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Low dielectric constant (k) polymers with excellent comprehensive properties are useful materials in the microelectronics industry as matrix resins or encapsulation layers. With the inherent low polarization, high reactivity, good processability, and low cost, poly(dicyclopentadiene) (PDCPD) has received considerable attention as low‐k materials. However, its practical application is limited by the relatively high thermal expansion and k value. Herein, three norbornene‐functionalized polyhedral oligomeric silsesquioxanes (POSSs) with T8, T10, and T12 polyhedral cores are synthesized and employed for enhancing the dielectric and comprehensive properties of PDCPD via reactive blending. The results show that these POSSs have good compatibility with PDCPD matrix and nano‐dispersed POSSs particles could be obtained. As a result, the materials' properties can be largely enhanced by varying the POSS content and POSS size. Especially, PT12N12‐40 (40 wt% of T12N12) shows the lowest k value (2.1) and coefficient of thermal expansion (63.4 ppm°C−1), highest glass transition temperature (202.5 °C), yield strength (78.0 MPa), and elastic modulus (2.36 GPa), along with excellent hydrophobicity. This study highlights a useful strategy to fabricate high‐performance low‐k polymer nanocomposites by using larger POSS and reactive blending, which provides useful materials for the future microelectronic industry and high frequency communication. [ABSTRACT FROM AUTHOR]

Constructing stereocomplex (SC) crystallites at the interface of poly(L‐lactide) (PLLA)/elastomer blends represent a promising strategy to develop heat‐resistant and super‐tough PLLA materials because such SC crystallites can behave as not only nucleator to accelerate crystallization of PLLA matrix but also interfacial binder to strengthen interface. The properties of blends could be largely dominated by the SC interfacial layer, however, it is still unclear how the interfacial structure affects nucleating efficiency and interfacial strength. Herein, taking PLLA/poly(ethylene‐co‐methyl acrylate‐graft‐poly(D‐lactide)) (EMA‐g‐PDLA) blends as an example, EMA‐g‐PDLA bearing different chain lengths and grafting densities is prepared to tailor the size and packing density of interface‐localized SC crystallites. The results indicate that the interfacial structure and properties of the blends have been successfully manipulated. Compared with low‐graft‐density long PDLA chains, high‐graft‐density short ones can readily collaborate with PLLA chains to form numerous SC crystallites with smaller size and higher packing density at the interface and thus dramatically enhance the impact toughness and matrix crystallization rate. Moreover, the toughness is dominated by the content of SC crystallites, but the matrix crystallization is determined by their size and packing density. The work provides a new understanding of SC structure controlling the properties of PLLA/elastomer blends. [ABSTRACT FROM AUTHOR]

The nucleation efficiency (NE) of stereocomplex crystallites (SCs) formed in asymmetric poly(L‐lactide)/poly(D‐lactide) (PLLA/PDLA) blends is generally unsatisfactory because the competition between stereocomplexation and chain mixing involved in the melt‐mixing process can cause low formation efficiency and even severe aggregation of SCs. Herein, it is attempted to achieve high‐efficient formation of finely dispersed SCs particles by designing a unique melt‐mixing procedure, where the mixing of PLLA with 0.75 wt% PDLA is first performed at elevated temperatures (far above the melting temperature of SCs) to allow the homogeneous mixing of PLLA/PDLA chains and then at a low temperature (slightly above that of homocrystallites) to permit the full stereocomplexation of the premixed chains. It is found that the SCs formed in the blends exhibit unexpectedly low NEs (e.g., 54.5%), much inferior to that (73.6%) in the counterpart without undergoing premixing. This is because the introduction of premixing leads to a remarkable deterioration in the amount of SCs particles formed, despite decreased particle size, highlighting that the direct mixing at low temperatures of 170–180 °C (about 20–30 °C lower than that used in common melt‐processing of PLA) is more effective for the construction of SCs with superior NE. The mechanisms for these striking findings are discussed. [ABSTRACT FROM AUTHOR]

