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In this work, STO-coated NCM811 cathode materials were obtained through a facile wet chemical method, exhibiting excellent cyclic stability. Additionally, the STO-coated NCM811 could also mitigate the Li 2 CO 3 generation on the cathode surface by effective isolation from H 2 O and CO 2. Thus, higher specific capacity was retained after long-term storage in the air compared to the uncoated NCM811 sample. Our studies proposed an effective surface modification strategy to enhance the electrochemical performance of layered ternary oxides for high performance-cathodes in commercial LIBs. [Display omitted] Ni-rich layered oxides, such as LiNi 0.8 Co 0.1 Mn 0.1 O 2 (NCM811), are promising cathode materials for high-energy lithium-ion batteries. However, the relatively high reactivity of Ni in NCM811 cathodes results in severe capacity fading originating from the undesired side reactions that occur at the cathode-electrolyte interface during prolonged cycling. Therefore, the trade-off between high capacity and long cycle life can obstruct the commercialization process of Ni-rich cathodes in modern lithium-ion batteries (LIBs). In addition, high sensitivity toward air upon storage greatly limits the commercial application. Herein, a facile surface modification strategy is introduced to enhance the cycling and in-air storage stability of NCM811. The NCM811 with a uniform SrTiO 3 (STO) nano-coating layer exhibited outstanding electrochemical performances that could deliver a high discharge capacity of 173.5 mAh⋅g−1 after 200 cycles under 1C with a capacity retention of 90%. In contrast, the uncoated NCM811 only provided 65% capacity retention of 130.8 mAh⋅g−1 under the same conditions. Structural evolution analysis suggested that the STO coating acted as a buffer layer to suppress the dissolution of transition metal ions caused by the HF attack from the electrolyte and promote the lithium diffusion during the charge–discharge process. In addition, the constructed STO layer prevented the exposure of NCM811 to H 2 O and CO 2 and thus effectively improved the in-air storage stability. This work offers an effective way to enhance the performance stability of Ni-rich oxides for high-performance cathodes of lithium-ion batteries. [ABSTRACT FROM AUTHOR]

In this work, STO-coated NCM811 cathode materials were obtained through a facile wet chemical method, exhibiting excellent cyclic stability. Additionally, the STO-coated NCM811 could also mitigate the Li 2 CO 3 generation on the cathode surface by effective isolation from H 2 O and CO 2. Thus, higher specific capacity was retained after long-term storage in the air compared to the uncoated NCM811 sample. Our studies proposed an effective surface modification strategy to enhance the electrochemical performance of layered ternary oxides for high performance-cathodes in commercial LIBs. [Display omitted] Ni-rich layered oxides, such as LiNi 0.8 Co 0.1 Mn 0.1 O 2 (NCM811), are promising cathode materials for high-energy lithium-ion batteries. However, the relatively high reactivity of Ni in NCM811 cathodes results in severe capacity fading originating from the undesired side reactions that occur at the cathode-electrolyte interface during prolonged cycling. Therefore, the trade-off between high capacity and long cycle life can obstruct the commercialization process of Ni-rich cathodes in modern lithium-ion batteries (LIBs). In addition, high sensitivity toward air upon storage greatly limits the commercial application. Herein, a facile surface modification strategy is introduced to enhance the cycling and in-air storage stability of NCM811. The NCM811 with a uniform SrTiO 3 (STO) nano-coating layer exhibited outstanding electrochemical performances that could deliver a high discharge capacity of 173.5 mAh⋅g−1 after 200 cycles under 1C with a capacity retention of 90%. In contrast, the uncoated NCM811 only provided 65% capacity retention of 130.8 mAh⋅g−1 under the same conditions. Structural evolution analysis suggested that the STO coating acted as a buffer layer to suppress the dissolution of transition metal ions caused by the HF attack from the electrolyte and promote the lithium diffusion during the charge–discharge process. In addition, the constructed STO layer prevented the exposure of NCM811 to H 2 O and CO 2 and thus effectively improved the in-air storage stability. This work offers an effective way to enhance the performance stability of Ni-rich oxides for high-performance cathodes of lithium-ion batteries. [ABSTRACT FROM AUTHOR]

