Green synthesis of novel in-situ micro/submicron-Cu paste for semiconductor interconnection

A green method for the synthesis of in-situ Cu paste is developed. Cu particles are prepared through chemical reduction by selecting a special copper source, reducing agent, and solvent. Then the reaction solution is directly concentrated to obtain an in-situ Cu paste. The synthesis of Cu particles and the preparation of Cu paste are conducted simultaneously, and the process of separation, purification, drying, storage, and re-dispersion of powder are reduced. Particles are not directly exposed to air, thus the oxidation of micro/nano-Cu is effectively prevented, and the agglomeration of particles caused by drying and dispersion operations is simultaneously reduced. Furthermore, the proposed method has a certain universality, and different types of Cu sources can be used to prepare in-situ paste with different sizes and morphologies. The entire preparation process is simple, efficient, green, and the yield can reach 99.99%, which breaks through the bottleneck of the application of traditional micro/nano-Cu materials. Copper acetate based in-situ paste is sintered for 30 min at 260 °C and 2 MPa in a reducing atmosphere. The shear strength, resistivity, and thermal conductivity reach 55.26 MPa, 4.01 × 10-8 Ω·m, and 92.75 W/(m·K), respectively, which could meet the interconnection application of power semiconductor devices.

Synthesis of Copper–nitrogen Codoped Carbon Quantum Dots Using Frangipani as a Carbon Source and Application of Metronidazole Determination

High-fluorescence Cu/N codoped carbon quantum dots (Cu/NCQDs) were prepared by a one-step hydrothermal method using frangipani as the carbon source and copper acetate as the copper source. The Cu/NCQDs exhibited high-intensity, stable blue fluorescence that is independent of the excitation wavelength. Since metronidazole can effectively quench the fluorescence intensity of Cu/NCQDs, a metronidazole fluorescence-detection method using Cu/NCQDs as the fluorescence probe was developed, and the quenching mechanism was studied.The method has the advantages of simplicity, speed, and low cost. Besides,it has a wider linear range and detection limit. Further, the metronidazole content in actual samples was determined by this method, with good results.

Cu-Based Conductive MOF Grown in situ on Cu Foam as a Highly Selective and Stable Non-Enzymatic Glucose Sensor

A non-enzymatic electrochemical sensor for glucose detection is executed by using a conductive metal–organic framework (MOF) Cu-MOF, which is built from the 2,3,6,7,10,11-hexahydroxytriphenylene (HHTP) ligand and copper acetate by hydrothermal reaction. The Cu-MOF demonstrates superior electrocatalytic activity for glucose oxidation under alkaline pH conditions. As an excellent non-enzymatic sensor, the Cu-MOF grown on Cu foam (Cu-MOF/CF) displays an ultra-low detection limit of 0.076 μM through a wide concentration range (0.001–0.95 mM) and a strong sensitivity of 30,030 mA μM−1 cm−2. Overall, the Cu-MOF/CF exhibits a low detection limit, high selectivity, excellent stability, fast response time, and good practical application feasibility for glucose detection and can promote the development of MOF materials in the field of electrochemical sensors.

Corrosion performance and morphological analysis of activated zinc phosphate coating formed on steel surface

Purpose The purpose of this paper is to study the effect of different concentrations of pretreatment solution of copper acetate (1, 5 and 10 g/L) on the deposition, growth and protection ability of zinc phosphate coating. Design/methodology/approach Zinc phosphate coatings were deposited on steel surface by immersion method. Scanning electron microscopy (SEM) and energy-dispersive spectroscopy (EDS) were used to study the morphological evolution and chemical analysis of formed coatings. The electrochemical performance of the coatings was evaluated via potentiodynamic polarization curves, electrochemical impedance spectroscopy (EIS) and immersion test in an aerated 3.5% NaCl solution. Findings The results showed that the activation treatment accelerated the deposition of the phosphate coating and improved its surface coverage. A higher phosphate coating weight (7.35 g/m2) and more compact structure was obtained with pretreatment solution of 1 g/L copper acetate. Electrochemical results revealed that the protection ability of the phosphated substrates was markedly enhanced after the pretreatment, and the best corrosion protection was obtained with a concentration of 1 g/L copper acetate solution. The corrosion current density of phosphated substrate was reduced by 64.9% after activation treatment with 1 g/L copper acetate solution. Originality/value In this investigation, dense, stable and compact zinc phosphate layers with improved corrosion resistance were formed on a carbon steel surface after activation pretreatment with copper acetate solution prior to a phosphating step.

