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| 2. |
- Fan, Zhiwen, et al.
(författare)
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Porous Ionic Network/CNT Composite Separator as a Polysulfide Snaring Shield for High Performance Lithium–Sulfur Battery
- 2023
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Ingår i: Macromolecular rapid communications. - 1022-1336 .- 1521-3927. ; 44:24
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Tidskriftsartikel (refereegranskat)abstract
- Lithium–sulfur (Li–S) battery features a high theoretical energy density, but the shuttle of soluble polysulfides between the two electrodes often results in a rapid capacity decay. Herein, a straightforward electrostatic adsorption strategy based on a cross-linked polyimidazolium separator as a snaring shield of polysulfides is reported, which suppresses the undesirable migration of polysulfides to the anode. The porous ionic network (PIN)-modified carbon nanotubes (CNTs) are successfully prepared and coated onto a commercial porous polypropylene membrane in a vacuum-filtration step. The favorable affinity of the imidazolium ring toward polysulfide via the polar interaction and the electrostatic effect of ions mitigates the undesirable shuttle of polysulfides in the electrolyte, improving the Li─S battery in terms of rate performance and cycling life. Compared to the reference PIN-free CNT-coated separator, the PIN/CNT-coated one has an increased initial capacity of 1.3 folds (up to 1394.8 mAh g−1 for PIN/CNT/PP-3) at 0.1 C.
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| 3. |
- Guo, Han, et al.
(författare)
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Transition metal-catalysed molecular n-doping of organic semiconductors
- 2021
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Ingår i: Nature. - London, United Kingdom : Nature Publishing Group. - 0028-0836 .- 1476-4687. ; 599:7883, s. 67-73
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Tidskriftsartikel (refereegranskat)abstract
- Electron doping of organic semiconductors is typically inefficient, but here a precursor molecular dopant is used to deliver higher n-doping efficiency in a much shorter doping time. Chemical doping is a key process for investigating charge transport in organic semiconductors and improving certain (opto)electronic devices(1-9). N(electron)-doping is fundamentally more challenging than p(hole)-doping and typically achieves a very low doping efficiency (eta) of less than 10%(1,10). An efficient molecular n-dopant should simultaneously exhibit a high reducing power and air stability for broad applicability(1,5,6,9,11), which is very challenging. Here we show a general concept of catalysed n-doping of organic semiconductors using air-stable precursor-type molecular dopants. Incorporation of a transition metal (for example, Pt, Au, Pd) as vapour-deposited nanoparticles or solution-processable organometallic complexes (for example, Pd-2(dba)(3)) catalyses the reaction, as assessed by experimental and theoretical evidence, enabling greatly increased eta in a much shorter doping time and high electrical conductivities (above 100 S cm(-1); ref. (12)). This methodology has technological implications for realizing improved semiconductor devices and offers a broad exploration space of ternary systems comprising catalysts, molecular dopants and semiconductors, thus opening new opportunities in n-doping research and applications(12, 13).
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| 4. |
- Sun, Huiliang, et al.
(författare)
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A monothiophene unit incorporating both fluoro and ester substitution enabling high-performance donor polymers for non-fullerene solar cells with 16.4% efficiency
- 2019
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Ingår i: Energy & Environmental Science. - : ROYAL SOC CHEMISTRY. - 1754-5692 .- 1754-5706. ; 12:11, s. 3328-3337
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Tidskriftsartikel (refereegranskat)abstract
- Thiophene and its derivatives have been extensively used in organic electronics, particularly in the field of polymer solar cells (PSCs). Significant research efforts have been dedicated to modifying thiophene-based units by attaching electron-donating or withdrawing groups to tune the energy levels of conjugated materials. Herein, we report the design and synthesis of a novel thiophene derivative, FE-T, featuring a monothiophene functionalized with both an electron-withdrawing fluorine atom (F) and an ester group (E). The FE-T unit possesses distinctive advantages of both F and E groups, the synergistic effects of which enable significant downshifting of the energy levels and enhanced aggregation/crystallinity of the resulting organic materials. Shown in this work are a series of polymers obtained by incorporating the FE-T unit into a PM6 polymer to fine-tune the energetics and morphology of this high-performance PSC material. The optimal polymer in the series shows a downshifted HOMO and an improved morphology, leading to a high PCE of 16.4% with a small energy loss (0.53 eV) enabled by the reduced non-radiative energy loss (0.23 eV), which are among the best values reported for non-fullerene PSCs to date. This work shows that the FE-T unit is a promising building block to construct donor polymers for high-performance organic photovoltaic cells.
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| 5. |
- Tang, Yumin, et al.
(författare)
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Two Compatible Polymer Donors Enabling Ternary Organic Solar Cells with a Small Nonradiative Energy Loss and Broad Composition Tolerance
- 2020
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Ingår i: Solar RRL. - : Wiley-VCH Verlagsgesellschaft. - 2367-198X. ; 4:11
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Tidskriftsartikel (refereegranskat)abstract
- High-performance nonfullerene ternary organic solar cells (OSCs) with two polymer donors are less frequently reported because of the limited numbers of efficient polymer donors with good compatibility. Herein, a wide-bandgap polymer P1 with a deep-lying highest occupied molecular orbital (HOMO) level is incorporated as the third component into the benchmark PM6:Y6 binary system to fabricate ternary OSCs. The introduction of P1 not only leads to extended absorption coverage and forms a cascade-like energy level alignment but also shows excellent compatibility with PM6, resulting in a favorable morphology in the ternary blend. More importantly, P1 possesses a deeper HOMO level (-5.6 eV) than most well-known donor polymers, which enables resulting ternary OSCs with an improved open-circuit voltage. As a result, the optimized ternary OSCs with 40 wt% P1 in donors achieve a power conversion efficiency (PCE) of 16.2% with a small nonradiative recombination loss of 0.23 eV, which is among the highest values of ternary OSCs based on two polymer donors. In addition, the ternary OSCs show a broad composition tolerance with a high PCE of over 14% throughout the whole blend ratios. These results provide an effective approach to fabricate efficient ternary OSCs by synergizing two wide-bandgap polymer donors.
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| 6. |
- Yang, Weijia, 1989-, et al.
(författare)
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Experimental investigation of theoretical stability regions for ultra-low frequency oscillations of hydropower generating systems
- 2019
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Ingår i: Energy. - : PERGAMON-ELSEVIER SCIENCE LTD. - 0360-5442 .- 1873-6785. ; 186
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Tidskriftsartikel (refereegranskat)abstract
- With the increasing momentum towards flexible power systems based on renewables, the role of hydropower has great importance, especially for providing balancing power. In this paper, a fundamental study on the operating stability of hydropower generating systems is conducted to reveal the practical characteristics for the newly emergent issue of ultra-low frequency oscillations. A unique study methodology is adapted by combing the theoretical analysis and the physical model experiment. In this paper, first, the set-up of the integral experiment platform for the transient processes of the pumped storage plants is presented. Second, a mathematical model of hydropower generating systems is built, and the theoretical stability analysis is conducted based on the Routh-Hurwitz criterion and the stability margin region. The model experiments related to the frequency stability of hydropower generating systems were conducted with reference to the stability region from theoretical analysis. The results demonstrate the sustained ultra-low frequency oscillations and frequency instability of hydropower units in experiments for the first time. Attenuation characteristics of the oscillations are theoretically derived based on the stability margin region, and then quantitatively identified by experiments. The experiment accorded with theoretical stability region within a reasonable tolerance that corresponded to the +/- 0.1 stability margin. (C) 2019 Elsevier Ltd. All rights reserved.
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