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Träfflista för sökning "WFRF:(Li Yingping) "

Sökning: WFRF:(Li Yingping)

  • Resultat 1-10 av 11
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1.
  • Kristanl, Matej, et al. (författare)
  • The Seventh Visual Object Tracking VOT2019 Challenge Results
  • 2019
  • Ingår i: 2019 IEEE/CVF INTERNATIONAL CONFERENCE ON COMPUTER VISION WORKSHOPS (ICCVW). - : IEEE COMPUTER SOC. - 9781728150239 ; , s. 2206-2241
  • Konferensbidrag (refereegranskat)abstract
    • The Visual Object Tracking challenge VOT2019 is the seventh annual tracker benchmarking activity organized by the VOT initiative. Results of 81 trackers are presented; many are state-of-the-art trackers published at major computer vision conferences or in journals in the recent years. The evaluation included the standard VOT and other popular methodologies for short-term tracking analysis as well as the standard VOT methodology for long-term tracking analysis. The VOT2019 challenge was composed of five challenges focusing on different tracking domains: (i) VOT-ST2019 challenge focused on short-term tracking in RGB, (ii) VOT-RT2019 challenge focused on "real-time" short-term tracking in RGB, (iii) VOT-LT2019 focused on long-term tracking namely coping with target disappearance and reappearance. Two new challenges have been introduced: (iv) VOT-RGBT2019 challenge focused on short-term tracking in RGB and thermal imagery and (v) VOT-RGBD2019 challenge focused on long-term tracking in RGB and depth imagery. The VOT-ST2019, VOT-RT2019 and VOT-LT2019 datasets were refreshed while new datasets were introduced for VOT-RGBT2019 and VOT-RGBD2019. The VOT toolkit has been updated to support both standard short-term, long-term tracking and tracking with multi-channel imagery. 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 dataset, the evaluation kit and the results are publicly available at the challenge website(1).
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2.
  • Zhu, Can, et al. (författare)
  • Tuning the electron-deficient core of a non-fullerene acceptor to achieve over 17% efficiency in a single-junction organic solar cell
  • 2020
  • Ingår i: Energy & Environmental Science. - : ROYAL SOC CHEMISTRY. - 1754-5692 .- 1754-5706. ; 13:8, s. 2459-2466
  • Tidskriftsartikel (refereegranskat)abstract
    • Finding effective molecular design strategies to enable efficient charge generation and small energy loss is among the long-standing challenges in developing high performance non-fullerene organic solar cells (OSCs). Recently, we reported Y-series non-fullerene acceptors with an electron-deficient-core-based fused structure (typically Y6), opening a new door to achieve high external quantum efficiency (∼80%) while maintaining low energy loss (∼0.57 eV). On this basis, further reducing the energy losses and ultimately improving the performance of OSCs has become a research hotspot. In this paper, we design and synthesize a new member of the Y-series acceptor family, Y18, which adopts a fused benzotriazole segment with unique luminescence properties as its electron-deficient core. Compared to Y6, the benzotriazole-based acceptor Y18 exhibits extended optical absorption and higher voltage. Consequently, the device delivers a promising power conversion efficiency of 16.52% with a very low energy loss of 0.53 eV. Further device optimization by exploiting a ternary blend strategy allowed us to achieve a high efficiency of 17.11% (certified as 16.76% by NREL). Y18 may become one of the most important candidate materials for its broader absorption spectra and higher voltage of Y18 (compared to Y6) in the OSCs field.
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3.
