Development of composite separators by coating hydrochloric acid-treated halloysite nanotubes on polypropylene separators for lithium-ion batteries.

In this study, polypropylene/halloysite nanotube (PP/HNT) composite separators were prepared by coating HNTs treated with hydrochloric acid (HCl) of different concentrations on both sides of a PP separator. The effect of HNTs treated with hydrochloric acid (HCl) of different concentrations on the properties of PP/HNT composite separators was investigated. The results indicate that the PP/HNT composite separator exhibits higher electrolyte uptake and wettability than a commercial PP separator, resulting in a better electrochemical performance in Li/LiFePO4 cells. In particular, the PP/HNTs-1.2 M composite separator with HNTs treated with 1.2 M HCl exhibits the highest electrolyte uptake (384%) and ionic conductivity (1.03 mS cm-1). The cells assembled with a PP/HNTs-1.2 M composite separator deliver discharge capacities of 166 mA h g-1 (0.5 C) and 131 mA h g-1 (3 C) with attractive cycling performance (87.6% capacity retention after 100 cycles). HNTs treated with HCl of appropriate concentrations can significantly improve the properties of PP/HNT composite separators for application in lithium-ion batteries.

Effectively Regulating More Robust Amorphous Li Clusters for Ultrastable Dendrite-Free Cycling.

A disordered phase in Li-deposit nanostructure is greatly attractive, but plagued by the uncontrollable and unstable growth, and the nanoscale characterization in the structure. Here, fully characterized in cryogenic transmission electron microscopy (cryo-TEM), more robust amorphous-Li (ALi) clusters are revealed and effectively regulated on heteroatom-activating electronegative sites and an advanced solid electrolyte interphase (SEI) layer. Heteroatom-activating electronegative sites capably enhance the electrostatic interaction of Li+ and heteroatom-doping graphene-like film (HDGs), meaning lower Li diffusion barrier and larger binding energy that is confirmed by small nucleation overpotentials of 13.9 and 10 mV at 0.1 mA cm-2 in the fluoroethylene carbonate-adding ester-based (FEC-ester) and LiNO3 -adding ether-based (LiNO3 -ether) electrolytes. Orderly multilayer SEI structure comprised of inorganic-rich components enables fast ion transports and durable capabilities to construct highly reversible and long-term plating/stripping cycling. ALi cluster anodes exhibit non-crystalline morphologies and perform ultrastable dendrite-free cycling over 2800 times. Stable ALi clusters are also grown in LiFePO4 (LFP) (LFP-ALi-HDGs-N||LiFePO4 [LFP]) full cells with advantageous capacities up to 165.5 and 164.3 mAh g-1 in these optimized electrolytes at 0.1 C; the remarkable capacity retentions maintain to 93% and 91% after 150 cycles at 0.2 C. Structure viability, electrochemical reversibility, and excellent performance in ALi clusters are effectively regulated.

In Situ Construction of a Multifunctional Quasi-Gel Layer for Long-Life Aqueous Zinc Metal Anodes.

Aqueous zinc (Zn)-ion batteries are considered very promising in grid-scale energy storage systems. However, the dendrite, corrosion, and H2 evolution issues of Zn anode have restricted their further applications. Herein, to solve these issues, a hydrophilic layer, consisting of a covalent organic polymer (COP) and carboxylmethyl cellulose (CMC), is designed to in situ construct a multifunctional quasi-gel (COP-CMC/QG) interface between Zn metal and the electrolyte. The COP-CMC/QG interface can significantly improve the rechargeability of the Zn anode through enhancing Zn2+ transport kinetics, guiding uniform nucleation, and suppressing Zn corrosion and H2 evolution. As a result, the COP-CMC-Zn anode exhibits a reduced overpotential (12 mV at 0.25 mA cm-2), prolonged cycle life (over 4000 h at 0.25 mA cm-2 and 2000 h at 5 mA cm-2 in symmetrical cells), and elevated full-cell (Zn/MnO2) performance. This work provides an efficient approach to achieve long-life Zn metal anodes and paves the way toward high-performance Zn-based and other metal-ion batteries.

Characterization of Two Novel Bacillus thuringiensis Cry8 Toxins Reveal Differential Specificity of Protoxins or Activated Toxins against Chrysomeloidea Coleopteran Superfamily.

