Designing Polymer-in-Salt Electrolyte and Fully Infiltrated 3D Electrode for Integrated Solid-State Lithium Batteries.

Solid-state lithium batteries (SSLBs) are promising owing to enhanced safety and high energy density but plagued by the relatively low ionic conductivity of solid-state electrolytes and large electrolyte-electrode interfacial resistance. Herein, we design a poly(vinylidene fluoride-co-hexafluoropropylene) (PVDF-HFP)-based polymer-in-salt solid electrolyte (PISSE) with high room-temperature ionic conductivity (1.24×10-4  S cm-1 ) and construct a model integrated TiO2 /Li SSLB with 3D fully infiltration of solid electrolyte. With forming aggregated ion clusters, unique ionic channels are generated in the PISSE, providing much faster Li+ transport than common polymer electrolytes. The integrated device achieves maximized interfacial contact and electrochemical and mechanical stability, with performance close to liquid electrolyte. A pouch cell made of 2 SSLB units in series shows high voltage plateau (3.7 V) and volumetric energy density comparable to many commercial thin-film batteries.

Filler-Integrated Composite Polymer Electrolyte for Solid-State Lithium Batteries.

Composite polymer electrolytes (CPEs) utilizing fillers as the promoting component bridge the gap between solid polymer electrolytes and inorganic solid electrolytes. The integration of fillers into the polymer matrices is demonstrated as a prevailing strategy to enhance Li-ion transport and assist in constructing Li+ -conducting electrode-electrolyte interface layer, which addresses the two key barriers of solid-state lithium batteries (SSLBs): low ionic conductivity of electrolyte and high interfacial impedance. Recent review articles have largely focused on the performance of a broad spectrum of CPEs and the general effects of fillers on SSLBs device. Recognizing this, in this review, after briefly presenting the categories of fillers (traditional and emerged) and the promoted ionic conducting mechanisms in CPEs, the progress in the interfacial structure design principle, with the emphasis on the crucial influence of filler size, concentration, and hybridization strategies on filler-polymer interface that is the most critical to Li-ion transport is assessed. The latest exciting advances on filler-enabled in situ generation of a Li+ -conductive layer at the electrode-electrolyte interface to greatly reduce the interfacial impedance are further elaborated. Finally, this review discusses the challenges to be addressed, outlines research directions, and provides a future vision for developing advanced CPEs for high-performing SSLBs.

Electrolyte Concentration Regulation Boosting Zinc Storage Stability of High-Capacity K0.486V2O5 Cathode for Bendable Quasi-Solid-State Zinc Ion Batteries.

Vanadium-based cathodes have attracted great interest in aqueous zinc ion batteries (AZIBs) due to their large capacities, good rate performance and facile synthesis in large scale. However, their practical application is greatly hampered by vanadium dissolution issue in conventional dilute electrolytes. Herein, taking a new potassium vanadate K0.486V2O5 (KVO) cathode with large interlayer spacing (~ 0.95 nm) and high capacity as an example, we propose that the cycle life of vanadates can be greatly upgraded in AZIBs by regulating the concentration of ZnCl2 electrolyte, but with no need to approach "water-in-salt" threshold. With the optimized moderate concentration of 15 m ZnCl2 electrolyte, the KVO exhibits the best cycling stability with ~ 95.02% capacity retention after 1400 cycles. We further design a novel sodium carboxymethyl cellulose (CMC)-moderate concentration ZnCl2 gel electrolyte with high ionic conductivity of 10.08 mS cm-1 for the first time and assemble a quasi-solid-state AZIB. This device is bendable with remarkable energy density (268.2 Wh kg-1), excellent stability (97.35% after 2800 cycles), low self-discharge rate, and good environmental (temperature, pressure) suitability, and is capable of powering small electronics. The device also exhibits good electrochemical performance with high KVO mass loading (5 and 10 mg cm-2). Our work sheds light on the feasibility of using moderately concentrated electrolyte to address the stability issue of aqueous soluble electrode materials.

Bioaccumulation of endocrine disrupting compounds in fish with different feeding habits along the largest subtropical river, China.

