Electronic structure of multiquantum giant vortex states in mesoscopic superconducting disks

We report self-consistent calculations of the microscopic electronic structure of the so-called giant vortex states. These novel multiquantum vortex states, detected by recent magnetization measurements on submicron disks, are qualitatively different from the Abrikosov vortices in the bulk. We find that, in addition to multiple branches of bound states in the core region, the local tunneling density of states exhibits Tomasch oscillations due to the single-particle interference arising from quantum confinement. These features should be directly observable by scanning tunneling spectroscopy.Comment: 5 pages, 4 figure

Single-molecule photochemical reactions of Auger-ionized quantum dots

Photoinduced electron transfer in donor-acceptor systems composed of quantum dots (QDs) and electron donors or acceptors is a subject of considerable recent research interest due to the potential applications of such systems in both solar energy harvesting and degradation of organic pollutants. Herein, we employed single-molecule imaging and spectroscopy techniques for the detection of photochemical reactions between 1,4-diaminobutane (DAB) and CdSe/ZnS single QDs. We investigated the reactions by analyzing photoluminescence (PL) intensity and lifetime of QDs at ensemble and single-molecule levels. While DAB was applied to single QDs tethered on a cover slip or QDs dispersed in a solution, PL intensity of QD continuously decreased with a concomitant increase in the PL lifetime. Interestingly, these changes in the PL properties of QD were predominant under high-intensity photoactivation. We hypothesize that the above changes in the PL properties surface due to the transfer of an electron from DAB to Auger-ionized QD followed by elimination of a proton from DAB and the formation of a QD-DAB adduct. Thus, a continuous decrease in the PL intensity of QDs under high-intensity photoactivation is attributed to continuous photochemical reactions of DAB with single QDs and the formation of QD-(DAB)n adducts. We believe that detection and analysis of such photochemical reactions of single QDs with amines will be of considerable broad interest due to the significant impact of photoinduced electron transfer reactions in energy management and environmental remediation

Reply to: “Impact of marine processes on flow dynamics of northern Antarctic Peninsula outlet glaciers” by Rott et al.

Replying to Rott et al. Nature Communications https://doi.org/10.1038/s41467-020-16658-y (2020)Publisher PDFPeer reviewe

Nuclear Forensics and Attribution for Improved Energy Security: The Use of Taggants in Nuclear Fuel

The Global Nuclear Energy Partnership (GNEP), recently announced by DOE Secretary Bodman, poses significant new challenges with regard to securing, safeguarding, monitoring and tracking nuclear materials. In order to reduce the risk of nuclear proliferation, new technologies must be developed to reduce the risk that nuclear material can be diverted from its intended use. Regardless of the specific nature of the fuel cycle, nuclear forensics and attribution will play key roles to ensure the effectiveness of nonproliferation controls and to deter the likelihood of illicit activities. As the leader of the DHS nuclear and radiological pre-detonation attribution program, LLNL is uniquely positioned to play a national leadership role in this effort. Ensuring that individuals or organizations engaged in illicit trafficking are rapidly identified and apprehended following theft or diversion of nuclear material provides a strong deterrent against unlawful activities. Key to establishing this deterrent is developing the ability to rapidly and accurately determine the identity, source and prior use history of any interdicted nuclear material. Taggants offer one potentially effective means for positively identifying lost or stolen nuclear fuels. Taggants are materials that can be encoded with a unique signature and introduced into nuclear fuel during fuel fabrication. During a nuclear forensics investigation, the taggant signature can be recovered and the nuclear material identified through comparison with information stored in an appropriate database. Unlike serial numbers or barcodes, microtaggants can provide positive identification with only partial recovery, providing extreme resistance to any attempt to delete or alter them

