SPECTROCHIMICA ACTA PART A-MOLECULAR AND BIOMOLECULAR SPECTROSCOPY
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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.
研究领域:
分析化学
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生物医学
·
材料科学
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DOI
高影响因子
SENSORS AND ACTUATORS B-CHEMICAL
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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.
研究领域:
生物化学
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医学检测
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分析化学
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产品关联
DOI
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
研究领域:
材料科学
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分析化学
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电化学
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产品关联
DOI
高影响因子
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.
研究领域:
分析化学
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纳米材料
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质谱分析
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临床诊断
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传感器
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产品关联
DOI
PubMed
高影响因子
Journal of Materials Chemistry A
·
2022
·Vol. 10
·期 29
·15543-15553
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IF 14.511
Weibin Chen,Yuxin Xie,Xuehui Gao,Lei Li,Zhan Lin
Multiple electronic structure modification is propitious for constructing strong metal–support interaction and then improving the electrocatalytic activity of supported catalysts, yet remains a great challenge due to the lack of facile protocols. Herein, we report a CoIr alloy supported on two dimensional (2D) graphitic-N doped carbon (CoIr@CN) through a one-step annealing process from an Ir-doped 2D Co-MOF, which exhibits a remarkably reduced Ir loading (2.69 wt%) and enhanced electrocatalytic activity for oxygen evolution reaction (OER) and hydrogen evolution reaction (HER). Ir plays an essential role of optimizing the properties of metal nanoparticles and simultaneously effecting the calcining process to adjust the N-doping structure, eventually modulating the synergetic effect between alloy nanoparticles and the N-doped carbon support. Owing to the positive effect of such multiple electronic structure optimization, the electron transfer between alloy nanoparticles and N-doped carbon is promoted to enable more moderate adsorption energies of reaction intermediates in both the OER and HER. Impressively, CoIr@CN exhibits a low OER/HER overpotential of 269 mV/70 mV to achieve a current density of 10 mA cm−2 in 1.0 M KOH, and 25 mV in 0.5 M H2SO4 for HER, as well as a negligible decay of catalytic activity after long-term stability measurements for OER/HER. This study offers an effective way for designing strong metal–support interaction through multiple electronic structure modification, which effectively improves the OER/HER performance of supported catalysts.
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产品关联
DOI
高影响因子
JOURNAL OF PHOTOCHEMISTRY AND PHOTOBIOLOGY A-CHEMISTRY
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2020
·
IF 3.306
Xiaoye Wen,Li Yan,Zhefeng Fan
A novel and simple probe (denoted LN-1) with AIE property based on malononitrile and 4-diethylaminobenzaldehyde was designed and synthesized. The use of two different mechanisms for the independent detection of Fe 3+ and CN − is more convenient and efficient than the continuous detection of anions and cations. The detection mechanism was verified by mass spectrometry (MS), nuclear magnetic resonance (NMR) spectrum, and particle size distribution. Under optimized experimental conditions, excellent calibration curves were obtained for the LN-1-Fe 3+ and the LN-1-CN − with detection limits of 0.17 and 0.39 μM, respectively. This method was successfully applied to detect the content of Fe 3+ and total inorganic iron in actual samples. Owing to its low cytotoxicity, good biocompatibility, and enhanced orange emission in aqueous solution, the LN-1 was successfully applied for CN − imaging in live cells. In addition, Fe 3+ and EDTA incorporation into the LN-1 changed the fluorescent intensity, which is beneficial in constructing ultrasensitive INHIBIT logic gate.
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DOI
高影响因子
EcoMat
·
2024
·
IF 10.7
Junming Shi,Guoyang Gao,Can Jin,Hongqing Wu,Weizhen Wang,Yulong An,Zhen Zhou,Zhanhua Huang,Wenshuai Chen
Value-added conversion of lignocellulose is a sustainable approach. Photo-refining biomass is in line with current environmental protection strategies. However, photo-reforming biomass suffers from poor catalyst stability and low conversion efficiency. Here, we designed fructose as a lignocellulosic model. The heterogeneous structure of Prussian blue coating was constructed with a special covalent bond structure of Co CN Zn. This structure has a catalytic conversion mechanism that can accelerate electron transfer. Fructose was simultaneously converted to value-added platform compounds (5-HMF and formic acid) and gaseous fuels (CO, CH 4 ) with a conversion rate of up to 92.5%, which is more than 1.7 times than that of catalysts without adding Prussian blue. Hydrogen transfer and carbon transfer on the carbon atoms of fructose facilitates the production and accelerates the spillover of CO from formic acid. This work provides new ideas for the development of Prussian blue catalysts and the conversion of pentose.
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产品关联
DOI
高影响因子
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.
研究领域:
材料科学
·
电化学
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DOI
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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产品关联
DOI
高影响因子
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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产品关联
DOI
高影响因子
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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产品关联
DOI
PubMed
高影响因子
JOURNAL OF CATALYSIS
·
2021
·
IF 7.92
Yunchao Feng,Sishi Long,Guihua Yan,Wenlong Jia,Yong Sun,Xing Tang,Zehui Zhang,Xianhai Zeng,Lu Lin
Developing the active and environmentally friendly non-noble nano-catalysts is highly desired to transform biomass-derived platform into value chemicals. Herein, we report a low-cost and sustainable cobalt/nitrogen-doped carbon catalyst containing both metallic Co and Co-N components exhibits satisfying activity for the oxidative esterification of 5-hydroxymethylfurfural and other investigated alcohols in methanol without the base additive under mild conditions. Experimental results show that an appropriate ratio of Co to Co-N is responsible for the high activity of the Co/Co-N/CN catalysts towards oxidative esterification. Theoretical computational results demonstrate that the Co/Co-N group synergistically promotes electron transfer from the Co adatom to the surface oxygen atoms, facilitates O 2 adsorption and activation on the Co sites, and further reduces the energy barrier for the oxidation of alcohols to aldehydes, all of which contribute to the overall activity of oxidative esterification of alcohols to the corresponding esters. In addition to exhibiting superior intrinsic activity, the as-prepared Co/Co-N/CN catalyst also shows excellent stability and recyclability.
研究领域:
催化
·
材料科学
·
化学工程
·
环境科学
✓ 已验证
DOI
高影响因子
危险品化学品经营许可证（带存储）