APPLIED CATALYSIS B-ENVIRONMENTAL
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2024
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IF 20.2
Mingjie Cheng,Bo Gao,Xiaoli Zheng,Wenzhuo Wu,Weiqian Kong,Pengfei Yan,Zubin Wang,Bin An,Yunpeng Zhang,Qingchao Li,Qun Xu
Exploring a facile, rapid and efficient route to produce metal-organic frameworks (MOFs) with highly accessible active sites is of great importance for catalysis. Here we demonstrate the CO 2 coordination can drive low temperature rapid synthesis of porphyrin-based bismuth-MOFs (Bi-PMOFs) by utilizing synergistic physical and chemical properties of supercritical CO 2 (SC-Bi-PMOFs). The molecular-level role of scCO 2 in the synthesis of SC-Bi-PMOFs have been investigated through a series of characterizations including in-situ time-dependent infrared spectroscopy, wherein chemical coordination of CO 2 promotes to fabricate 2D SC-Bi-PMOFs nanosheets. Moreover, the formation of Cu-PMOFs and Fe-PMOFs proves the universal scCO 2 strategy for synthesizing PMOFs. Density functional theory (DFT) calculations together with experiments results confirm the SC-Bi-PMOFs with abundant active sites guarantee efficient ligand-to-metal charge transfer and reduction efficiency of CO 2 . The high-efficiency utilization of CO 2 for synthesizing a series of MOFs and subsequent catalysis on photocatalytic CO 2 reduction for valuable chemicals realize the carbon recycle.
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ACS Applied Nano Materials
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2024
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IF 5.3
Yapeng Yao,Xiaodong Gou,Wei Liu,Zihang Liang,Jiangbo Zhang,Zhongliang Ma
Integrating energetic materials into microelectromechanical system (MEMS) to enhance their energy output characteristics has shown extensive potential across aerospace, defense, and civilian applications. Within this study, the MEMS compatible Cu/DNBT (DNBT = [5,5′-dinitro-3,3′-bi(1,2,4-triazole)]) and Cu/DNBT@nano-Al energetic films were successfully synthesized on the copper substrate using an electrochemical method and a drip coating method. The scanning electron microscope (SEM), X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR), differential thermal analyses (DTA), and a pulse laser ignition test were used to analyze the morphology, composition, thermal performance, and ignition properties of the prepared samples. The findings indicate that the prepared Cu/DNBT and Cu/DNBT@nano-Al energetic films exhibit a nanostructure, and their morphology can be effectively regulated via modifications to the deposition voltage, deposition time, and aluminum plating frequency. Furthermore, the energetic properties of Cu/DNBT@nano-Al films can be adjusted after the deposition of nano-Al. Their heat release, flame height and ignition duration can reach up to 1823.1 J·g–1, 13.5 mm, and 400 μs, respectively. These findings suggest that Cu/DNBT@nano-Al energetic films being a prime contender for initiating powders in MEMS pyrotechnics. In summary, this work offers valuable insights into the integration and application of energetic materials in MEMS ignition devices.
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ADVANCED MATERIALS
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2024
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IF 27.4
Qingquan Han,Xigang Gao,Chao Zhang,Yajie Tian,Sen Liang,Xin Li,Yafeng Jing,Milin Zhang,Anhe Wang,Shuo Bai
Conducting polymer hydrogels have gained attention in the bioelectronics field due to their unique combination of biocompatibility and customizable mechanical properties. However, achieving both excellent conductivity and mechanical strength in a hydrogel remains a significant challenge, primarily because of the inherent conflict between the hydrophobic nature of conducting polymers and the hydrophilic characteristics of hydrogels. To address this issue, this work proposes a simple one-step acid-induced approach that not only promotes the gelation of hydrophilic polymers but also facilitates the in situ phase separation of hydrophobic conducting polymers under mild conditions. This results in a distinctive bi-continuous phase structure with exceptional electrical property (906 mS cm −1 ) and mechanical performance (fracture strain of 1103%). The hydrogel forms robust percolating networks that maintain structural integrity under mechanical stress due to their entropic elasticity, providing remarkable strain insensitivity, low mechanical hysteresis, and an impressive resilience (95%). Electrodes fabricated from the conductive hydrogel exhibit stable and minimal interfacial contact impedance with skin (1–6 kilohms at 1–100 Hz) and significantly lower noise power (4.9 µV 2 ). This work believes that the motion-insensitive characteristics and mechanical robustness of this hydrogel will enable efficient and reliable monitoring of biological signals, establishing a new benchmark in the bioelectronics.