Enhanced carrier multiplication in engineered quasi-type-II quantum dots

Sem informaçãoOne process limiting the performance of solar cells is rapid cooling (thermalization) of hot carriers generated by higher-energy solar photons. In principle, the thermalization losses can be reduced by converting the kinetic energy of energetic carriers into additional electron-hole pairs via carrier multiplication (CM). While being inefficient in bulk semiconductors this process is enhanced in quantum dots, although not sufficiently high to considerably boost the power output of practical devices. Here we demonstrate that thick-shell PbSe/CdSe nanostructures can show almost a fourfold increase in the CM yield over conventional PbSe quantum dots, accompanied by a considerable reduction of the CM threshold. These structures enhance a valence-band CM channel due to effective capture of energetic holes into long-lived shell-localized states. The attainment of the regime of slowed cooling responsible for CM enhancement is indicated by the development of shell-related emission in the visible observed simultaneously with infrared emission from the core.518Sem informaçãoSem informaçãoSem informaçãoC. M. C., L. A. P., K. A. V., I. R., J.M.P. and V. I. K acknowledge support of the Center for Advanced Solar Photophysics (CASP), an Energy Frontier Research Center (EFRC) funded by the US Department of Energy (DOE), Office of Science, Office of Basic Energy Sciences (BES). N.S.M. is a CASP member supported by LANL Director's Postdoctoral Fellowship. Q. L. and H. L. are CASP affiliates supported by the New Mexico Consortium and Los Alamos National Laboratory

3D characterization of CdSe nanoparticles attached to carbon nanotubes

The crystallographic structure of CdSe nanoparticles attached to carbon nanotubes has been elucidated by means of high resolution transmission electron microscopy and high angle annular dark field scanning transmission electron microscopy tomography. CdSe rod-like nanoparticles, grown in solution together with carbon nanotubes, undergo a morphological transformation and become attached to the carbon surface. Electron tomography reveals that the nanoparticles are hexagonal-based with the (001) planes epitaxially matched to the outer graphene layer.Comment: 7 pages, 8 figure

Noninjection Synthesis of CdS and Alloyed CdSxSe1−xNanocrystals Without Nucleation Initiators

CdS and alloyed CdSxSe1−x nanocrystals were prepared by a simple noninjection method without nucleation initiators. Oleic acid (OA) was used to stabilize the growth of the CdS nanocrystals. The size of the CdS nanocrystals can be tuned by changing the OA/Cd molar ratios. On the basis of the successful synthesis of CdS nanocrystals, alloyed CdSxSe1−x nanocrystals can also be prepared by simply replacing certain amount of S precursor with equal amount of Se precursor, verified by TEM, XRD, EDX as well as UV–Vis absorption analysis. The optical properties of the alloyed CdSxSe1−x nanocrystals can be tuned by adjusting the S/Se feed molar ratios. This synthetic approach developed is highly reproducible and can be readily scaled up for potential industrial production

The Swift Surge of Perovskite Photovoltaics

The breakthrough early 1990s dye sensitization of mesoscopic TiO2 films along with a regenerative iodide redox couple led to the explosive growth of dye-sensitized solar cell (DSC) research. The pioneering work of Grätzel and colleagues also made it possible to develop a solid-state DSSC with spiro-oMETAD as the hole conductor and thus replace the liquid electrolyte in the cell. Research efforts of Konenkamp and others further initiated the search for the “extremely thin absorber” (ETA) nanostructured solar cell, using TiO2 as the electron conductor, an inorganic absorber, and a hole conductor. Another major research thrust was by Weller, Kamat, Zaban, Nozik, Hodes, and others, who employed inorganic quantum dots (e.g., CdS and CdSe) as sensitizers. While discussing developments in sensitized solar cells, it is important to note the contributions of early visionaries like Gerischer, Sutin, and Bard, who were first to establish the concepts of sensitization using dye molecules and semiconductor nanostructures

Low-Cost Flexible Nano-Sulfide/Carbon Composite Counter Electrode for Quantum-Dot-Sensitized Solar Cell

Cu2S nanocrystal particles were in situ deposited on graphite paper to prepare nano-sulfide/carbon composite counter electrode for CdS/CdSe quantum-dot-sensitized solar cell (QDSC). By optimization of deposition time, photovoltaic conversion efficiency up to 3.08% was obtained. In the meantime, this composite counter electrode was superior to the commonly used Pt, Au and carbon counter electrodes. Electrochemical impedance spectra further confirmed that low charge transfer resistance at counter electrode/electrolyte interface was responsible for this, implied the potential application of this composite counter electrode in high-efficiency QDSC