Sodium‐ion batteries (SIBs) are still confronted with several major challenges, including low energy and power densities, short‐term cycle life, and poor low‐temperature performance, which severely ...hinder their practical applications. Here, a high‐voltage cathode composed of Na3V2(PO4)2O2F nano‐tetraprisms (NVPF‐NTP) is proposed to enhance the energy density of SIBs. The prepared NVPF‐NTP exhibits two high working plateaux at about 4.01 and 3.60 V versus the Na+/Na with a specific capacity of 127.8 mA h g−1. The energy density of NVPF‐NTP reaches up to 486 W h kg−1, which is higher than the majority of other cathode materials previously reported for SIBs. Moreover, due to the low strain (≈2.56% volumetric variation) and superior Na transport kinetics in Na intercalation/extraction processes, as demonstrated by in situ X‐ray diffraction, galvanostatic intermittent titration technique, and cyclic voltammetry at varied scan rates, the NVPF‐NTP shows long‐term cycle life, superior low‐temperature performance, and outstanding high‐rate capabilities. The comparison of Ragone plots further discloses that NVPF‐NTP presents the best power performance among the state‐of‐the‐art cathode materials for SIBs. More importantly, when coupled with an Sb‐based anode, the fabricated sodium‐ion full‐cells also exhibit excellent rate and cycling performances, thus providing a preview of their practical application.
A high‐voltage sodium‐super‐ion‐conductor‐type cathode significantly enhances the energy density of sodium‐ion batteries. Its low‐strain crystal lattice during the successive (de‐)sodiation and superior Na transport kinetics promise high‐rate capabilities, long‐term cycle life, superior low‐temperature performance, and excellent full‐cell performance, providing a preview of their practical applications.
Conventional ion batteries utilizing metallic ions as the single charge carriers are limited by the insufficient abundance of metal resources. Although supercapacitors apply both cations and anions ...to store energy through absorption and/or Faradic reactions occurring at the interfaces of the electrode/electrolyte, the inherent low energy density hinders its application. The graphite‐cathode‐based dual‐ion battery possesses a higher energy density due to its high working potential of nearly 5 V. However, such a battery configuration suffers from severe electrolyte decomposition and exfoliation of the graphite cathode, rendering an inferior cycle life. Herein, a new surface‐modification strategy is developed to protect the graphite cathode from the anion salvation effect and the deposition derived from electrolyte decomposition by generating an artificial solid electrolyte interphase (SEI). Such SEI‐modified graphite exhibits superior cycling stability with 96% capacity retention after 500 cycles under 200 mA g−1 at the upper cutoff voltage of 5.0 V, which is much improved compared with the pristine graphite electrode. Through several ex situ studies, it is revealed that the artificial SEI greatly stabilizes the interfaces of the electrode/electrolyte after reconstruction and gradual establishment of the optimal anion‐transport path. The findings shed light on a new avenue toward promoting the performance of the dual‐ion battery (DIB) and hence to make it practical finally.
An artificial layer of a solid electrolyte interphase is fabricated on a graphite cathode for a dual‐ion battery (DIB). Such surface modification can alleviate the electrolyte decomposition at the high working voltage of the anion de‐/intercalation processes and the solvation effect of anions, much improving the cycling stability of the Li//graphite DIB.
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•Sludge reduction via microbial metabolism without extra energy and resource inputs.•The sludge reduction strategy is environmentally sustainable.•Thermodynamics and stoichiometry on ...the sludge reduction strategy were discussed.•Sludge reduction was reviewed based on substrate allocation and energy conversion.•Opportunities and challenges for the sludge reduction strategy were presented.
