Journal of Energy Storage
·
2026
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IF 10.7
Pindu Chen,Xiaochun Wen,Jia Chen,Xiang Xu,Jianeng Huang,Li'’An Ma,Xiaoyun Ye,Hongxiang Chen
Manganese-based halides like Li 2 MnCl 4 are attractive for their cost-effectiveness and inverse spinel structure with ion channels. Their use as solid-state electrolytes is limited by low ionic conductivity at room-temperature and poor stability at the lithium interface. Current strategies focus on single-cation doping, which often offers limited conductivity improvements or causes side effects. This study proposes a dual-site cation-anion co-doping strategy to modify lattice defects and Li + migration pathways, thereby enhancing interfacial stability with metallic lithium. Lattice distortion is greatly induced, and Li + vacancy concentration is optimized in Li 1.7 Al 0.1 MnCl 4- x F x ( x = 0–0.7) by substituting Al 3+ at octahedral sites and partially replacing Cl − with F − . Structural and electrochemical tests show that moderate co-doping maintains the cubic structure and greatly improves Li + transport. The best Li 1.7 Al 0.1 MnCl 3.9 F 0.1 exhibits a room-temperature ionic conductivity of 5.2 × 10 −5 S cm −1 , nearly ten times higher than pristine Li 2 MnCl 4 , with a reduced activation energy of 0.45 eV. The distribution of relaxation time analysis further reveals that interface-related relaxation processes remain relatively stable over long time scales. Stable lithium stripping/deposition was demonstrated for hundreds of hours at 0.1 mA cm −2 in lithium-symmetric batteries. However, polarization during long cycling indicates challenges with interfacial stability. This work underscores the impact of dual-site co-doping in developing low-cost, high-performance manganese-based halide solid-state electrolytes.
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MATERIALS CHEMISTRY AND PHYSICS
·
2023
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IF 4.6
Yatao Pan,Guangjing Hou,Xiaojuan Wang,Xia Ran,Pingan Liu,Lijun Guo
Developing novel inhibitors for the fibrillization of amyloid peptides and understanding the relevant assembly processes are essential for biomedical and biomaterial sciences. Herein, we have synthesized and characterized the nitrogen and fluorine co-doped graphene quantum dots (N, F-GQDs), and investigated their inhibition of the fibrillization of Amyloid-beta peptide (1–42) (Aβ 42 ) by monitoring the assembly morphologies in the Aβ 42 /N, F-GQDs systems. Our results indicate that the N, F-GQDs functionalized with multiple surface groups effectively inhibits the fibrillization of amyloid Aβ 42 . The strong adsorption of Aβ 42 on N, F-GQDs significantly reduces the generation of β-sheet structures and the cytotoxicity of Aβ 42 /N, F-GQDs aggregates. Accordingly, a morphological evolution from the long fibrils of Aβ 42 to the spherical particles and unique closed-loop structures of Aβ 42 /N, F-GQDs have been captured. A possible interpretation for the observed phenomena in the presence of N, F-GQDs has been proposed by combining the different inhibition effects of other GQDs on the fibrillization of Aβ 42 and the results from various control experiments. Moreover, the inhibition activity of N, F-GQDs demonstrates good adaptability to resist the fluctuation of pH value and the interference of divalent metal ions , facilitating their practical applications in the future.
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MATERIALS CHEMISTRY AND PHYSICS
·
2023
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IF 4.6
Xia Zhao,Hong Hao,Haixia Pang,Min Jiang,Yanping Duan
Emulsifier-free polymerization was employed to prepare the submicron spherical PSA (the copolymer of styrene and acrylic acid), then SiO 2 was grown on the surface of the PSA by sol-gel method to form F–SiO 2 @PSA particles. It was found that when styrene: acrylic acid = 2.5:1 and tetraethyl orthosilicate : PSA was between 2.17:1 and 6.38:1, a perfect raspberry-like structure could be obtained. The coating based on F–SiO 2 @PSA particles exhibited contact angles of 167.3 ± 1.4°, 152.1 ± 1.5°,150.3 ± 1.6°, 150.9 ± 1.6°, 142.2 ± 1.7°, 143.7 ± 1.5° and 146.6 ± 1.9° to water, diiodomethane, soybean oil, rapeseed oil, hexadecane, kerosene, and waste engine oil , respectively. The F–SiO 2 @PSA coating could reduce the adsorption of protein by 90% compared with the control surface . It was observed that bacteria and platelets could hardly adhere to the coating surface after 24 h of E. coli culture and 3 h of platelet-rich plasma immersion. The anti-adhesion to proteins, platelets, and bacteria will give the coating a promising application in the medical field.
