| 1. |
- Yang, Chaoran, et al.
(författare)
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Alternate-stacked Li4Ti5O12 nanosheets/d-Ti3C2 flexible film as a current collector-free, high-capacity and robust cathode for rechargeable Mg batteries
- 2020
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Ingår i: Nano select. - : John Wiley & Sons. - 2688-4011. ; 1:1, s. 1-11
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Tidskriftsartikel (refereegranskat)abstract
- Rechargeable magnesium batteries (RMBs) have gained increasing attention owing to its high volumetric capacity, crust abundance, and safety from dendrite-free characteristic. However, the lack of development of high-performance cathode materials with long cycling stability and satisfactory capacity has greatly restricted the development of RMBs. Herein, a self-supported, current collector-free and soft electrode is prepared with delaminated Ti3C2 (d-Ti3C2) and Li4Ti5O12 nanosheets by simple vacuum filtration as flexible cathode in RMBs. Fabricated into a full cell with hybrid AlCl3/MgCl2/Mg(TFSI)2 electrolyte and Mg anode (a thin Mg foil with thickness of 50 μm), the flexible cathode shows high initial specific capacity of 320 mAh g−1 at 20 mA g−1, excellent cycling stability (good retention even after 1000 cycles) and outstanding rate performance. Detailed mechanistic studies reveal that introduction of d-Ti3C2 provide fast transport paths for electrons and Mg2+. The enlarged layer spacing of composited d-Ti3C2 accounts for significant increment in capacity. Benefiting from above-mentioned advantages, the best performance among Ti-based electrode materials is realized and make wearable devices powered by RMBs possible, thus circumventing the safety issues of lithium batteries.
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| 2. |
- Bao, Qinye, et al.
(författare)
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The Effect of Oxygen Uptake on Charge Injection Barriers in Conjugated Polymer Films
- 2018
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Ingår i: ACS Applied Materials and Interfaces. - : AMER CHEMICAL SOC. - 1944-8244 .- 1944-8252. ; 10:7, s. 6491-6497
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Tidskriftsartikel (refereegranskat)abstract
- The energy offset between the electrode Fermi level and organic semiconductor transport levels is a key parameter controlling the charge injection barrier and hence efficiency of organic electronic devices. Here, we systematically explore the effect of in situ oxygen exposure on energetics in n-type conjugated polymer P(NDI2OD-T2) films. The analysis reveals that an interfacial potential step is introduced for a series of P(NDI2OD-T2) electrode contacts, causing a nearly constant downshift of the vacuum level, while the ionization energies versus vacuum level remain constant. These findings are attributed to the establishment of a so-called double-dipole step via motion of charged molecules and will modify the charge injection barriers at electrode contact. We further demonstrate that the same behavior occurs when oxygen interacts with p-type polymer TQ1 films, indicating it is possible to be a universal effect for organic semiconductOrs.
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| 3. |
- Li, Danqin, et al.
(författare)
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Enhanced and Balanced Charge Transport Boosting Ternary Solar Cells Over 17% Efficiency
- 2020
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Ingår i: Advanced Materials. - : WILEY-V C H VERLAG GMBH. - 0935-9648 .- 1521-4095. ; 32:34
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Tidskriftsartikel (refereegranskat)abstract
- Ternary architecture is one of the most effective strategies to boost the power conversion efficiency (PCE) of organic solar cells (OSCs). Here, an OSC with a ternary architecture featuring a highly crystalline molecular donor DRTB-T-C4 as a third component to the host binary system consisting of a polymer donor PM6 and a nonfullerene acceptor Y6 is reported. The third component is used to achieve enhanced and balanced charge transport, contributing to an improved fill factor (FF) of 0.813 and yielding an impressive PCE of 17.13%. The heterojunctions are designed using so-called pinning energies to promote exciton separation and reduce recombination loss. In addition, the preferential location of DRTB-T-C4 at the interface between PM6 and Y6 plays an important role in optimizing the morphology of the active layer.
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| 4. |
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| 5. |
- Lv, Wanzhi, et al.
