Journal of Advanced Ceramics
·
2022
·Vol. 11
·期 5
·742-753
·
IF 11.534
Guo Meng,Liu Yufeng,Zhang Fengnian,Cheng Fuhao,Cheng Chufei,Miao Yang,Gao Feng,Yu Jun
A series of high-entropy perovskite oxides (HEPOs) La(CoCrFeMnNiAl x ) 1/(5+ x ) O 3− δ ( x = 0.4, 0.5, 0.6, and 0.7) have been synthesized by coprecipitation method combined with calcination process and explored as electrodes for supercapacitors. The crystal structure, microstructure, and elemental composition of HEPOs were investigated by X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), and energy-dispersive X-ray spectroscopy (EDS) in detail. The electrochemical properties of HEPOs as supercapacitor electrodes were elucidated. The specific capacitances of HEPOs ( x = 0.4, 0.5, 0.6, and 0.7) are 281.84, 353.65, 325.60, and 259.30 F/g at the current density of 1 A/g, respectively. After 2000 cycles, the specific capacitances of HEPOs ( x = 0.4, 0.5, 0.6, and 0.7) remain 85.01%, 88.61%, 86.37%, and 91.25%, respectively. Such outstanding electrochemical properties can be attributed to the entropy-stabilized structure caused by mixed six cations in B-site and the Al 3+ -doping suppressing active ion aggregation during charge—discharge process. This research highlights the potential of HEPOs as electrodes for supercapacitors.
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JOURNAL OF MOLECULAR LIQUIDS
·
2022
·
IF 6.633
Xiaohan Jin,Jingbao Wang,Siyuan Zheng,Jianan Li,Xuemei Ma,Li Feng,Hailin Zhu,Zhiyong Hu
Three triazine-based surfactants with different hydrophobic chain lengths were synthesized and characterized, namely, 2-(n-Hexylamino)-4,6-bis (3-N, N-dimethylaminopropyl) amino-1,3,5-triazine, 2-(n-Octylamino)-4,6-bis (3-N, N-dimethylaminopropyl) amino-1,3,5-triazine and 2-(n-n-Dodecylamino)-4,6-bis (3-N, N-dimethylaminopropyl) amino-1,3,5-triazine, labelled C 6 , C 8 and C 12 respectively. The chemical structure was confirmed by FTIR and 1 H NMR. The surface activity was evaluated by surface tension. C 12 had a lower critical micelle concentration (CMC) value (0.5 mM) than C 6 and C 8 , which suggested that a lower concentration was required to reach interfacial adsorption saturation, representing better inhibition performance. The corrosion inhibition of surfactants for 45 # carbon steel in 1.0 M HCl was studied by static weight loss measurement, electrochemical impedance spectroscopy (EIS), and potentiodynamic polarization. Inhibition results showed that C 12 was better than C 6 and C 8 with the maximum inhibition efficiency of 96% at 0.1 mM. The surface analysis had given a clear view of the mechanism of surfactants in inhibiting the corrosion process. Moreover, the Freundlich adsorption isotherm was the best description for the adsorption process of surfactants on 45 # carbon steel in 1.0 M HCl.
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JOURNAL OF MEMBRANE SCIENCE
·
2020
·
IF 7.183
Yingying Liu,Wentao Yan,Zhi Wang,Huihui Wang,Song Zhao,Jixiao Wang,Peng Zhang,Xingzhong Cao
A novel aqueous solution additive, 1-methylimidazole (1-MI), was applied to prepare aromatic polyamide (PA) reverse osmosis (RO) membranes with excellent performance by interfacial polymerization of trimesoyl chloride (TMC) and m-phenylenediamine. The RO membrane structure and performance were characterized in detail. The results indicated that the addition of 1-MI was beneficial to forming the membrane with a dense and thin PA layer. This is because 1-MI could react with TMC, which is in favor of the formation of back surface structure with more pores. The product generated by 1-MI and TMC was hydrolyzed easily, and then endowed the membrane with more carboxylic acid groups. The membrane desalination performance for feeds with different NaCl concentration was evaluated. The membrane prepared with 1-MI possessed a higher flux and rejection because of the thinner and denser PA layer and more carboxylic acid groups. Considering that the membranes inevitably face chemical cleaning with acid or alkaline solutions in the real processes, the RO membranes were exposed to acidic-alkaline solution, and the results showed that the membrane prepared with 1-MI had good pH stability. This study offers a new route for preparing an excellent-performance RO membrane via using 1-MI as an additive.