[Display omitted] • Long life silver-zinc (Ag-Zn) fibrous batteries have been developed. • A bifunctional gel electrolyte is designed by introducing graphene oxide. • The undesired Zn dendrite growth and Ag migration during cycling are suppressed. • The battery can maintain its performance and power electronics under deformations. Silver-zinc (Ag-Zn) fibrous batteries are considered as a promising power source for next-generation flexible/wearable electronics because of their superior safety, high energy density, and stable output voltage. Nevertheless, the widespread application of Ag-Zn batteries is hindered by their limited cycle life, primarily caused by Zn dendrite growth and Ag migration. Herein, we develop a flexible mild Ag-Zn fibrous battery with outstanding cycle performance via designing a bifunctional gel electrolyte. The graphene oxide (GO) introduced into the electrolyte provides dual enhancement in suppressing the growth of Zn dendrite and migration of Ag, leading to improved structural integrity and long cycle life. The designed fibrous battery demonstrates a high capacity of 0.85 mAh cm−1 and it can retain 90% (77.4%) of the initial capacity after 250 cycles under current density of 0.5 (5) mA cm−1. Additionally, the battery can maintain its performance under various deformations and a four-battery set is employed as the power source for LED patterns and wearable sensors. This work provides a rational way to design advanced gel electrolytes for high-performance flexible batteries. [ABSTRACT FROM AUTHOR]

The world is currently facing a serious health burden of waterborne diseases, including diarrhea, gastrointestinal diseases, and systemic illnesses. The control of these infectious diseases ultimately depends on the access to safe drinking water, properly managed sanitation, and hygiene practices. Therefore, ultrasensitive, rapid, and specific monitoring platforms for bacterial pathogens in ambient waters at the point of sample collection are urgently needed. We conducted a literature review on state-of-the-art research of rapid in-field aquatic bacteria detection methods, including cell-based methods, nucleic acid amplification detection methods, and biosensors. The detection performance, the advantages, and the disadvantages of the technologies are critically discussed. We envision that promising monitoring approaches should be automated, real-time, and target-multiplexed, thus allowing comprehensive evaluation of exposure risks attributable to waterborne pathogens and even emerging microbial contaminants such as antibiotic resistance genes, which leads to better protection of public health. [ABSTRACT FROM AUTHOR]

Silver nanowire (Ag NW)-based flexible and transparent electrodes are a promising candidate for various electronic and optoelectronic applications. However, thermal and electrical instabilities of Ag NW networks during operation and post treatments need to be improved for practical applications. In this work, Ag NW/Graphene Oxide (GO) hybrid films with a multilayer structure were developed, in which transparent GO sheets were inserted between Ag NWs. For the pristine Ag NW networks, contacted NWs exhibited poorer thermal stability than individual NWs as faster Ag diffusion between NWs led to the breakage of the junctions at working temperatures, hence leading to the overall device failure. In contrast, the GO intermediate layers hindered the Ag diffusion between NWs in the Ag NW/Graphene Oxide hybrid films and maintained the junction structure, giving rise to enhanced thermal stability compared to the pristine networks and the GO-covered samples. For electrical tests, unlike the network degradation under annealing treatments, a local deterioration perpendicular to the current flow was directly observed after electrical breakdown, which was attributed to high local temperature under large applied voltage. The electrical failure of the devices was related to the network structure and defects. Furthermore, the pristine devices showed notable variation of failure voltage, which in the hybrid devices is more uniform and improved in general. [ABSTRACT FROM AUTHOR]

