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ACS Applied Nano Materials · 2024 · IF 5.3

Colorimetric Agarose Gel Sensors Based on Cu-Doped Carbon Nanowires

Yu-Ying Wang,Xiao-Yang Zhang,Shu-Lan Li,Feng-Lei Jiang,Peng Jiang,Yi Liu

The colorimetric sensor has made great achievements in glucose sensing and diabetes prediction due to its simplicity, visualization, and lack of need for sophisticated instruments. The noninvasive sampling method has received more attention. Herein, a colorimetric agarose gel sensor was constructed by combining Cu-doped carbon nanowires (CuCNWs) with excellent peroxidase-like activity and glucose oxidase (GOx). CuCNWs can effectively catalyze the oxidation of 3,3′,5,5′-tetramethylbenzidine (TMB) with a maximum catalytic rate of 12.5 × 10–8 M s–1, which is superior to most nanomaterials reported. The modification by PVP can significantly improve the stability of CuCNWs under physiological conditions without affecting their catalytic activity. By introducing GOx, the sensitive detections of hydrogen peroxide (H2O2) and glucose in a wide range with the limit of detection as low as 30 nM and 0.2 μM can be achieved. Notably, the colorimetric agarose gel sensor exhibits a higher sensitivity than commercial test strips in detecting glucose in solution. Furthermore, it was applied to the detection of urine glucose. Diabetic urine can be easily distinguished from normal urine by judging color changes with the naked eye. This work is of great significance in guiding the construction of colorimetric agarose gel sensors and expands the applications of nanozymes in the biosensing fields.

CAS / MDL: 70-18-8 54827-17-7
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CERAMICS INTERNATIONAL · 2024 · IF 5.1

Functional modification of TC4 by Cu-containing titanium dioxide films

Zhiwei Su,Yi Ren,Yanwen Zhou,Caibo Yan,Tingdong Ren

To improve the biological fouling and corrosion resistance of Ti6Al4V (TC4) in marine environments, copper-containing titanium dioxide (TiO 2 (Cu)) films were prepared by magnetron sputtering TiO 2 (Cu) powder targets. The morphologies of the films showed that they became rough and coarse from 1.6 nm of the TiO 2 film to approximately 9 nm of the TiO 2 (Cu) films, which might be owing to the increase in the deposition rates from 1.33 to 2.08 nm/min. No diffraction orientations of the TiO 2 and Cu phases were found compared to those of the TiO 2 (Cu) powder. Ti, O, and Cu were detected using X-ray photoelectron spectroscopy to confirm the composition of the films. The ratio of Cu 2+ increased as the Cu content of the films increased, whereas that of Cu/Cu  +  scarcely changed. The TiO 2 and TiO 2 (Cu) films exhibited photocatalytic effects and their photocatalytic intensities decreased as the Cu content increased. Hydrophobicity was enhanced by the addition of Cu to the film. The antibiological fouling effect of the TiO 2 (Cu) films remained unchanged as the Cu/Ti ratio varied. Compared with those of TC4 , the corrosion current densities of the TiO 2 (Cu) films decreased by one order of magnitude and the corrosion potentials increased by 350 mV in artificial seawater , indicating that the corrosion resistance of TiO 2 (Cu)/TC4 was improved. Importantly, Cu was in abundance in the films for both antibiological and corrosion resistance functions owing to the saturated ratio of Cu/Cu + irrespective of the Cu/Ti ratio in the films.

CAS / MDL: 13463-67-7 111-30-8
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JOURNAL OF THE ELECTROCHEMICAL SOCIETY · 2024 ·Vol. 171 ·期 5 ·053507 · IF 3.1

Fabrication of Cu-Ni Alloy Microcomponents using Localized Electrochemical Deposition

Wenzheng Wu,Xiaojie Tang,Jing Wang,Chenghan Zhao

With the rapid development of electronics, additive manufacturing of complex three-dimensional microscale metal and alloy structures has emerged as one of the future directions for advanced technologies. In this study, a localized electrochemical deposition technique was developed which enables the fabrication of microscale three-dimensional metal structures in an ambient environment. Notably, we investigated the effects of voltage, initial electrode gap, and electrolyte composition on the deposition of Cu-Ni alloy. Furthermore, we successfully fabricated Cu-Ni equiatomic micro-columns, providing possibilities for the micro/nanoscale fabrication of commercial K-Monel copper. Finally, based on these foundations, we successfully shaped overhanging structures with various angles as well as an "H" structure using a rotating cathode substrate, demonstrating their potential in the fabrication of Cu-Ni alloy micro components.

