Moungi G. Bawendi

Bio: Moungi G. Bawendi is an academic researcher from Massachusetts Institute of Technology. The author has contributed to research in topics: Quantum dot & Nanocrystal. The author has an hindex of 165, co-authored 626 publications receiving 118108 citations. Previous affiliations of Moungi G. Bawendi include United States Department of the Navy & United States Naval Research Laboratory.

Direct observation of rapid discrete spectral dynamics in single colloidal CdSe-CdS core-shell quantum dots.

Abstract: We measure the anomalous spectral diffusion of single colloidal quantum dots over eight temporal decades simultaneously by combining single-molecule spectroscopy and photon-correlation Fourier spectroscopy. Our technique distinguishes between discrete and continuous dynamics and directly reveals that the quasicontinuous spectral diffusion observed using conventional spectroscopy is composed of rapid, discrete spectral jumps. Despite their multiple time scales, these dynamics can be captured by a single mechanism whose parameters vary widely between dots and over time in individual dots.

Temperature-, gate-, and photoinduced conductance of close-packed CdTe nanocrystal films

Abstract: We measure the conductance of close-packed films of $\mathrm{CdTe}$ nanocrystals in field-effect structures in the dark and in the presence of light. We find that the majority carriers are holes, that they are injected from gold electrodes into the $\mathrm{CdTe}$ nanocrystal films, and that the hole density can be modulated with gate voltage. Secondary photocurrents have a photoconductive gain of $\ensuremath{\sim}10$ at ${10}^{6}\phantom{\rule{0.3em}{0ex}}\mathrm{V}∕\mathrm{cm}$ showing that the hole mobility is higher than the electron mobility. A single phenomenological description of the field dependence of the hole mobility can explain the dependence of current on source-drain voltage for both dark and light currents.

Synthesis cost dictates the commercial viability of lead sulfide and perovskite quantum dot photovoltaics

Abstract: Any new solar photovoltaic (PV) technology must reach low production costs to compete with today's market-leading crystalline silicon and commercial thin-film PV technologies. Colloidal quantum dots (QDs) could open up new applications by enabling lightweight and flexible PV modules. However, the cost of synthesizing nanocrystals at the large scale needed for PV module production has not previously been investigated. Based on our experience with commercial QD scale-up, we develop a Monte Carlo model to analyze the cost of synthesizing lead sulfide and metal halide perovskite QDs using 8 different reported synthetic methods. We also analyze the cost of solution-phase ligand exchange for preparing deposition-ready PbS QD inks, as well as the manufacturing cost for roll-to-roll solution-processed PV modules using these materials. We find that present QD synthesis costs are prohibitively high for PV applications, with median costs of 11 to 59 $ per g for PbS QDs (0.15 to 0.84 $ per W for a 20% efficient cell) and 73 $ per g for CsPbI3 QDs (0.74 $ per W). QD ink preparation adds 6.3 $ per g (0.09 $ per W). In total, QD materials contribute up to 55% of the total module cost, making even roll-to-roll-processed QDPV modules significantly more expensive than silicon PV modules. These results suggest that the development of new low-cost synthetic methods is critically important for the commercial relevance of QD photovoltaics. Using our cost model, we identify strategies for reducing synthetic cost and propose a cost target of 5 $ per g to move QD solar cells closer to commercial viability.

疟原虫var基因转换速率变化导致抗原变异[英]／Paul H, Robert P, Christodoulou Z, et al//Proc Natl Acad Sci U S A

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。

Gold nanoparticles: assembly, supramolecular chemistry, quantum-size-related properties, and applications toward biology, catalysis, and nanotechnology.

Abstract: Although gold is the subject of one of the most ancient themes of investigation in science, its renaissance now leads to an exponentially increasing number of publications, especially in the context of emerging nanoscience and nanotechnology with nanoparticles and self-assembled monolayers (SAMs). We will limit the present review to gold nanoparticles (AuNPs), also called gold colloids. AuNPs are the most stable metal nanoparticles, and they present fascinating aspects such as their assembly of multiple types involving materials science, the behavior of the individual particles, size-related electronic, magnetic and optical properties (quantum size effect), and their applications to catalysis and biology. Their promises are in these fields as well as in the bottom-up approach of nanotechnology, and they will be key materials and building block in the 21st century. Whereas the extraction of gold started in the 5th millennium B.C. near Varna (Bulgaria) and reached 10 tons per year in Egypt around 1200-1300 B.C. when the marvelous statue of Touthankamon was constructed, it is probable that “soluble” gold appeared around the 5th or 4th century B.C. in Egypt and China. In antiquity, materials were used in an ecological sense for both aesthetic and curative purposes. Colloidal gold was used to make ruby glass 293 Chem. Rev. 2004, 104, 293−346

Semiconductor Clusters, Nanocrystals, and Quantum Dots

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.

Phd by thesis

Abstract: Deposits of clastic carbonate-dominated (calciclastic) sedimentary slope systems in the rock record have been identified mostly as linearly-consistent carbonate apron deposits, even though most ancient clastic carbonate slope deposits fit the submarine fan systems better. Calciclastic submarine fans are consequently rarely described and are poorly understood. Subsequently, very little is known especially in mud-dominated calciclastic submarine fan systems. Presented in this study are a sedimentological core and petrographic characterisation of samples from eleven boreholes from the Lower Carboniferous of Bowland Basin (Northwest England) that reveals a >250 m thick calciturbidite complex deposited in a calciclastic submarine fan setting. Seven facies are recognised from core and thin section characterisation and are grouped into three carbonate turbidite sequences. They include: 1) Calciturbidites, comprising mostly of highto low-density, wavy-laminated bioclast-rich facies; 2) low-density densite mudstones which are characterised by planar laminated and unlaminated muddominated facies; and 3) Calcidebrites which are muddy or hyper-concentrated debrisflow deposits occurring as poorly-sorted, chaotic, mud-supported floatstones. These

Probing Single Molecules and Single Nanoparticles by Surface-Enhanced Raman Scattering

Abstract: Optical detection and spectroscopy of single molecules and single nanoparticles have been achieved at room temperature with the use of surface-enhanced Raman scattering. Individual silver colloidal nanoparticles were screened from a large heterogeneous population for special size-dependent properties and were then used to amplify the spectroscopic signatures of adsorbed molecules. For single rhodamine 6G molecules adsorbed on the selected nanoparticles, the intrinsic Raman enhancement factors were on the order of 10 14 to 10 15 , much larger than the ensemble-averaged values derived from conventional measurements. This enormous enhancement leads to vibrational Raman signals that are more intense and more stable than single-molecule fluorescence.