Scarabaeoidea and Chrysomeloidea insects are agriculture-destructive coleopteran pests. Few effective Bacillus thuringiensis (Bt) insecticidal proteins against these species have been described. Bt isolate BtSU4 was found to be active against coleopteran insects. Genome sequencing revealed two new cry8 genes in BtSU4, designated as cry8Ha1 and cry8Ia1. Both genes expressed a 135 kDa protoxin forming irregular shape crystals. Bioassays performed with Cry8Ha1 protoxin showed that it was toxic to both larvae and adult stages of Holotrichia parallela, also to Holotrichia oblita adults and to Anoplophora glabripennis larvae, but was not toxic to larval stages of H. oblita or Colaphellus bowringi. The Cry8Ia1 protoxin only showed toxicity against H. parallela larvae. After activation with chymotrypsin, the Cry8Ha1 activated toxin lost its insecticidal activity against H. oblita adults and reduced its activity on H. parallela adults, but gained toxicity against C. bowringi larvae, a Chrysomeloidea insect pest that feeds on crucifer crops. The chymotrypsin activated Cry8Ia1 toxin did not show toxicity to any one of these insects. These data show that Cry8Ha1 and Cry8Ia1 protoxin and activated toxin proteins have differential toxicity to diverse coleopteran species, and that protoxin is a more robust protein for the control of coleopteran insects.

Effects of SpoIVA on the formation of spores and crystal protein in Bacillus thuringiensis.

In addition to forming spores, Bacillus thuringiensis (Bt) 4.0718 can produce toxins, insecticidal crystal protein (ICP) and vegetative insecticidal protein (Vip). The Bt spoIVA was successfully knocked out by gene recombination and was shown to inhibit sporulation. The mutant strain also exhibited significantly decreased growth and crystal formation, which inhibited spore formation and partially reduced the rate of crystal synthesis. The 50 % lethal concentrations (LC50) values of Bt 4.0718, replacement, complementation and multi-copy mutant strains against the fourth larval stage of H. armigera was determined as 5.422, 6.776, 6.223 and 5.018 µg/mL, respectively. A total of 1814 proteins were identified through isobaric tags for relative and absolute protein (iTRAQ), with 41 and 54 up and downregulated proteins observed. Gene ontology enrichment analysis showed that differentially expressed proteins were primarily involved in the biological process and molecular function. Quantitative real-time PCR analysis confirmed that 9 differential expressed genes exhibited a positive correlation between changes at transcriptional and translational levels. The results of this study provide a basis for further studies of the metabolic regulatory network of spores and crystal protein formation. Moreover, they can be used to ecologically safe insecticide of farmland production because the constructed Bt spoIVA mutants did not produce spores.Provides new ideas for the targeted improvement and application of environmentally friendly spore-free strains.

Room-Temperature Fabrication of a Liquid NaK Alloy-Based Membrane Electrode for Sodium-Ion Batteries.

The room-temperature liquid anode is a feasible method for building dendrite-free alkali-metal-based batteries. The Na-K phase diagram shows a eutectic point as low as 260.53 K with a long liquid range below 298 K with the molar fraction of potassium ranging from 30.48 to 84.99%. However, the NaK alloy exhibits a very high surface tension preventing it from wetting the current collector surface. Herein, a novel homogeneous dual solid-liquid composite in which the liquid alloy is fixed by the solid Na15Sn4 phase and perfectly stuffed into the grid of the mesh has been designed and fabricated. Based on the liquid range of the NaK alloy, the Na-K-Sn mixture possesses a theoretical specific capacity of 768 mAh g-1. The symmetric cells of the Na-K-Sn@mesh electrodes cycled at 2.0 mA cm-2 with 1.0 mAh cm-2 showed little fluctuations with the stable overpotential of ∼200 mV for 550 h, and the full cell coupled with Na3V2(PO4)3 showed an initial discharge capacity of 103 mAh g-1 at 2 C with a retention of 90% after 800 cycles. When the high-loading Na3V2(PO4)3 electrode is applied in the full cell, a stable cycling life is still maintained with a good capacity retention of 86% over 190 cycles (2.7 mAh cm-2) and 91% over 60 cycles (5.2 mAh cm-2).

Sex-dependent neurofunctional predictors of long-term maintenance of visual word learning.

A previous study has revealed sex-dependent neurofunctional predictors of visual word learning [C. Chen, G. Xue, Q. Dong, Z. Jin, T. Li, F. Xue, L. Zhao, Y. Guo, Sex determines the neurofunctional predictors of visual word learning, Neuropsychologia 45 (2007) 741-747]. The present study aimed to extend that study to investigate sex-dependent neurofunctional predictors of long-term maintenance. Twenty-three Chinese college students trained in the previous study were followed up twice: immediately (T1) and 6 months after the training (T2). At both T1 and T2, subjects were tested with the simultaneously presented same-different judgment task. Compared with the T1 performance, subjects (both males and females) showed a small but significant amount of forgetting (i.e., longer reaction times) at T2. Consistent with our hypothesis, males' performance at both T1 and T2 was predicted by the pre-training left-lateralized fusiform activation, whereas females' performance was predicted by symmetrical bilateral fusiform activation.