Enhanced Ion Conductivity in Conducting Polymer Binder for High‐Performance Silicon Anodes in Advanced Lithium‐Ion Batteries

Polymer binders with high ion and electron conductivities are prepared by assembling ionic polymers (polyethylene oxide and polyethylenimine) onto the electrically conducting polymer poly(3,4‐ethylenedioxythiophene): poly(styrenesulfonate) chains. Crosslinking, chemical reductions, and electrostatics increase the modulus of the binders and maintain the integrity of the anode. The polymer binder shows lithium‐ion diffusivity and electron conductivity that are 14 and 90 times higher than those of the widely used carboxymethyl cellulose (with acetylene black) binder, respectively. The silicon anode with the polymer binder has a high reversible capacity of over 2000 mA h g^?1 after 500 cycles at a current density of 1.0 A g^?1 and maintains a superior capacity of 1500 mA h g^?1 at a high current density of 8.0 A g^?1.     

Mapping Nonfullerene Acceptors with a Novel Wide Bandgap Polymer for High Performance Polymer Solar Cells

A new weak electron‐deficient building block, bis(2‐ethylhexyl) 2,5‐bis(5‐bromothiophen‐2‐yl) thieno[3,2‐b]thiophene‐3,6‐dicarboxylate ( TT‐Th ), is incorporated to construct a wide‐bandgap (1.88 eV) polymer PBDT‐TT for nonfullerene polymer solar cells (NF‐PSCs). PBDT‐TT possesses suitable energy levels and complementary absorption when blended with both ITIC analogues ( ITIC and IT‐M ) and a near‐infrared (NIR) acceptor ( 6TIC ). Moreover, PBDT‐TT exhibits good conjugated planarity and preferable face‐on orientation in the blended thin film, which are beneficial for charge transfer and carrier transport. The PSCs based on PBDT‐TT : IT‐M and PBDT‐TT : 6TIC blend films yield high power conversion efficiencies of 11.38% and 11.03%, respectively. To the best of the authors' knowledge, the PCE of 11.03% for PBDT‐TT : 6TIC‐ based device is one of the highest values reported for NIR NF‐PSCs. This work demonstrates that TT‐Th is a useful new electron‐accepting building block for making p‐type wide bandgap polymers for efficient NIR NF‐PSCs.     

Toward High Efficiency Polymer Solar Cells: Rearranging the Backbone Units into a Readily Accessible Random Tetrapolymer

Two donor–acceptor (D–A) conjugated polymers composed of the same ratio of 5‐fluorobenzothiadiazole and thiophene subunits are synthesized through different routes, providing a precisely regioregular ( 2TRR ) and a random ( 2TRA ) polymer structures. Detailed structural analyses indicate that the backbone of regioregular 2TRR has only one donor segment of bithiophene, while the backbone of random 2TRA consists of three different donor segments: thiophene, bithiophene, and terthiophene (in a ratio of 0.16:0.68:0.16). Synergetic contributions from these segments allow the “tetrapolymer” 2TRA to achieve more favorable film morphology and a higher hole‐mobility relative to 2TRR . Consequently, the random polymer 2TRA achieves a substantially higher power conversion efficiency (8.8%) than the regioregular polymer 2TRR (5.1%). Notably, the “tetrapolymer” 2TRA is readily synthesized from two monomers, rather than through complex conventional preparation required for similar multipolymers. These findings provide a novel route toward the design and synthesis of multipolymeric materials and demonstrate their potential advantages in high‐performance organic electronic applications.     

Superelastic Hybrid CNT/Graphene Fibers for Wearable Energy Storage

The demands for wearable technologies continue to grow and novel approaches for powering these devices are being enabled by the advent of new electromaterials and novel fabrication strategies. Herein, a novel approach is reported to develop superelastic wet‐spun hybrid carbon nanotube graphene fibers followed by electrodeposition of polyaniline to achieve a high‐performance fiber‐based supercapacitor. It is found that the specific capacitance of hybrid carbon nanotube (CNT)/graphene fiber is enhanced up to ≈39% using a graphene to CNT fiber ratio of 1:3. Fabrication of spring‐like coiled fiber coated with an elastic polymer shows an extraordinary elasticity capable of 800% strain while affording a specific capacitance of ≈138 F g^?1. The elastic rubber coating enables extreme stretchability and enabling cycles with up to 500% strain for thousands of cycles with no significant change in its performance. Multiple supercapacitors can be easily assembled in series or parallel to meet specific energy and power needs.     

Bandgap Engineering of Organic Semiconductors for Highly Efficient Photocatalytic Water Splitting

The bandgap engineering of semiconductors, in particular low‐cost organic/polymeric photocatalysts could directly influence their behavior in visible photon harvesting. However, an effective and rational pathway to stepwise change of the bandgap of an organic/polymeric photocatalyst is still very challenging. An efficient strategy is demonstrated to tailor the bandgap from 2.7 eV to 1.9 eV of organic photocatalysts by carefully manipulating the linker/terminal atoms in the chains via innovatively designed polymerization. These polymers work in a stable and efficient manner for both H₂ and O₂ evolution at ambient conditions (420 nm < λ < 710 nm), exhibiting up to 18 times higher hydrogen evolution rate (HER) than a reference photocatalyst g‐C₃N₄ and leading to high apparent quantum yields (AQYs) of 8.6%/2.5% at 420/500 nm, respectively. For the oxygen evolution rate (OER), the optimal polymer shows 19 times higher activity compared to g‐C₃N₄ with excellent AQYs of 4.3%/1.0% at 420/500 nm. Both theoretical modeling and spectroscopic results indicate that such remarkable enhancement is due to the increased light harvesting and improved charge separation. This strategy thus paves a novel avenue to fabricate highly efficient organic/polymeric photocatalysts with precisely tunable operation windows and enhanced charge separation.     

