High-Efficiency Hybrid Sulfur Cathode Based on Electroactive Niobium Tungsten Oxide and Conductive Carbon Nanotubes for All-Solid-State Lithium-Sulfur Batteries.

All-solid-state lithium-sulfur batteries (ASSLSBs) have become a promising candidate because of their high energy density and safety. To ensure the high utilization and electrochemical capacity of sulfur in all-solid-state batteries, both the electronic and ionic conductivities of the sulfur cathode should be as high as possible. In this work, an intercalation-conversion hybrid cathode is proposed by distributing sulfur evenly on electroactive niobium tungsten oxide (Nb18W16O93) and conductive carbon nanotubes (CNTs) for achieving high performance ASSLSBs. Herein, Nb18W16O93 shows good electrochemical lithium storage in the hybrid cathode, which could serve as an effective Li-ion/electron conductor for the conversion of sulfur in the discharge/charge processes to achieve a high utilization of sulfur. However, CNTs could further increase the electronic conductivity of the hybrid cathode by constructing good conductive frameworks and suppress the volumetric fluctuation during the interconversion of sulfur and Li2S. With this strategy, the S/Nb18W16O93/CNT cathode achieves a high sulfur utilization of 91% after one cycle activation with a high gravimetric capacity of 1526 mA h g-1. In addition, excellent rate performance is also obtained at 0.5 C with a reversible capacity of 1262 mA h g-1 after 1000 cycles. This work offers a new perspective to develop ASSLSBs.

Congener Substitution Reinforced Li7P2.9Sb0.1S10.75O0.25 Glass-Ceramic Electrolytes for All-Solid-State Lithium-Sulfur Batteries.

Glass-ceramic sulfide solid electrolytes like Li7P3S11 are practicable propellants for safe and high-performance all-solid-state lithium-sulfur batteries (ASSLSBs); however, the stability and conductivity issues remain unsatisfactory. Herein, we propose a congener substitution strategy to optimize Li7P3S11 as Li7P2.9Sb0.1S10.75O0.25 via chemical bond and structure regulation. Specifically, Li7P2.9Sb0.1S10.75O0.25 is obtained by a Sb2O5 dopant to achieve partial Sb/P and O/S substitution. Benefiting from the strengthened oxysulfide structural unit of POS33- and P2OS64- with bridging oxygen atoms and a distorted lattice configuration of the Sb-S tetrahedron, the Li7P2.9Sb0.1S10.75O0.25 electrolyte exhibits prominent chemical stability and high ionic conductivity. Besides the improved air stability, the ionic conductivity of Li7P2.9Sb0.1S10.75O0.25 could reach 1.61 × 10-3 S cm-1 at room temperature with a wide electrochemical window of up to 5 V (vs Li/Li+), as well as good stability against Li and Li-In alloy anodes. Consequently, the ASSLSB with the Li7P2.9Sb0.1S10.75O0.25 electrolyte shows high discharge capacities of 1374.4 mAh g-1 (0.05C, 50th cycle) at room temperature and 1365.4 mAh g-1 (0.1C, 100th cycle) at 60 °C. The battery also presents remarkable rate performance (1158.3 mAh g-1 at 1C) and high Coulombic efficiency (>99.8%). This work provides a feasible technical route for fabricating ASSLSBs.

[Expression and enzyme activity analysis of Djtry in planarian Dugesia japonica].

The cDNA Djtry, encoding a planarian trypsin, was identified from the cDNA library of Dugesia japonica. Multiple alignment analysis showed that the Tryps_SPc domain contained the incompletely conserved catalytic triad in which the first amino acid His was substituted by Lys. Phylogenetic analysis indicateed that Djtry protein falls at the base of other animal trypsins. The Djtry cDNA was cloned into a bacterial vector pET-28a and was transferred into E. coli BL21. The His-tagged Djtry fusion protein expression was induced by IPTG. SDS-PAGE analysis revealed that the Djtry was expressed as inclusion bodies in E. coli BL21 with the estimated molecular weight of approximately 26 kDa. Western blotting with His-tag antibody showed that the antibody was reacted with the fusion protein after refolding. Compared to bovine trypsin using BAEE as special substrate of trypsin, the enzyme activity of Djtry was measured. These results indicate that Djtry represents the archetype of animal trypsins, and this type of mutational trypsin Djtry still performs the trypsin nature with slightly weaker activity.

Analyzing S-adenosylhomocysteine hydrolase gene sequences in deuterostome genomes.

S-adenosylhomocysteine hydrolase (SAHH) gene sequences of sea-urchin, two amphioxus, sea-squirt and eight vertebrates are comparatively analyzed in the current analysis. Although SAHH protein sequences are highly conserved in these species, their nucleotide sequences are much different, ranging from 5,446 bp in amphioxus to 40,174 bp in zebra fish. The length divergence is mainly caused by distinct introns in some species. SAHH genes in amphioxus (or sea-urchin), sea-squirt and vertebrates are composed of eight, nine and ten exons, respectively. Sequence alignment shows that exon 3 in amphioxus and sea-urchin is similar to exons 3 + 4 in vertebrates, exon 5 in amphioxus and sea-urchin is similar to exons 5 + 6 in sea-squirt, and the two exons are fused into exon 6 in vertebrates. Furthermore, exon 7 in sea-squirt is similar to exons 7 + 8 in vertebrates, indicating that exon-fission and exon-fusion events have been taken place during the evolution of deuterostome SAHH genes. Active sites and NAD+-binding sites are located in exons 2 7 in amphioxus, which are dispersed into much more exons along with the evolution of vertebrates. It is speculated that ten-exon organization of SAHH gene occurred after the separation of invertebrates and vertebrates. Synonymous and non-synonymous substitution analysis shows that negative selection plays a dominant role in the evolution of SAHH genes. Phylogenetic analysis shows that SAHH genes in amphioxus, sea-urchin and sea-squirt form a cluster and locate at the base of neighbor-joining tree, suggesting that they are the archetype of vertebrate SAHH genes.

[Toxic effects of nonylphenol on the gonad of adult rosy barb].

Acute and sub-acute toxicities of nonylphenol (NP) on fish were investigated with adult rosy barb (Puntius conchonius). The acute toxicity of NP to adult rosy barb was determined in semi-static bioassays. Median lethal concentration (LC50) value of NP was (1.72 +/- 0.06) micromol/L for 96 h exposure. The effects of sub-toxicity of NP (0.17, 0.34 and 0.68 micromol/L) on the adult rosy barb were studied after 21 d exposure. It showed that testis somatic index (TSI) and ovary somatic index (OSI) were reduced significantly by NP in a dose-dependent manner. The histopathological examination showed that the gland structures were impaired by NP as evidenced by hypertrophied Sertoli cells, a loss of germinal cells in testis, retardation of eggs development and increase in atresia in the follicles of ovary. These suggest that NP exerts adverse effects on the testis and the ovary, and disturbs the development of sperm and eggs. In addition, due to rosy barb high sensitivity to NP, it is also possible to apply rosy barb as a potential fish model to the toxicity of NP.