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ANALYTICA CHIMICA ACTA · 2025 · IF 6

Simultaneous Detection of Cu+ and Cu2+ Using Dual-functionalized Glass Micropipette Sensors

Guofeng Wang,Shiwei Xu,Chao Deng,Yueyue Feng,Liying Huang,Qin Guo,Yajun Wang,Min Zhang,Qian Shi,Nannan Liu

Copper ions (Cu + and Cu 2+ ) are vital for physiological functions, and their imbalance is implicated in disease progression. However, simultaneous detection of both species is challenging due to their similar properties. Here, we report a dual-functionalized glass micropipette sensor enabling independent detection of Cu + and Cu 2+ . UiO-66-NH 2 was grown in situ on the inner wall to capture Cu 2+ via amino coordination, reducing ionic current. Glutathione-functionalized carbon nanotubes (GCNTs) coated on the outer surface bind Cu + , increasing SERS signal via enhanced surface defects. The sensor exhibits a wide detection range (10 -1 –10 5 μM), a detection limit of 0.1 μM, and allows simultaneous monitoring of Cu + /Cu 2+ in the physiological range (2–10 μM). It further distinguishes copper ion levels in MCF-10A and MCF-7 cells, revealing altered copper homeostasis in cancer. This platform offers a sensitive, selective tool for studying copper in biological systems.

CAS / MDL: 25952-53-8 6066-82-6
✓ 已验证 产品关联 DOI PubMed 高影响因子
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CATALYSIS LETTERS · 2025 ·Vol. 155 ·期 6 ·1-14 · IF 2.4

Schottky Heterojunction of Core–Shell Cu/CuO/Cu2O for Efficient Photocatalytic Degradation

Yang Ke,Zhou Bo,Dong Kun,Wu Yan,Huang Qu,Lv Jingbo,Wan Ziyi,Yang Mingzhu

With the acceleration of industrialization and urbanization, the treatment of organic pollutants in water bodies has become a global problem. Photocatalytic technology is regarded as an ideal solution due to its green and efficient characteristics. However, traditional powder catalysts have the problem of difficult recovery. Using copper foam as the substrate to load photocatalysts is a feasible solution. Cu/CuO/Cu 2 O with a core–shell structure was prepared by a simple solvothermal method based on copper foam. Under visible light irradiation, the Cu/CuO/Cu 2 O catalyst has a high catalytic efficiency for Congo red (95% within 180 min) and a significant adsorption and degradation ability for tetracycline hydrochloride. The results of the density functional theory calculation and electrochemical tests reveal that a Schottky heterojunction forms between Cu 2 O and CuO, the band gap of Cu 2 O is 0.57 eV, and the free energy of Cu/CuO/Cu 2 O is 0.24 eV, close to 0 eV, revealing the ternary composite’s possibility to evolve hydrogen. The heterojunction generated by Cu 2 O and CuO improves the material’s charge transport efficiency. Furthermore, this ternary composite based on copper foam easy to recycle and reuse, and can maintain nearly 90% degradation efficiency after 8 cycles. This concept offers a method for planning and building interfaces in nanocomposite structures. Graphical

✓ 已验证 DOI 高影响因子
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Nano Research · 2021 ·Vol. 14 ·期 8 ·2831-2836 · IF 8.897

Cu2Sb decorated Cu nanowire arrays for selective electrocatalytic CO2 to CO conversion

Mou Shiyong,Li Yonghao,Yue Luchao,Liang Jie,Luo Yonglan,Liu Qian,Li Tingshuai,Lu Siyu,Asiri Abdullah M.,Xiong Xiaoli,Ma Dongwei,Sun Xuping

The advancement of cost-effective and selective electrocatalyst towards CO 2 to CO conversion is crucial for renewable energy conversion and storage, thus to achieve carbon-neutral cycle in a sustainable manner. In this communication, we report that Cu 2 Sb decorated Cu nanowire arrays on Cu foil act as a highly active and selective electrocatalyst for CO 2 to CO conversion. In CO 2 -saturated 0.1 M KHCO 3 , it achieves a high Faraday efficiency (FE) of 86.5% for CO, at −0.90 V vs. reversible hydrogen electrode (RHE). The H 2 /CO ratio is tunable from 0.08:1 to 5.9:1 by adjusting the potential. It is worth noting that HCOO − product was totally suppressed on such catalyst, compared with Sb counterpart. The improving selectivity for CO could be attributed to the bimetallic effect and nanowire arrays structure.