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JOURNAL OF ALLOYS AND COMPOUNDS
·
2022
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IF 6.371
Wenjing Zhao,Peng Wang,Fan Zhang,Yinshen Liu,Xuan Jin,Shijun Yuan,Qi Fan,Xing Guo,Qingyu Xu
Cation-disordered rock-salt cathodes have attracted extensive attention due to their high capacity and energy density . However, the excessive redox reaction of O 2- causes a severe impairment of Ni capacity and the release of O 2 , leading to the poor cycle stability and voltage decay for Li-Ni-Nb-O cathodes. In our work, the oxyfluoride compounds Li 1.23 Ni 0.3 Nb x Fe y O 2- z F z with various doping concentrations of Fe and F are successfully synthesized by solid state reaction using high-energy ball milling. Apart from observing the plateau at around 4 V with the redox reaction of Ni, a new plateau at approximately 2.6 V is observed due to the redox reaction of Fe. The doping of Fe on Nb increases the discharge capability and the co-doping of F on O further improves cycle stability. With the optimized doping amount of Fe ( y = 0.16) and F ( z = 0.15), Li 1.23 Ni 0.3 Nb 0.30 Fe 0.16 O 0.85 F 0.15 can deliver a discharge capacity of 347.1 mAh/g at a current density of 20 mA/g after the activation process in subsequent cycles. After 20 cycles at 20 mA/g, the capacity retention is 181.6 mAh/g, and after 100 cycles at 50 mA/g, the discharge capacity remains 102.2 mAh/g.
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APPLIED MICROBIOLOGY AND BIOTECHNOLOGY
·
2022
·Vol. 106
·期 18
·6277-6287
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IF 5.56
Yin Ru,Zhang Xue,Wang Beijia,Jia Jianbo,Wang Nana,Xie Chunyan,Su Peiyang,Xiao Pengfei,Wang Jianqiao,Xiao Tangfu,Yan Bing,Hirai Hirofumi
Abstract Environmental bisphenol F (BPF) has a cyclic endocrine disruption effect, seriously threatening animal and human health. It is frequently detected in environmental samples worldwide. For BPF remediation, biological methods are more environmentally friendly than physicochemical methods. White-rot fungi have been increasingly studied due to their potential capability to degrade environmental pollutants. Phanerochaete sordida YK-624 has been shown to degrade BPF by ligninolytic enzymes under ligninolytic conditions. In the present study, degradation of BPF under non-ligninolytic conditions (no production of ligninolytic enzymes) was investigated. Our results showed that BPF could be completely removed after 7-d incubation. A metabolite of BPF, 4,4’-dihydroxybenzophenone (DHBP) was identified by mass spectrometry and nuclear magnetic resonance, and DHBP was further degraded by this fungus to form 4-hydroxyphenyl 4-hydroxybenzoate (HPHB). DHBP and HPHB were the intermediate metabolites of BPF and would be further degraded by P. sordida YK-624. We also found that cytochrome P450s played an important role in BPF degradation. Additionally, transcriptomic analysis further supported the involvement of these enzymes in the action of BPF degradation. Therefore, BPF is transformed to DHBP and then to HPHB likely oxidized by cytochrome P450s in P. sordida YK-624. Furthermore, the toxicological studies demonstrated that the order of endocrine-disrupting activity for BPF and its metabolites was HPHB > BPF > DHBP. Key points
• White-rot fungus Phanerochaete sordida YK-624 could degrade BPF.
• Cytochrome P450s were involved in the BPF degradation.
• The order of endocrine disrupting activity was: HPHB > BPF > DHBP.
Graphical abstract
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JOURNAL OF HAZARDOUS MATERIALS
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2023
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IF 13.6
Xiaolan Zhang,Shufang Xu,Zhimin Liu,Zhigang Xu,Qinpeng Shen,Shiyun Tang,Zhihua Liu,Xiaoxi Si
Bisphenol F (BPF) has evoked global attentions due to its ubiquity and detrimental effects. Herein, a flexible molecularly imprinted fiber library was firstly proposed for the metabolic analysis of BPF in aquatic ecosystems . The library includes flexible single fibers and fiber arrays to precisely identify BPF and its metabolites with a wide range of polarities. Compared to commercial polyacrylate , the performance increased 11.56–570.98-fold. The adsorption capacity and the Log K ow value were positively related. These arrays were used for the acquisition of environmental metabolomics data from aquatic ecosystems. In-depth data analysis showed that risk quotient was lower than 0.76, and bioaccumulation factor was lower than 2000 L/kg. Distribution concentration of BPF and its metabolites changed seasonally, and accumulation in sediment was much larger than that in surface water and hydrobionts. The risk is gradually increasing in sediment, but it does not reach high risk. The likelihood of bioaccumulation of parent compounds was greater than its metabolites. The library can be used in the metabolic diagnosis of pollutants with a broad range of polarities, providing a new method to acquire data for further ecological risk assessment , and offering a revolutionary strategy for environmental metabolomics investigation in aquatic ecosystems.
