Flexible Composite Electrolyte Membranes with Fast Ion Transport Channels for Solid-State Lithium Batteries.

Numerous endeavors have been dedicated to the development of composite polymer electrolyte (CPE) membranes for all-solid-state batteries (SSBs). However, insufficient ionic conductivity and mechanical properties still pose great challenges in practical applications. In this study, a flexible composite electrolyte membrane (FCPE) with fast ion transport channels was prepared using a phase conversion process combined with in situ polymerization. The polyvinylidene fluoride-hexafluoro propylene (PVDF-HFP) polymer matrix incorporated with lithium lanthanum zirconate (LLZTO) formed a 3D net-like structure, and the in situ polymerized polyvinyl ethylene carbonate (PVEC) enhanced the interface connection. This 3D network, with multiple rapid pathways for Li+ that effectively control Li+ flux, led to uniform lithium deposition. Moreover, the symmetrical lithium cells that used FCPE exhibited high stability after 1200 h of cycling at 0.1 mA cm-2. Specifically, all-solid-state lithium batteries coupled with LiFePO4 cathodes can stably cycle for over 100 cycles at room temperature with high Coulombic efficiencies. Furthermore, after 100 cycles, the infrared spectrum shows that the structure of FCPE remains stable. This work demonstrates a novel insight for designing a flexible composite electrolyte for highly safe SSBs.

Synthesis of Monodisperse Mesoporous Carbon Spheres/EPDM Rubber Composites and Their Enhancement Mechanical Properties.

Monodisperse mesoporous carbon spheres (MCS) were synthesized and their potential applications in ethylene propylene diene monomer (EPDM) foam were evaluated. The obtained MCS exhibited a high specific surface area ranging from 621-to 735 m2/g along with large pore sizes. It was observed that the incorporation of MCS into EPDM foam rubber significantly enhances its mechanical properties. The prepared MCS-40 rubber composites exhibit the highest tear strength of 210 N/m and tensile strength of 132.72 kPa, surpassing those of other samples. The enhancement mechanism was further investigated by employing computer simulation technology. The pores within the MCS allowed for the infiltration of EPDM molecular chains, thereby strengthening the interaction forces between the filler and matrix. Moreover, a higher specific surface area resulted in greater adsorption of molecular chains onto the surface of these carbon spheres. This research offers novel insights for understanding the enhancement mechanism of monodisperse mesoporous particles/polymer composites (MCS/EPDM) and highlights their potential application in high-performance rubber composites.

Ultrafine platinum nanoparticles supported on N,S-codoped porous carbon nanofibers as efficient multifunctional materials for noticeable oxygen reduction reaction and water splitting performance.

The design of highly active, stable and durable platinum-based electrocatalysts towards the oxygen reduction reaction (ORR), oxygen evolution reaction (OER), hydrogen evolution reaction (HER), and hydrogen adsorption has a high and urgent demand in fuel cells, water splitting and hydrogen storage. Herein, ultrafine platinum nanoparticles (Pt NPs) supported on N,S-codoped porous carbon nanofibers (Pt-N,S-pCNFs) hybrids were prepared through the electrospinning method coupled with hydrothermal and carbonation processes. The ultrafine Pt NPs are sufficiently dispersed and loaded on pCNFs and codoped with N and S, which can improve oxygen adsorption, afford more active sites, and greatly enhance electron mobility. The Pt-N,S-pCNFs hybrid achieves excellent activity and stability for ORR with ∼70 mV positive shift of onset potential compared to the commercial Pt/C-20 wt% electrocatalyst. The long-term catalytic durability with 89.5% current retention after a 10 000 s test indicates its remarkable ORR behavior. Pt-N,S-pCNFs also exhibits excellent HER and OER performance, and can be used as an efficient catalyst for water splitting. In addition, Pt-N,S-pCNFs exhibits an excellent hydrogen storage capacity of 0.76 wt% at 20 °C and 10 MPa. This work provides novel design strategies for the development of multifunctional materials as high-performance ORR catalysts, water splitting electrocatalysts and hydrogen storage materials.

Fe/Co/N-C/graphene derived from Fe/ZIF-67/graphene oxide three dimensional frameworks as a remarkably efficient and stable catalyst for the oxygen reduction reaction.

The development of non-noble metal catalysts with high-performance, long stability and low-cost is of great importance for fuel cells, to promote the oxygen reduction reaction (ORR). Herein, Fe/Co/N-C/graphene composites were easily prepared by using Fe/ZIF-67 loaded on graphene oxide (GO). The Fe/Co/porous carbon nanoparticles were uniformly dispersed on graphene with high specific surface area and large porosity, which endow high nitrogen doping and many more active sites with better ORR performance than the commercial 20 wt% Pt/C. Therefore, Fe/Co/N-C/graphene composites exhibited excellent ORR activity in alkaline media, with higher initial potential (0.91 V) and four electron process. They also showed remarkable long-term catalytic stability with 96.5% current retention after 12 000 s, and outstanding methanol resistance, compared with that of 20 wt% Pt/C catalysts. This work provides an effective strategy for the preparation of non-noble metal-based catalysts, which could have significant potential applications, such as in lithium-air batteries and water-splitting devices.

