Materials Research Express
·
2016
·Vol. 3
·期 6
·065018
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IF 0.968
Pinhua Zhang,Guangliang Cui,Chuanhai Xiao,Mingzhe Zhang,Li Chen,Changmin Shi
We fabricated an Ag decorated Cu (Ag@Cu) nano/microstructure ordered array by facile template-free 2D electrodeposition combined with a galvanic reduction method for SERS applications. The Cu nano/microstructure ordered arrays were first synthesized by a 2D electrodeposition method, then Ag nanocubes were decorated on the arrays by galvanic reduction without any capping agent. The pollution-free surface and edge-to-face heterostructure of Ag nanocubes and Cu nano/microstructure arrays provide the powerful field-enhancements for SERS performance. The results verified that the Ag@Cu nano/microstructure ordered arrays have excellent activity for 4-Mercaptopyridine, and the sensitivity limit is as low as 10−8 M. Therefore, this facile route provides a useful platform for the fabrication of a SERS substrate based on nano/microstructure ordered arrays.
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RSC Advances
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2016
·Vol. 6
·期 94
·91394-91400
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IF 3.289
Jie Xue,Jizhong Song,Yousheng Zou,Chengxue Huo,Yuhui Dong,Leimeng Xu,Jianhai Li,Haibo Zeng
Compared to monometallic counterparts, core–shell structured nanowires may possess additional performances or even new properties because of synergistic effects between two components. Particularly, the alloying shell may bring the advantage that we can adjust its components and sizes to achieve the desired performance. Here, we mainly study Ni-dependent electric stability and opto-electrical performances of Cu@CuNi NW electrodes. And we find that the increase of nickel content has little effect on optical performance, but effectively improves the stability of Cu@CuNi NW electrodes. We can also achieve ideal performance through regulating the nickel content and outstanding performance may come from the particular structure. Hence we studied Ni-dependent microstructure variations of Cu@CuNi NWs with the corresponding properties. The high stability NWs with a high nickel content have smooth CuNi alloying shells which effectively protect the NWs from oxidation. At the same time, the large length diameter ratio and high degree of crystallinity of Cu@CuNi NWs are the reasons for good transparent conductive properties. These demonstrations of controlling the composition of alloying shells for oxidation resistance of the NWs could bring forth great opportunities for transparent, flexible, stretchable, and wearable electronic and optoelectronic devices.
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Asia-Pacific Journal of Chemical Engineering
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2017
·Vol. 12
·期 3
·422-431
·
IF 0.836
Yuan Wang,Wei Zhu,Shengya Sang,Lijing Gao,Guomin Xiao
Aqueous-phase processing of biomass-derived furfural is one of the promising ways to convert biomass into useful chemicals. Supported metal catalysts are crucial in the aqueous-phase hydrogenation of furfural. Understanding the effect of acid and basic properties of supports on the performance of the catalysts will help understand the reaction pathways and develop more efficient catalysts. Here, a series of Cu-based catalysts with different supports (Al 2 O 3 , ZnO, SiO 2 , MgO, and ZSM-5) have been investigated in hydrogenation of furfural in aqueous phase. The properties of the supports have been characterized by X-ray diffraction, N 2 adsorption–desorption, transmission electron microscope, H 2 temperature-programmed reduction, and CO 2 and NH 3 temperature-programmed desorption. The results show that pure acid support leads to the formation of oligomers and pure basic support results in furfuryl alcohol as the main product. And the mass balance in reaction system catalyzed by Cu-based catalysts with higher acidity amount is lower. © 2017 Curtin University of Technology and John Wiley & Sons, Ltd.