(författare)
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Lipoxin A4 attenuation of endothelial inflammation response mimicking pancreatitis-induced lung injury
- 2013
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Ingår i: Experimental Biology and Medicine. - : SAGE Publications. - 1535-3702 .- 1535-3699. ; 238:12, s. 1388-1395
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Tidskriftsartikel (refereegranskat)abstract
- Lipoxins (LXs) and their analogues are known to display potent anti-inflammatory actions. Previously, we reported that lipoxin A4 (LXA4) possessed powerful anti-inflammatory properties in acute pancreatitis in rats and that it may ameliorate the concomitant acute lung injury by reducing cytokine generation and inhibiting neutrophil activation. Considering that the vascular endothelium plays an important role during adherence, migration and activation of leukocytes, the present study was designed to investigate the effects of LXA4 on the inflammatory response induced by tumor necrosis factor a (TNF-alpha) in human pulmonary microvascular endothelial cells (HPMECs) and explore the potential mechanisms involved in these processes. We found that LXA4 markedly down-regulated the expression of monocyte chemotactic protein-1 (MCP-1), E-selectin, and interleukin-6 (IL-6) mRNA, as well as intercellular adhesion molecule-1 (ICAM-1) in TNF-alpha-exposed HPMECs. Moreover, LXA4 inhibited the phosphorylation and nuclear translocation of nuclear factor-kappa B/p65 (NF-kappa B/p65) and phosphorylation of p38 mitogen-activated protein kinase (p38 MAPK) in HPMECs following TNF-alpha stimulation. Heme oxygenase-1 (HO-1), a cytoprotective enzyme, was up-regulated by LXA4 in both non- and TNF-alpha-stimulated HPMECs. In conclusion, the protective effects of LXA4 to ALI may be executed through inhibition inflammation pathways of NF-kappa B and p38 MAPK and up-regulation of cytoprotective HO-1.
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| 6. |
- Xiao, Wei, et al.
(författare)
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Exploring Red, Green, and Blue Light-Activated Degradation of Perovskite Films and Solar Cells for Near Space Applications
- 2020
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Ingår i: Solar RRL. - : Wiley-VCH Verlagsgesellschaft. - 2367-198X. ; 4:3
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Tidskriftsartikel (refereegranskat)abstract
- Hybrid perovskite solar cells with a high specific power have great potential to become promising power sources mounted on spacecrafts in space applications. However, there is a lack of study on their photostability as light absorbers in those conditions. Herein, the stability of the perovskite films and solar cells under red, green, and blue (RGB) light illumination in medium vacuum that belongs to near space is explored. The perovskite active layers exhibit different degradations from morphological, chemical, and structural points of view. This is attributed to the strong coupling between photoexcited carriers and the crystal lattice and the diversity of RGB light absorption in the perovskite films. Device characterizations reveal that the efficiency loss of perovskite solar cells results from not only perovskite degradation, but also the photoexcited carriers reducing the energy barrier of ion migration and accelerating the migration to generate more deep-level trap defects. Moreover, comparative devices suggest that the well encapsulation can weaken the effect of vacuum on stability.
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| 7. |
- Xiong, Shaobing, et al.
(författare)
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Additive-Induced Synergies of Defect Passivation and Energetic Modification toward Highly Efficient Perovskite Solar Cells
- 2021
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Ingår i: Advanced Energy Materials. - : WILEY-V C H VERLAG GMBH. - 1614-6832 .- 1614-6840. ; 11:29
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Tidskriftsartikel (refereegranskat)abstract
- Defect passivation via additive and energetic modification via interface engineering are two effective strategies for achieving high-performance perovskite solar cells (PSCs). Here, the synergies of pentafluorophenyl acrylate when used as additive, in which it not only passivates surface defect states but also simultaneously modifies the energetics at the perovskite/Spiro-OMeTAD interface to promote charge transport, are shown. The additive-induced synergy effect significantly suppresses both defect-assisted recombination and interface carrier recombination, resulting in a device efficiency of 22.42% and an open-circuit voltage of 1.193 V with excellent device stability. The two photovoltaic parameters are among the highest values for polycrystalline CsFormamidinium/Methylammonium (FAMA)/FAMA based n-i-p structural PSCs using low-cost silver electrodes reported to date. The findings provide a promising approach by choosing the dual functional additive to enhance efficiency and stability of PSCs.