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CATALYSIS TODAY
·
2019
·
IF 4.888
Hongxia Chen,Runduo Zhang,Wenjing Bao,Hao Wang,Zhoujun Wang,Ying Wei
The catalytic removal of HCHO with low noble-metal loading at room temperature is meaningful and challenging work. Herein, high performance catalysts x Pt/TS-1 (Si/Ti = 30, x = 0.1, 0.3, and 0.6 wt%) for HCHO oxidation were synthesized by polyvinyl alcohol-protected NaBH 4 reduction method. The Pt/TS-1 sample loading with 0.3 wt% Pt nanoparticles (NPs) could completely remove 120 ppm HCHO at space velocity (SV) of 60,000 mL/(g h) at 20 °C. Moreover, the 0.3Pt/TS-1 sample remained outstanding activity and stability in humid air with 35–75% water vapor and at high SV with a range between 60,000 and 240,000 mL/(g h). Based on the results of UV–vis, Raman, NH 3 -TPD, Contact angle measurement, CO chemisorption , and O 2 -TPD, the excellent catalytic performance of Pt/TS-1 was mostly attributed to high Pt dispersion and high concentration of adsorbed oxygen species. This work expands the field of utilization of zeolite supported noble-metal catalysts for the purification of indoor pollutants.
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IONICS
·
2016
·Vol. 22
·期 10
·1947-1955
·
IF 2.119
Zhuo Kelei,Ma Xueli,Chen Yujuan,Wang Congyue,Li Aoqi,Yan Changling
The molecular imprinting technique is powerful to prepare functional materials with molecular recognition properties. In this work, a potentiometric sensor was fabricated by dispersing molecularly imprinted polymers (MIPs) into plasticized PVC matrix and used for the determination of 1-hexyl-3-methylimidazolium cation ([C 6 mim] + ) in aqueous solution. The MIPs were synthesized by precipitation polymerization using 1-hexyl-3-methylimidazolium chloride ([C 6 mim]Cl) as the template molecule, methacrylic acid (MAA) and ethylene glycol dimethacrylat (EGDMA) as the functional monomers, and EGDMA also as the cross-linking agent. The as-prepared electrode exhibited a Nernstian response (58.87 ± 0.3 mV per decade) to [C 6 mim] + in a concentration range from 1.0 × 10 −6 to 0.1 mol kg −1 with a low detection limit of 2.8 × 10 −7 mol kg −1 , high selectivity, and little pH influence. The as-prepared electrode was used for the detection of the [C 6 mim] + in distilled water, tap water, and river water with a good recovery. It was also successfully applied in the determination of mean activity coefficients of [C 6 mim]Br in fructose + water systems based on the potentiometric method at 298.15 K.