Reduced nicotinamide adenine dinucleotide (NADH) is a kind of coenzyme and widely works as a biomarker in cancer cells. It plays a crucial role in many cellular metabolic processes, especially NADH in mitochondria is indispensable for the mitochondrial respiration chain that produces ATP. Herein, we designed a fluorescent probe Mito-FCC based on an ethylene-bridging dual-salt structure, in which benzo[e]indolium fluorophore was used as the mitochondria-targeting group and 1-methylquinolinium moiety as the NADH recognition unit. Mito-FCC exhibited high sensitivity and selectivity for NADH with a rapid "turn-on" fluorescence signal. The dual-salt structure endowed the probe with a reliable mitochondria-targeted ability even after the recognition unit was reduced by NADH. With the help of the probe, the fluctuations of endogenous NADH induced by glucose or pyruvate were imaged. Besides, Mito-FCC had a capability to make a distinction between cancer cells and normal cells due that the content of NADH in cancer cells was distinctly higher than that in normal ones. Notably, the visualization of tumor in vivo through monitoring NADH using Mito-FCC was realized successfully. These experimental results showed that Mito-FCC hold a great perspective in study of mitochondrial function and potential diagnosis of cancer diseases. A mitochondria-targeted fluorescent probe for visualizing the fluctuation of endogenous NADH in mitochondria, differentiating cancer cells from normal cells, and imaging tumor precisely in vivo has been developed. [Display omitted] • A dual-salt specific fluorescent probe was designed to monitor mitochondrial NADH. • The probe can image the fluctuation of endogenous NADH in mitochondria. • The probe had the ability to distinguish cancer cells from normal cells. • The probe can be used for precise visualization of tumor in vivo. [ABSTRACT FROM AUTHOR]

Background The objective of the study was to observe the efficacy and safety of pulsatile administration of high-dose gefitinib or erlotinib in patients with advanced non-small cell lung cancer ( NSCLC) with secondary drug resistance to standard doses of tyrosine kinase inhibitor ( TKI) treatment. Materials and methods We recruited 42 NSCLC patients from our hospital, between August 2014 and December 2015, who had experienced drug resistance after one year of conventional treatment with gefitinib or erlotinib. The gefitinib group (29 patients) received one dose of 1000 mg gefitinib every four days. The erlotinib group (13 patients) received one dose of 450 mg erlotinib every three days. Treatments continued until disease progression according to Response Evaluation Criteria In Solid Tumors 1.1 or development of intolerable toxicity. Results Median progression-free survival ( PFS) was 30 months (gefitinib vs. erlotinib: 31 vs. 24 months; P > 0.05). After high-dose pulsatile administration, eight patients achieved a partial response ( PR), 11 had stable disease ( SD), and 23 had progressive disease ( PD; relative risk 19.0%; disease control rate 45.2%; median PFS six months). Patients were categorized based on epidermal growth factor receptor gene mutation: exon 19 (no patients achieved complete response [ CR], 4 PR, 6 SD, and 17 PD) and exon 21 mutation groups (no patients achieved CR, 4 PR, 5 SD, and 6 PD). Conclusion High-dose TKI pulsatile treatment is safe, efficient, and can improve prognoses for certain patients with advanced NSCLC. [ABSTRACT FROM AUTHOR]

Evaporation‐driven electricity generators have been proposed to generate electricity by water interacting with nanostructured materials. However, several proposed mechanisms, such as intrinsic gradient of polar functional groups principle and electrokinetic effect perspective, are in wide discrepancy. Here, through the combination of theoretical calculations involving time dimension on material's moisturizing process and experimental analyses, it is revealed the working principle through the water molecule triple roles in driving moisture electric generators (MEGs): 1) intrinsic H2O absorption on the material surface and splitting into hydroxy group and proton due to the polarizability of the material surface determined by the static electric potential of the materials. This process induces the electrochemical potential difference of the materials via the work function changes; 2) freely diffused protons derived from the H2O splitting work as the ions charge carriers; 3) via the hydrogen bond of the water molecules to drive charge carriers diffuse between opposite electrodes, maintaining the internal circuit current flow. It is successfully unveiled that anatase TiO2 based materials for output voltage changes correlated to the domains’ work function's difference, tuning by the surface adsorption species (H, Cl, OH) and anisotropic exposed crystal facets of the material. This work unveils MEG's general working principle. [ABSTRACT FROM AUTHOR]

