Novel zinc anodes are synthesized via electroplating with organic additives in the plating solution. The selected organic additives are cetyltrimethylammonium bromide (CTAB), sodium dodecyl sulfate (SDS), polyethylene-glycol (PEG-8000), and thiourea (TU). The synthesized zinc anode materials, namely, Zn-CTAB, Zn-SDS, Zn-PEG, and Zn-TU, are characterized by powder X-ray diffraction and scanning electron microscopy. The results show that each additive produces distinctively different crystallographic orientation and surface texture. The surface electrochemical activity is characterized by linear polarization when the zinc is in contact with the battery's electrolyte. Tafel fitting on the linear polarization data reveals that the synthetic zinc materials using organic additives all exhibit 6-30 times lower corrosion currents. When using Zn-SDS as the anode in the rechargeable hybrid aqueous battery, the float current decreases as much as 2.5 times. The batteries with Zn-SDS, Zn-PEG, and Zn-TU anodes display the capacity retention of 79%, 76%, and 80% after 1000 cycles of charge-discharge at 4C rate, whereas only 67% obtained from the batteries using the anode prepared from commercial zinc foil. Among these electroplated anodes, Zn-SDS is the most suitable for aqueous batteries thanks to its low corrosion rate, low dendrite formation, low float current, and high capacity retention after 1000 cycles.

Nanostructured Li 4 Ti 5 O 12 /CNT composite particles were synthesized using an aerosol spray drying process followed by thermal annealing. After assembling into CNT networks, lightweight, flexible and binder-free Li 4 Ti 5 O 12 /CNT anodes were fabricated for lithium-ion batteries. Electrodes fabricated from these nanocomposites showed effective electron and ion transport and, more importantly, more robust structure compared to traditional binder-bonded electrodes. The electrodes delivered a high reversible capacity and superior rate performance up to an extremely high rate of 100 C. Moreover, ultralong cycling stability was attained through 8000 rapid charge-discharge cycles with 89 % capacity retention. These results demonstrate the feasibility of ultrafast batteries.

Nanostructured Fe2O3-nanomesh graphene (NMG) composites containing ∼3 nm Fe2O3 nanoparticles (NPs) uniformly distributed in the nanopores of NMG are synthesized by an adsorption-precipitation process. As anodes for Li ion batteries (LIBs), the 10%Fe2O3-NMG composite exhibits an upward trend in the capacity and delivers a reversible specific capacity of 1567 mA h g(-1) after 50 cycles at 150 mA g(-1), and 883 mA h g(-1) after 100 cycles at 1000 mA g(-1), much higher than the corresponding values for the NMG electrode. The significant capacity enhancement of the 10%Fe-NMG composite is attributed to the positive synergistic effect between NMG and Fe2O3 NPs due to the catalytic activity of Fe2O3 NPs for decomposition of the solid electrolyte interface film. Our results indicate that decoration of ultrasmall Fe2O3 NPs can significantly change the surface condition of graphene. This synthesis strategy is simple, effective, and broadly applicable for constructing other electrode materials for LIBs.

Here, we report a new approach to synthesizing S-doped porous carbons and achieving both a high capacity and a high Coulombic efficiency in the first cycle for carbon nanostructures as anodes for Li ion batteries. S-doped porous carbons (S-PCs) were synthesized by carbonization of pitch using magnesium sulfate whiskers as both templates and S source, and a S doping up to 10.1 atom % (corresponding to 22.5 wt %) was obtained via a S doping reaction. Removal of functional groups or highly active C atoms during the S doping has led to formation of much thinner solid-electrolyte interface layer and hence significantly enhanced the Coulombic efficiency in the first cycle from 39.6% (for the undoped porous carbon) to 81.0%. The Li storage capacity of the S-PCs is up to 1781 mA h g(-1) at the current density of 50 mA g(-1), more than doubling that of the undoped porous carbon. Due to the enhanced conductivity, the hierarchically porous structure and the excellent stability, the S-PC anodes exhibit excellent rate capability and reliable cycling stability. Our results indicate that S doping can efficiently promote the Li storage capacity and reduce the irreversible Li combination for carbon nanostructures.

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Background and AimsIn mammalian spermatogenesis, glial cell line-derived neurotrophic factor (GDNF) is one of the major Sertoli cell-derived factors which regulates the maintenance of undifferentiated spermatogonia including spermatogonial stem cells (SSCs) through GDNF family receptor α1 (GFRα1). It remains unclear as to when, where and how GDNF molecules are produced and exposed to the GFRα1-positive spermatogonia in vivo.Methodology and Principal FindingsHere we show the cyclical and patch-like distribution of immunoreactive GDNF-positive signals and their close co-localization with a subpopulation of GFRα1-positive spermatogonia along the basal surface of Sertoli cells in mice and hamsters. Anti-GDNF section immunostaining revealed that GDNF-positive signals are mainly cytoplasmic and observed specifically in the Sertoli cells in a species-specific as well as a seminiferous cycle- and spermatogenic activity-dependent manner. In contrast to the ubiquitous GDNF signals in mouse testes, high levels of its signals were cyclically observed in hamster testes prior to spermiation. Whole-mount anti-GDNF staining of the seminiferous tubules successfully visualized the cyclical and patch-like extracellular distribution of GDNF-positive granular deposits along the basal surface of Sertoli cells in both species. Double-staining of GDNF and GFRα1 demonstrated the close co-localization of GDNF deposits and a subpopulation of GFRα1-positive spermatogonia. In both species, GFRα1-positive cells showed a slender bipolar shape as well as a tendency for increased cell numbers in the GDNF-enriched area, as compared with those in the GDNF-low/negative area of the seminiferous tubules.Conclusion/SignificanceOur data provide direct evidence of regionally defined patch-like GDNF-positive signal site in which GFRα1-positive spermatogonia possibly interact with GDNF in the basal compartment of the seminiferous tubules.

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