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JOURNAL OF ELECTRONIC MATERIALS
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2017
·Vol. 46
·期 7
·4676-4681
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IF 1.579
Han Wensong
Third-generation hyperbranched polyester (HBPE3) was synthesized by stepwise polymerization with N , N -diethylol-3-amine methylpropionate as AB 2 monomer and pentaerythritol as core molecule. Then, Cu particles were prepared by reduction of copper nitrate with ascorbic acid in aqueous solution using HBPE3 as template. Finally, Cu/SiO 2 particles were prepared by coating silica on the surface of Cu particles. The structure and morphology of the samples were characterized by Fourier-transform infrared (FT-IR) spectrometry, x-ray diffraction (XRD) analysis, transmission electron microscopy (TEM), scanning electron microscopy (SEM), and thermogravimetric analysis (TGA). The results confirmed the formation of the silica coating on the surface of Cu and that the Cu/SiO 2 particles had spherical shape with particle size in the range of 0.8 μ m to 2 μ m. Compared with pure Cu, the synthesized Cu/SiO 2 core–shell particles exhibited better oxidation resistance at high temperature. Moreover, the oxidation resistance of the Cu/SiO 2 particles increased significantly with increasing tetraethyl orthosilicate (TEOS) concentration.
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JOURNAL OF MAGNETISM AND MAGNETIC MATERIALS
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2016
·
IF 2.357
Cuicui Wang,Heyi Ge,Yueying Zhao,Shanshan Liu,Yu Zou,Wenbo Zhang
The folic acid functionalized magnetic graphene oxide (FA-mGO) as a new adsorbent has been synthesized in this work for the elimination of Cu(II) from waste water. The as-prepared FA-mGO was tested by SEM, TEM , particle size analyzer, FTIR, XRD, Roman spectrum, TGA and magnetic properties analyzer. Some factors, such as adsorbent dose, pH, contact time, initial concentration of adsorbate and temperature were explored. The results showed that the FA-mGO had the better adsorption performance than mGO. After 40 min, the adsorption equilibrium could be reached. Furthermore, the adsorption property obeyed the pseudo-second order kinetic model and the Temkin isotherms well. The maximum adsorption capacity was 283.29 mg/g for Cu(II) from Pseudo-second-order model at pH=5 and 318 K. The chelation action between FA and Cu(II) along with electrostatic incorporation between GO and Cu(II) determined the favourable adsorption property. Besides, thermodynamic studies results ∆G 0 <0, ∆H 0 >0, ∆S 0 >0 suggested that the adsorption mechanism was an endothermic and spontaneous process essentially. Finally, desorption and reusability studies imply FA-mGO has an excellent reproducibility and is benefit to environmental protection and resource conservation.
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CARBOHYDRATE POLYMERS
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2017
·
IF 4.811
Shidong Dai,Nana Prempeh,Dagang Liu,Yimin Fan,Mingyue Gu,Yu Chang
With the increasing demand of environmental monitoring for toxic and odorous ammonia gas it is desired to develop specific green, cost-effective and in situ passive colorimetric alternatives to current complex instrumentations. In this work, we designed an ammonia gas sensor based on cholesteric liquid crystal films of copper(II)-doped cellulose nanocrystals (CNC Cu(II)) whose structure, optical and sensing properties were investigated. The hybrid films using the low doping Cu(II) as a color-tuning agent inherited the chiral nematic signature and optical activity of CNCs, suggesting a strong chelation between copper ions and negatively charged CNCs. The sensing performance illustrates that the CNC Cu(II)125 film was sensitive to ammonia gas which could merge into nematic layers of CNCs and trigger-sensed to copper ions chelated on CNCs, consequently arousing a red-shift of reflective wavelength as well as an effective colorimetric transition. Such a hybrid film is anticipated to boost a new gas sensing regime for fast and effective on-site qualitative investigations.
