SENSORS AND ACTUATORS B-CHEMICAL
·
2025
·
IF 7.7
Xiaotong Wang,Tongtong Ye,Shaohui Geng,Shuna Ren,Xuming Zhao,Lihua Chen
A dual-signal strategy was developed based on a coordination reaction between iron(II) ions (Fe 2+ ) and potassium hexacyanoferrate(III) (K 3 [Fe(CN) 6 ]) to distinguish between brucella vaccine and wild strain. Utilizing metal-organic frameworks (MOFs), MOF Al (aluminum) @Fe 2+ @P 1 and MOF Fe @P 2 were synthesized and affixed to a hyaluronic acid (HA)-doped electrode. Hairpin probe 1 (P 1 ) has a common sequence (P 1 ') recognizing a fragment (T 1 ) in vaccines and wild strains. In contrast, hairpin probe 2 (P 2 ) has a differential sequence (P 2 ') only targeting a specific fragment (T 2 ) in the wild strain. Experimental findings indicated that activation of T 1 led to the dissociation of P 1 from MOF Al @Fe 2+ @P 1 , which released Fe 2+ into a buffer containing trace Fe 2+ . Following this, the addition of hydrogen peroxide (H 2 O 2 ) and K 3 [Fe(CN) 6 ] resulted in the formation of KFe[Fe(CN) 6 ] (PB). In contrast, specific activation of T 2 caused the detachment of P 2 from MOF Fe , thereby exposing its catalytic site. In H 2 O 2 , this catalytic site facilitated the conversion of trace Fe 2+ in buffer to Fe 3+ , with no PB generated after the addition of K 3 [Fe(CN) 6 ]. Simultaneous activation of T 1 and T 2 promoted the oxidation of Fe 2+ released from MOF Al by the exposed catalytic site of MOF Fe . The ratio of K 3 [Fe(CN) 6 ] to PB exhibited dynamic changes. Specifically, the ratio below 2.37 ± 0.05 indicated a Brucella-positive sample, whereas a ratio under 0.9 ± 0.02 suggested a sample derived from the vaccine. The scarcity of dual-signal sensors employing coordination reactions underscores the significance of this approach. Moreover, it addressed the challenges associated with brucella detection, demonstrating robust analytical performance.
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高影响因子
JOURNAL OF ELECTROANALYTICAL CHEMISTRY
·
2025
·
IF 4.1
Sumin Xu,Wenjing Liu,Jiajia Zhang,Jianying Qu
In this work, a MOF-on-MOF synthesis strategy was employed to successfully prepare (ZIF-8)-on-(CoCu-MOF) composites, which were further pyrolyzed at high temperature to obtain CoCu-CN nanomaterials. The morphological and structural properties of the materials were systematically investigated using SEM, FTIR, XRD and XPS. A novel sensor of CoCu-CN/GCE was constructed at a glassy carbon (GC) substrate, which exhibited excellent electrocatalytic activity to redox reactions of acetaminophen (PA) and p-aminophenol (4-AP). Under optimal conditions, the CoCu-CN/GCE sensor can be employed to detect simultaneously PA and 4-AP in the wider linear ranges of 0.05–270.00 μM and 0.05–170.00 μM, respectively with the lower detection limits of 0.020 μM and 0.019 μM respectively. Practical sample analysis for pharmaceutical and lake water gave satisfactory results. The proposed sensor displays excellent selectivity and stability with potential analytical applications
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ANALYTICAL CHEMISTRY
·
2025
·
IF 6.7
Yangyang Li,Yongqi Wang,Dumei Ma,Chuan-Fan Ding,Yinghua Yan
Enhancing the ionization efficiency of saccharides remains a significant challenge in matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI-TOF MS). Herein, novel MOF-derived erythrocyte-like CuO/Cu2O@ZnO–CN nanomaterials were designed as a MALDI matrix for various saccharides’ detection. The ZIF-8-derived ZnO framework maintained its intrinsic porosity while gaining uniformly distributed C/N-doped catalytic sites. Copper oxides integration further induced an erythrocyte-like morphology with a substantially larger surface area. The CuO/Cu2O@ZnO–CN matrix demonstrated superior performance over conventional CHCA and DHB in LDI-MS analysis of saccharides (Xyl, Glc, and Malt), featuring the advantages of excellent conductivity and stability, minimum background interference, excellent ionization efficiency, high salt and protein tolerance, and remarkable specificity. The developed method enabled accurate glucose quantification in human serum (0.5–9 mM linear range, R2 = 0.998) with a low limit of detection (LOD) of 0.28 mM via internal standardization. Good reproducibility and reliability of the method were verified by intraday (1.7–5.6%) and interday precision (2.2–8.2%) and accuracy (93.8 to 101.6%). Analysis of glucose of human serum from healthy people and diabetes patients indicated the matrix’s potential application in clinical analysis.