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DALTON TRANSACTIONS
·
2017
·Vol. 46
·期 8
·2643-2652
·
IF 4.029
Aimin Wu,Jing Li,Baodan Liu,Wenjin Yang,Yanan Jiang,Lusheng Liu,Xinglai Zhang,Changmin Xiong,Xin Jiang
(GaN)1−x(ZnO)x solid solution has attracted extensive attention due to its feasible band-gap tunability and excellent photocatalytic performance in overall water splitting. However, its potential application in the photodegradation of organic pollutants and environmental processing has rarely been reported. In this study, we developed a rapid synthesis process to fabricate porous (GaN)1−x(ZnO)x solid solution with a tunable band gap in the range of 2.38–2.76 eV for phenol photodegradation. Under visible-light irradiation, (GaN)0.75(ZnO)0.25 solid solution achieved the highest photocatalytic performance compared to other (GaN)1−x(ZnO)x solid solutions with x = 0.45, 0.65 and 0.85 due to its higher redox capability and lower lattice deformation. Slight Ag decoration with a content of 1 wt% on the surface of the (GaN)0.75(ZnO)0.25 solid solution leads to a significant enhancement in phenol degradation, with a reaction rate eight times faster than that of pristine (GaN)0.75(ZnO)0.25. Interestingly, phenol in aqueous solution (10 mg L−1) can also be completely degraded within 60 min, even under the direct exposure of sunlight irradiation. The photocurrent response indicates that the enhanced photocatalytic activity of (GaN)0.75(ZnO)0.25/Ag is directly induced by the improved transfer efficiency of the photogenerated electrons at the interface. The excellent phenol degradation performance of (GaN)1−x(ZnO)x/Ag further broadens their promising photocatalytic utilization in environmental processing, besides in overall water splitting for hydrogen production.
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高影响因子
DALTON TRANSACTIONS
·
2022
·Vol. 51
·期 31
·11703-11712
·
IF 4.569
Jun Sun,Minghui Zhou,Bei Zhang,Youjie Hua,Feifei Huang,Hongping Ma,Renguang Ye,Shiqing Xu
A series of Rb1−yKyNa3(Li3SiO4)4:Eu2+(0 ≤ y ≤ 1) phosphors were successfully synthesized through a high-temperature solid-state reaction. The introduction of K+ into the RbNa3(Li3SiO4)4:Eu2+ phosphor to partially or completely replace Rb+ allows the emission spectrum to be modulated from blue (λ = 473 nm, FWHM = 22.5 nm) to a narrow cyan band (λ = 485 nm, FWHM = 21.1 nm). As the K+ ion content increases, the space group of the phosphor evolves from I4/M to I41/A. The complete replacement of Rb+ by K+ results in the KNa3(Li3SiO4)4:Eu2+ cyan phosphor, which shows excellent thermal stability (the comprehensive emission loss is only 8% at 150 °C) and can be used to fill the cyan light gap in white LED devices. By adding the KNa3(Li3SiO4)4:Eu2+ cyan phosphor in packaging with yellow and red phosphors, the color rendering index is increased from 90.2 to 97.1 and the correlated color temperature improved to 3658 K. These results indicate that the cyan phosphor has important application value in full-spectrum white LEDs.
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Frontiers of Environmental Science & Engineering
·
2025
·Vol. 19
·期 12
·1-16
·
IF 6.4
Zhao Biyi,Chen Wei,Chen Geng,Zhao Feng,Xiao Yong
Electroactive microorganisms are integral to biogeochemical cycles through extracellular electron transfer and have potential applications in environmental remediation. However, their long-term competitive interactions and evolutionary dynamics with non-electroactive microorganisms remain poorly understood. In this study, we conducted a 320-day cultivation experiment in which monocultures of the electroactive Shewanella oneidensis MR-1, the non-electroactive Citrobacter freundii An1, and their cocultures were compared under three single electron acceptor conditions: anaerobic (no exogenous electron acceptor), ferrihydrite, or oxygen. After 320 d, S. oneidensis MR-1 presented the highest relative abundance of 30.94% ± 0.74% in the ferrihydrite cocultures. S. oneidensis MR-1 maintained ferrihydrite reduction capacity after cultivation under all three conditions, indicating the long-term stability of its extracellular electron transfer. Moreover, no other phenotypic evolution was observed in S. oneidensis MR-1 after ferrihydrite or anaerobic cultivation. In contrast, both monocultured and cocultured S. oneidensis MR-1 exhibited enhanced adaptation to oxygen, characterized by increased growth rates, metabolic activity, and reduced cell aggregation. Notably, substrate consumption increased in monocultures but decreased in cocultures, suggesting an optimization of metabolic efficiency in the latter. Genome sequencing revealed mutations in genes associated with cell division, adenosine triphosphate synthesis, lactate metabolism, and flagellar/pilus expression in S. oneidensis MR-1. Interestingly, the ferrihydrite-adapted groups also exhibited enhanced adaptation to oxygen. 83.96% of mutations were shared across all culture systems and enriched in environmental signal-sensing pathways, indicating that parallel genomic evolution facilitated cross-environmental adaptation. Our findings reveal the ecological evolution of electroactive microorganisms in diverse redox environments and establish a foundation for engineering electroactive communities.