  • Chen, Min, et al. (författare)
  • Yeast increases glycolytic flux to support higher growth rates accompanied by decreased metabolite regulation and lower protein phosphorylation
  • 2023
  • Ingår i: Proceedings of the National Academy of Sciences of the United States of America. - 0027-8424 .- 1091-6490. ; 120:25
  • Tidskriftsartikel (refereegranskat)abstract
    • Supply of Gibbs free energy and precursors are vital for cellular function and cell metabolism have evolved to be tightly regulated to balance their supply and consumption. Precursors and Gibbs free energy are generated in the central carbon metabolism (CCM), and fluxes through these pathways are precisely regulated. However, how fluxes through CCM pathways are affected by posttranslational modification and allosteric regulation remains poorly understood. Here, we integrated multi-omics data collected under nine different chemostat conditions to explore how fluxes in the CCM are regulated in the yeast Saccharomyces cerevisiae. We deduced a pathway- and metabolism-specific CCM flux regulation mechanism using hierarchical analysis combined with mathematical modeling. We found that increased glycolytic flux associated with an increased specific growth rate was accompanied by a decrease in flux regulation by metabolite concentrations, including the concentration of allosteric effectors, and a decrease in the phosphorylation level of glycolytic enzymes.
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4.
  • Chen, Xian-Kai, et al. (författare)
  • A unified description of non-radiative voltage losses in organic solar cells
  • 2021
  • Ingår i: Nature Energy. - : Springer Nature. - 2058-7546. ; 6:8, s. 799-806
  • Tidskriftsartikel (refereegranskat)abstract
    • Organic solar cells based on non-fullerene acceptors have enabled high efficiencies yet their charge dynamics and its impact on the photovoltaic parameters are not fully understood. Now, Chen et al. provide a general description of non-radiative voltage losses in both fullerene and non-fullerene solar cells. Recent advances in organic solar cells based on non-fullerene acceptors (NFAs) come with reduced non-radiative voltage losses (Delta V-nr). Here we show that, in contrast to the energy-gap-law dependence observed in conventional donor:fullerene blends, the Delta V-nr values in state-of-the-art donor:NFA organic solar cells show no correlation with the energies of charge-transfer electronic states at donor:acceptor interfaces. By combining temperature-dependent electroluminescence experiments and dynamic vibronic simulations, we provide a unified description of Delta V-nr for both fullerene- and NFA-based devices. We highlight the critical role that the thermal population of local exciton states plays in low-Delta V-nr systems. An important finding is that the photoluminescence yield of the pristine materials defines the lower limit of Delta V-nr. We also demonstrate that the reduction in Delta V-nr (for example, <0.2 V) can be obtained without sacrificing charge generation efficiency. Our work suggests designing donor and acceptor materials with high luminescence efficiency and complementary optical absorption bands extending into the near-infrared region.
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5.
  • Hu, Jinghua, et al. (författare)
  • Synthesis and First-principle Calculation of TiO2 Rutile Nanowire Electrodes for Dye-sensitized Solar Cells
  • 2017
  • Ingår i: International Journal of Electrochemical Science. - : Electrochemical Science Group. - 1452-3981. ; 12:10, s. 9725-9735
  • Tidskriftsartikel (refereegranskat)abstract
    • In this paper, a TiO2 nanowire film synthesized via a hydrothermal method was prepared as a photoanode for dye-sensitized solar cells (DSSCs). The synthesized TiO2 nanowires were characterized by transmission electron microscopy and X-ray diffraction. The TiO2 nanowire film greatly improved the efficiency of the DSSC owing to the rapid interfacial electron transport in the one-dimensional TiO2 nanowires. The light absorption and interfacial electron transport, which play important roles in the efficiency of DSSCs, were investigated by UV-vis absorption spectroscopy and electrochemical impedance spectroscopy. The energy band structure and electron density of states of the rutile nanowire were calculated using a first-principles method and compared to bulk anatase and rutile TiO2 phases. The band gap of the rutile TiO2 nanowire was found to be less than that of anatase TiO2 by 0.6 eV. Further calculations using GGA+U yielded a similar band gap reduction. In addition to the redshift of the absorption edge originating from the smaller band gap, the larger surface area of the TiO2 nanowire compared to the bulk material is expected to facilitate the migration of photogenerated electrons and holes from inside to the surface of the material. This would result in a considerable improvement of the photocatalytic efficiency of TiO2.
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6.