In view of the drawbacks of high-cost and inherent brittleness of indium tin oxide (ITO) based transparent electrodes, silver nanowires (AgNW) networks have been considered as promising alternatives owing to their excellent optical transparency, mechanical flexibility, and compatibility with large scale printing process. AgNWs have been applied as transparent electrodes in many electronic devices, however, in many cases, they inevitably interact with the surrounding media (e.g., temperature, electric field, UV light irradiation, etc.) which will cause performance degradation. For instance, AgNWs show a typical Rayleigh instability phenomenon when the external temperature is higher than a critical point. Moreover, a specific range of UV light or/and intensive current density can accelerate the partial breakage of AgNW networks. To develop highly stable AgNW based transparent electrodes for flexible electronic devices, intensive research works have been conducted to mitigate the degeneration issues. In this review, the degradation mechanisms of AgNW based transparent electrodes have been systematically studied. Furthermore, the mainstream strategies for mitigating the deterioration of AgNW based transparent electrodes have been analyzed. Finally, the present challenges in current materials processing, and future research directions have been discussed. [ABSTRACT FROM AUTHOR]

Cell lysis is an essential step for the nucleic acid-based surveillance of bacteriological water quality. Recently, electrochemical cell lysis (ECL), which is based on the local generation of hydroxide at a cathode surface, has been reported to be a rapid and reagent-free method for cell lysis. Herein, we describe the development of a milliliter-output ECL device and its performance characterization with respect to the DNA extraction efficiency for gram-negative bacteria (Escherichia coli and Salmonella Typhi) and gram-positive bacteria (Enterococcus durans and Bacillus subtilis). Both gram-negative and gram-positive bacteria were successfully lysed within a short but optimal duration of 1 min at a low voltage of ∼5 V. The ECL method described herein, is demonstrated to be applicable to various environmental water sample types, including pond water, treated wastewater, and untreated wastewater with DNA extraction efficiencies similar to a commercial DNA extraction kit. The ECL system outperformed homogeneous chemical lysis in terms of reaction times and DNA extraction efficiencies, due in part to the high pH generated at the cathode surface, which was predicted by simulations of the hydroxide transport in the cathodic chamber. Our work indicates that the ECL method for DNA extraction is rapid, simplified and low-cost with no need for complex instrumentation. It has demonstrable potential as a prelude to PCR analyses of waterborne bacteria in the field, especially for the gram-negative ones. An electrochemical lysis device has been developed for DNA extraction of gram-positive and gram-negative bacteria from varied environmental samples. Image 1 • An electrochemical cell lysis (ECL) device was developed based on local high pH at cathode surface. • Different bacteria were successfully lysed with an optimal duration of 1 min at a low voltage of ∼5 V. • Various environmental water samples were demonstrated with high DNA extraction efficiencies. [ABSTRACT FROM AUTHOR]

