Highly stable and reversible Zn anodes enabled by an electrolyte additive of sucrose.

Aqueous zinc-ion batteries (ZIBs) are one of the most promising candidates for electric energy storage devices due to their merits of low cost and high safety. However, the notorious side reactions and dendrite formation on zinc anodes impede the commercialization of ZIBs. In this work, a cheap and edible electrolyte additive sucrose is applied to address the above issues. Sucrose with hydroxyl groups can react as zincophilic sites to adsorb Zn2+. As verified by Raman and FT-IR spectroscopy, the solvation structure of Zn2+ and the hydrogen bonds can be regulated by the sucrose molecule. The weakened solvated structure of Zn2+ and lowered coupling degree between Zn2+ and SO42- can inhibit the hydrogen evolution reaction (HER) and the generation of the sulfate by-product. Furthermore, a solid electrolyte interphase (SEI)-like ion buffer layer is formed because of the preferentially adsorbed sucrose, which can increase the nucleation overpotential and equalize the ion distribution. The enriched Zn nucleation sites and inhibited 2D diffusion of Zn2+ resulting from the sucrose additive enable uniform Zn deposition. Thus, improved performances of symmetric Zn||Zn, asymmetric Zn||Cu and Zn||VO2 cells are realized. The Zn||Zn cell exhibits a highly reversible cycling performance for 1200 h and 400 h at 5 mA cm-2/1 mA h cm-2 and 10 mA cm-2/5 mA h cm-2, respectively. This work provides a readily available and edible additive to improve the performance of ZIBs.

Prenatal, perinatal, and postnatal factors associated with autism spectrum disorder cases in Xuzhou, China.

BACKGROUND: The aim of the present study was to explore the prenatal, perinatal, and postnatal risk factors in children with autism spectrum disorder (ASD) from Xuzhou, China by comparing them with healthy children. METHODS: Children with ASD who received rehabilitation training at special education schools and rehabilitation institutions in Xuzhou were selected as the ASD group, and healthy children during the same period were selected as the healthy non-ASD group. A questionnaire based on the possible causes and susceptibility factors of ASD in children was issued and given to all children in this study. RESULTS: The findings of the present study revealed a higher prevalence of prenatal, perinatal, and postnatal factors in children with ASD compared with healthy children. There were significantly more males than females in the ASD group, and the proportion of boys to girls was 5.81:1 (P<0.05). Logistic regression analysis suggested that the risk factors of male children developing ASD were feeding difficulties, poor living environment during pregnancy, maternal exposure to cigarette smoking during pregnancy, and perinatal hypoxia. Factors associated with ASD risk among were identified, such as living environment during pregnancy, delivery method, feeding difficulties, and epilepsy (P<0.05). Feeding difficulties and living in the countryside during pregnancy might be risk factors for ASD in girls according to the logistic regression analysis. CONCLUSIONS: This survey confirmed the high prevalence of prenatal, perinatal, and postnatal factors in children with ASD. Some of these factors may be effective entry points for the prevention and treatment of ASD.

Solid-Solution Anion-Enhanced Electrochemical Performances of Metal Sulfides/Selenides for Sodium-Ion Capacitors: The Case of FeS2- xSe x.

Transition-metal sulfides/selenides are explored as advanced electrode materials for nonaqueous sodium-ion capacitors, using FeS2- xSe x as an example. A solid solution of S/Se in FeS2- xSe x allows it to combine the high capacity of FeS2 and the good diffusion kinetics of FeSe2 together, thereby exhibiting excellent cycle stability (∼220 mA h g-1 after 6000 cycles at 2 A g-1) and superior rate capability (∼210 mA h g-1 at 40 A g-1) within 0.8-3.0 V. These results are much better than those of FeS2 and FeSe2, confirming the advantages of S/Se solid solution, as supported by EIS spectra, DFT calculations, and electronic conductivity. As FeS2- xSe x is paired with the activated carbon (AC) as Na-ion capacitors, this device is also better than sodium-ion batteries of FeS2- xSe x//Na3V2(PO4)3 and sodium-ion capacitors of metal oxides//AC, particularly at high rates. These results open a new door for the applications of sulfides/selenides in another device of electrochemical energy storage.

Biphase-Interface Enhanced Sodium Storage and Accelerated Charge Transfer: Flower-Like Anatase/Bronze TiO2/C as an Advanced Anode Material for Na-Ion Batteries.

Flower-like assembly of ultrathin nanosheets composed of anatase and bronze TiO2 embedded in carbon is successfully synthesized by a simple solvothermal reaction, followed with a high-temperature annealing. As an anode material in sodium-ion batteries, this composite exhibits outstanding electrochemical performances. It delivers a reversible capacity of 120 mA h g-1 over 6000 cycles at 10 C. Even at 100 C, there is still a capacity of 104 mA h g-1. Besides carbon matrix and hierarchical structure, abundant interfaces between anatase and bronze greatly enhance the performance by offering additional sites for reversible Na+ storage and improving the charge-transfer kinetics. The interface enhancements are confirmed by discharge/charge profiles, rate performances, electrochemical impedance spectra, and first-principle calculations. These results offer a new pathway to upgrade the performances of anode materials in sodium-ion batteries.

Mesoporous Amorphous Silicon: A Simple Synthesis of a High-Rate and Long-Life Anode Material for Lithium-Ion Batteries.

Amorphous Si (a-Si) shows potential advantages over crystalline Si (c-Si) in lithium-ion batteries, owing to its high lithiation potential and good tolerance to intrinsic strain/stress. Herein, porous a-Si has been synthesized by a simple process, without the uses of dangerous or expensive reagents, sophisticated equipment, and strong acids that potential cause environment risks. These porous a-Si particles exhibit excellent electrochemical performances, owing to their porous structure, amorphous nature, and surface modification. They deliver a capacity of 1025 mAh g-1 at 3 A g-1 after 700 cycles. Moreover, the reversible capacity after electrochemical activation, is quite stable throughout the cycling, resulting in a capacity retention about around 88 %. The direct comparison between a-Si and c-Si anodes clearly supports the advantages of a-Si in lithium-ion batteries.