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MATERIALS CHEMISTRY AND PHYSICS · 2019 · IF 2.781

Catalytic reduction of 4-nitrophenol over graphene supported Cu@Ni bimetallic nanowires

Zhiqiang Xu,Xianhua He,Mingwei Liang,Lijuan Sun,Di Li,Kenan Xie,Li Liao

Catalytic reduction of 4-nitrophenol (4-NP) to 4-aminophenol (4-AP) over high-performance non-noble metal catalysts is attracting intensive attention. Herein, we report a graphene supported Cu@Ni bimetallic nanowires catalyst by a facile liquid phase reduction method with the assistance of an external magnetic field. The morphology and structure of the composite are studied by SEM, TEM and XPS. The vibrating sample magnetometer (VSM) is used to analyze its magnetic properties . Owing to the synergistic effect of graphene and bimetallic nanowires, the catalyst shows superior catalytic performance and excellent stability. The results of catalysis exhibit an extraordinary rate constant (1.16 min −1 ) and activity factor (5.81 min −1  mg −1 ) at room temperature, which are much higher than a majority of non-noble metal catalysts, even noble metal catalysts. Also, compared with noble metal catalyst, the novel catalyst possesses ferromagnetism , which facilitates the separation of catalyst and reaction system, and guarantees recyclability. Moreover, a possible synergistic catalytic mechanism based on the fact that electron transfer between copper-nickel nanowires and graphene has been proposed. It is believed that the novel catalyst has a great importance for the application of nanowires in the field of catalysis.

✓ 已验证 DOI 高影响因子
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MOLECULES · 2022 ·Vol. 27 ·期 9 ·2933 · IF 4.927

Cations Modulated Assembly of Triol-Ligand Modified Cu-Centered Anderson-Evans Polyanions

Yiran Wang,Fengxue Duan,Xiaoting Liu,Bao Li

Counter-cations are essential components of polyoxometalates (POMs), which have a distinct influence on the solubility, stabilization, self-assembly, and functionality of POMs. To investigate the roles of cations in the packing of POMs, as a systematic investigation, herein, a series of triol-ligand covalently modified Cu-centered Anderson-Evans POMs with different counter ions were prepared in an aqueous solution and characterized by various techniques including single-crystal X-ray diffraction. Using the strategy of controlling Mo sources, in the presence of triol ligand, NH4+, Cu2+and Na+were introduced successfully into POMs. When (NH4)6Mo7O24was selected, the counter cations of the produced POMs were ammonium ions, which resulted in the existence of clusters in the discrete state. Additionally, with the modulation of the pH of the solutions, the modified sites of triol ligands on the cluster can be controlled to form δ- or χ-isomers. By applying MoO3in the same reaction, Cu2+ions served as linkers to connect triol-ligand modified polyanions into chains. When Na4Mo8O26was employed as the Mo source to react with triol ligands in the presence of CuCl2, two 2-D networks were obtained with {Na4(H2O)14} or {{Na2(H2O)4} sub-clusters as linkers, where the building blocks were δ/δ- and χ/χ-isomers, respectively. The present investigation reveals that the charges, sizes and coordination manners of the counter cations have an obvious influence on the assembled structure of polyanions.Keywords:polyoxometalate;Anderson-Evans;triol ligand;cation-modulation

✓ 已验证 DOI PubMed 高影响因子
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Catalysis Science & Technology · 2020 ·Vol. 10 ·期 21 ·7378-7385 · IF 5.721

Photoelectrocatalytic bacterial inactivation of Acinetobacter baumannii on Cu2O/TiO2@Cu mesh photoanodes

Mengna Ding,Fengyan Shi,Huijuan Zhu,Yuping Yang,Jiahui Zhong,Liulin Luo,Yuning Huo,Hexing Li

A hybrid Cu2O/TiO2 composite loaded on a Cu mesh (Cu2O/TiO2@Cu mesh) was developed via a supercritical solvothermal route. A uniformly distributed Cu2O/TiO2 p–n hetero-junction was stably coated on a Cu mesh, benefiting the visible-light harvesting. In comparison to electrochemistry and visible-light photocatalysis, the photoelectrochemistry process on the photoanode of the Cu2O/TiO2@Cu mesh presented improved bacterial inactivation activity for Acinetobacter baumannii. By means of the main active species of ˙O2− radicals, the photoelectrocatalytic process on the Cu2O/TiO2@Cu mesh also realized complete leakage of K+ ions, much stronger mineralization of the cell membrane and more efficient elimination of the self-recovery function, finally leading to cell death. In comparison, the electrochemistry process only led to the leakage of K+ ions without inactivation of bacteria, and the visible-light photocatalysis process induced partial leakage of K+ ions and cell mineralization after the death of most bacteria.