Dual modification enabled by a thermally treated STO layer served multiple beneficial functions: 1) it prevented direct contact between the Ni-rich cathode and the organic electrolyte, thereby minimizing side reactions and enlarging the cathode lifespan; 2) it improved Li+ conductivity by defining clear Li-ion diffusion pathways, leading to low interfacial resistance and excellent electrochemical performance. [Display omitted] • Dual modifications are achieved with optimized thermal treatment of SrTiO 3 coated Ni-rich cathode material. • The specific capacity, cyclic stability and rate performance of Ni-rich cathode materials are significantly improved. • The SrTiO 3 coating not only protects NCM811 from parasitic reactions and facilitates Li+ diffusion enabled by the Ti interfacial doping. • The electrochemical polarization and internal cracking are reduced with the dual modification. Ni-rich layered structure ternary oxides, such as LiNi 0.8 Co 0.1 Mn 0.1 O 2 (NCM811), are promising cathode materials for high-energy lithium-ion batteries (LIBs). However, a trade-off between high capacity and long cycle life still obstructs the commercialization of Ni-rich cathodes in modern LIBs. Herein, a facile dual modification approach for improving the electrochemical performance of NCM811 was enabled by a typical perovskite oxide: strontium titanate (SrTiO 3). With a suitable thermal treatment, the modified cathode exhibited an outstanding electrochemical performance that could deliver a high discharge capacity of 188.5 mAh/g after 200 cycles under 1C with a capacity retention of 90%. The SrTiO 3 (STO) protective layer can effectively suppress the side reaction between the NCM811 and the electrolyte. In the meantime, the pillar effect provided by interfacial Ti doping could effectively reduce the Li+/Ni2+ mixing ratio on the NCM811 surface and offer more efficient Li+ migration between the cathode and the coating layer after post-thermal treatment (≥600 °C). This dual modification strategy not only significantly improves the structural stability of Ni-rich layered structure but also enhances the electrochemical kinetics via increasing diffusion rate of Li+. The electrochemical measurement results further disclosed that the 3 wt% STO coated NCM811 with 600 °C annealing exhibits the best performance compared with other control samples, suggesting an appropriate temperature range for STO coated NCM811 cathode is critical for maintaining a stable structure for the whole system. This work may offer an effective option to enhance the electrochemical performance of Ni-rich cathodes for high-performance LIBs. [ABSTRACT FROM AUTHOR]

This study was carried out to demonstrate the prognostic value of CD274 (PD-L1 promoter gene) methylation in bladder cancer patients. UCSC Xena database was searched for relevant information on PD-L1 (CD274) methylation and PD-L1 mRNA expression in bladder cancer. 407 bladder patients were included in our analyses. Multivariate analysis revealed that PD-L1 methylation was an independent predictor for OS (P = 0.037). Moreover, PD-L1 methylation might be a prognostic biomarker for immunotherapy response. However, PD-L1 methylation and PD-L1 mRNA expression was not statistically associated with chemotherapy response. In conclusion, PD-L1 methylation was an independent prognostic factor for bladder cancer patients. [ABSTRACT FROM AUTHOR]

• A portable, hand-pressed 3D-printed system with SAP microspheres was developed. • This system could achieve efficient concentration of environmental microorganisms. • Superior performance was achieved with varying ionic strengths in a short time. • Optimized SAP microspheres could be reused 20 times with simple procedures. Even though numerous methods have been developed for the detection and quantification of waterborne pathogens, the application of these methods is often hindered by the very low pathogen concentrations in natural waters. Therefore, rapid and efficient sample concentration methods are urgently needed. Here we present a novel method to pre-concentrate microbial pathogens in water using a portable 3D-printed system with super-absorbent polymer (SAP) microspheres, which can effectively reduce the actual volume of water in a collected sample. The SAP microspheres absorb water while excluding bacteria and viruses by size exclusion and charge repulsion. To improve the water absorption capacity of SAP in varying ionic strength waters (0–100 mM), we optimized the formulation of SAP to 180 g⋅L−1 Acrylamide, 75 g⋅L−1 Itaconic Acid and 4.0 g⋅L−1 Bis-Acrylamide for the highest ionic strength water as a function of the extent of cross-linking and the concentration of counter ions. Fluorescence microscopy and double-layer agar plating respectively showed that the 3D-printed system with optimally-designed SAP microspheres could rapidly achieve a 10-fold increase in the concentration of Escherichia coli (E. coli) and bacteriophage MS2 within 20 min with concentration efficiencies of 87% and 96%, respectively. Fold changes between concentrated and original samples from qPCR and RT-qPCR results were found to be respectively 11.34–22.27 for E. coli with original concentrations from 104 to 106 cell·mL−1, and 8.20–13.81 for MS2 with original concentrations from 104 to 106 PFU·mL−1. Furthermore, SAP microspheres can be reused for 20 times without performance loss, significantly decreasing the cost of our concentration system. [ABSTRACT FROM AUTHOR]