composition were synthesized and examined for hydrodeoxygenation (HDO) of 5-hydroxymethylfurfural (HMF).
Abstract: Carbon-supported, Pt and PtCo nanocrystals (NCs) with controlled size and composition were synthesized and examined for hydrodeoxygenation (HDO) of 5-hydroxymethylfurfural (HMF). Experiments in a continuous flow reactor with 1-propanol solvent, at 120 to 160 °C and 33 bar H2, demonstrated that reaction is sequential on both Pt and PtCo alloys, with 2,5-dimethylfuran (DMF) formed as an intermediate product. However, the reaction of DMF is greatly suppressed on the alloys, such that a Pt3Co2 catalyst achieved DMF yields as high as 98%. XRD and XAS data indicate that the Pt3Co2 catalyst consists of a Pt-rich core and a Co oxide surface monolayer whose structure differs substantially from that of bulk Co oxide. Density functional theory (DFT) calculations reveal that the oxide monolayer interacts weakly with the furan ring to prevent side reactions, including overhydrogenation and ring opening, while providing sites for effective HDO to the desired product, DMF. We demonstrate that control over metal nanopart...

115 citations


Cited by
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28 Jul 2005
TL;DR: PfPMP1)与感染红细胞、树突状组胞以及胎盘的单个或多个受体作用,在黏附及免疫逃避中起关键的作�ly.
Abstract: 抗原变异可使得多种致病微生物易于逃避宿主免疫应答。表达在感染红细胞表面的恶性疟原虫红细胞表面蛋白1(PfPMP1)与感染红细胞、内皮细胞、树突状细胞以及胎盘的单个或多个受体作用,在黏附及免疫逃避中起关键的作用。每个单倍体基因组var基因家族编码约60种成员,通过启动转录不同的var基因变异体为抗原变异提供了分子基础。

18,940 citations

Journal ArticleDOI
16 Feb 1996-Science
TL;DR: In this article, the authors focus on the properties of quantum dots and their ability to join the dots into complex assemblies creates many opportunities for scientific discovery, such as the ability of joining the dots to complex assemblies.
Abstract: Current research into semiconductor clusters is focused on the properties of quantum dots-fragments of semiconductor consisting of hundreds to many thousands of atoms-with the bulk bonding geometry and with surface states eliminated by enclosure in a material that has a larger band gap. Quantum dots exhibit strongly size-dependent optical and electrical properties. The ability to join the dots into complex assemblies creates many opportunities for scientific discovery.

10,737 citations

Journal ArticleDOI
25 Sep 1998-Science
TL;DR: Highly luminescent semiconductor quantum dots (zinc sulfide-capped cadmium selenide) have been covalently coupled to biomolecules for use in ultrasensitive biological detection and these nanometer-sized conjugates are water-soluble and biocompatible.
Abstract: Highly luminescent semiconductor quantum dots (zinc sulfide-capped cadmium selenide) have been covalently coupled to biomolecules for use in ultrasensitive biological detection. In comparison with organic dyes such as rhodamine, this class of luminescent labels is 20 times as bright, 100 times as stable against photobleaching, and one-third as wide in spectral linewidth. These nanometer-sized conjugates are water-soluble and biocompatible. Quantum dots that were labeled with the protein transferrin underwent receptor-mediated endocytosis in cultured HeLa cells, and those dots that were labeled with immunomolecules recognized specific antibodies or antigens.

7,393 citations