✓ 已验证 DOI 高影响因子
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Polymer Chemistry · 2021 ·Vol. 12 ·期 30 ·4347-4358 · IF 5.582

Cu-Catalyzed four-component polymerization of alkynes, sulfonyl azides, nucleophiles and electrophiles

Junnan He,Nan Zheng,Ming Li,YuBin Zheng,Wangze Song

Multicomponent polymerization has emerged as a promising strategy to develop functional polymers with versatile structures. In this work, a Cu-catalyzed four-component polymerization was developed using diynes, sulfonyl azides, nucleophiles, and a variety of electrophiles including alkyl glyoxylates, nitroalkenes, and Morita–Baylis–Hillman adducts to successfully synthesize a library of α-functionalized poly(N-sulfonylimidates)s with a wide substrate scope and high molecular weights (up to 20 000 g mol−1) in high yields (up to 86%). Such α-functionalized poly(N-sulfonylimidates)s could be further post-modified or utilized for the design of multi-functional and biodegradable polymers.

✓ 已验证 DOI 高影响因子
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RSC Advances · 2016 ·Vol. 6 ·期 20 ·16177-16182 · IF 3.289

N-Doped and Cu-doped TiO2-B nanowires with enhanced photoelectrochemical activity

Jingjie Su,Zhaodong Li,Yongquan Zhang,Yingjin Wei,Xudong Wang

TiO2-B is a metastable phase of titania with an interesting crystal structure and electrochemical properties. N-Doped and Cu-doped TiO2-B nanowires (NWs) were synthesized by hydrothermal and microwave-assisted hydrothermal methods, respectively. All the NWs are single crystal with the same crystal orientation regardless of the synthesis method and doping situation. The doped NWs together with their corresponding pristine NWs were fabricated into a photoelectrochemical (PEC) anode for water oxidation and their photoactivity performances were studied and compared under different illumination wavelength ranges. The Cu-doped TiO2-B NWs exhibited a significantly higher photocurrent density than all the other samples under direct Xe lamp illumination; while their performance rapidly dropped below the hydrothermal NWs when the UV illumination was cut off. On the contrary, N-doped TiO2-B NWs exhibited significantly enhanced photoactivity particularly in the visible light range. X-ray photoelectron spectroscopy revealed that N-doping could narrow the electronic bandgap of TiO2, while the Cu-doping had little impact on the bandgap but rather improved the electrical conductivity. This research provides a new insight into elemental and phase control of TiO2-based solar energy harvesters.

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Chem Catalysis · 2022 · IF 0

Boosting electrosynthesis of urea from N2 and CO2 by defective Cu-Bi

Wenjie Wu,Yulu Yang,Yitong Wang,Tiantian Lu,Qingsong Dong,Junwei Zhao,Jingyang Niu,Qingchao Liu,Zhaomin Hao,Shuyan Song

Electrosynthesis of urea from N 2 and CO 2 molecules is of immense significance but has so far been plagued by the lack of a universal design principle to guide the search for new catalysts. Herein, as exemplified by the Cu-Bi catalyst, our findings revealed that the defective Cu-Bi catalyst could offer a maximum urea concentration of 0.45 ± 0.06 mg L −1 and the largest faradaic efficiency of 8.7% ± 1.7% at −0.4 V (versus reversible hydrogen electrode [RHE]), exhibiting outstanding activity in contrast to monometallic (Cu and Bi) and bimetallic (Cu-Bi mixture and intact Cu-Bi) catalysts. Moreover, the evidence from isotope tracing experiments, in situ Raman spectroscopy, and density functional theory (DFT) calculations suggested that it is a promising strategy for the co-reduction of N 2 and CO 2 by defective Cu-Bi catalysts, switching on a light to the application of defects in electrosynthesis of urea.