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CHEMICAL ENGINEERING JOURNAL
·
2023
·
IF 15.1
Weirui Chen,Siyou Fu,Xukai Li,Jing Wang,Xunan Ning,Liying Bin,Ping Li,Bing Tang,Laisheng Li
Photocatalytic ozonation (PCO) was a novel water treatment method, but the low photo-generated electron ( e - ) utilization and ambiguous ROS formation mechanism restrained its performance. Herein, C vacancy and F co-decorated g-C 3 N 4 (FCN_Cv) was designed to accelerate the PCO performance with sodium p -perfluorinated nonoxybenzenesulfonate (OBS) acting as model pollutant. Comparative characterizations revealed that FCN_Cv remained the inherent structure of g-C 3 N 4 (BCN), and had an enhanced conduction band potential, narrower band gap and longer e - lifetime. FCN_Cv exhibited the greater activity over BCN, with 99.3 % OBS removal in 30 min but only 78.3 % for BCN during PCO process. •OH was the main ROS for degrading OBS. The greater •OH yield was obtained by FCN_Cv PCO process because of the increase of e - utilization. On one hand, the two electrons reduction of O 2 into H 2 O 2 on FCN_Cv was accelerated, which triggered the peroxone reaction between photogenerated-H 2 O 2 and O 3 . On the other hand, the direct one electron reduction of O 3 by e - also accounted for •OH generation. 17 kinds of intermediates were detected and the OBS degradation routes were inferred, which was involved with hydroxylation, C-O cleavage and aromatic ring opening reactions. Overall, this study demonstrated the feasibility of decorating F element and C vacancy on g-C 3 N 4 in enhancing e - utilization and •OH generation during PCO process as well as deepened the understanding of fate of OBS in PCO process.
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Small
·
2023
·Vol. 20
·期 13
·2306561
·
IF 13.3
Yanling Zhuang,Quan Zong,Yuanzhe Wu,Chaofeng Liu,Qilong Zhang,Daiwen Tao,Jingji Zhang,Jiangying Wang,Guozhong Cao
The electrochemical properties of vanadium-based materials as cathode materials for aqueous zinc ion batteries are still restricted by low conductivity, sluggish reaction kinetics, and poor structural stability. Herein, the [VO 6 ] octahedron, as the basic unit of vanadium-oxide layer of ammonium vanadates (NH 4 V 4 O 10 , denoted as NVO), is incorporated by F atoms to regulate the coordinated environment of vanadium. Density functional theory (DFT) calculations and experimental results show that both physicochemical and electrochemical properties of NVO are improved by F-doping. The enhanced electronic conductivity accelerates the electron transfer and the expanded interlayer spacing expedites the diffusion kinetics of zinc ions. As a result, the F-doped NVO (F-NVO) electrode shows a high discharge capacity (465 mAh g −1 at 0.1 A g −1 ), good rate capability (260 mAh g −1 at 5 A g −1 ), and long-term cycling stability (88% capacity retention over 2000 cycles at 4 A g −1 ). The reaction kinetics and energy storage mechanism of F-NVO are further validated by in situ and ex situ characterizations.
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COLLOIDS AND SURFACES A-PHYSICOCHEMICAL AND ENGINEERING ASPECTS
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2023
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IF 5.2
Bochen Jiang,Yanhua Lei,Kai Sun,Qing Chen,Fei Zhang,Yan An,Yuliang Zhang,Yi Lin,Yuan Yuan,Tao Liu,Xiaofeng Li
Ice accumulation is an important challenge for daily life and industrial production. The photothermal effect offers a promising approach for active de-icing to address this issue. While the photothermal effect of polyphenol-metal ion complex is extensively studied in photothermal cancer therapy, its application in de-icing remains relatively unexplored. Herein, a durable photothermal superhydrophobic coating was designed by combining F-SiO 2 @Tp/Fe (Tea polyphenol-Fe 3+ ) nanoparticles and silicone resin using a one-step spray method. Due to the unique micro-nano structure, the resulting coating exhibited excellent superhydrophobicity, characterized by water contact angle (CA) of up to 159° and sliding angle (SA) of less than 2.5°. Additionally, the coating demonstrated reliable mechanical durability and chemical stability, as evidenced by its good performance in sandpaper abrasion, tape peeling and electrochemical corrosion tests. Moreover, owing to the efficient photothermal conversion of F-SiO 2 @Tp/Fe nanoparticles , surface temperature of the coating can quickly reach 81 ℃ under 1 kW/m 2 simulated sunlight irradiation (1 Sun). The prepared coating exhibits over three times delayed icing time under 1 sun irradiation at − 25 °C in comparison to the absence of light. And the coating also exhibits stable de-icing and defrosting cycle performance. These findings demonstrate effective synergistic effect of anti-icing and de-icing in the F-SiO 2 @Tp/Fe photothermal superhydrophobic coating, showcasing its promising application potential in practical engineering.
