Institution
Donghua University
Education•Shanghai, China•
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.
Topics: Fiber, Nanofiber, Membrane, Electrospinning, Catalysis
Papers published on a yearly basis
Papers
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TL;DR: In this article, the effect of different salts on electrospinning of polyacrlonitrile (PAN) polymer solution was investigated, and the results showed that when the salts were added, respectively, into different concentrations of PAN solution, the order of conductant was LiCl > NaNO3 > CaCl2 > NaCl > no salt added.
Abstract: Electrospinning is a relatively simple method to produce submicron fibers from solutions of different polymers and polymer blends. If the solution is absolutely insulating, or the applied voltage is not high enough that electrostatic force cannot overcome the surface tension, then no fiber can be produced by electrospinning; however, if some salt is added in the solution, the problem can be overcome. The effect of different salts on electrospinning of polyacrlonitrile (PAN) polymer solution was investigated in this article. The various inorganic salts used in this work include LiCl, NaNO3, NaCl, and CaCl2.The results show that when the salts were added, respectively, into different concentrations of PAN solution, the order of conductant was LiCl > NaNO3 > CaCl2 > NaCl > no salt added. Viscosity and shearing strength of electrospinning solutions are slightly affected by the adding of salts and mainly affected by the changes in concentration of PAN electrospinning solutions. The diameter of nanofibers electrospun by solutions with different salts size down as follows: LiCl > NaNO3 > CaCl2 > NaCl. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 103: 3865–3870, 2007
139 citations
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TL;DR: In this article, a 3D-printed TENG (3DP-TENGs) is designed and readily fabricated by a single integrated process without additional assembling steps, and the TENGs contain poly(glycerol sebacate) and carbon nanotubes (CNTs) as the two electrification components.
Abstract: Triboelectric nanogenerator (TENG) devices have gotten great attention in wearable power sources and physiological monitoring. However, the complicated assembling and the molding processing retard their applications. Here, 3D-printed TENGs (3DP-TENGs) are designed and readily fabricated by a single integrated process without additional assembling steps. The TENGs contain poly(glycerol sebacate) (PGS) and carbon nanotubes (CNTs) as the two electrification components. Conductive CNTs also serve as electrodes. Elastic PGS matrix makes TENGs intrinsically responsive to biomechanical motions leading to robust energy outputs. The hierarchical porous structure of the 3DP-TENG results in higher output efficiency than traditional molded microporous TENG counterparts. TENGs with different 3D shapes are readily fabricated for different applications. The 3DP-TENG insole efficiently harvests biomechanical energy to drive electronics. A ring-shaped TENG acts as a self-powered sensor to monitor the motion of fingers. Furthermore, the use of bio-based and biodegradable PGS matrix combining with efficient recycle of CNTs makes 3DP-TENGs favorable from sustainable perspective. This work provides a new strategy to design and tailor 3D TENGs that will be very useful for diverse electronic applications.
139 citations
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TL;DR: In this paper, a humidity-resisting triboelectric nanogenerator (HR-TENG) was proposed to harvest energy from human biomechanical movements for wearable electronics.
139 citations
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TL;DR: Novel doughnut-shaped multi-layered drug delivery devices (DDDs) were developed with local variations of the drug and release-retardant material for providing linear release profiles and 3DP is capable of offering novel strategies for developing DDDs with complex design features for desired drug release profiles.
139 citations
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TL;DR: In this article, a comprehensive overview of the reported strategies for PSC devices with flexible, stable and large-scale properties is presented, where the authors focus on the recent advancements in the aspects of flexibility, stability and large scale of PSCs.
Abstract: Recent progress in organic–inorganic halide perovskite solar cells (PSCs) has attracted great attention due to their impressive photovoltaic properties, and easy device manufacturing with facile layer deposition by solution processes, suggesting their great potential for large-scale applications. Remarkably, the power conversion efficiencies (PCEs) of PSCs have jumped from 3.8% of methyl ammonium lead halide, CH3NH3PbX3 (X = Br, I), sensitized liquid solar cells in 2009, to more than 20% of all solid-state solar cells in 2015. Just over the past 6 years, numerous efforts have contributed to promote PSCs with more attractive properties, in preparation for future commercial applications, such as high PCE, high stability, high flexibility, large area, low cost, environmental friendliness, etc. In this review, we will concentrate on the recent advancements in the aspects of flexibility, stability and large scale of PSCs. We strive to present a comprehensive overview and show a deep understanding of the reported strategies for PSC devices with flexible, stable and large-scale properties.
139 citations
Authors
Showing all 21321 results
Name | H-index | Papers | Citations |
---|---|---|---|
Dongyuan Zhao | 160 | 872 | 106451 |
Xiang Zhang | 154 | 1733 | 117576 |
Seeram Ramakrishna | 147 | 1552 | 99284 |
Kuo-Chen Chou | 143 | 487 | 57711 |
Shuai Liu | 129 | 1095 | 80823 |
Chao Zhang | 127 | 3119 | 84711 |
Tao Zhang | 123 | 2772 | 83866 |
Zidong Wang | 122 | 914 | 50717 |
Xinchen Wang | 120 | 349 | 65072 |
Zhenyu Zhang | 118 | 1167 | 64887 |
Benjamin S. Hsiao | 108 | 602 | 41071 |
Qian Wang | 108 | 2148 | 65557 |
Jian Zhang | 107 | 3064 | 69715 |
Yan Zhang | 107 | 2410 | 57758 |
Richard B. Kaner | 106 | 557 | 66862 |