Copper acetate-facilitated transfer-free growth of high-quality graphene advancing hydrovoltaic electricity generators

ABSTRACT Direct synthesis of high-quality graphene on dielectric substrates without a transfer process is of vital importance to aim at a variety of applications. Current strategies for boosting high-quality graphene growth, such as remote metal catalyzation otherwise are limited by poor performance with respect to the release of metal catalysts and hence suffer from the problem of metal residues. Herein, we report an effective approach that utilizes a metal-containing species, copper acetate, to continuously supply copper clusters in a gaseous form to aid transfer-free growth of graphene over a wafer scale. The thus-derived graphene films were found to show reduced multilayer density and improved electrical performance and exhibited a carrier mobility of 8500 cm2 V−1 s−1. Furthermore, droplet-based hydrovoltaic electricity generator devices based on directly grown graphene were found to exhibit robust voltage output and long cyclic stability, in stark contrast to their counterpart based on transferred graphene, demonstrating its potential for emerging energy harvesting applications. The work presented here offers a promising solution to organize the metal catalytic booster toward the transfer-free synthesis of high-quality graphene and enable smart energy generation.

Synthesis of CuAl2O4 Nanoparticle and Its Conversion to CuO Nanorods

The molten salt approach was used to convert CuAl2O4 nanoparticles to CuO nanorods in this study. Molten hydroxide (NaOH) synthesis was chosen over molten salts (NaCl/KCl) for removing aluminium oxide from copper aluminate at low temperatures. The molten salt process is environmentally beneficial. Polymeric precursors were used to make nanosized copper aluminates. Alginic acid polymer is used to gel aqueous solutions of copper acetate and aluminium nitrate, yielding precursor after further heating. The precursor provides 14 nm nanosized copper aluminates after being heated at 900°C for 5 hours. XRD, FTIR, SEM, and TEM were used to characterize the nanosized copper aluminate powder. Solid state mixing and solution technique were used to investigate molten hydroxide treatment of spinel CuAl2O4. The products of the reaction were identified using XRD. FTIR and SEM are also used to analyze the sample. Using UV-DRS absorbance spectrum analysis, the optical characteristics of CuAl2O4 and CuO nanorods were examined. Using the Tauc plot method, the band gaps of CuAl2O4 and CuO were calculated to be 4.3 and 3.93 eV.

Tyrosinase@HKUST-1: A Super Stable Biocatalyst Efficient for Catecholic Product Synthesis

Although metal-organic frameworks (MOFs) have been considered as promising matrices for enzyme immobilization, HKUST-1, constructed from copper acetate (CuAc2) and benzene 1,3,5-tricarboxylate (BTC), has rarely been explored for this application. In this study, mushroom tyrosinase (EC 1.14.18.1) was immobilized in the form of tyrosinase@HKUST-1 following a simple reaction procedure we developed. The order of mixing BTC with the enzyme prior to addition of CuAc2 is believed to be responsible for the super stability exhibited by the immobilized enzyme so formed. The resultant biocatalyst was characterized in both structural features and catalytic properties. Upon incorporation into the HKUST-1 frameworks, the enzyme gained a prominent enhancement in stability against pH, temperature and storage: When incubated at 50 oC and pH 6.0, tyrosinase@HKUST-1 presented a half-life of 32.6 h, which is 77-fold and over 10-fold higher than that of the free enzyme and its other immobilization forms, respectively; and the catalyst fully maintained its activity for at least 2 months when stored at 30 oC. The applicability of this new biocatalyst was demonstrated by employing it as catalyst for regioselective ortho-hydroxylation reactions to produce catecholic products with huge pharmacological effects, i.e., hydroxytyrosol and L-DOPA, with excellent yields and productivities. This study has thus offered a facile immobilization method to prepare a novel biocatalyst with super stability, and tyrosinase@HKUST-1 so formed from crude mushroom extract provides an efficient catalyst which can be applied to the production of catecholic products with health benefits.

Antimicrobial materials produced by incorporating copper acetate into ethylene-vinyl alcohol copolymer for its use in personal care and cosmetic packaging

Currently, there is a great demand for functional materials with effective pathogen-killing properties. In this research, we describe the use of green technology “reactive extrusion” for the synthesis of potent antimicrobial materials based on Ethylene-vinyl alcohol copolymer (EVOH). Herein, the antimicrobial agent, copper (II) acetate was used without pretreatment and introduced into the EVOH matrices at high temperatures. The thermal reaction of copper (II) acetate within the EVOH matrices and their effect on the thermal and thermomechanical properties of the polymer were investigated in regards to their concentration. The physicochemical, thermal, and rheological features, as well as, metal salt release kinetics were reported. The antimicrobial agent had significant effects on the properties of the matrix. Results showed a reduction in the glass transition temperatures and storage modulus of the materials in response to the incorporation of copper (II) acetate. Finally, the antimicrobial activity of the products was studied and demonstrated a possibility to create antimicrobial materials in a one-step, solvent-free extrusion process.