Fe, B, and N Codoped Carbon Nanoribbons Derived from Heteroatom Polymers as High-Performance Oxygen Reduction Reaction Electrocatalysts for Zinc-Air Batteries.

For zinc-air batteries, it is of great importance to heighten the oxygen reduction reaction (ORR) activity of cathode electrocatalysts. Herein, we synthesized carbon nanoribbons doped with Fe, B, and N as high-activity ORR electrocatalysts by a templating method. Benefiting from the melamine fiber (MF) and B doping, the as-prepared carbon nanoribbon has a high specific surface area, and the improved turnover frequency of Fe sites increases the ORR activity. The as-synthesized Fe-B-N-C electrocatalyst shows an improved half-wave potential and limited current density compared to Fe-N-C, B-N-C, and N-C. Moreover, zinc-air batteries with the Fe-B-N-C electrocatalyst exhibit a higher specific capacity and better long-term durability compared to those with commercial Pt/C. This work provides an effective strategy to synthesize noble-metal-free electrocatalysts for wide applications of zinc-air batteries.

Uniformly dispersed platinum nanoparticles over nitrogen-doped reduced graphene oxide as an efficient electrocatalyst for the oxygen reduction reaction.

Oxygen reduction reaction (ORR) with efficient activity and stability is significant for fuel cells. Herein, platinum (Pt) nanoparticles dispersed on nitrogen-doped reduced graphene oxide (N-rGO) were prepared by a hydrothermal and carbonized approach for the electrocatalysis of ORR. Polyvinylpyrrolidone plays a significant role in the reduction and dispersion of platinum particles (about 2 nm). The obtained Pt-N-rGO hybrids exhibited superior activity with an electron transfer number of ∼4.0, onset potential 0.90 eV of ORR, good stability and methanol tolerance in alkaline media. These results reveal the interactions between Pt-N-rGO and oxygen molecules, which may represent an oxygen modified growth in catalyst preparation. The excellent electrocatalysis may lead to the decreased consumption of expensive Pt and open up new opportunities for applications in lithium air batteries.

Li-fluorine codoped electrospun carbon nanofibers for enhanced hydrogen storage.

Carbon materials have attracted increasing attention for hydrogen storage due to their great specific surface areas, low weights, and excellent mechanical properties. However, the performance of carbon materials for hydrogen absorption is hindered by weak physisorption. To improve the hydrogen absorption performance of carbon materials, nanoporous structures, doped heteroatoms, and decorated metal nanoparticles, among other strategies, are adopted to increase the specific surface area, number of hydrogen storage sites, and metal catalytic activity. Herein, Li-fluorine codoped porous carbon nanofibers (Li-F-PCNFs) were synthesized to enhance hydrogen storage performance. Especially, perfluorinated sulfonic acid (PFSA) polymers not only served as a fluorine precursor, but also inhibited the agglomeration of lithium nanoparticles during the carbonization process. Li-F-PCNFs showed an excellent hydrogen storage capacity, up to 2.4 wt% at 0 °C and 10 MPa, which is almost 24 times higher than that of the pure porous carbon nanofibers. It is noted that the high electronegativity gap between fluorine and lithium facilitates the electrons of the hydrogen molecules being attracted to the PCNFs, which enhanced the hydrogen adsorption capacity. In addition, Li-F-PCNFs may have huge potential for application in fuel cells.

Clustering-Triggered Emission and Luminescence Regulation by Molecular Arrangement of Nonaromatic Polyamide-6.

Photoluminescent polymers with merely nonaromatic chromophores have attracted rapidly growing attention owing to their importance in the significant fundamental, encryption, and anticounterfeiting fields. Based on the clustering-triggered emission mechanism, through-space conjugation and conformational rigidification of nonaromatic chromophores are crucial to photoluminescence, which are also dependent on molecular arrangement. Herein, polyamide-6 (PA-6) with well-defined molecular arrangements was thus studied. The luminescence from the PA-6 solution is enhanced upon aggregation from solution to amorphous solid and further boosted with the formation of highly regular molecular arrangement. More importantly, both blue and green fluorescence from PA-6/formic acid (FA) solutions were observed because of the variable clusters formed among PA-6 and FA. To make clear of this, PA-6 cast film (PCF) and PA-6 electrospun film (PEF) were prepared and belonged to α- (antiparallel molecular arrangement) and γ (parallel molecular arrangement)-form crystals, as confirmed by Fourier transform infrared, X-ray diffraction, and Raman measurements. The relationship between molecular arrangement and luminescence of PA-6 molecules was clarified by their photophysical properties in solids and solutions. Notably, color-tunable cryogenic phosphorescence of PA-6 solids was also detected. Such aggregation-enhanced emission and tunable phosphorescence of PA-6 solids are ascribed to the formation of diversified amide clusters together with remarkably rigidified molecular conformations owing to the highly regular molecular arrangement in the aggregated states.

