| 1. |
- Li, Wenxiong, et al.
(författare)
-
Can the Helium-detonation Model Explain the Observed Diversity of Type Ia Supernovae?
- 2021
-
Ingår i: Astrophysical Journal. - : American Astronomical Society. - 0004-637X .- 1538-4357. ; 906:2
-
Tidskriftsartikel (refereegranskat)abstract
- We study a sample of 16 Type Ia supernovae (SNe Ia) having both spectroscopic and photometric observations within 2-3 days after the first light. The early B - V colors of such a sample tend to show a continuous distribution. For objects with normal ejecta velocity (NV), the C ii lambda 6580 feature is always visible in the early spectra, while it is absent or very weak in the high-velocity (HV) counterpart. Moreover, the velocities of the detached high-velocity features (HVFs) of the Ca II near-IR triplet (CaIR3) above the photosphere are found to be much higher in HV objects than in NV objects, with typical values exceeding 30,000 km s(-1) at 2-3 days. We further analyze the relation between the velocity shift of late-time [Fe II] lines (v([Fe II])) and host galaxy mass. We find that all HV objects have redshifted v([Fe II]), while NV objects have both blue- and redshifted v([Fe II]). It is interesting to point out that the objects with redshifted v([Fe II]) are all located in massive galaxies, implying that HV and a portion of NV objects may have similar progenitor metallicities and explosion mechanisms. We propose that, with a geometric/projected effect, the He-detonation model may account for the similarity in birthplace environment and the differences seen in some SNe Ia, including B - V colors, C II features, CaIR3 HVFs at early times, and v([Fe II]) in the nebular phase. Nevertheless, some features predicted by He-detonation simulation, such as the rapidly decreasing light curve, deviate from the observations, and some NV objects with blueshifted nebular v([Fe II]) may involve other explosion mechanisms.
|
|
| 2. |
- Kristan, Matej, et al.
(författare)
-
The Visual Object Tracking VOT2017 challenge results
- 2017
-
Ingår i: 2017 IEEE INTERNATIONAL CONFERENCE ON COMPUTER VISION WORKSHOPS (ICCVW 2017). - : IEEE. - 9781538610343 ; , s. 1949-1972
-
Konferensbidrag (refereegranskat)abstract
- The Visual Object Tracking challenge VOT2017 is the fifth annual tracker benchmarking activity organized by the VOT initiative. Results of 51 trackers are presented; many are state-of-the-art published at major computer vision conferences or journals in recent years. The evaluation included the standard VOT and other popular methodologies and a new "real-time" experiment simulating a situation where a tracker processes images as if provided by a continuously running sensor. Performance of the tested trackers typically by far exceeds standard baselines. The source code for most of the trackers is publicly available from the VOT page. The VOT2017 goes beyond its predecessors by (i) improving the VOT public dataset and introducing a separate VOT2017 sequestered dataset, (ii) introducing a realtime tracking experiment and (iii) releasing a redesigned toolkit that supports complex experiments. The dataset, the evaluation kit and the results are publicly available at the challenge website(1).
|
|
| 3. |
- Tan, Yeshu, et al.
(författare)
-
Highly Luminescent and Stable Perovskite Nanocrystals with Octylphosphonic Acid as a Ligand for Efficient Light-Emitting Diodes
- 2018
-
Ingår i: ACS Applied Materials and Interfaces. - : AMER CHEMICAL SOC. - 1944-8244 .- 1944-8252. ; 10:4, s. 3784-3792
-
Tidskriftsartikel (refereegranskat)abstract
- All inorganic perovskite nanocrystals (NCs) of CsPbX3 (X = Cl, Br, I, or their mixture) are regarded as promising candidates for high-performance light-emitting diode (LED) owing to their high photoluminescence (PL) quantum yield (QY) and easy synthetic process. However, CsPbX3 NCs synthesized by the existing methods, where oleic acid (OA) and oleylamine (OLA) are generally used as surface-chelating ligands, suffer from poor stability due to the ligand loss, which drastically deteriorates their PL QY, as well as dispersibility in solvents. Herein, the OA/OLA ligands are replaced with octylphosphonic acid (OPA), which dramatically enhances the CsPbX3 stability. Owing to a strong interaction between OPA and lead atoms, the OPA-capped CsPbX3 (OPA-CsPbX3) NCs not only preserve their high PL QY (amp;gt;90%) but also achieve a high-quality dispersion in solvents after multiple purification processes. Moreover, the organic residue in purified OPA-CsPbBr3 is only similar to 4.6%, which is much lower than similar to 29.7% in OA/OLA-CsPbBr3. Thereby, a uniform and compact OPA-CsPbBr3 film is obtained for LED application. A green LED with a current efficiency of 18.13 cd A(-1), corresponding to an external quantum efficiency of 6.5%, is obtained. Our research provides a path to prepare high-quality perovskite NCs for high-performance optoelectronic devices.
|
|
| 4. |
- Zhang, Tiankai, et al.