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ENVIRONMENTAL RESEARCH
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2024
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IF 7.7
Suo Wang,Changyu Li,Huanshun Yin,Bin Gao,Zhengkun Yu,Yunlei Zhou,Jun Wang,Hongxia Xu,Jichun Wu,Yuanyuan Sun
Currently, achieving dual applications of Bi 2 O 2 CO 3 -based photocatalysts in photocatalytic degradation and sterilization under visible-light conditions is challenging. In this study, a novel Ag/Bi/Bi 2 O 2 CO 3 visible-light photocatalyst with bimetallic doping and rich oxygen vacancies was successfully synthesized using a one-pot hydrothermal crystallization method. The existence of oxygen vacancies was verified by X-ray photoelectron spectroscopy (XPS) and Electron spin resonance (ESR) analysis. The experimental results showed that Ag/Bi/Bi 2 O 2 CO 3 killed ∼100% (log 7) of antibiotic-resistant Escherichia coli (AR- E. coli ) within 60 min and degraded 83.81% of tetracycline (TC) within 180 min under visible light irradiation. Moreover, Ag/Bi/Bi 2 O 2 CO 3 can still remove 61.07% of TC in water after 5 cycles, showing excellent photocatalytic cycle stability and reusability. The possible degradation pathway of TC was determined by liquid chromatography-mass spectrometry. It was found that the main active substances in the photocatalytic disinfection of AR- E. coli were 1 O 2 , h + , and ·OH, while 1 O 2 was the dominant active species in the photocatalytic degradation of TC. This study presents a promising Bi 2 O 2 CO 3 -based visible light photocatalyst for treating both antibiotics (TC) and antibiotic-resistant bacteria (AR- E. coli ) in water.
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DESALINATION
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2025
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IF 9.8
Fei Yu,Haoyuan Yin,Jie Li,Tianjie Chen,Liping Sun,Jie Ma
Developing bismuth-carbon composites that can alleviate the stress concentration and volume expansion problems during the Bi/BiOCl conversion reaction is crucial for electrochemical desalination, especially Cl − removal technology, but it is still a great challenge. Here, we report a B/N co-doped bismuth encapsulated in carbon tubes. Using CAU-17 as a template, a carbon tubular material with multiple carbon layer structures was successfully synthesized by co-pyrolysis with BCN nanosheets, which achieved effective encapsulation of Bi. As the pyrolysis temperature increased, the continuous evaporation of Bi prompted the transformation of the carbon tube structure from a soft carbon to a hard carbon structure interconnected by multi-layered short graphene flakes. This alleviated the instability of the electrode caused by the volume expansion during the Bi/BiOCl transformation reaction and also provided additional ion storage capacity. When applied to the CDI dechlorination anode, Bi@BCN-900 exhibited a high desalination capacity of 145.96 mg g −1 and low energy consumption of 0.53 kWh kg −1 NaCl at an applied voltage of 1.2 V. Moreover, Bi@BCN-900 showed good stability over long-term cycling tests. This work expands the application of CAU-17 and offers new research insights for the design of bismuth-based materials for CDI dechlorination anodes.
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CHEMICAL ENGINEERING JOURNAL
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2024
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IF 13.3
Shen Wang,Meng Rong,Lin-Bing Sun,Yunze Zhao,Huifang Xing,Liangrong Yang
Indeed, the efficient and sustainable recovery of lithium from highly concentrated sodium-containing mother liquors of Li 2 CO 3 and salt-lake brines remains a significant challenge. Herein, two typical Li + recognition receptors, namely benzo-12-crown-4 and thenoyltrifluoroacetone, were separately introduced into the cationic and anionic parts to successfully synthesize novel bi-functionalized task-specific ionic liquids [(B12C4)C n im][TTA] (n = 4, 6, 8). A new, green, and high-efficiency extraction system has been developed by dissolving [(B12C4)C 6 im][TTA] in commercial room-temperature ionic liquid 1-hexyl-3-methyl-imdazolium bis(trifluromethylsulfonyl)imide [C 6 mim][NTf 2 ], without the addition of any other co-extractants. The newly developed [(B12C4)C 6 im][TTA]-[C 6 mim][NTf 2 ] extraction system exhibited a wide pH working range (4.0–11.0), high lithium extraction efficiency (95.4 %), as well as superior separation factors of Li/Na (β Li/Na = 2154.0) and Li/K (β Li/K =757.2). The extraction mechanism involving cation exchange was determined through slope analysis, ion chromatography, UV–vis spectroscopy and FT-IR spectra measurement, indicating that one [(B12C4)C 6 im][TTA] molecule can interact with two lithium ions and form a 1:2 complex. Moreover, the [(B12C4)C 6 im][TTA]-[C 6 mim][NTf 2 ] extraction system also demonstrated fast extraction kinetics, facile stripping and regeneration, along with good cycling performance. Furthermore, a multi-stage countercurrent extraction process to extract lithium from the simulated mother liquor of Li 2 CO 3 was evaluated. When the volume ratio (O/A) of oil phase (O) to water phase (A) was 1.0, only two theoretical extraction stages were needed to extract 91.4 % of lithium into the organic phase. Thus, the [(B12C4)C 6 im][TTA]-[C 6 mim][NTf 2 ] extraction system is promising for lithium extraction from mother liquor of Li 2 CO 3 and salt-lake brines. This study also opens the avenue for designing cationic and anionic bi-functionalized ionic liquids for metal ion separation.
