Improving on mapping long-term surface water with a novel framework based on the Landsat imagery series.

Surface water plays a crucial role in the ecological environment and societal development. Remote sensing detection serves as a significant approach to understand the temporal and spatial change in surface water series (SWS) and to directly construct long-term SWS. Limited by various factors such as cloud, cloud shadow, and problematic satellite sensor monitoring, the existent surface water mapping datasets might be short and incomplete due to losing raw information on certain dates. Improved algorithms are desired to increase the completeness and quality of SWS datasets. The present study proposes an automated framework to detect SWS, based on the Google Earth Engine and Landsat satellite imagery. This framework incorporates implementing a raw image filtering algorithm to increase available images, thereby expanding the completeness. It improves OTSU thresholding by replacing anomaly thresholds with the median value, thus enhancing the accuracy of SWS datasets. Gaps caused by Landsat7 ETM + SLC-off are respired with the random forest algorithm and morphological operations. The results show that this novel framework effectively expands the long-term series of SWS for three surface water bodies with distinct geomorphological patterns. The evaluation of confusion matrices suggests the good performance of extracting surface water, with the overall accuracy ranging from 0.96 to 0.97, and user's accuracy between 0.96 and 0.98, producer's accuracy ranging from 0.83 to 0.89, and Matthews correlation coefficient ranging from 0.87 to 0.9 for several spectral water indices (NDWI, MNDWI, ANNDWI, and AWEI). Compared with the Global Reservoirs Surface Area Dynamics (GRSAD) dataset, our constructed datasets promote greater completeness of SWS datasets by 27.01%-91.89% for the selected water bodies. The proposed framework for detecting SWS shows good potential in enlarging and completing long-term global-scale SWS datasets, capable of supporting assessments of surface-water-related environmental management and disaster prevention.

Morphological environment survey and hydrodynamic modeling of a large bifurcation-confluence complex in Yangtze River, China.

Since the establishment of the world-class Three Gorges Dam (TGD) across the Yangtze River, China, the downstream reach has experienced a long-term adjustment with regard to the river morphology and hydrodynamics, imposing a profound impact on the environmental conditions of human living and aquatic ecosystem. This study presents an investigation on the river channel morphological characteristics and hydrodynamic environment of a large bifurcation-confluence complex downstream of the TGD through detailed field survey and numerical modeling. Results show that the main stem, before being bifurcated into two sub-channels (the North Channel and the South Channel), experiences a meander, leading to the severe bed scouring near the outer bank (pools) resulted from a high flow mass flux and bed shear stress. Because of being bifurcated, the river width with largely growing may result in the reduction of flow velocity and sediment deposition (riffles), and thereby two plugbars are formed near the entrance of two sub-channels. In the meantime, the velocity-reversal phenomenon (flow velocity and friction velocity) is identified when low flows are transited into high flows. The flow mass flux, however, is always larger in pool regions, which is highly related to water depth. As a result, the topographic steering of flows by riffles, bars and floodplains may have more impact on flow path under low flow conditions, while the bankline shape would become more important under high flows. Furthermore, the topographic steering could play a key role in the pattern of flow separations near the confluence. More interestingly, the confluence flow separation only occurs under low flow conditions and its occurring location shifts upwards the tributary (the North Channel), which differs from observations in previous studies. The visualized numerical results of friction velocity distribution indicate that sediment is more likely to deposit in the North Channel (entrance) with lower friction velocity, implying the potential closure of the sub-channel.

Rational Design of an Electron/Ion Dual-Conductive Cathode Framework for High-Performance All-Solid-State Lithium Batteries.