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PubMed
高影响因子
SPECTROCHIMICA ACTA PART A-MOLECULAR AND BIOMOLECULAR SPECTROSCOPY
·
2021
·
IF 4.098
Liangqiang Wu,Yan Liu,Xiaodong Wu,Yapeng Li,Jianshi Du,Shaolong Qi,Qingbiao Yang,Hai Xu,Yaoxian Li
We have successfully synthesized NIRF as a near-infrared fluorescence probe for relay recognition of zinc and cyanide ions. The probe possesses well selectivity and anti-interference ability over common ions towards Zn 2+ and CN – . The results showed that Zn 2+ and the probe formed [NIRF-Zn 2+ ] complex after added Zn 2+ into the probe NIRF solution, which emited red fluorescence. The probe can be used for quantitative detection of Zn 2+ with a detection limit of 4.61 × 10 −8 M. It was determined that the binding stoichiometry between the NIRF and Zn 2+ was 1:1 according to the job , s curve. Subsequently, CN – was added to the NIRF-Zn 2+ solution, CN – combined with Zn 2+ to generate [Zn(CN – ) x ] 1-x due to the stronger binding ability between zinc ion and cyanogen, which lead to the red fluorescence disappeared. The quantitative detection of CN – was realized with a detection limit of 7.9 × 10 *7 M. In addition, the probe has excellent specificity and selectivity for Zn 2+ and CN – . And the probe can be stable in a wide range of pH. Through biological experiments, we found that it can complete cell imaging in macrophages and imaging of living mice, which has application prospects in Bioimaging. In addition, the probe NIRF has good applicability for Zn 2+ and CN – detection in actual samples.
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高影响因子
JOURNAL OF ALLOYS AND COMPOUNDS
·
2023
·
IF 6.2
Min Wang,Dehua Xin,Wei Zhang,Dan Luo,Guoqiang Tan
The optimization of the photogenerated carriers’ relaxation dynamics process is critical for the improvement of photocatalytic performance. Herein, a ternary heterojunction with multilevel charge transfer channels was constructed by coupling plasma Ag, nitrogen vacancies carbon nitride (NVs-CN) and Bi 2 O 2-δ CO 3 . Ag/NVs-CN/Bi 2 O 2-δ CO 3 heterojunction showed the S-scheme mechanism, which not only promoted the interfacial charge transfer, but also enhanced the driving force for redox reactions. The defect states induced by nitrogen vacancies and oxygen vacancies provided an additional energy level platforms for hot electrons relaxation of plasma Ag, resulting in the improved separation efficiency and utilization rate of the high-energy hot carriers. Hence, the prepared Ag/NVs-CN/Bi 2-δ O 2 CO 3 heterojunction exhibited the markedly boosted full-spectrum driven catalytic activity for antibiotics degradation. 80.5% and 83.8% of tetracycline and ciprofloxacin could be mineralized into H 2 O and CO 2 by the optimal heterojunction under visible light irradiation, and the corresponding mineralization efficiencies could reach 81.7% and 81.5% under NIR light irradiation. The proposed multichannel charge transfer mechanism provided a new insight into the design and preparation of high-active full-spectrum responsive heterojunction photocatalysts.