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BIOSENSORS & BIOELECTRONICS
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2025
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IF 10.5
Haizhi Huang,Hefei Wang,Keyu Du,Xiaoping Yu,Xuping Shentu
Lateral flow immunoassay (LFIA) is an affordable and rapid technique for detecting veterinary drugs such as sulfonamides (SAs). However, balancing accuracy, sensitivity, and convenience remains a challenge. To address this, a microfluidic chip-based LFIA utilizing a zirconium-based organic framework, PCN-222@liposome, was developed to simultaneously detect four Sas: sulfamethizole, sulfamethoxazole, sulfamethoxydiazine, and sulfathiazole, with both colorimetric and fluorescent dual-signal detection. In this study, PCN-222 was modified with liposomes to enhance its biocompatibility and water solubility. Characterization through scanning electron microscopy, transmission electron microscopy, powder X-ray diffraction, and Fourier-transform infrared spectroscopy, confirmed the successful incorporation of liposomes with PCN-222. Under optimized conditions, the PCN-222@liposome-LFIA demonstrated high sensitivity, with detection limits ranging from 0.01 to 0.05 μg/L using fluorescent signals—10 times more sensitive than conventional gold nanoparticle-based LFIA. Finally, the PCN-222@liposome-LFIA integrated with the microfluidic chip successfully detected the four SAs in chicken, shrimp, and milk samples, with recoveries ranging from 89.65 % to 118.78 %. This study presents a simple, sensitive, and efficient method for the rapid detection of veterinary drug residues.
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BIOSENSORS & BIOELECTRONICS
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2024
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IF 10.7
Chunli Yang,Yanan Shi,Yuqing Zhang,Jiayang He,Zhihan Zhang,Xinyue Jia,Ruo Yuan,Wenju Xu
Constructing label-free bivariate fluorescence biosensor would be intriguing and desired for the recognizable and accurate detection of two specific DNA segments, yet the design of functional DNA structures with low overlapped interference might be challenging. Herein in this work, a double-faced J anus D NA n ano a rchitecture ( J DNA) with bi-responsive recognition regions on opposite sides was assembled, which consisted of two substrate strands and two template strands for loading green-/red-emissive Ag nanoclusters ( g AgNC and r AgNC) as bivariate signaling reporters. Of note, the hybridized double helix in the middle rationally oriented two flank faces and stabilized the rigid conformation of J DNA, while the template sequences of bicolor clusters were blocked to minimize non-specific background leakage. Upon inputting two targets, the discernible hairpins lost their hairpin structures due to forming two dsDNA complexes. They were executed to simultaneously invade J DNA for activating two individual target-recycled strand displacement (TRSD) events, guiding signal transduction and efficient amplification. Consequently, the clustering templates were unlocked via the tailored conformation switch of J DNA, in which g AgNC and r AgNC were in situ synthesized in two diagonal positions, thereby significantly emitting bi-responsive signal without cross interference. Benefited from the logic integration of double-faced J DNA and TRSD, a label-free, sensitive and specific bivariate fluorescence approach was developed, which would open a new avenue for the potential application in biosensing and bioanalysis.
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JOURNAL OF POWER SOURCES
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2024
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IF 8.1
Huan Shi,Tuo Li,Yang Liu,Tong Yu,Zhenxiang Zhao,Linrui Hou,Changzhou Yuan
Sodium metal batteries (SMBs) have been widely investigated recently due to the low price of Na metal, satisfactory energy density and similar chemical properties to lithium. However, SMBs also face challenges like low Na utilization, dendrite growth, dead sodium accumulation, unstable solid electrolyte interphase and massive bubble generation. To improve their safety and cycling stability, herein, we fabricate a porous hybrid framework, i.e. , fine Bi nanoparticles anchored in porous N-doped carbon matrix (Bi@PNC), as a modified layer upon Cu collector toward stable SMBs. Upon electrochemical activation, the nanoscale Bi-derived Na–Bi alloy with high sodiophilicity reduces the nucleation overpotential of Na, inhibits the formation of Na dendrites, and decreases the loss of Na during cycling. Thanks to these striking merits, the half cells assembled with Na undergo 1600 cycles (3200 h) at 1 mA cm −2 , 1 mAh cm −2 with the average Coulombic efficiency of 99.95%. The optimized Bi@PNC based symmetric cells still maintain the overpotential of ∼9.2 mV under 1 mA cm −2 and depth of discharge of 16.7% after cycling for 2420 h. Furthermore, the assembled less-Na full SMBs exhibit superb electrochemical properties. Our strategy here provides meaningful avenue to construct stable less-Na metallic anodes for advanced SMBs.