N, F-Codoped Microporous Carbon Nanofibers as Efficient Metal-Free Electrocatalysts for ORR.

Currently, the oxygen reduction reaction (ORR) mainly depends on precious metal platinum (Pt) catalysts. However, Pt-based catalysts have several shortcomings, such as high cost, scarcity, and poor long-term stability. Therefore, development of efficient metal-free electrocatalysts to replace Pt-based electrocatalysts is important. In this study, we successfully prepared nitrogen- and fluorine-codoped microporous carbon nanofibers (N, F-MCFs) via electrospinning polyacrylonitrile/polyvinylidene fluoride/polyvinylpyrrolidone (PAN/PVDF/PVP) tricomponent polymers followed by a hydrothermal process and thermal treatment, which was achieved for the first time in the literature. The results indicated that N, F-MCFs exhibit a high catalytic activity (Eonset: 0.94 V vs. RHE, E1/2: 0.81 V vs. RHE, and electron transfer number: 4.0) and considerably better stability and methanol tolerance for ORR in alkaline solutions as compared to commercial Pt/carbon (Pt/C, 20 wt%) catalysts. Furthermore, in acidic media, N, F-MCFs showed a four-electron transfer pathway for ORR. This study provides a new strategy for in situ synthesis of N, F-MCFs as highly efficient metal-free electrocatalysts for ORR in fuel cells.

A facile and general approach for the direct fabrication of N-rGO-metal(metal oxides)-Pt composites as electrocatalyst for oxygen reduction reactions.

Nitrogen-doped reduced graphene oxide-metal(metal oxides) nanoparticle (N-rGO-M(MO) NPs, M = Fe, MO: M = Co, Mn) composites were prepared through a facile and general method at high temperature (800 °C). M(MO) were well-dispersed and tightly anchored on graphene sheets, which were doped with nitrogen simultaneously and further loaded with Pt nanoparticles. Those results showed a more positive onset potential, higher cathodic density, and higher electron transfer number for the ORR in alkaline media. Furthermore, N-rGO-metal(metal oxides)-Pt (N-rGO-M(MO)-Pt) nanoparticles show better durability than the commercial Pt/C catalyst, and can be used as promising potential materials in practical applications.

Restoration of orbicularis oculi muscle function in rabbits with peripheral facial paralysis via an implantable artificial facial nerve system.

The purpose of the present study was to restore orbicularis oculi muscle function using the implantable artificial facial nerve system (IAFNS). The in vivo part of the IAFNS was implanted into 12 rabbits that were facially paralyzed on the right side of the face to restore the function of the orbicularis oculi muscle, which was indicated by closure of the paralyzed eye when the contralateral side was closed. Wireless communication links were established between the in vivo part (the processing chip and microelectrode) and the external part (System Controller program) of the system, which were used to set the working parameters and indicate the working state of the processing chip and microelectrode implanted in the body. A disturbance field strength test of the IAFNS processing chip was performed in a magnetic field dark room to test its electromagnetic radiation safety. Test distances investigated were 0, 1, 3 and 10 m, and levels of radiation intensity were evaluated in the horizontal and vertical planes. Anti-interference experiments were performed to test the stability of the processing chip under the interference of electromagnetic radiation. The fully implanted IAFNS was run for 5 h per day for 30 consecutive days to evaluate the accuracy and precision as well as the long-term stability and effectiveness of wireless communication. The stimulus intensity (range, 0-8 mA) was set every 3 days to confirm the minimum stimulation intensity which could indicate the movement of the paralyzed side was set. Effective stimulation rate was also tested by comparing the number of eye-close movements on both sides. The results of the present study indicated that the IAFNS could rebuild the reflex arc, inducing the experimental rabbits to close the eye of the paralyzed side. The System Controller program was able to reflect the in vivo part of the artificial facial nerve system in real-time and adjust the working pattern, stimulation intensity and frequency, range of wave and stimulation time. No significant differences in the stimulus intensities were observed during 30 days. The artificial facial nerve system chip operation stable in the anti-interference test, and the radiation field strength of the system was in a safe range according to the national standard. The IAFNS functioned without any interference and was able to restore functionality to facially paralyzed rabbits over the course of 30 days.