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JOURNAL OF ALLOYS AND COMPOUNDS
·
2023
·
IF 6.2
Pengfei Zhu,Xiaolong Wu,Xingyang Xiao,Ming Duan,Dan Luo,Jinru Lin
In this work, Bi 12 O 17 Cl 2 and ZIF-8 were synthesized via a facile in-situ precipitation method, while ZnO-CN was obtained through the pyrolysis of ZIF-8. Then, a novel Bi 12 O 17 Cl 2 /ZnO-CN composite catalyst with Z-scheme heterojunction was prepared by mechanical mixing-low temperature activation method. When the ZnO-CN is pyrolyzed at 550 ℃ and accounts for 10 wt% in the Bi 12 O 17 Cl 2 /ZnO-CN composite, the composite exhibited a significantly higher degradation rate for levofloxacin hydrochloride (LVX) (94.50%) compared to Bi 12 O 17 Cl 2 (67.30%) and ZnO-CN (36.80%), while also achieving a high removal rate of Cr(VI) under acidic conditions (92.00%). And the toxicity of LVX to wheat decreased significantly after photocatalytic degradation. Meanwhile, the Bi 12 O 17 Cl 2 /ZnO-CN has good universality, salt resistance and reuse stability. The experimental results of sample characterization show that the improved photocatalytic performance of Bi 12 O 17 Cl 2 /ZnO-CN composite can be attributed to the high-efficiency separation of electron-hole pairs (e - -h + ), enhanced light absorption in the visible region, increased specific surface area and active sites. Both the free radical capture experiment and electron paramagnetic resonance (EPR) test indicate that •O 2 - and h + are the primary active species in the process of degrading LVX by Bi 12 O 17 Cl 2 /ZnO-CN. Combined with mechanism exploration experiment and iquid chromatography-mass spectrometry (LC-MS) analysis, a possible direct Z-scheme heterojunction electron transfer mechanism and photocatalytic degradation pathways for LVX was proposed. This work enhances the photocatalytic performance of Bi 12 O 17 Cl 2 and provides an idea for antibiotic or Cr(VI) wastewater treatment.
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Inorganic Chemistry Frontiers
·
2023
·Vol. 10
·期 24
·7274-7284
·
IF 7
Yulin Kong,Yawei Xiao,Shutao Zhang,Liang Chen,Zhaoping Liu,Yude Wang
Aqueous zinc-ion batteries (AZIBs) are considered promising energy storage devices for future large-scale energy storage systems due to their high safety, low production cost, and non-combustibility. However, low operating voltage and energy output are still drawbacks in their practical applications. Herein, we develop a cubic aluminum hexacyanoferrate/graphene high-voltage cathode material for rechargeable AZIBs, and it exhibits an activation process and can deliver a high output voltage of 1.8 V (vs. Zn/Zn2+) with a specific energy density of 125.56 W h kg−1. The voltage is increased by stretching the Fe–C bonds in the Fe–CN–Al covalent structure. The reversible phase transformation between cubic AlFe(CN)6 and cubic–orthorhombic–monoclinic Zn0.5AlFe(CN)6 occurs with the intercalation/extraction of zinc ions, and the coordination environment of Al plays a decisive role in this key process. This work will provide a feasible reference for the structural design of high-voltage Prussian blue analog cathode materials.
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Small Methods
·
2022
·Vol. 6
·期 8
·2200404
·
IF 15.367
Chun-Mei Xu,Jian Peng,Xiao-Hao Liu,Wei-Hong Lai,Xiang-Xi He,Zhuo Yang,Jia-Zhao Wang,Yun Qiao,Li Li,Shu-Lei Chou
Prussian blue analogues (PBAs) have attracted extensive attention as cathode materials in sodium-ion batteries (SIBs) due to their low cost, high theoretical capacity, and facile synthesis process. However, it is of great challenge to control the crystal vacancies and interstitial water formed during the aqueous co-precipitation method, which are also the key factors in determining the electrochemical performance. Herein, an antioxidant and chelating agent co-assisted non-aqueous ball-milling method to generate highly-crystallized Na 2- x Fe[Fe(CN) 6 ] y with hollow structure is proposed by suppressing the speed and space of crystal growth. The as-prepared Na 2- x Fe[Fe(CN) 6 ] y hollow nanospheres show low vacancies and interstitial water content, leading to a high sodium content. As a result, the Na-rich Na 1.51 Fe[Fe(CN) 6 ] 0.87 ·1.83H 2 O hollow nanospheres exhibit a high initial Coulombic efficiency, excellent cycling stability, and rate performance via a highly reversible two-phase transition reaction confirmed by in situ X-ray diffraction. It delivers a specific capacity of 124.2 mAh g −1 at 17 mA g −1 , presenting ultra-high rate capability (84.1 mAh g −1 at 3400 mA g −1 ) and cycling stability (65.3% capacity retention after 1000 cycles at 170 mA g −1 ). Furthermore, the as-reported non-aqueous ball-milling method could be regarded as a promising method for the scalable production of PBAs as cathode materials for high-performance SIBs.