Sludge reduction via microbial metabolism does not require extra energy and resource inputs and thus merits attention as an alternative approach for sustainable wastewater treatment. This review presents a summary and analysis of the existing literatures on sludge reduction based on microbial metabolism, as well as interprets these sludge reduction mechanisms using bacterial thermodynamics and stoichiometry. Future efforts should be directed toward using advanced analytical techniques to further reveal sludge reduction mechanisms. The feasibility of coupling sludge reduction and nutrient removal by microorganism metabolism needs to be further evaluated to minimize the effect of sludge reduction on nutrient removal. A comprehensive life cycle assessment of sludge reduction strategies is recommended to effectively confirm their sustainability. Full-scale research is needed to verify the results obtained from bench- and pilot-scale experiments. This review presents the future opportunities and challenges for sludge reduction based on microbial metabolism in the excess sludge disposal.
Intricately interwoven topologies are continually being synthesized and are ultimately equally versatile and significant at the nanoscale level; however, reports concerning ravel structures, which ...are highly entwined new topological species, are extremely rare and fraught with tremendous synthesis challenges. To solve the synthesis problem, a tetrapodontic pyridine ligand L1 with two types of olefinic bond units and two Cp*M‐based building blocks (E1, M=Rh; E2, M=Ir) featuring large conjugated planes was prepared to perform the self‐assembly. Two unprecedented 5+10 icosanuclear molecular 4‐ravels containing four crossings were obtained by parallel‐displaced π⋅⋅⋅π interactions in a single‐step strategy. Remarkably, reversible structural transformations between the 4‐ravel and the corresponding metallocage could be realized by concentration changes and solvent‐ and guest‐induced effects. X‐ray crystallographic data and NMR spectroscopy provide full confirmation of these phenomena.
Two unprecedented 5+10 icosanuclear molecular 4‐ravels containing four crossings have been generated using a single‐step strategy. This topology is achieved by utilizing parallel‐displaced π⋅⋅⋅π interactions with carefully selected naphthoquinoyl Cp*M building blocks and X‐shaped pyridyl ligands.
Data on the associations between esophageal histological lesions and risk of esophageal squamous cell carcinoma (ESCC) in general populations are limited. We aimed to investigate these associations ...in a large Chinese general population to inform future Chinese ESCC screening guidelines.
We performed endoscopic screening of 21,111 participants aged 40-69 years from 3 high-risk areas of China in 2005-2009, and followed the cohort through 2016. Cumulative incidence and mortality rates of ESCC were calculated by baseline histological diagnosis, and hazard ratios of ESCC, overall and by age and sex, were assessed using the Cox proportional hazards models.
We identified 143 new ESCC cases (0.68%) and 62 ESCC deaths (0.29%) during a median follow-up of 8.5 years. Increasing grades of squamous dysplasia were associated with the increasing risk of ESCC incidence and mortality. The cumulative ESCC incidence rates for severe dysplasia/carcinoma in situ, moderate dysplasia (MD), and mild dysplasia were 15.5%, 4.5%, and 1.4%, respectively. Older individuals (50-69 years) had 3.1 times higher ESCC incidence than younger individuals (40-49 years), and men had 2.4 times higher ESCC incidence than women.
This study confirmed that increasing grades of squamous dysplasia are associated with increasing risk of ESCC and that severe dysplasia and carcinoma in situ require clinical treatment. This study suggests that in high-risk areas of China, patients with endoscopically worrisome MD should also receive therapy, the first screening can be postponed to 50 years, and endoscopic surveillance intervals for unremarkable MD and mild dysplasia can be lengthened to 3 and 5 years, respectively.