All-solid-state lithium batteries (ASSLBs) have been paid increasing attention because of the better security compared with conventional lithium-ion batteries with flammable organic electrolytes. However, the poor ion transport between the cathode materials greatly hinders the capacity performance of ASSLBs. Herein, an electron/ion dual-conductive electrode framework is proposed for superior performance ASSLBs. Highly electronic conductive reduced graphene oxide and carbon nanotubes interconnect with active materials in the cathodes, constructing a three-dimensional continuous electron transport network. The composite electrolyte penetrates into the porous structure of the electrode, forming a consecutive ionic conductive framework. Furthermore, the thin electrolyte film formed on the surface of the cathode effectively lowers the interfacial resistance with the electrolyte membrane. Highly electron/ion conductive electrodes, combined with the polyethylene oxide-Li6.4La3Zr1.4Ta0.6O12 (PEO-LLZTO) composite electrolyte, show excellent capacity performance for both LiFePO4 and sulfur (lithium-sulfur battery) active materials. In addition, the LiFePO4 cathode demonstrates superior capacity performance and rate capability at room temperature. Furthermore, the relationship between the low Coulombic efficiency and Li dendrite growth has been revealed in this work. An effective layer is formed on the surface of Li metal by the simple modification of cupric fluoride (CuF2), which can stabilize the electrolyte/anode interface. Finally, high-performance ASSLBs with high Coulombic efficiency can be achieved.

IL-4 functionalized titanium dioxide nanotubes modulate the inflammatory response of macrophages.

Inflammatory response is an essential part of optimal tissue-implant integration and the regeneration process. Due to their highly plastic properties, macrophages display phenotypic changes during inflammatory signaling. Investigating these changes on implant surfaces is essential for evaluating implant stability and longevity. In order to control macrophage polarization, IL-4 was conjugated to titanium dioxide nanotubes (TNTs) through polydopamine, and successful fabrication was checked by scanning electron microscopy (SEM), atomic force microscopy (AFM), X-ray photoelectron spectroscopy (XPS) and contact angle, respectively. In vitro experiments including immunofluorescence staining, cell proliferation, the expression of genes associated with pro-inflammatory M1 phenotype (tumor necrosis factor-alpha (TNF-α), Interleukin-18 (IL-18)) and cytokines related to the anti-inflammatory M2 phenotype (IL-4 and IL-10), and the production of nitric oxide (NO) and cytokines TNF-α, IL-10 were detected. Macrophage response showed that IL-4 functionalized TNTs favored macrophage polarization towards an anti-inflammatory M2-phenotype. This study provides a new strategy for use in medical devices and the development of advanced nano-biomaterials in immunotherapy applications.

TiO2 nanotubes promote osteogenic differentiation of mesenchymal stem cells via regulation of lncRNA CCL3-AS.

Titanium (Ti) is widely used as orthopedic implant materials. TiO2 nanotubes (TNTs) further improve the bioactivity of Ti, which enhance the osteogenic differentiation of mesenchymal stem cells (MSCs). However, the underlying mechanism is still unclear. In this study, we verified the response of MSCs on Ti and TNT substrates and explored the regulatory mechanism of long non-coding RNAs (lncRNAs). LncRNA and mRNA expression profiles were analyzed via RNA sequencing. Differential lncRNA and mRNA expression and predicted target genes of lncRNAs were performed by bioinformatics analysis. 1075 up-regulated and 1301 down-regulated genes, 26 up-regulated and 35 down-regulated lncRNAs were obtained according to the RNA-Seq. Expression of 8 lncRNAs were verified by qPCR, which was consistent with the sequencing data. To explore the function and target gene of lncRNA, lncRNA CCL3-AS and gene CCL3 were selected for further investigation. The fluorescence staining, alkaline phosphatase (ALP) activity and CCK-8 assay were performed. Besides, expressions of runt-related transcription factor 2 (Runx2), collagen type I (Col I), osteopontin (OPN) were detected by qPCR and western blot. These results indicate that lncRNA CCL3-AS could inhibit the osteogenic differentiation and enhance cell viability of MSCs on the TNT substrates, which was dependent on the regulation of CCL3. This study supplied a comprehensive understanding for further study using lncRNA modulators to surface design of titanium for enhancing osseointegration.

A New Intermetallic NiSn5 Phase: Induced Synthesis, Crystal Structure Resolution, and Investigation of Its Mechanism.