CAS / MDL: 7786-81-4 68-04-2
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FREE RADICAL BIOLOGY AND MEDICINE · 2024 · IF 7.1

Identification of tanshinone I as a natural Cu(II) ionophore

Ya-Long Zheng,Yuan Ji,Yan Li,Shuai Yan,Xiao-Rong Ren,Wei Tang,Fang Dai,Bo Zhou

The development of Cu(II) ionophores for targeted disruption of aberrant redox homeostasis in cancer cells has been considered an appealing strategy in the field of anticancer research. This study presents the first identification of tanshinone I ( Ts1 ), a natural o -quinone, as a Cu(II) ionophore. Structure-activity relationship studies on tanshinones and mechanistic investigations reveal that the presence of Cu(II) effectively promotes the tautomerization of Ts1 from its diketo to keto-enol forms, thereby facilitating its sequential proton-loss Cu(II) chelation, and enabling it to function as a Cu(II) ionophore due to its structural features including the presence of an o -quinone moiety, a benzyl hydrogen, and a large conjugated system. The unique property allows Ts1 to preferentially induce copper accumulation in human hepatoma HepG2 cells over human umbilical vein endothelial cells, by releasing copper driven by reduced glutathione (GSH). This copper accumulation leads to a reduction in the GSH-to-oxidized glutathione ratio and the generation of reactive oxygen species, ultimately triggering apoptosis of HepG2 cells. The findings not only provide support for o -quinones as innovative types of anticancer Cu(II) ionophores, but also shed light on the previously unrecognized role of Ts1 as a potent Cu(II) ionophore for eradicating cancer cells by selectively disrupting their redox regulation programs, resembling a "Trojan horse".

CAS / MDL: 35825-57-1 568-72-9
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TALANTA · 2025 · IF 6.1

Nonenzymatic glucose electrochemical sensor based on Pd–Cu bimetallic aerogels

Zhanhong Li,Mengyi Jiang,Dingxi Lu,Yuwei Wang,Haotian Li,Wen Sun,Jianjun Long,Itthipon Jeerapan,Jean Louis Marty,Zhigang Zhu

This study introduces a novel nonenzymatic glucose electrochemical sensor based on palladium-copper bimetallic aerogels (Pd–Cu BMA) synthesized through a facile self-assembly reduction method. The Pd–Cu BMA exhibits a three-dimensional network structure formed by interconnected nanowires, which facilitates rapid electron transfer and offers abundant active sites for catalysis. Benefiting from the synergistic effect of Pd and Cu, the Pd–Cu (2:1) aerogels demonstrates remarkable electrocatalytic activity and stability under neutral conditions. Specifically, this sensor achieves a rapid response to glucose oxidation at an applied potential of 0 V, with a linear detection range up to 20 mM and a limit of detection as low as 43.4 μM. Notably, it maintains high catalytic activity over one month and shows excellent anti-interference performance against common physiological interferents. For practical application, the sensor can accurately detect additional glucose in diluted serum within the concentration range of 1–20 mM and in undiluted serum from 1 to 4 mM, thereby validating its potential for real-time monitoring of glucose levels in physiological samples. This innovative design of Pd–Cu bimetallic aerogels not only enhances the performance of nonenzymatic glucose sensors but also paves the way for the development of advanced materials for point-of-care diagnostics.

CAS / MDL: 16919-73-6
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MATERIALS SCIENCE FORUM · 2018 · IF 0

A Facile Method of Preparing Core/Shell Cu@Mo Powders

De Zhi Wang,Yu Qing Zhang,Bo Hua Duan

In this work, Molybdenum trioxide and conventional copper particles were used as precursors, reduced in hydrogen atmosphere. Then Cu@Mo Powders were successfully synthesized. Effects of reduction temperature on the microstructure of the composite powders and the performance of the intermediate product (molybdenum dioxide) were investigated. Results show that 700°C is the optimal reduction temperature, because Mo is reduced from its oxide and forms a coating layer on the surface of copper particles tightly without serious crack. Mo-20wt.% Cu composite powders where Cu is coated uniformly with continuous molybdenum layer are successfully obtained by co-reduction method.