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| 8. |
- Xiong, Shaobing, et al.
(författare)
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Defect passivation by nontoxic biomaterial yields 21% efficiency perovskite solar cells
- 2021
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Ingår i: Journal of Energy Challenges and Mechanics. - : ELSEVIER. - 2056-9386. ; 55, s. 265-271
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Tidskriftsartikel (refereegranskat)abstract
- Defect passivation is one of the most important strategies to boost both the efficiency and stability of perovskite solar cells (PSCs). Here, nontoxic and sustainable forest-based biomaterial, betulin, is first introduced into perovskites. The experiments and calculations reveal that betulin can effectively passivate the uncoordinated lead ions in perovskites via sharing the lone pair electrons of hydroxyl group, promoting charge transport. As a result, the power conversion efficiencies of the p-i-n planar PSCs remarkably increase from 19.14% to 21.15%, with the improvement of other parameters. The hydrogen bonds of betulin lock methylamine and halogen ions along the grain boundaries and on the film surface and thus suppress ion migration, further stabilizing perovskite crystal structures. These positive effects enable the PSCs to maintain 90% of the initial efficiency after 30 days in ambient air with 60%+/- 5% relative humidity, 75% after 300 h aging at 85 degrees C, and 55% after 250 h light soaking, respectively. This work opens a new pathway for using nontoxic and low-cost biomaterials from forest to make highly efficient and stable PSCs. (C) 2020 Science Press and Dalian Institute of Chemical Physics, Chinese Academy of Sciences. Published by ELSEVIER B.V. and Science Press. All rights reserved.
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| 9. |
- Xiong, Shaobing, et al.
(författare)
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Defect-Passivation Using Organic Dyes for Enhanced Efficiency and Stability of Perovskite Solar Cells
- 2020
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Ingår i: Solar RRL. - : WILEY-V C H VERLAG GMBH. - 2367-198X. ; 4:5
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Tidskriftsartikel (refereegranskat)abstract
- Perovskite solar cells are a highly competitive candidate for next-generation photovoltaic technology. Defects in the perovskite grain boundaries and on the film surfaces however have significant impacts on both the device efficiency and environmental stability. Herein, a strategy using organic dyes as additives to passivate the defect states and produce more n-type perovskite films, thereby improving charge transport and decreasing charge recombination, is reported. Based on this strategy, the power conversion efficiency of the perovskite solar cell is significantly increased from 18.13% to 20.18% with a negligible hysteresis. Furthermore, the rich hydrogen bonds and carbonyl structures in the organic dye can significantly enhance device stability both in terms of humidity and thermal stress. The results present a promising pathway using abundant and colorful organic dyes as additives to achieve high-performance perovskite solar cells.
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| 10. |
- Xiong, Shaobing, et al.
(författare)
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Direct Observation on p- to n-Type Transformation of Perovskite Surface Region during Defect Passivation Driving High Photovoltaic Efficiency
- 2021
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Ingår i: Joule. - : CELL PRESS. - 2542-4351. ; 5:2, s. 467-480
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Tidskriftsartikel (refereegranskat)abstract
- Perovskite solar cells (PSCs) suffer from significant nonradiative recombination, limiting their power conversion efficiencies. Here, for the first time, we directly observe a complete transformation of perovskite MAPbI(3) surface region energetics from p- to n-type during defect passivation caused by natural additive capsaicin, attributed to the spontaneous formation of a p-n homojunction in perovskite active layer. We demonstrate that the p-n homojunction locates at similar to 100 nm below perovskite surface. The energetics transformation and defect passivation promote charge transport in bulk perovskite layer and at perovskite/PCBM interface, suppressing both defect-assisted recombination and interface carrier recombination. As a result, an efficiency of 21.88% and a fill factor of 83.81% with excellent device stability are achieved, both values are the highest records for polycrystalline MAPbI(3) based p-i-n PSCs reported to date. The proposed new concept of synergetic defect passivation and energetic modification via additive provides a huge potential for further improvement of PSC performance.
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