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高影响因子
Food Bioscience
·
2026
·
IF 6.2
Zixian Xia,Xiaoyan Guan,Rui Liu,Yeting Wu,Yingying Li,Mengmeng Liu,Yifeng Ding,Xiaohong Wang,Youyou Lu
Bifidobacterium faces major challenges in the gastrointestinal tract, including inactivation under acidic conditions and insufficient targeted release. In this study, three novel heterologous dual-protein complex systems were constructed by lactoferrin (LF) with α-lactalbumin (ALA), β-lactoglobulin (BLG), casein (CN). Subsequently, sodium alginate (SA) -cross-linked gel microcapsules loaded with these dual-protein complexes and B. animalis F1-7. The optimal preparation conditions for the dual-protein were as follows: ALA/LF = 1.5, 50 °C; BLG/LF = 2, 50 °C; CN/LF = 0.5, 25 °C. Incorporation of SA and endogenous emulsification method enabled efficient encapsulation of B . animalis F1-7, achieving encapsulation efficiency exceeding 90%. B. animalis F1-7@SA-(LF-ALA/BLG/CN) exhibited strong acid resistance, favorable intestinal responsiveness, and significantly improved microbial viability. The microcapsules enhanced gastric acid tolerance primarily through a spatial barrier effect, while the incorporation of dual-protein components contributed to matrix structural reinforcement and digestion-responsive release behavior. This integrated “physical protection-structural modulation” strategy also conferred excellent 28-day storage stability. In vitro experiments by mice/human feces, combined with 16S rRNA and metabolomics analysis, revealed that the composite microcapsules effectively regulated the structure of the microbial community and altered metabolite profiles (e.g. , pathways involved in nitrogen metabolism). Overall, this study provided reproducible preparation parameters and a theoretical basis for SA-based dual-protein composite encapsulation delivery systems, and offered a promising strategy to address the coordinated challenges of activity, controlled release, and storage stability of sensitive food bioactive microorganisms or nutrients.
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高影响因子
CATALYSIS LETTERS
·
2025
·Vol. 155
·期 11
·1-12
·
IF 2.4
Lu Wei,Zhou Liang
Photocatalytic regeneration of nicotinamide adenine dinucleotide (NADH) is indispensable for the sustainability of enzyme-driven industrial processes. In this study, we developed a Z-scheme heterogeneous photocatalyst consisting of CdS and g-C 3 N 4 , which markedly enhanced visible-light absorption and photogenerated charge separation efficiency, and applied it to an in situ visible-light-driven NADH regeneration system. The synthesized catalyst afforded an exceptional NADH regeneration yield of 97.88% within just 15 min. Additionally, enzyme activity assays utilizing alcohol dehydrogenase (ADH) demonstrated that 67.60% of NAD + was successfully converted into the enzymatically fraction, 1,4-NADH. Furthermore, formate dehydrogenase (FDH) immobilized on ZIF-8 was integrated into this NADH regeneration system, enabling highly sustainable biosynthesis of formic acid. During a 2 h continuous reaction, the integrated system successfully accumulated a total formic acid concentration of 0.88 mM. This novel Z-scheme photocatalytic system thus presented a highly effective solution for regenerating active NADH, providing valuable insights and promoting the development of photocatalysis-driven enzymatic systems for sustainable solar-to-chemical energy conversion. Graphical
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高影响因子
MICROCHIMICA ACTA
·
2022
·Vol. 189
·期 11
·1-10
·
IF 6.408
Fan Ru,Tian Jinrong,Wang Huili,Wang Xuedong,Zhou Peipei