Benefiting from the nanoscale effect, some metastable compounds can be synthesized in nanoparticles under normal conditions. The new intermetallic NiSn5 phase is synthesized by us for the first time by using a seed crystal induction method. This tetragonal phase in the P4/ mcc space group has stoichiometric Ni atom defects, yielding Ni0.62Sn5. A study of the growth mechanism reveals that the FeSn5/CoSn5 seed crystal plays a vital role in the formation of the NiSn5 phase. An investigation of the phase evolution during lithiation/delithiation processes indicates the irreversibility of NiSn5 as an anode for lithium ion batteries.

Rational Design of Porous N-Ti3C2 MXene@CNT Microspheres for High Cycling Stability in Li-S Battery.

Herein, N-Ti3C2@CNT microspheres are successfully synthesized by the simple spray drying method. In the preparation process, HCl-treated melamine (HTM) is selected as the sources of carbon and nitrogen. It not only realizes in situ growth of CNTs on the surface of MXene nanosheets with the catalysis of Ni, but also introduces efficient N-doping in both MXene and CNTs. Within the microsphere, MXene nanosheets interconnect with CNTs to form porous and conductive network. In addition, N-doped MXene and CNTs can provide strong chemical immobilization for polysulfides and effectively entrap them within the porous microspheres. Above-mentioned merits enable N-Ti3C2@CNT microspheres to be ideal sulfur host. When used in lithium-sulfur (Li-S) battery, the N-Ti3C2@CNT microspheres/S cathode delivers initial specific capacity of 927 mAh g-1 at 1 C and retains high capacity of 775 mAh g-1 after 1000 cycles with extremely low fading rate (FR) of 0.016% per cycle. Furthermore, the cathode still shows high cycling stability at high C-rate of 4 C (capacity of 647 mAh g-1 after 650 cycles, FR 0.027%) and high sulfur loading of 3 and 6 mg cm-2 for Li-S batteries.

Facile Synthesis of rGO/g-C3N4/CNT Microspheres via an Ethanol-Assisted Spray-Drying Method for High-Performance Lithium-Sulfur Batteries.

rGO/g-C3N4 and rGO/g-C3N4/CNT microspheres are synthesized through the simple ethanol-assisted spray-drying method. The ethanol, as the additive, changes the structure of the rGO/g-C3N4 or rGO/g-C3N4/CNT composite from sheet clusters to regular microspheres. In the microspheres, the pores formed by reduced graphene oxide (rGO), g-C3N4, and carbon nanotube (CNT) stacking provide physical confinement for lithium polysulfides (LiPSs). In addition, enriched nitrogen (N) atoms of g-C3N4 offer strong chemical adhesion to anchor LiPSs. The dual immobilization mechanism can effectively alleviate the notorious "shuttle effect" of the lithium-sulfur battery. Meanwhile, the cathode with high cyclic stability can be achieved. The rGO/g-C3N4/CNT/S cathode delivers a discharge capacity of 620 mA h g-1 after 500 cycles with a low capacity fading rate of only 0.03% per cycle at 1 C. Even, the cathode shows a retained capacity of 712 mA h g-1 over 300 cycles with a high sulfur loading (4.2 mg cm-2) at 0.2 C.

The controlled naringin release from TiO2 nanotubes to regulate osteoblast differentiation.

To design titanium (Ti)-based biomaterials with controlled drug-releasing bioactive property, TiO2 nanotubes with a diameter of approximately 110 nm was fabricated by electrochemical anodization. TiO2 nanotubes were then loaded with naringin by direct dropping and coated with chitosan layers. The surface morphologies, chemical compositions and wettability of different substrates were characterized by field emission scanning electron microscopy, atomic force microscope, X-ray photoelectron spectroscopy and contact angle measurement, respectively. The in vitro release behavior of naringin was evaluated by UV-visible-spectrophotometer. The biological properties of osteoblasts on different substrates were investigated in vitro. Our results indicate that the chitosan-coated naringin-loaded TiO2 nanotubes enhanced osteoblast spreading, proliferation, alkaline phosphatase activity and late-stage osteoblast mineralization. This study provides a platform to help enhance osteointegration between the bone and implant surface in clinical applications.

Ultra-stable binder-free rechargeable Li/I2 batteries enabled by "Betadine" chemical interaction.