Bacterial surface properties fundamentally affect the stability and aggregation of anammox granular sludge. The variation in the surface properties of the granular sludge at different salinities were ...investigated to further clarify the effect of salinity on the aggregation of anammox granular sludge in this study. High anammox activity was obtained at a salinity of 30 g/L NaCl, and the average removal efficiency of NH4+N, NO2−-N and TN reached 91.9% ± 1.4%, 97.3% ± 0.4% and 86.3% ± 0.9%, respectively. The sludge particle size in Reactor 1 (with 0 g/L NaCl as control) and Reactor 2 (with 0, 15 and 30 g/L NaCl) increased from 1.62 ± 0.16 mm and 1.59 ± 0.12 mm to 2.71 ± 0.23 mm and 2.44 ± 0.19 mm, respectively, during total operation. PN gradually decreased from 30.58 ± 2.5 mg/g to 18.11 ± 2.1 mg/g, and PS sharply increased from 1.48 ± 0.09 mg/g to 10.52 ± 0.50 mg/g with the increase in salinity. The PS/PN ratio of extracellular polymeric substances (EPS) rapidly increased from 0.05 to 0.58 with an increase of salinity. Fourier transform infra-red spectroscopy (FTIR) and X-ray photoelectron spectroscopy (XPS) results showed that salinity inhibited the expression of anammox sludge hydrophobicity by changing surface groups. Binding between multivalent metal ions and EPS was significantly hindered by the high Na+ concentration. The results of this study provided a better understanding of the effect of salinity on the stability and aggregation of anammox granular sludge in saline wastewater treatment.
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•High anammox activity and nitrogen removal were obtained at 30 g/L NaCl.•Salinity modified the surface properties of anammox biomass.•Salinity inhibited the anammox sludge hydrophobicity by changing surface groups.•Composition changes in EPS went against the aggregation of anammox biomass.•Replacement of multivalent metal ions by Na+ hindered anammox sludge granulation.
WRKYs are important regulators in plant development and stress responses. However, knowledge of this superfamily in soybean is limited. In this study, we characterized the drought- and salt-induced ...gene
based on RNA-Seq and qRT-PCR.
, which is 714 bp in length, encoded 237 amino acids and grouped into WRKY II. The promoter region of
included ABER4, MYB, MYC, GT-1, W-box and DPBF
-elements, which possibly participate in abscisic acid (ABA), drought and salt stress responses.
was minimally expressed in different tissues under normal conditions but highly expressed under drought and salt treatments. As a nucleus protein,
was responsive to drought, salt, ABA and salicylic acid (SA) stresses. Using a transgenic hairy root assay, we further characterized the roles of
in abiotic stress tolerance. Compared with control (Williams 82), overexpression of
enhanced drought and salt tolerance, increased proline (Pro) content and decreased malondialdehyde (MDA) content under drought and salt treatment in transgenic soybean seedlings. These results may provide a basis to understand the functions of
in abiotic stress responses in soybean.
Circular RNAs (circRNAs) are pivotal regulators of various human cancers and circ-ERBB2 is abnormally expressed in breast cancer cells. However, the role and mechanism of circ-ERBB2 in HER2-positive ...breast cancer are still unknown.
The circ-ERBB2 expressions in the tumor tissues of HER2-positive breast cancer patients were tested using quantitative real-time PCR. The circ-ERBB2 function was investigated by cell counting kit 8 assay, Transwell, flow cytometry and Western blot. Mechanistically, fluorescence in situ hybridization, RNA immunoprecipitation, RNA pull-down and dual-luciferase reporter gene assays were conducted to confirm the interaction between circ-ERBB2 and miR-136-5p or miR-198 in HER2-positive breast cancer cells.
Circ-ERBB2 was elevated in the tumor tissues of HER2-positive breast cancer patients. Functionally, the interference with circ-ERBB2 repressed HER2-positive breast cancer cell proliferation, migration, invasion and accelerated cell apoptosis. Furthermore, the mechanistic analysis corroborated that circ-ERBB2 acted as a competing endogenous RNA for miR-136-5p or miR-198 to relieve the repressive influence of miR-136-5p or miR-198 on its target transcription factor activator protein 2C (TFAP2C). Meanwhile, in vivo assays further corroborated the oncogenic function of circ-ERBB2 in HER2-positive breast cancer.
Circ-ERBB2 accelerated HER2-positive breast cancer progression through the circ-ERBB2/miR-136-5p/TFAP2C axis or the circ-ERBB2/miR-198/TFAP2C axis.