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Journal of Environmental Chemical Engineering
·
2025
·
IF 7.2
Arif Nawaz,Mahnoor Amjad,Jalwa Afreeq,Tauseef Khan,Linke Zhao,Fazli Wahid,Haifa Zhai
Advanced oxidation processes (AOPs), particularly photocatalysis catalyzed by efficient and economical photocatalysts, is an emerging and sustainable approach. Band gap engineering, and spin polarization induction by anchoring spatially adjacent redox sites (metal cation vacancies) in the material is an excellent way for ensuring enhanced photocatalytic performance. Inspired by this, herein a novel and effective Sn rich Co co-doped Co 0.5 Sn 2 Mn 0.5 O 3 (C-SMO 3 ) oxide perovskite photocatalyst has been designed to accelerate charge separation and inhibit charge carrier recombination at redox intimate interfaces and defective Co, Mn 3 + /Mn 4+ dual sites for photocatalysis. The synthesized photocatalyst has been confirmed by various characterizations such as UV-Vis spectrophotometry, FTIR, XRD, SEM, TEM, HR-TEM, Raman, XPS, etc. The FTIR shows characteristics peaks of all constituent components. The crystalline morphology, d-spacing and shape of composite materials deduced from SEM, TEM, HR-TEM and XRD are all in agreement with each other hence the formation Co doped Sn rich SnMnO 3 has been confirmed. The experimental results demonstrate C-SMO 3 a potential dynamic dual site contender for wastewater decontamination. The spatially adjacent redox sites Co (1- x) - Mn 3+ /Mn 4+ inhibit photo-exciton recombination and accelerates charge carrier responsible for photocatalytic degradation of contaminants synchronized by light harvesting efficiency. The dual redox half reactions synergized photoinduced charge carriers dynamically enhanced the Sn 2 Mn 0.5 O 3 /Co (1- x) photodegradation property and performed 98 % breakdown of EB in 50 min, 96.7 % of CV dye in 90 min, and 90.9 % of CEF antibiotics under visible light irradiations optimized by RSM. The photocatalyst was recycled and reused due to its convenient recyclability, resulting in nearly stable degradation efficiency.
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TOXICOLOGY AND APPLIED PHARMACOLOGY
·
2025
·
IF 3.4
Han Lin,Ying Yan,Chenyu Qiu,Junqi Wang,Wenying Fu,Chongchong Shu,Yinghua Chen,Chenxin Xu,Shaotang Li,Yiqun Xia,Jundixia Chen,Yunzhi Chen,Peng Zou,Ri Cui,Daoyong Ni
Glutamyl-prolyl-tRNA synthetase 1 (EPRS1) is a key enzyme in protein synthesis and is implicated in various diseases, including inflammation, fibrosis, and cancer. Here, we found that EPRS1 is highly expressed in patients with colon cancer and is positively correlated with poor prognosis. Halofuginone, a derivative of febrifugine extracted from the traditional Chinese herb Dichroa febrifuga , was previously identified as a specific inhibitor of EPRS1. Our research found that halofuginone significantly inhibit the growth of colon cancer cells. Mechanistic investigations demonstrated that halofuginone treatment activates the ATF4-CHOP and JNK signaling pathways in colon cancer cells. Further research revealed that halofuginone inhibits the expression of NRF2, and that high NRF2 expression can reverse halofuginone's anti-colon cancer activity. Importantly, the inhibition of NRF2, along with the activation of the ATF4-CHOP and JNK signaling pathways caused by halofuginone, can be substantially reversed by proline. Additionally, we observed a synergistic antitumor effect when halofuginone was combined with bortezomib, a well-established proteasome inhibitor, in colon cancer cells. These results imply that the halofuginone-bortezomib combination could offer a promising therapeutic option for colon cancer treatment. In summary, our research comprehensively elucidates the molecular mechanisms underlying halofuginone's action against colon cancer and provides new insights into halofuginone-based combination therapies.