An activated carbon cloth/polymer-iodine (ACC/PVP-I2) composite was prepared by the "Betadine" method and employed as a high-performance cathode for rechargeable Li/I2 batteries. Due to the synergistic effect of ACC and PVP-I2, Li/I2 cells with ACC/PVP-I2 as the cathode exhibited superior electrochemical performance.

The response of bone cells to titanium surfaces modified by simvastatin-loaded multilayered films.

The aim of this study was to enhance cytocompatibility of titanium substrates by loading a multilayer film of chitosan (Chi), gelatin (Gel) and simvastatin (SV). This was fabricated using a spin-assisted layer-by-layer (LBL) technique. The surface properties of the different substrates were characterized by field emission scanning electron microscopy (FE-SEM), atomic force microscope (AFM), X-ray photoelectron spectroscopy (XPS) and contact angle measurement, respectively. Simvastatin release in vitro was measured by ultraviolet-visible spectrophotometer. A well morphology with filopodia extensions was observed in mesenchymal stem cells (MSCs) grown on simvastatin loaded multilayered films-modified titanium substrates. After 7, 14 and 21 days of culture, the simvastatin loaded multilayered films increased cell proliferation, improved osteoblastic differentiation of alkaline phosphatase (ALP) and mineralization. Additionally, osteoclast diffentiation marker tartrate-resistant acid phosphatase (TRAP) was decreased in simvastatin loaded multilayered films. This study provides a new insight for the fabrication of titanium-based implants to enhance osseointegration especially for osteoporosis patients in orthopedic application.

Fibronectin modified TiO2 nanotubes modulate endothelial cell behavior.

Cardiovascular disease has become a great threat to the health of mankind; current titanium (Ti) stents fail due to late stent thrombosis caused by the lack of re-endothelialization of the Ti stent. The objective of this study was to design a novel cardiovascular Ti implant with improved surface biocompatibility. TiO2 nanotubes with a diameter of 110 nm were anodized at a constant voltage of 30 V, and fibronectin was immobilized onto the TiO2 nanotubes using polydopamine. The element composition, morphology, and wettability of the different substrate surfaces were characterized by x-ray photoelectron spectroscopy (XPS), field-emission scanning electron microscopy (FE-SEM), atomic force microscopy (AFM), and contact angle measurements, respectively, confirming the successful immobilization of fibronectin. In vitro experiments including immunofluorescence staining, Cell Counting Kit-8 (CCK-8), and nitric oxide (NO) and prostacyclin (PGI2) release demonstrate that fibronectin modified TiO2 nanotubes supported cell adhesion, proliferation, and normal cellular functions of human umbilical vein endothelial cells (HUVECs). These methodologies can be applied for future fabrication of cardiovascular stents.

Polyiodide-Shuttle Restricting Polymer Cathode for Rechargeable Lithium/Iodine Battery with Ultralong Cycle Life.

Rechargeable lithium/iodine (Li/I2) batteries have attracted much attention because of their high gravimetric/volumetric energy densities, natural abundance and low cost. However, problems of the system, such as highly unstable iodine species under high temperature, their subsequent dissolution in electrolyte and continually reacting with lithium anode prevent the practical use of rechargeable Li/I2 cells. A polymer-iodine composite (polyvinylpyrrolidone-iodine) with high thermostability is employed as cathode material in rechargeable Li/I2 battery with an organic electrolyte. Because of the chemical interaction between polyvinylpyrrolidone (PVP) and polyiodide, most of the polyiodide in the cathode could be effectively trapped during charging/discharging. In-situ Raman observation revealed the evolution of iodine species in this system could be controlled during the process of I5- ↔ I3- ↔ I-. Herein, the Li/I2 battery delivered a high discharge capacity of 278 mAh g-1 at 0.2 C and exhibited a very low capacity decay rate of 0.019% per cycle for prolonged 1100 charge/discharge cycles at 2 C. More importantly, a high areal capacity of 4.1 mAh cm-2 was achieved for the electrode with high iodine loading of 21.2 mg cm-2. This work may inspire new approach to design the Li/I2 (or Li/polyiodide) system with long cycle life.