Endocrine disrupting compounds (EDCs) are becoming an increasing concern regarding bioaccumulation in aquatic biota. However, the effects of regional pollution levels and specific feeding habits on the bioaccumulation of EDCs in fish are rarely reported. 4-Nonylphenol (4-NP), bisphenol A (BPA), 4-tert-octylphenol (4-t-OP), triclocarban (TCC) and triclosan (TCS) were determined in abiotic compartments [water, sediment, suspended particulate matter (SPM)] and fish with different feeding habits along the Pearl River, China. EDCs in abiotic compartments exhibited significant (p < 0.05) spatial variations, forming five zones clustered based on site-specific EDC concentrations. 4-NP was the dominant compound, contributing 58-98% of the EDCs in fish, followed by BPA (<41%), 4-t-OP (<13%), and TCC and TCS (<4.7%). The concentrations of 4-NP and 4-t-OP, BPA, and TCC and TCS were the highest in brackish carnivorous, planktivorous, and detritivorous fish, respectively. The bioaccumulation factors (BAFs) showed that 4-NP accumulated (BAF > 5000) in all fish except for suck-feeding detritivores, while 4-t-OP and TCC accumulated in filter-feeding planktivores. The concentration of 4-NP in carnivores was significantly higher than that in detritivores, indicating the potential biomagnification of 4-NP along food chains. EDCs in sediment and SPM and those in water were most positively correlated with those in detritivores and planktivores, respectively, suggesting the potential of fish with these two feeding habits to act as bioindicators of EDC pollutants.

[Spatio-Temporal Patterns and Environmental Risk of Endocrine Disrupting Chemicals in the Liuxi River].

This study aimed to investigate the occurrence and spatio-temporal distribution of 4-tert-octylphenol (4-t-OP), 4-nonylphenol (4-NP), triclosan (TCS), estrone (E1), 17ß-estradiol (E2), and bisphenol-A (BPA) as endocrine disrupting chemicals (EDCs) in the water of the Liuxi River and to evaluate the risks for estrogenic activity. The results showed that EDCs had been detected at the 14 monitoring sites and the total concentration ranged from 26.07 ng·L-1 to 7109.5 ng·L-1, with the highest contribution rate coming from 4-NP (78.62%), followed by BPA (11.91%), and the other four EDCs (≤ 4.92%). On a spatial and temporal scale, the EDC contents increased longitudinally from upstream to downstream, especially in the heavily-polluted Baiyun section where the water quality was lower than level Ⅴ. The EDC contents in the tributaries were much higher than those in the main channels. Influenced by the monsoon precipitation, the contents of 4-NP, 4-t-OP, and total EDCs in the rainy season were significantly (P<0.05) higher than those in the dry season, while the seasonal changes of E1 and E2 followed the opposite tendency. A Pearson correlation analysis showed that DO was significantly negatively correlated with all the EDCs, suggesting that the EDCs and reductive organic pollutants might coexist. As TN, TP, NH4+-N, permanganate index, and EC were significantly positively correlated with E1, E2, BPA, and TCS but not obviously correlated with 4-NP (P>0.05), we presumed that the pollution source of E1, E2, BPA, and TCS might be the same with nitrogen and phosphorus nutrition, originating from the point source emission of the domestic sewage, industrial, and agricultural wastewater. In contrast, 4-NP and 4-t-OP more likely originated from the non-point source pollution from agriculture. RDA results showed that the variation of the EDCs contents by season was more obvious than that in space (RDA1 56.14%>RDA2 14.20%), which was much more influenced by 4-NP in the rainy season and by BPA in the dry season. As E1, E2, and TCS were positively correlated with the Cu, Zn, cyanide, and fecal coliform, these three target compounds could be used to indicate the multiple pollution components for water quality. Compared with the worldwide reported EDC contents in waters, 4-NP, BPA, and TCS contents in the middle and lower reaches of the Liuxi River were at higher levels, while E1, E2, and 4-t-OP were at the middle and lower levels. The risk assessment for estrogenic activity showed that the RQ values in the middle and lower reaches of the Liuxi River were all greater than 1, indicating that the downstream river sections were under high risk for estrogenic activity. As a result, appropriate precautions are needed to improve environmental management.