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PubMed
高影响因子
Nature Communications
·
2025
·Vol. 16
·期 1
·1-14
·
IF 15.7
Wang Peng,Zhao Danyang,Zhang Peng,Hui Xiaobin,Zhang Zhiwei,Wang Rutao,Wang Chengxiang,Ge Xiaoli,Liu Xiaojing,Li Yuguang C.,Yin Longwei
The metallic phase MoS 2 (1T-MoS 2 ) supported metal-nanocatalyst is an appealing material system for accelerating the redox kinetics of non-aqueous Li | |O 2 batteries. However, the drawbacks associated with the surface orbital steric effect and the internal electron coupling results in a detrimental effect for the stability of 1T-MoS 2 , especially for the interface charge transfer. This makes it difficult to incorporate guest metal nanoparticles without compromising the 1 T phase support. To circumvent these issues, here we propose a p-block element (In-O) doping strategy to stabilize the 1 T phase MoS 2 by moderating the surface orbital steric effect and strengthening the internal chemical bonding, and thus for the epitaxial Ru nanocatalyst graft on the stabilized 1T-MoS 2 for Li | |O 2 batteries. The experimental and theoretical analyzes indicate that the In-O-MoS 2 @Ru enhances the O 2 dissociation and facilitates the adsorption of LiO 2 intermediates. This effect promotes the growth of weakly crystalline Li 2 O 2 films during oxygen reduction reaction, which can be more easily decomposed during the oxygen evolution reaction, thereby enhancing the bifunctional-catalytic kinetics. When employed at the positive electrode for non-aqueous Li | |O 2 batteries, In-O-MoS 2 @Ru shows an overpotential of 0.37 V and a cycling life of 284 cycles at 200 mA g −1 with a final discharge specific capacity of 1000 mAh g −1 at 25 °C.
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高影响因子
MOLECULES
·
2025
·Vol. 30
·期 3
·502
·
IF 4.6
Tian Lan,Xiaofan Ding,Qi Chen,Songtao Xiao,Taihong Yan,Tianchi Li,Weifang Zheng
Iodine is one of the key elements that must be removed from the off-gas systems of nuclear fuel reprocessing. This study systematically investigates the iodine vapor adsorption performance of the metal–organic framework (MOF) material HKUST-1(1-(2-methyl-4-(2-oxopyrrolidin-1-yl)phenyl)-3-morpholino-5,6-dihydropyridin-2(1H)-one), with particle sizes of 100 nm and 20 μm. HKUST-1 samples with varying particle sizes were synthesized via a hydrothermal method. The experimental results show that the 20 μm HKUST-1 exhibits superior crystallinity, a more intact pore structure, and a higher iodine adsorption capacity, reaching 700 mg/g, which is significantly greater than the 300 mg/g capacity of the 100 nm HKUST-1. Kinetic analysis reveals that the adsorption process follows the pseudo-second-order model, with physical adsorption as the predominant mechanism, where iodine molecules are accommodated within the pores. FTIR and XRD further confirm the structural stability of the HKUST-1 framework after iodine adsorption. However, desorption experiments show that iodine molecules are easily volatilized into the air, with a 20% weight loss observed within 10 h and a color change from black to green. The results provide experimental evidence for optimizing the application of HKUST-1 materials in iodine capture and suggest that material modification could enhance the long-term stability of iodine fixation.
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