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Journal of Inorganic and Organometallic Polymers and Materials
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2024
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IF 3.9
Ji Yufeng,Zou Congyang,Wang Yong,Zhou Zhuyou,Liu Menghe,Xu Ying,Liu Ruijie,Yang Minjie
In this study, a novel photocatalyst composed of silver phosphate (Ag 3 PO 4 ) and bismuth-based organic framework (Bi-MOF) were synthesized via chemical precipitation at room temperature, and the photocatalytic degradation of pollutants under visible light irradiation was conducted to evaluate their photocatalytic performance. The composite materials exhibited significantly enhanced photocatalytic activity compared to pure Bi-MOF and Ag 3 PO 4 , with APBM-1/1 performing the most effectively. The degradation efficiencies of rhodamine B (RhB) and tetracycline hydrochloride (TCH) were 99% and 86.9% within 50 min and 30 min of light exposure, respectively. The construction of a unique p-n heterojunction interface between Ag 3 PO 4 and Bi-MOF significantly enhanced the efficiency of interfacial charge separation, leading to exceptional photocatalytic activity. Capture experiments and electron paramagnetic resonance (EPR) were conducted, revealing that photogenerated holes (h + ) and superoxide radicals (·O 2 − ) were the primary active species involved in the degradation reaction. Based on these findings, a plausible mechanism for the photocatalytic process was proposed.
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JOURNAL OF CHROMATOGRAPHY A
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2024
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IF 3.8
Chengcheng Yang,Wen Deng,Fei Li,Mengting Gong,Hui Li,Xiaorong Mi,Sitong Ma
A pH/temperature bi-responsive gallic acid magnetic imprinted polymer (PTBG-MIP) was synthesized on a Fe 3 O 4 @SiO 2 @KH570 carrier using methacrylic acid (MAA), p-Vinylphenylboronic acid (p-VPBA), and N-isopropyl-acrylamide (NIPAAm) as complex functional monomers. The density functional theory (DFT) was employed to optimize the molar ratio of multi-functional monomers-template complex, which proved to be an effective tool for predicting complex configuration based on electrostatic potential (ESP) analysis and the lowest binding energy. DFT calculation and analysis determined the optimized molar ratio of 2:1:1:1 for GA-MAA-NIPAAm-p-VPBA, which showed good agreement with experimental results. The PTBG-MIP-4 obtained under the optimized conditions exhibited high pH- and temperature- dependence in rebinding the template, displaying a maximum adsorption capacity ( Q e ) of 62.26 mg g −1 and a highest selection factor (α) of 5.217. Additionally, the PTBG-MIP-4 exhibited exceptional physicochemical properties encompassing magnetization characteristics, morphology, surface sites distribution, and adsorption performance. The application efficiency of this imprinted composite in the extraction and purification of gallic acid from Galla chinensis was remarkably demonstrated.
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COMPOSITES PART B-ENGINEERING
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2025
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IF 14.2
Jixia Deng,Changlin Zhai,Lei Zhan,Kuihua Zhang,Tao Yang,Qinfei Ke,Chen Huang,Anlin Yin
The long-term reliability of small-diameter vascular grafts (SDVGs) is still largely confined by acute thrombosis, intimal hyperplasia and delayed endothelialization. In this study, a fibrous SDVG containing both physical and biochemical cues was developed to promote rapid endothelialization. The success of our method depends on the integration of a bi-oriented luminal surface with the conjugation of salvianolic acid B (Sal B) via aminolysis and subsequent amidation reaction. Specifically, longitudinally aligned poly (lactide acid-co-ε-caprolactone) (PLCL) microfibers having nano-grooved surface texture provided bi-oriented topographical cues to guide the elongation and migration of endothelial cells (ECs), whilst the incorporation of Sal B served as a biochemical signal to inhibit thrombosis, enhance EC growth and increase von Willebrand factor (vWF) expression in ECs. When implanted into a rat abdominal aorta defect model, the graft was able to facilitate luminal EC coverage, smooth muscle cells infiltration and collagen deposition without causing stenosis or thrombosis. The combination of bi-oriented topography with surface functionalization may become a platform design to maintain patency and accelerate in situ tissue regeneration of SDVG.
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