  • Huang, Kun, et al. (författare)
  • Enhanced peak growth of global vegetation and its key mechanisms
  • 2018
  • Ingår i: Nature Ecology and Evolution. - : Springer Science and Business Media LLC. - 2397-334X. ; 2:12, s. 1897-1905
  • Tidskriftsartikel (refereegranskat)abstract
    • The annual peak growth of vegetation is critical in characterizing the capacity of terrestrial ecosystem productivity and shaping the seasonality of atmospheric CO2 concentrations. The recent greening of global lands suggests an increasing trend of terrestrial vegetation growth, but whether or not the peak growth has been globally enhanced still remains unclear. Here, we use two global datasets of gross primary productivity (GPP) and a satellite-derived Normalized Difference Vegetation Index (NDVI) to characterize recent changes in annual peak vegetation growth (that is, GPPmax and NDVImax). We demonstrate that the peak in the growth of global vegetation has been linearly increasing during the past three decades. About 65% of the NDVImax variation is evenly explained by expanding croplands (21%), rising CO2 (22%) and intensifying nitrogen deposition (22%). The contribution of expanding croplands to the peak growth trend is substantiated by measurements from eddy-flux towers, sun-induced chlorophyll fluorescence and a global database of plant traits, all of which demonstrate that croplands have a higher photosynthetic capacity than other vegetation types. The large contribution of CO2 is also supported by a meta-analysis of 466 manipulative experiments and 15 terrestrial biosphere models. Furthermore, we show that the contribution of GPPmax to the change in annual GPP is less in the tropics than in other regions. These multiple lines of evidence reveal an increasing trend in the peak growth of global vegetation. The findings highlight the important roles of agricultural intensification and atmospheric changes in reshaping the seasonality of global vegetation growth.
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7.
  • Liu, Wei, et al. (författare)
  • A-pi-A structured non-fullerene acceptors for stable organic solar cells with efficiency over 17%
  • 2022
  • Ingår i: Science in China Series B. - : SCIENCE PRESS. - 1674-7291 .- 1869-1870. ; 65:7, s. 1374-1382
  • Tidskriftsartikel (refereegranskat)abstract
    • With the development of photovoltaic materials, especially the small molecule acceptors (SMAs), organic solar cells (OSCs) have made breakthroughs in power conversion efficiencies (PCEs). However, the stability of high-performance OSCs remains a critical challenge for future technological applications. To tackle the inherent instability of SMA materials under the ambient conditions, much effort has been made to improve OSCs stability, including device modification and new materials design. Here we proposed a new electron acceptor design strategy and developed a "quasi-macromolecule" (QM) with an A-pi-A structure, where the functionalized pi-bridge is used as a linker between two SMAs (A), to improve the long-term stability without deteriorating device efficiencies. Such type of QMs enables excellent synthetic flexibility to modulate their optical/electro-chemical properties, crystallization and aggregation behaviors by changing the A and pi units. Moreover, QMs possess a unique long conjugated backbone combining high molecular weight over 3.5 kDa with high purity. Compared with the corresponding SMA BTP-4F-OD (Y6-OD), the devices based on newly synthesized A-pi-A type acceptors QM1 and QM2 could exhibit better device stability and more promising PCEs of 17.05% and 16.36%, respectively. This kind of "molecular-framework" (A-pi-A) structure provides a new design strategy for developing high-efficiency and -stability photovoltaic materials.
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8.