(författare)
-
Ion-modulated radical doping of spiro-OMeTAD for more efficient and stable perovskite solar cells
- 2022
-
Ingår i: Science. - : AMER ASSOC ADVANCEMENT SCIENCE. - 0036-8075 .- 1095-9203. ; 377:6605, s. 495-501
-
Tidskriftsartikel (refereegranskat)abstract
- Record power conversion efficiencies (PCEs) of perovskite solar cells (PSCs) have been obtained with the organic hole transporter 2,2,7,7-tetrakis(N,N-di-p-methoxyphenyl-amine)9,9-spirobifluorene (spiro-OMeTAD). Conventional doping of spiro-OMeTAD with hygroscopic lithium salts and volatile 4-tert-butylpyridine is a time-consuming process and also leads to poor device stability. We developed a new doping strategy for spiro-OMeTAD that avoids post-oxidation by using stable organic radicals as the dopant and ionic salts as the doping modulator (referred to as ion-modulated radical doping). We achieved PCEs of >25% and much-improved device stability under harsh conditions. The radicals provide hole polarons that instantly increase the conductivity and work function (WF), and ionic salts further modulate the WF by affecting the energetics of the hole polarons. This organic semiconductor doping strategy, which decouples conductivity and WF tunability, could inspire further optimization in other optoelectronic devices.
|
|
| 5. |
- Duan, Sai, et al.
(författare)
-
Density functional theory study on the adsorption and decomposition of the formic acid catalyzed by highly active mushroom-like Au@Pd@Pt tri-metallic nanoparticles
- 2013
-
Ingår i: Physical Chemistry, Chemical Physics - PCCP. - : Royal Society of Chemistry (RSC). - 1463-9076 .- 1463-9084. ; 15:13, s. 4625-4633
-
Tidskriftsartikel (refereegranskat)abstract
- Local structures and adsorption energies of a formic acid molecule and its decomposed intermediates (H, O, OH, CO, HCOO, and COOH) on highly electrocatalytically active mushroom-like Au-core@Pd-shell@Pt-cluster nanoparticles with two atomic layers of the Pd shell and stoichiometric Pt coverage of around half-monolayer (Au@2 ML Pd@0.5 ML Pt) have been investigated by first principles calculations. The adsorption sites at the center (far away from the Pt cluster) and the edge (close to the Pt cluster) are considered and compared. Significant repulsive interaction between the edge sites and CO is observed. The calculated potential energy surfaces demonstrate that, with respect to the center sites, the CO2 pathway is considerably promoted in the edge area. Our results reveal that the unique edge structure of the Pt cluster is responsible for the experimentally observed high electrocatalytic activity of the Au@Pd@Pt nanoparticles toward formic acid oxidation. Such microscopic understanding should be useful for the design of new electrochemical catalysts.
|
|
| 6. |
- Li, C. -Y, et al.
(författare)
-
Observation of inhomogeneous plasmonic field distribution in a nanocavity
- 2020
-
Ingår i: Nature Nanotechnology. - : Nature Research. - 1748-3387 .- 1748-3395.
-
Tidskriftsartikel (refereegranskat)abstract
- The progress of plasmon-based technologies relies on an understanding of the properties of the enhanced electromagnetic fields generated by the coupling nanostrucutres1–6. Plasmon-enhanced applications include advanced spectroscopies7–10, optomechanics11, optomagnetics12 and biosensing13–17. However, precise determination of plasmon field intensity distribution within a nanogap remains challenging. Here, we demonstrate a molecular ruler made from a set of viologen-based, self-assembly monolayers with which we precisely measures field distribution within a plasmon nanocavity with ~2-Å spatial resolution. We observed an unusually large plasmon field intensity inhomogeneity that we attribute to the formation of a plasmonic comb in the nanocavity. As a consequence, we posit that the generally adopted continuous media approximation for molecular monolayers should be used carefully.
|
|
| 7. |
- Li, Daobin, et al.
(författare)
-
Atomically dispersed platinum supported on curved carbon supports for efficient electrocatalytic hydrogen evolution
- 2019
-
Ingår i: Nature Energy. - : Nature Publishing Group. - 2058-7546. ; 4:6, s. 512-518
-
Tidskriftsartikel (refereegranskat)abstract
- Dispersing catalytically active metals as single atoms on supports represents the ultimate in metal utilization efficiency and is increasingly being used as a strategy to design hydrogen evolution reaction (HER) electrocatalysts. Although platinum (Pt) is highly active for HER, given its high cost it is desirable to find ways to improve performance further while minimizing the Pt loading. Here, we use onion-like nanospheres of carbon (OLC) to anchor stable atomically dispersed Pt to act as a catalyst (Pt-1/OLC) for the HER. In acidic media, the performance of the Pt-1/OLC catalyst (0.27 wt% Pt) in terms of a low overpotential (38 mV at 10 mA cm(-2)) and high turnover frequencies (40.78 H-2 s(-1) at 100 mV) is better than that of a graphene-supported single-atom catalyst with a similar Pt loading, and comparable to a commercial Pt/C catalyst with 20 wt% Pt. First-principle calculations suggest that a tip-enhanced local electric field at the Pt site on the curved support promotes the reaction kinetics for hydrogen evolution.
|
|
| 8. |
- Neeraj, Kumar, et al.