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Catalysts · 2022 ·Vol. 12 ·期 12 ·1562 · IF 4.501

Promoting the Electrocatalytic Ethanol Oxidation Activity of Pt by Alloying with Cu

Di Liu,Hui-Zi Huang,Zhejiaji Zhu,Jiani Li,Li-Wei Chen,Xiao-Ting Jing,An-Xiang Yin

The development and commercialization of direct ethanol fuel cells requires active and durable electro-catalysts towards the ethanol oxidation reactions (EOR). Rational composition and morphology control of Pt-based alloy nanocrystals can not only enhance their EOR reactivity but also reduce the consumption of precious Pt. Herein, PtCu nanocubes (NCs)/CB enclosed by well-defined (100) facets were prepared by solution synthesis, exhibiting much higher mass activity (4.96 A mgPt−1) than PtCu nanoparticles (NPs)/CB with irregular shapes (3.26 A mgPt−1) and commercial Pt/C (1.67 A mgPt−1). CO stripping and in situ Fourier transform infrared spectroscopy (FTIR) experiments indicate that the alloying of Cu enhanced the adsorption of ethanol, accelerated the subsequent oxidation of intermediate species, and increased the resistance to CO poisoning of PtCu NCs/CB, as compared with commercial Pt/C. Therefore, alloying Pt with earth-abundant Cu under rational composition and surface control can optimize its surface and electronic structures and represents a promising strategy to promote the performance of electro-catalysts while reduce the use of precious metals.Keywords:Pt–Cu alloy;nanocubes;electrocatalysis;ethanol oxidation reaction;in situ FTIR

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CRYSTENGCOMM · 2014 ·Vol. 16 ·期 38 ·9054-9062 · IF 3.858

Stirring-induced growth of hierarchical Cu structures in the presence of diamine

Zongjian Liu,Yuanyuan Chen,Yifan Zheng

We propose a novel strategy for the synthesis of materials with a hierarchical structure. This strategy is based on in situ combination of two processes, namely, capping agent-mediated oriented growth and stirring-induced aggregation, and the growth of Cu crystals in the presence of linear alkyl diamines of short carbon chain length under vigorous stirring is shown to demonstrate its feasibility. Our experimental results have shown that the oriented growth of Cu nanowires can be significantly disturbed by vigorous stirring, resulting in large-scale growth of hierarchical dendritic Cu crystals. The morphology of grown dendritic Cu crystals has been found to vary with the stirring rate, type of diamine, and diamine concentration, which makes it possible to prepare hierarchical Cu structures of various morphologies. The growth mechanism of these hierarchical Cu structures is proposed based on the experimental observations. The present unique strategy offers a fresh way to fabricate materials with a hierarchical structure.

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SPECTROCHIMICA ACTA PART A-MOLECULAR AND BIOMOLECULAR SPECTROSCOPY · 2013 · IF 1.977

Fluorescent detection of hydrogen peroxide and glucose with polyethyleneimine-templated Cu nanoclusters

Yu Ling,Na Zhang,Fei Qu,Ting Wen,Zhong Feng Gao,Nian Bing Li,Hong Qun Luo

An interesting, simple, and label-free strategy for the detection of hydrogen peroxide and glucose has been developed with polyethyleneimine (PEI)-capped copper nanoclusters as a fluorescence probe in aqueous solution. The PEI-templated Cu nanoclusters which we have synthesized have an average diameter of 1.8   nm and show a blue emission at 480   nm. In the presence of hydrogen peroxide, the fluorescence of the Cu nanoclusters is quenched. Similarly, glucose oxidase catalyzes the oxidation of glucose to gluconic acid and H 2 O 2 , so we can also use this probe to detect glucose. Because of the high zymolyte specificity of glucose oxidase, the detection of glucose has good selectivity. Under the optimized experimental conditions, the linear ranges for H 2 O 2 and glucose are 0.5–10   μM and 10–100   μM, respectively. And the detection limits for H 2 O 2 and glucose are 0.4 and 8   μM, respectively. Furthermore, we discussed the mechanism of fluorescence quenching which is caused by the interaction between H 2 O 2 and Cu nanoclusters. This sensing system has been applied successfully to the detection of glucose in human serum samples.

✓ 已验证 DOI PubMed 高影响因子
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