  • Lu, Haibo, et al. (författare)
  • Comparing machine learning-derived global estimates of soil respiration and its components with those from terrestrial ecosystem models
  • 2021
  • Ingår i: Environmental Research Letters. - : IOP Publishing. - 1748-9318 .- 1748-9326. ; 16:5
  • Tidskriftsartikel (refereegranskat)abstract
    • The CO2 efflux from soil (soil respiration (SR)) is one of the largest fluxes in the global carbon (C) cycle and its response to climate change could strongly influence future atmospheric CO2 concentrations. Still, a large divergence of global SR estimates and its autotrophic (AR) and heterotrophic (HR) components exists among process based terrestrial ecosystem models. Therefore, alternatively derived global benchmark values are warranted for constraining the various ecosystem model output. In this study, we developed models based on the global soil respiration database (version 5.0), using the random forest (RF) method to generate the global benchmark distribution of total SR and its components. Benchmark values were then compared with the output of ten different global terrestrial ecosystem models. Our observationally derived global mean annual benchmark rates were 85.5 ± 40.4 (SD) Pg C yr-1 for SR, 50.3 ± 25.0 (SD) Pg C yr-1 for HR and 35.2 Pg C yr-1 for AR during 1982-2012, respectively. Evaluating against the observations, the RF models showed better performance in both of SR and HR simulations than all investigated terrestrial ecosystem models. Large divergences in simulating SR and its components were observed among the terrestrial ecosystem models. The estimated global SR and HR by the ecosystem models ranged from 61.4 to 91.7 Pg C yr-1 and 39.8 to 61.7 Pg C yr-1, respectively. The most discrepancy lays in the estimation of AR, the difference (12.0-42.3 Pg C yr-1) of estimates among the ecosystem models was up to 3.5 times. The contribution of AR to SR highly varied among the ecosystem models ranging from 18% to 48%, which differed with the estimate by RF (41%). This study generated global SR and its components (HR and AR) fluxes, which are useful benchmarks to constrain the performance of terrestrial ecosystem models.
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9.
  • Song, Jiage, et al. (författare)
  • Over 13% Efficient Organic Solar Cells Based on Low-Cost Pentacyclic A-DA D-A-Type Nonfullerene Acceptor
  • 2021
  • Ingår i: Solar RRL. - : Wiley-Blackwell. - 2367-198X. ; 5:8
  • Tidskriftsartikel (refereegranskat)abstract
    • Recent studies have almost focused on finding active layer materials with extended pi-conjugation structures for high-performance organic solar cells (OSCs). However, with the extension of conjugate length, the synthesis difficulty and cost of materials will increase. Achieving high efficiency while reducing material costs is a prerequisite for the commercialization of OSCs. Herein, two low-cost A-DA D-A-type (where A and D represent an electron-withdrawing unit and an electron-donating unit, respectively) nonfullerene acceptors (Y25,Y26) are synthesized with pentacyclic fused backbone as the DA D electron-deficient core and 5,6-difluoro-3-(dicyandiamethyl) indigo as the end groups. Compared with classical Y series acceptors with heptacyclic backbone, although Y25 and Y26 own the reduced conjugated length, they still show moderate performance (11.65% and 13.34%), and the cost of synthesis is significantly reduced. Therefore, we provide a new molecular design idea for commercially efficient nonfullerene OSCs acceptors. We also find that adding alkyl chains to the beta site of thiophenes is beneficial to obtaining the reduced energetic disorder, dominant molecular stacking, and desirable morphology, which can facilitate charge carrier transport and prompt higher short-circuit current density (J(sc)) as well as fill factor.
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10.
  • Yuan, Jun, et al. (författare)
  • Reducing Voltage Losses in the A-DAD-A Acceptor-Based Organic Solar Cells
  • 2020
  • Ingår i: Chem. - : CELL PRESS. - 2451-9308 .- 2451-9294. ; 6:9, s. 2147-2161
  • Tidskriftsartikel (refereegranskat)abstract
    • Power conversion efficiencies (PCEs) of solution-processed organic solar cells (OSCs) have recently reached 17.4% (certified) for single-junction devices. Crucial to this advancement is the development of non-fullerene acceptors (NFAs) since 2015. The recent A-DAD-A NFAs have attracted widespread attention because of their ladder-type electron-deficient-core-based central fused ring with improved transport properties and optimum energy levels. With the synergistic effect of electron-deficient-core and specific molecular geometry, the A-DADA molecules could achieve low voltage losses and high current generation at the same time, reaching new regimes of device physics and photophysics. This perspective will discuss the voltage losses in state-of-the-art A-DAD-A NFA-based OSCs and propose new molecular design strategies to achieve PCEs over 20% in OSCs based on these new acceptors by further decreasing their total voltage losses.
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