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JOURNAL OF LUMINESCENCE
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2017
·
IF 2.686
Jinshui Liu,Bin Wang,Meijiao Xu,Lizhen Wang,Zihan Zhou
Polyethyleneimine-capped Cu nanoclusters (PEI-CuNCs) with a mean diameter of 2.5 nm and that emitted blue light at 485 nm were synthesized. The fluorescence of PEI-CuNCs was strongly quenched when Au(III) ions were present. Because of this specific response, a PEI-CuNC-based fluorescent turn-off sensor was developed. Under optimum conditions, a good linear relationship (R 2 =0.993) was found between the relative fluorescence intensity ( F 0 / F ) and the Au(III) ion concentration between 0.5 and 15 µM. The detection limit for Au(III) ions was 0.06 µM. The quenching mechanism was assessed by performing X-ray photoelectron spectroscopy spectra studies. The fluorescence quenching was ascribed to photo-induced electron transfer from the PEI-CuNCs to the AuCl 4 − occur. Using The method described is a new way of quantifying Au(III) ions.
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JOURNAL OF MATERIALS SCIENCE-MATERIALS IN ELECTRONICS
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2016
·Vol. 27
·期 12
·13280-13287
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IF 1.798
Liu Jingdong,Ji Hongjun,Wang Shuai,Li Mingyu
In this study, we present a new simple method using formic acid pretreatment to achieve low temperature sintering of Cu nanoparticles, and the Cu nanoparticles have been successfully prepared with a modified polyol method. For formic acid pretreatment, the spherical Cu nanoparticles with an average size of 30 nm were saturated with a mixed solution of formic acid and absolute ethanol directly. The surface composition analysis indicated that the initial oxide on the surface of Cu nanoparticles was completely removed, and formate was generated as a by-product which could decompose at low temperature. According to the thermal analysis results, it was found that the sintering temperature of Cu nanoparticles with formic acid pretreatment was reduced to 160 °C. And the corresponding microstructures further demonstrated that the emerging small exothermic peak of thermal curve over the temperature range between 120 and 160 °C was caused by the formation of sintering necks. The formic acid treated Cu nanoparticle films sintered at 260 and 320 °C exhibited an electrical resistivity of 6.1 and 3.6 μΩ cm respectively.
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SURFACE & COATINGS TECHNOLOGY
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2024
·
IF 5.3
Guangyin Liu,Yuhui Zhang,Chaofan Ma,Qin Tang,Hanbing Li,Shiqi Chen,Jun Shen
The gallium (Ga) base liquid metal (LM) with high thermal conductivity and deformability is applied widely in thermal management in electrical systems. However, Ga readily reacts with Cu to form intermetallic compounds (IMCs), which can cause failure in electronic devices. Herein, the thermal interface material (TIM) with Ga and diamond is prepared to analyze the reaction behavior of TIM and Cu/Ni-plated Cu under an aging test at 125 °C. The results show that Ga reacts with Cu substrate and forms CuGa 2 bulk. Moreover, Ni coating can inhibit the corrosion of Ga and Cu. However, the as-volcano IMC structures were generated, also. The thermal resistance increased from 2.24 mm 2 ·K·W −1 to 14.47 mm 2 ·K·W −1 from initial time to 200 h. The interfacial corrosion behavior between TIM and Cu substrate is studied by first-principles molecular dynamics simulation. The diffusion coefficient in the z direction of Cu is 0.04 × 10 −5 cm 2 /s. In a word, the work could provide the guidelines for the further design of high-performance corrosion resistance in the region where Ga was used for thermal management on electronic products.
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ACS Applied Energy Materials
·
2024
·
IF 5.4
Xiang Li,Zhitao Liu,Liyuan Zeng,Wanyi Ye,Guangxing Yang,Qiao Zhang,Shengjun Du,Zhiting Liu,Feng Peng
The CO2 electrochemical reduction (CO2ER) to produce valuable multicarbon products represents a promising approach for enhancing CO2 conversion. While previous research has investigated the impact of Cu electrode surface topography on C2 production, it is important to note that other parameters were also altered concurrently with changes in roughness. To isolate the specific effect of surface texture on CO2 electroreduction, this study prepared Cu layers with varying textures using the sputtering method with a varied sputtering time. To characterize the surface features of the sputtered Cu layers, the developed interfacial area ratio (Sdr), known as areal parameter, was introduced, with the aim of correlating it with C2 product selectivity. The results of this study indicate that the improved selectivity of C2 products can be attributed to higher Sdr values, primarily due to a rougher and finer surface texture that increases the local concentration of CO and OH–. This research underscores the significance of surface topography and offers perspectives for designing efficient Cu electrodes for the CO2ER.
