Donghua University

About: Donghua University is a education organization based out in Shanghai, China. It is known for research contribution in the topics: Fiber & Nanofiber. The organization has 21155 authors who have published 21841 publications receiving 393091 citations. The organization is also known as: Dōnghuá Dàxué & China Textile University.

Use of dynamic rheological behavior to estimate the dispersion of carbon nanotubes in carbon nanotube/polymer composites.

Abstract: Well-dispersed multiwalled carbon nanotube (MWNT)/polystyrene composites have been prepared. Transmission and scanning electron microscopy were employed to observe the distribution of the MWNTs in the composites in a microscopic scale, indicating a nanotube network formed in the matrix. The dispersion of the nanotubes in the polymer was monitored by oscillatory rheology. It was found that the addition of MWNTs in the polymer had a drastic influence on the rheological behavior of the composites. As the MWNT loading increased, Newtonian behavior disappeared at low frequency, suggesting a transition from liquid-like to solid-like viscoelastic behavior. A more homogeneous dispersion or a greater loading of the nanotubes in the matrix produced stronger solid-like and nonterminal behavior, and the composites exhibited less temperature dependence at elevated temperature, compared to the matrix melt.

Oriented arrays of polyaniline nanorods grown on graphite nanosheets for an electrochemical supercapacitor.

Abstract: Oriented arrays of polyaniline (PANI) nanorods grown on expanded graphite (EG) nanosheets are fabricated by in situ polymerization to achieve excellent electrochemical properties for applications as supercapacitor electrodes. EG serves as an excellent 3D conductive skeleton that supports a highly electrolytic accessible surface area of redox-active PANI and provides a direct path for electrons. The porous and ordered nanostructure provides a larger contact surface area for the intercalation/deintercalation of protons into/out of active materials and shortens the path length for electrolyte ion transport. The maximum specific capacitance of 1665 F g–1 at 1 A g–1 is observed in the PANI/EG electrode with 10% EG content. The composite electrode material also exhibits significant rate capability and good long-term cycling stability. The results demonstrate that PANI is effectively utilized with the assistance of EG conductive skeletons in the electrode. Such 3D composite nanoarchitecture is very promising for...

Solution-Processed Organic Solar Cells with High Open-Circuit Voltage of 1.3 V and Low Non-Radiative Voltage Loss of 0.16 V.

Abstract: Compared with inorganic or perovskite solar cells, the relatively large non-radiative recombination voltage losses (ΔVnon-rad ) in organic solar cells (OSCs) limit the improvement of the open-circuit voltage (Voc ). Herein, OSCs are fabricated by adopting two pairs of D-π-A polymers (PBT1-C/PBT1-C-2Cl and PBDB-T/PBDB-T-2Cl) as electron donors and a wide-bandgap molecule BTA3 as the electron acceptor. In these blends, a charge-transfer state energy (ECT ) as high as 1.70-1.76 eV is achieved, leading to small energetic differences between the singlet excited states and charge-transfer states (ΔECT ≈ 0.1 eV). In addition, after introducing chlorine atoms into the π-bridge or the side chain of benzodithiophene (BDT) unit, electroluminescence external quantum efficiencies as high as 1.9 × 10-3 and 1.0 × 10-3 are realized in OSCs based on PBTI-C-2Cl and PBDB-T-2Cl, respectively. Their corresponding ΔVnon-rad are 0.16 and 0.17 V, which are lower than those of OSCs based on the analog polymers without a chlorine atom (0.21 and 0.24 V for PBT1-C and PBDB-T, respectively), resulting in high Voc of 1.3 V. The ΔVnon-rad of 0.16 V and Voc of 1.3 V achieved in PBT1-C-2Cl:BTA3 OSCs are thought to represent the best values for solution-processed OSCs reported in the literature so far.

In situ Visualization of State-of-Charge Heterogeneity within a LiCoO2 Particle that Evolves upon Cycling at Different Rates

Abstract: For designing new battery systems with higher energy density and longer cycle life, it is important to understand the degradation mechanism of the electrode material, especially at the individual particle level. Using in situ transmission X-ray microscopy (TXM) coupled to a pouch cell setup, the inhomogeneous Li distribution as well as the formation, population, and evolution of inactive domains in a single LiCoO2 particle were visualized as it was cycled for many times. It is found that the percentage of the particle that fully recovered to the pristine state is strongly related to the cycling rate. Interestingly, we also observed the evolution of the inactive region within the particle during long-term cycling. The relationship between morphological degradation and chemical inhomogeneity, including the formation of unanticipated Co metal phase, is also observed. Our work highlights the capability of in situ TXM for studying the degradation mechanism of materials in LIBs.