CAS / MDL: 1313-27-5
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ACS Applied Materials & Interfaces · 2017 · IF 7.504

Cu(II)-Doped Polydopamine-Coated Gold Nanorods for Tumor Theranostics

Shuwei Liu,Lu Wang,Min Lin,Dandan Wang,Ziqi Song,Shuyao Li,Rui Ge,Xue Zhang,Yi Liu,Zhimin Li,Hongchen Sun,Bai Yang,Hao Zhang

Gold nanorods (AuNRs) are potentially useful in tumor theranostics, but the poor stability, high toxicity, and rapid removal by the immune system seriously limit their theranostic applications. In our study, we demonstrate the fabrication of Cu(II)-doped polydopamine-coated AuNR (AuNR@CuPDA), which significantly improves the potentials in tumor theranostics. Besides the improvement of physiological stability and biocompatibility, the PDA shell increases the photothermal performance and prolongs the blood circulation time of AuNRs. The half-life of AuNRs during blood circulation increases from 0.7 to 4.5 h after PDA coating, and the injected dose per gram of tumor tissue is 4.6% ID g–1 for AuNR@CuPDA. In addition to computer tomography imaging, the loading of Cu(II) in PDA shell endows AuNR@CuPDA with magnetic resonance imaging function. Cu(II) doped in PDA shell also exhibits chemotherapeutic behavior, and the tumor inhibitor rate is 31.2%. Further combining 808 nm laser-driven photothermal therapy, tumors were completely ablated, and no recurrence was observed. Liver and renal functions tests and histological analysis of major organs confirm that AuNR@CuPDA is in good safety.

CAS / MDL: 57-09-0 151-21-3
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ACS Applied Nano Materials · 2025 · IF 5.5

Cu Nanocrystals on Carbon Nitride for the CO2 Reduction Reaction

Pengxuan Wu,Wanbing Ma,Yuxin Ge,Jinbao Xu,Minglei Lu,Xia Li,Liang Ma,Song Bai,Tiejun Wang

A facile one-step method was developed to promote the carbon dioxide reduction reaction (CRR) activities to form the C2 products (C2H4 and C2H5OH) via the capping agent and organic solvent-free involvement of copper (Cu) on graphitic carbon nitride (GCN). By tuning the using amount of the Cu precursor, Cu-GCN-0.2 exhibited a total Faradaic efficiency (FE) of more than 86.69 ± 0.73% for the C1 species (CO, CH4, HCOOH) and C2 species (C2H5OH, C2H4) as the CRR products when the electrolysis was carried out at an overpotential of 0.7 V (vs RHE) even after 12 h electrocatalysis and at a ratio of about 1:1 for C2/C1. Further investigation confirms that the enhanced CRR activities can be ascribed to three aspects: Firstl’y, smartl’y regulation of the Cu involvement during the synthesis of GCN created the CRR active site, which enables more CO2 to be adsorbed and activated at a lower overpotential to participate in the C–C couple procedures. Secondly, the neglected HER active site was formed when Cu was involved, which enables the well-maintained proton generation and adsorption activities for the proton-coupled electron transfer procedures, leading to the promoted C2/C1 ratio. Thirdly, the decreased electronic resistance accelerates the electronic transfer speed, which enables a faster reaction rate and a promoted long-term durability performance. This research provides a facile method for the rational construction and preparation of the electrocatalyst toward large-scale utilization in sustainable conversion and application.

CAS / MDL: 57-13-6 298-14-6
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COLLOIDS AND SURFACES A-PHYSICOCHEMICAL AND ENGINEERING ASPECTS · 2024 · IF 4.9

CuFe nanoparticles coupled Cu–Nx for enhancing oxygen reduction reaction

Xiaoting Cao,Lvzhou Li,Xu Dong,Xi Wang,Xiaoshuang Zhou,Jiangnan Li,Ningyi Yuan,Jianning Ding

For the large-scale development of zinc-air batteries (ZABs), designing efficient, and cost-effective oxygen reduction reaction (ORR) electrocatalysts is crucial yet challenging. Herein, CuFe nanoparticles coupled with Cu–N x active sites co-anchored on 2D nitrogen–doped porous carbon nanosheets (CuFe@Cu–N–C) were obtained by the pyrolysis of Cu–MOF–74, nitrogen source, and ferric salt. The 2D porous carbon structure and the coupling effect between CuFe nanoparticles and Cu–Nx active sites endowed the CuFe@Cu–N–C electrocatalyst with excellent ORR electrocatalytic performance. Consequently, the CuFe@Cu–N–C electrocatalyst exhibited enhanced ORR activity with a higher half–wave potential than Cu–N–C, surpassing even that of the commercial 20 % Pt/C by 21 mV in alkaline media. Additionally, the CuFe@Cu–N–C electrocatalyst exhibited superior ORR stability to commercial 20 % Pt/C. Primary ZABs assembled with the CuFe@Cu–N–C as the cathode ORR electrocatalyst also showed excellent electrochemical properties. The work shows that the prepared CuFe@Cu–N–C electrocatalyst can serve as an ideal alternative to Pt-based catalysts for ZABs.