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Journal of Environmental Sciences
·
2025
·
IF 6.3
Yansen Qu,Xin Li,Yingjie Xia,Haosheng Lan,Le Ding,Jing Zhong,Xinghua Chang
Accelerated industrialization combined with over-applied nitrogen fertilizers results in serious nitrate pollution in surface and ground water, disrupting the balance of the global nitrogen cycle. Electrochemical nitrate reduction (eNO 3 RR) emerges as an attractive strategy to simultaneously enable nitrate removal and decentralized ammonia fabrication, restoring the globally perturbed nitrogen cycle. However, complex deoxygenation-hydrogenation processes and sluggish proton-electron transfer kinetics significantly hinder practical application of eNO 3 RR. In this study, we developed carbon-coated Cu-Ni bimetallic catalysts derived from metal-organic frameworks (MOFs) to facilitate eNO 3 RR. The unique structural features of catalyst promote enhanced synergy between Cu and Ni, effectively addressing critical challenges in nitrate reduction. Comprehensive structural and electrochemical analysis demonstrate that electrochemical nitrate-to-nitrite conversion mainly takes place on active Cu sites, the introduction of Ni could efficiently accelerate the generation of aquatic active hydrogen, promoting the hydrogenation of oxynitrides during eNO 3 RR. In addition, Ni introduction could push up the d-band center of the catalyst, thus enhancing the adsorption and activation of nitrate and the corresponding intermediates. Detailed reaction pathways for nitrate-to-ammonia conversion are illuminated by rotating disk electrode (RDE), in-situ Fourier-transform infrared spectroscopy, in-situ Raman spectrum and electrochemical impedance spectroscopy (EIS). Benefiting from the synergistic effect of Cu and Ni, optimum catalyst exhibited excellent nitrate reduction performance. This work provides a new idea for elucidating the underlying eNO 3 RR reaction mechanisms and contributes a promising strategy for designing efficient bimetallic electrocatalysts.
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ACS Nanoscience Au
·
2024
·
IF 4.8
Dan Luo,Zhiheng Xie,Shuangqun Chen,Tianyi Yang,Yalin Guo,Ying Liu,Zhouhao Zhu,Liyong Gan,Lingmei Liu,Jianfeng Huang
Electrochemical semihydrogenation (ESH) of alkynes to alkenes is an appealing technique for producing pharmaceutical precursors and polymer monomers, while also preventing catalyst poisoning by alkyne impurities. Cu is recognized as a cost-effective and highly selective catalyst for ESH, whereas its activity is somewhat limited. Here, from a mechanistic standpoint, we hypothesize that electron-deficient Cu can enhance ESH activity by promoting the rate-determining step of alkene desorption. We test this hypothesis by utilizing Cu–Ag hybrids as electrocatalysts, developed through a welding process of Ag nanoparticles with Cu nanowires. Our findings reveal that these rationally engineered Cu–Ag hybrids exhibit a notable enhancement (2–4 times greater) in alkyne conversion rates compared to isolated Ag NPs or Cu NWs, while maintaining over 99% selectivity for alkene products. Through a combination of operando and computational studies, we verify that the electron-depleted Cu sites, resulting from electron transfer between Ag nanoparticles and Cu nanowires, effectively weaken the adsorption of alkenes, thereby substantially boosting ESH activity. This work not only provides mechanistic insights into ESH but also stimulates compelling strategies involving hybridizing distinct metals to optimize ESH activity.
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