(författare)
-
Inertial spin dynamics in ferromagnets
- 2021
-
Ingår i: Nature Physics. - : Springer Science and Business Media LLC. - 1745-2473 .- 1745-2481. ; 17, s. 245-250
-
Tidskriftsartikel (refereegranskat)abstract
- The understanding of how spins move and can be manipulated at pico- and femtosecond timescales has implications for ultrafast and energy-efficient data-processing and storage applications. However, the possibility of realizing commercial technologies based on ultrafast spin dynamics has been hampered by our limited knowledge of the physics behind processes on this timescale. Recently, it has been suggested that inertial effects should be considered in the full description of the spin dynamics at these ultrafast timescales, but a clear observation of such effects in ferromagnets is still lacking. Here, we report direct experimental evidence of intrinsic inertial spin dynamics in ferromagnetic thin films in the form of a nutation of the magnetization at a frequency of ~0.5 THz. This allows us to reveal that the angular momentum relaxation time in ferromagnets is on the order of 10 ps.
|
|
| 9. |
- Zhang, Qun, et al.
(författare)
-
The Realistic Domain Structure of As-Synthesized Graphene Oxide from Ultrafast Spectroscopy
- 2013
-
Ingår i: Journal of the American Chemical Society. - : American Chemical Society (ACS). - 0002-7863 .- 1520-5126. ; 135:33, s. 12468-12474
-
Tidskriftsartikel (refereegranskat)abstract
- Graphene oxide (GO) is an attractive alternative for large-scale production of graphene, but its general structure is still under debate due to its complicated nonstoichiometric nature. Here we perform a set of femto-second pump-probe experiments on as-synthesized GO to extrapolate structural information in situ. Remarkably, it is observed that, in these highly oxidized GO samples, the ultrafast graphene-like dynamics intrinsic to pristine graphene is completely dominant over a wide energy region and can be modified by the localized impurity states and the electron-phonon coupling under certain conditions. These observations, combined with the X-ray photoelectron spectroscopy analysis and control experiments, lead to an important conclusion that GO consists of two types of domain, namely the carbon-rich graphene-like domain and the oxygen-rich domain. This study creates a new understanding of the realistic domain structure and properties of as-synthesized GO, offering useful guidance for future applications based on chemically modified/functionalized graphenes.
|
|
| 10. |
- Ai-Xi, Chen, et al.
(författare)
-
Potential-Induced Phase Transition of N-Isobutyryl-L-cysteine Monolayers on Au(111) Surfaces
- 2017
-
Ingår i: Wuli huaxue xuebao. - : PEKING UNIV PRESS. - 1000-6818. ; 33:5, s. 1010-1016
-
Tidskriftsartikel (refereegranskat)abstract
- Functional solid substrates modified by self-assembled monolayers (SAMs) have potential applications in biosensors, chromatography, and biocompatible materials. The potential-induced phase transition of N-isobutyryl-L-cysteine (L-NIBC) SAMs on Au(111) surfaces was investigated by in-situ electrochemical scanning tunneling microscopy (EC-STM) in 0.1 mol.L-1 H2SO4 solution. The NIBC SAMs with two distinct structures (alpha phase and beta phase) can be prepared by immersing the Au(111) substrate in pure NIBC aqueous solution and NIBC solution controlled by phosphate buffer at pH 7, respectively. The as-prepared a phase and beta phase of NIBC SAMs show various structural changes under the control of electrochemical potentials of the Au(111) in H2SO4 solution. The a phase NIBC SAMs exhibit structural changes from ordered to disordered structures with potential changes from 0.7 V (vs saturated calomel electrode, SCE) to 0.2 V. However, the beta phase NIBC SAMs undergo structural changes from disordered structures (E < 0.3 V) to y phase (0.4 V < E < 0.5 V) and finally to the beta phase (0.5 V < E < 0.7 V). EC-STM images also indicate that the phase transition from the alpha phase NIBC SAMs to the a phase occurs at positive potential. Combined with density functional theory (DFT) calculations, the phase transition from the beta phase to the a phase is explained by the potential-induced break of bonding interactions between -COO- and the negatively charged gold surfaces.
|
|