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JOURNAL OF FOOD COMPOSITION AND ANALYSIS
·
2021
·
IF 4.556
Wei Jia,Yinghuan Yang,Shuxing Liu,Lin Shi
Irradiation technology has been shown to be a possible preservation technology used to prolong the shelf life and provide microbial decontamination of spices. In this study, the molecular mechanisms of the irradiation-induced accumulation of polyphenols in star anise were explored using metabolomics combined with ultra-high-performance liquid chromatography quadrupole-Orbitrap (UHPLC-Q-Orbitrap) high-resolution mass spectrometry. Fifty-six star anise samples from different areas processed with 2–10 kGy doses of irradiation were compared. The effect of post irradiation storage times ranging from 0 to 70 days was also evaluated. A total of 161 metabolites with variable importance on projection greater than 1 were characterized, and significant differences in flavonoid content in star anise were observed after irradiation. Absolute quantification was used for the quantification of distinctive compounds, and the limit of quantitation of the components was 1.90–6.53 μg/kg. The flavonoid content was stable on the 28th day of storage. The average content of flavonoids increased by 2–9 times due to the breaking of glycoside bonds in star anise by irradiation. C 15 H 11 O 7 + m/z 303.13045 and C 3 H 3 O 2 + m/z 71.01276 were defined as the characteristic fragments of flavonoids according to the mechanism of fragmentation. Checking the extraction ion chromatogram (EIC) characteristic fragments allows straightforward screening of untargeted flavonoids.
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PROGRESS IN ORGANIC COATINGS
·
2020
·
IF 4.469
Pengying Wan,Nie Zhao,Fugang Qi,Biao Zhang,Hailong Xiong,Heng Yuan,Bin Liao,Xiaoping Ouyang
A novel PDA-BN@f-Al 2 O 3 nanohybrid was synthesized by depositing Al 2 O 3 nanoparticles modified with γ -Aminopropyltriethoxysilane (KH550) on the surface of hexagonal boron-nitride (h-BN) sheets covered with polydopamine (PDA). Then, PDA-BN@f-Al 2 O 3 hybrids was dispersed in epoxy resin to prepare composite coating samples. Many characterizations revealed that the functionalized Al 2 O 3 successfully deposited on the surface of PDA-BN platelets and PDA-BN@f-Al 2 O 3 hybrids showed good dispersibility in the epoxy resin, and the interfacial adhesion between hybrids and epoxy matrix was improved. Furthermore, the effects of Al 2 O 3 , h-BN and various mixtures of PDA-BN@f-Al 2 O 3 hybrids at a low weight fraction of 1 % on the corrosion resistance of epoxy coating were studied by electrochemical measurement and salt spray test. The potentiodynamic polarization test revealed that PDA-BN@f-Al 2 O 3 hybrids have a corrosion inhibitive performance. Moreover, the coating resistance of PDA-BN@f-Al 2 O 3 (3:1)/epoxy was enhanced by three orders of magnitude compared with neat epoxy after 5 d immersion. This study provides a promising application prospect for the development of superior metal protective organic coatings.
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SPECTROCHIMICA ACTA PART A-MOLECULAR AND BIOMOLECULAR SPECTROSCOPY
·
2019
·
IF 2.931
Dongwei Miao,Dongkui Liu,Yanbo Zeng,Guobao Zhou,Wei Xie,Yiwen Yang,Hailong Wang,Jian Zhang,Yunyun Zhai,Zulei Zhang,Lei Li
A novel fluorescent biosensor based on dabcyl [(E)-4-((4-(dimethylamino) phenyl) diazenyl)benzoic acid] -modified anti-Mb aptamer (D-AMA) and 6-FAM(6-carboxyfluorescein) -modified complementary short chain (F-CSC)for the specific and sensitive detection of Mb levels is presented in this study. In PBS buffer solution, D-AMA bound to F-CSC, and then dabcyl quenched the fluorescence of 6-FAM. After adding Mb into the system, D-AMA bound to Mb and separated from F-CSC. The fluorescence of 6-FAM was restored after it separated from dabcyl. The assay exhibited high specificity and sensitivity toward Mb, with a low limit of detection of 0.07 ng/mL (S/N = 3) and linear relationships of 0.1–5 ng/mL. It was further applied to detect Mb levels in spiked human blood sera samples.
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