Toughening modification of poly(l‐lactide) (PLLA) with rubber particles is often realized at the cost of transparency, mechanical strength, and modulus because high rubber loadings are generally required for toughening. In this work, a promising strategy to simultaneously improve the transparency and stiffness–toughness performance of poly(butyl acrylate)‐poly(methyl methacrylate) (BAMMA) core‐shell rubber nanoparticles toughened PLLA blends by utilizing the stereocomplex (SC) crystallization between PLLA and poly(d‐lactide) (PDLA) is devised. The results reveal that the construction of SC crystallites in PLLA matrix via melt‐mixing PLLA/BAMMA blends with PDLA can prevent BAMMA nanoparticles from aggregation and promote them to form network‐like structure at lower contents. As a result, not only higher toughening efficiency with less rubber contents but also superior transparency is achieved in the PLLA/PDLA/BAMMA blends as compared with the PLLA/BAMMA ones where large aggregated BAMMA clusters are formed. Moreover, the outstanding reinforcement of SC crystallites network for PLLA can impart an enhanced tensile strength and modulus to PLLA/PDLA/BAMMA blends, thus improving the stiffness–toughness performance of PLLA/PDLA/BAMMA blends to a higher degree. This work demonstrates that SC crystallization is a promising solution to solve the contradiction between transparency and mechanical properties and then obtain superior comprehensive performances in rubber toughened PLLA blends. [ABSTRACT FROM AUTHOR]

Abstract: Stereocomplex (SC) crystallization between poly( l‐lactide) (PLLA) and poly( d‐lactide) (PDLA) exhibits tremendous potential to improve the properties of polylactide (PLA), but the practical processing of SC‐type PLA (SC‐PLA) is significantly hindered by the insufficient melt stability and serious degradation after complete melting of SC crystallites over 240 °C. In a previous work, powder metallurgy inspired low‐temperature (180–210 °C) compression sintering is proposed to fabricate SC‐PLA products from its nascent powder. However, its industrial application is still challenging mainly due to the low production efficiency (half an hour is required) as well as the weak ability to fabricate products with complex shapes. In this work, an effort to rapidly fabricate complex‐shaped SC‐PLA products using low‐temperature injection molding technology is reported, where SC‐PLA nascent powder is partially melted. To ensure appropriate powder flowability, small amounts of glyceryl monostearate are incorporated as a lubricant. The results show that, both the self‐nucleation and flow‐induced nucleation effects facilitate the SC crystallization across the interfaces between adjacent unmelted powder particles, which considerably shortens the sintering cycle to about 2 min. In this way, complex‐shaped SC‐PLA products (such as gears) with superb performance are successfully fabricated by injection molding for the first time. [ABSTRACT FROM AUTHOR]

A novel three-tier hierarchical cluster lithium-ion battery (LIB) anode is reported here, consisting of 1) carbon-coated Li4Ti5O12 crystals as the first nano-tier (ca. 10 nm) for high-rate capability; 2) submicron spheres consisting of Li4Ti5O12 crystals as the second submicron tier (100-300 nm), facilitating electrolyte infiltration and Li+ diffusion; and 3) clusters comprising Li4Ti5O12 spheres as the third micron-sized tier (1-2 μm) to increase the packing density of active materials for high-power LIBs. The submicron tier acts as a transition zone between the nano-tier and micro-tier to further benefit Li+ diffusion, electrolyte infiltration, and electron transport. The carbon coating on Li4Ti5O12 forms a uniform and continuous conductive network for fast electron transport and Li+ diffusion to address the low electronic conductivity obstacle of the Li4Ti5O12 anode. The three-tier hierarchical clusters maximize the close contact between the electrolytes and the active materials for excellent electrochemical performance. [ABSTRACT FROM AUTHOR]

Using electrospinning, specially prepared Ti and Sr precursor TiO2/ SrTiO3 composite nanofibers were successfully fabricated. This would ensure the close and uniform contact between TiO2 and SrTiO3, which significantly contributes to the electrons transfer at the interface between the two semiconductors with different band gaps. Meanwhile, the long fibrous structure of TiO2/ SrTiO3 composite nanofibers would further ease the electron transfer, enlarge the specific surface area, and enhance the light absorption capability thus leading to the improvement of photocatalytic efficiency. Because of the above-mentioned advantages, the TiO2/ SrTiO3 composite nanofibers exhibited higher photocatalytic H2 generation efficiency over bare TiO2 nanofibers in a water/methanol sacrificial reagent system under the irradiation of UV light. [ABSTRACT FROM AUTHOR]