Theoretical Investigation of 2D Conductive Microporous Coordination Polymers as Li–S Battery Cathode with Ultrahigh Energy Density

Even though tremendous achievement has been made experimentally in the performance of lithium–sulfur (Li–S) battery, theoretical studies in this area are lagging behind due to the complexity of the Li–S systems and the effects of solvent. For this purpose, a new methodology is developed for investigating the 2D hexaaminobenzene‐based coordination polymers (2D‐HAB‐CPs) as cathode candidate materials for Li–S batteries via density functional theory calculations in combination with an in‐house developed charge polarized solvent model and a genetic algorithm structure global search code. With high ratios of transition metal atoms and two‐coordinated nitrogen atoms, excellent electric conductivity, and structural porosity, the 2D‐HAB‐CP is able to address all of the three main challenges facing Li–S batteries: confining the lithium polysulfides from dissolution, facilitating the electron conductivity and buffering the volumetric expansion during the lithiation process. In addition, the theoretical energy density of this system is as high as 1395 Wh kg^?1. These results demonstrate that the 2D‐HAB‐CP is a promising cathode material for Li–S batteries. The proposed computational framework not only opens a new avenue for understanding the key role played by solution and liquid electrolytes in Li–S batteries, but also can be generally applied to other processes with liquids involved.     

Laccase from Aspergillus niger: A novel tool to graft multifunctional materials of interests and their characterization

In the present study, we propose a green route to prepare poly(3-hydroxybutyrate) [(P(3HB)] grafted ethyl cellulose (EC) based green composites with novel characteristics through laccase-assisted grafting. P(3HB) was used as a side chain whereas, EC as a backbone material under ambient processing conditions. A novel laccase obtained from Aspergillus niger through its heterologous expression in Saccharomyces cerevisiae was used as a green catalyst for grafting purposes without the use of additional initiator and/or cross-linking agents. Subsequently, the resulting P(3HB)-g-EC composites were characterized using a range of analytical and imagining techniques. Fourier transform infrared spectroscopy (FT-IR) spectra showed an increase in the hydrogen-bonding type interactions between the side chains of P(3HB) and backbone material of EC. Evidently, X-ray diffraction (XRD) analysis revealed a decrease in the crystallinity of the P(3HB)-g-EC composites as compared to the pristine individual polymers. A homogeneous P(3HB) distribution was also achieved in case of the graft composite prepared in the presence of 2,2′-azino-bis(3-ethylbenzothiazoline-6-sulphonic acid) (ABTS) as a mediator along with laccase as compared to the composite prepared using pure laccase alone. A substantial improvement in the thermal and mechanical characteristics was observed for grafted composites up to the different extent as compared to the pristine counterparts. The hydrophobic/hydrophilic properties of the grafted composites were better than those of the pristine counterparts.     

Inferior Olive HCN1 Channels Coordinate Synaptic Integration and Complex Spike Timing

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Comparison of Plastic Packaging Waste Management Options: Feedstock Recycling versus Energy Recovery in Germany

Plastics recycling, especially as prescribed by the German Ordinance on Packaging Waste (Verpackungsverordnung), is a conspicuous example of closing material loops on a large scale. In Germany, an industry‐financed system (Duales System Deutschland) was established in 1991 to collect and recycle packaging waste from households. To cope with mixed plastics, various “feedstock‐recycling” processes were developed. We discuss the environmental benefits and the cost‐benefit ratio of the system relative to municipal solid waste (MSW) incineration, based on previously published life‐cycle assessment (LCA) studies. Included is a first‐time investigation of energy recovery in all German incinerators, the optimization opportunities, the impact on energy production and substitution processes, an estimation of the costs, and a cost‐benefit assessment. In an LCA, the total environmental impact of MSW incineration is mainly determined by the energy recovery ratio, which was found on average to reach 39% in current German incineration plants. Due to low revenues from additional energy generation, it is not cost‐effective to optimize the plants energetically. Energy from plastic incineration substitutes for a specific mixture of electric base‐load power, district heating, and process steam generation. Any additional energy from waste incineration will replace, in the long term, mainly natural gas, rather than coal. Incineration of plastic is compared with feedstock recycling methods in different scenarios. In all scenarios, the incineration of plastic leads to an increase of CO2 emissions compared to landfill, whereas feedstock recycling reduces CO2 emissions and saves energy resources. The costs of waste incineration are assumed to decrease by about 30% in the medium term. Today, the calculated costs of CO2 reduction in feedstock recycling are very high, but are ex‐pected to decline in the near future. Relative to incineration, the costs for conserving energy via feedstock recycling are 50% higher, but this gap will close in the near future if automatic sorting and processing are implemented in Germany.     

基于能值-生态足迹模型的东北老工业基地生态安全评价——以辽宁省为例

采用能值-生态足迹模型,对辽宁省2003—2012年生态安全状况进行时间序列的定量分析与评价,并采用灰色动力学模型预测其动态变化趋势.结果表明: 研究期内辽宁省人均能值生态承载力从3.13 hm²下降到3.07 hm²,人均能值生态足迹由13.88 hm²增加到21.96 hm²,处于生态赤字状态,且赤字增大趋势明显;生态压力指数由4.43增长到7.16,生态安全预警等级由轻警过渡到中警程度.照此发展,2013—2022年辽宁省人均能值生态承载力将由3.04 hm²下降到2.98 hm²,人均能值生态足迹将由22.72 hm²上升到35.87 hm²;生态赤字将越来越大,生态压力指数将由7.46上升到12.04,生态安全等级将由较安全变为轻度不安全状态,并呈现由中警到重警的生态安全预警等级,生态安全问题亟待解决.