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ACS Applied Nano Materials · 2024 · IF 5.3

Au–Cu Janus Nanostructures as NIR-II Photothermal Antibacterial Agents

Qiuping Yang,Haixia Kong,Liwei Tang,Yanyun Ma,Feng Liu,Maochang Liu,Yi Wang,Pu Zhang,Yiqun Zheng

Metal nanoparticles have been found to exhibit a broad spectrum of antibacterial activities, yet not all metals possess the captivating plasmonic properties necessary for effective interaction with incident light. In this study, we demonstrate the feasibility of synergistically enhancing the Cu-induced antibacterial activity through the incorporation of plasmonic photothermal therapy by hybridlike anchoring the Cu component on a gold (Au) nanoplate that can effectively absorb near-infrared light. To fabricate the Janus structure, plate-like Au seeds were mixed with copper(ii) nitrate, cetyltrimethylammonium bromide, ascorbic acid, and hexamethylenetetramine, resulting in the formation of Au–Cu Janus nanostructures (JNSs). Notably, the plasmonic absorption of Au was preserved without being hindered by the Cu coating. Photothermal measurements revealed that the temperature rise of Au–Cu JNSs aqueous suspensions could reach up to 28.3 °C in just 10 min when exposed to 1064 nm laser light at a power density of 1 W·cm–2, with a photothermal conversion efficiency of 42.14%. Additionally, they show broad-spectrum antibacterial properties, making them potential contenders for addressing a wide range of bacterial infections. Our findings demonstrate that the antibacterial performance of metal nanoparticles composed of less plasmon-active components but with exceptional antibacterial properties can be significantly enhanced by coupling them with a plasmon-active nano-antenna through a Janus architecture. The Au–Cu JNSs possess potential application prospects in photothermal therapy, broad-spectrum antibacterial treatments, biomedical imaging, targeted drug delivery, sensitive diagnostics, and the development of advanced materials.

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MATERIALS RESEARCH BULLETIN · 2017 · IF 2.446

Optical properties of bimetallic Au-Cu nanocrystals embedded in glass

Yijun Zhang,Yu Jin,Meiling He,Lei Zhou,Tao Xu,Rongrong Yuan,Sai Lin,Weidong Xiang,Xiaojuan Liang

Bimetallic gold-copper and gold-copper solid solutions nanocrystals (NCs) with orthorhombic morphologies were successfully embedded in sodium borosilicate glass; these materials were fabricated via a facile and synthetic sol-gel technique. Microstructural investigations demonstrate that the Au-Cu intermetallic nanostructure is generated in the glass host. Z-scan technique was applied to reveal the third-order nonlinear optical properties of the as-obtained glasses at the wavelength of 800   nm. The as-synthesized glasses exhibit similar nonlinear behaviors with reverse saturation absorption effects and self-focusing performances. The third-order nonlinear susceptibility χ (3) values were optimized by tuning the sizes of the Au-Cu NCs. The χ (3) of Au-Cu(1), Au-Cu(2) and Au-Cu(3) measured to be 3.1   ×   10 −12 , 5.4   ×   10 −12 , and 4.4   ×   10 −12   esu for the single-pulse energy of 1   μJ. We have discussed the nonlinear optical mechanism of Au-Cu sodium borosilicate glass that may be due to the quantum confinement effects and surface plasmon resonance effects.

CAS / MDL: 10031-43-3 16961-25-4
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MATERIALS RESEARCH BULLETIN · 2025 · IF 5.7

Flexible pressure sensor based on Cu mesh/ZnO nanorod/graphene

Panting Zheng,Pengfei Zhao,Jijun Ding,Haixia Chen,Yongfeng Qu

Flexible pressure sensors have wide range of applications in fields such as electronic skin, medical detection and wearable devices. In this paper, a flexible piezoresistive pressure sensor based on Cu mesh/ZnO nanorod/graphene pressure-active layer is designed. Cu mesh is used as the conductive substrate, which not only enhances sensor performance but also expands the detection range of the sensor with its interlaced grid structure. To enhance the stability of the sensor, the graphene-functionalized polyvinylidene fluoride (PVDF) film is inserted between this active layer and the bottom electrodes, which prevents the direct contact between the Cu mesh and the electrodes, increases the electron transport channel and enhances the responsiveness of the sensor. The sensor shows sensitivity of 0.4 kPa -1 over pressure range of 0-0.5 kPa, as well as response time of 413 ms. Based on the excellent characteristics, a 4×4 pressure sensor array is constructed for the application of pressure sensors in daily life and human activity detection, which enables high-resolution detection and provides a reliable idea for the design of flexible sensors in the future.

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