By employing NH 2 -MIL-88 as a template, we synthesized the intermediate Fe@CN under high-temperature calcination and further fabricated the FeS 2 @CN nanocomposites in the presence of sulfur powder. Under varying temperatures (300–600 °C) and Fe@CN-to-S ratios (1:3–6), FeS 2 @CN 500-5 nanocomposites had the highest peroxidase-mimetic activity. Under optimized conditions (incubation temperature 40 °C; solution pH 4.0 and nanocomposite concentration 10 μg/mL; 652-nm absorption), the Michaelis-Menten constant ( K m ) of FeS 2 @CN was much lower than that of horseradish peroxidase (HRP), therefore demonstrating that it had a higher affinity for both chromogenic substrates than conventional HRP. The limits of detection for H 2 O 2 and glucose were 0.15 and 0.30 μmol/L, respectively, and the recoveries for glucose were 91.8–103% with RSDs <5.2%. The novelty of this study lies in (1) the FeS 2 @CN was confirmed to possess stronger enzyme-mimetic activity than its precursors (NH 2 -MIL-88 and Fe@CN); (2) the enhanced activity resulted from the unsaturated sites of N and S doping and the plentiful defects on the porous carbon surface; and (3) free radical trapping experiments evidenced that •OH played a major role in the catalytic reaction, while h + and •O 2 − simultaneously participated in the catalytic process. These convincing performance metrics lead us to postulate that the FeS 2 @CN-based colorimetric biosensor provides a promising approach for several real-world applications, such as point-of-care diagnosis and workplace health evaluations. Graphical abstract
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高影响因子
Inorganic Chemistry Frontiers
·
2026
·
IF 6.2
Maxim V. Mikhailenko,Tatiana Yu. Astakhova,Elena N. Timokhina,Maxim A. Faraonov,Alexey V. Kuzmin,Salavat S. Khasanov,Denis V. Korchagin,Gennady V. Shilov,Akihiro Otsuka,Hiroshi Kitagawa,Dmitri V. Konarev
A series of anionic bi- and trinuclear complexes of CoII, FeII and MnII with hexaazatrinaphthylene (HATNA) and hexaazatriphenylenehexacarbonitrile (HAT(CN)6), incorporating paramagnetic Cp*2Fe+ cations (S = 1/2), were obtained. It was demonstrated that even a mild Cp*2Fe reductant can be used to reduce metal complexes of HAT-type ligands. Metal iodides were transferred from the pristine powder to the complexes in a non-coordinating solvent via complex formation with spiropyran or tetrabutylammonium iodide. The isostructural complexes (Cp*2Fe+)[(MIII2)2·HATNA]−·C6H4Cl2·0.5C6H14 (M = Co (1), Fe (2) and Mn (3)) contain monoanionic [(MIII2)2·HATNA]− units, which alternate in π-stacks with Cp*2Fe+ cations and also form π-stacked [(MIII2)2·HATNA−]2 dimers. Metal ion coordination is asymmetric, featuring one short and one long M–N bond. The short M–N bonds are 1.973(6) Å for CoII (1), 2.039(4) Å for FeII (2), and 2.115(4) Å for MnII (3); these are the shortest bonds reported to date among studied HAT-based complexes for CoII and FeII. These complexes exhibit very strong antiferromagnetic metal–radical coupling, which isolates their high-spin ground states at high temperatures. To the best of our knowledge, the exchange coupling value of −300 cm−1 observed for 3 is the highest among MnII-containing complexes based on a radical ligand with delocalized spin. Compound (Cp*2Fe+)[(FeIII2)3·HATNA]−·C6H4Cl2 (4) is unique due to its magnetic behavior, which is severely different from that previously observed for similar trinuclear radical FeII-containing HAT-based complexes. Instead of a smooth increase in the χMT value with a temperature decrease, attributed to the formation of a high-spin system, a rapid increase below 30 K is observed. Trinuclear trianionic species [(FeIII2)3·HAT(CN)6]3− are isolated in (Cp*2Fe+)3[(FeIII2)3·HAT(CN)6]3−·4C6H4Cl2 (5) and do not participate in intermolecular exchange coupling. The unusual magnetic behavior of 5 can only be described by a model implying different signs of D for metal ions in the complex. Such a feature arises from the substantial difference in the coordination geometry of one Fe1 ion compared to the other two Fe2 ions.
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