MiR‐1283 has been identified as a tumor suppressor in some malignancies. Whereas, the role of miR‐1283 in HER2‐positive (HER2+) breast cancer, particularly its role in regulating cell proliferation, ...one of the most significant features of tumor progression, is unclear. The related microRNA screened by the breast cancer sample GSE131599 dataset were detected in HER2+ breast cancer tissues and cell lines. Then, the obtained miR‐1283 was overexpressed in SKBR3 and BT‐474 cells followed by relevant functional assays concerning cell proliferation and apoptosis. The xenograft mouse model was induced and the effect of miR‐1283 on tumor growth and cell proliferation was examined. The target of miR‐1283 and the transcription factor regulating miR‐1283 were predicted and identified. Finally, the influence of transcription factor KLF14 on cell proliferation and apoptosis was investigated. An integrated analysis confirmed that miR‐1283 expression was significantly decreased in HER2+ breast cancer tissues. Also, by q‐RT‐PCR detection, miR‐1283 expression was markedly reduced in HER2+ breast cancer tissues and cell lines. The miR‐1283 overexpression prevented the proliferation and enhanced apoptosis of HER2+ breast cancer cells, as well as inhibited tumor growth. Mechanistically, miR‐1283 inhibited TFAP2C expression by targeting the 3′‐untranslated regions of TFAP2C messenger RNA, and the KLF14 enhanced miR‐1283 level via binding to its promoter. The result subsequently confirmed the KLF14/miR‐1283 signaling suppressed cell proliferation in HER2+ breast cancer. Our results suggested that the KLF14/miR‐1283/TFAP2C axis inhibited HER2+ breast cancer progression, which might provide novel insight into mechanical exploration for this disease.
As a cathode for sodium‐ion batteries (SIBs), Na3V2(PO4)2F3 (NVPF) with 3D open framework is a promising candidate due to its high working voltage and large theoretical capacity. However, the severe ...capacity degradation and poor rate capability hinder its practical applications. The present study demonstrated the optimization of Na‐storage performance of NVPF via delicate lattice modulation. Aliovalent substitution of V3+ at Na+ in NVPF induces the generation of electronic defects and expansion of Na+‐migration channels, resulting in the enhancement in electronic conductivity and acceleration of Na+‐migration kinetics. It is disclosed that the formed stronger NaO bonds with high ionicity than VO bonds lead to the significant increase in structural stability and ionicity in the Na+‐substituted NVPF (NVPF‐Nax). The aforementioned effects of Na+ substitution achieve the unprecedented electrochemical performance in the optimized Na3.14V1.93Na0.07(PO4)2F3 (NVPF‐Na0.07). As a result, NVPF‐Na0.07 delivers a high‐rate capability (77.5 mAh g−1 at 20 C) and ultralong cycle life (only 0.027% capacity decay per cycle over 1000 cycles at 10 C). Sodium‐ion full cells are designed using NVPF‐Na0.07 as cathode and Se@reduced graphene oxide as anode. The full cells exhibit excellent wide‐temperature electrochemical performance from −25 to 25°C with an outstanding rate capability (96.3 mAh g−1 at 20 C). Furthermore, it delivered an excellent cycling performance over 300 cycles with a capacity retention exceeding 90% at 0.5 C under different temperatures. This study demonstrates a feasible strategy for the development of advanced cathode materials with excellent electrochemical properties to achieve high‐efficiency energy storage.
An advanced Na3.14V1.93Na0.07(PO4)2F3 cathode with high ionicity and excellent energy‐storage performance is prepared via aliovalent substitution of V3+ at Na+ sites. It exhibits the higher structural stability and improved electron/ion‐transport kinetics than the pristine Na3V2(PO4)2F3 owing to the stronger NaO and VO bonds, thereby extending the cycle life of NASICON cathode materials.
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