scholarly journals Fundamental Mechanisms of Copper CMP – Passivation Kinetics of Copper in CMP Slurry Constituents

2009 ◽  
Vol 1157 ◽  
Author(s):  
Shantanu Tripathi ◽  
Fiona M. Doyle ◽  
David A. Dornfeld

AbstractDuring copper CMP, abrasives and asperities interact with the copper at the nano-scale, partially removing protective films. The local Cu oxidation rate increases, then decays with time as the protective film reforms. In order to estimate the copper removal rate and other Cu-CMP output parameters with a mechanistic model, the passivation kinetics of Cu, i.e. the decay of the oxidation current with time after an abrasive/copper interaction, are needed. For the first time in studying Cu-CMP, microelectrodes were used to reduce interference from capacitive charging, IR drops and low diffusion limited currents, problems typical with traditional macroelectrodes. Electrochemical impedance spectroscopy (EIS) was used to obtain the equivalent circuit elements associated with different electrochemical phenomena (capacitive, kinetics, diffusion etc.) at different polarization potentials. These circuit elements were used to interpret potential-step chronoamperometry results in inhibiting and passivating solutions, notably to distinguish between capacitive charging and Faradaic currents.Chronoamperometry of Cu in acidic aqueous glycine solution containing the corrosion inhibitor benzotriazole (BTA) displayed a very consistent current decay behavior at all potentials, indicating that the rate of current decay was controlled by diffusion of BTA to the surface. In basic aqueous glycine solution, Cu (which undergoes passivation by a mechanism similar to that operating in weakly acidic hydrogen peroxide slurries) displayed similar chronoamperometric behavior for the first second or so at all anodic potentials. Thereafter, the current densities at active potentials settled to values around those expected from polarization curves, whereas the current densities at passive potentials continued to decline. Oxidized Cu species typically formed at ‘active’ potentials were found to cause significant current decay at active potentials and at passive potentials before more protective passive films form. This was established from galvanostatic experiments.

Coatings ◽  
2021 ◽  
Vol 11 (1) ◽  
pp. 106
Author(s):  
Akbar Ali Samsath Begum ◽  
Raja Mohamed Abdul Vahith ◽  
Vijay Kotra ◽  
Mohammed Rafi Shaik ◽  
Abdelatty Abdelgawad ◽  
...  

In the present study, the corrosion inhibition effect of Spilanthes acmella aqueous leaves extract (SA-LE) on mild steel was investigated in 1.0 M HCl solution at different temperature using weight loss, Tafel polarization, linear polarization resistance (LPR), and electrochemical impedance (EIS) measurements. Adsorption of inhibitor on the surface of the mild steel obeyed both Langmuir and Temkin adsorption isotherms. The thermodynamic and kinetic parameters were also calculated to determine the mechanism of corrosion inhibition. The inhibition efficiency was found to increase with an increase in the inhibitor concentration i.e., Spilanthes acmella aqueous leaves extract, however, the inhibition efficiency decreased with an increase in the temperature. The phytochemical constituents with functional groups including electronegative hetero atoms such as N, O, and S in the extract adsorbed on the metal surface are found responsible for the effective performance of the inhibitor, which was confirmed by Fourier-transform infrared spectroscopy (FT-IR) and ultraviolet–visible spectroscopic (UV-Vis) studies. Protective film formation against corrosion was confirmed by scanning electron microscopy (SEM), atomic force microscopy (AFM), and contact angle studies. The result shows that the leaves extract acts as corrosion inhibitor and is able to promote surface protection by blocking active sites on the metal.


Hydrogen ◽  
2020 ◽  
Vol 1 (1) ◽  
pp. 11-21
Author(s):  
Youyi Sun ◽  
Alexey Y. Ganin

Metal alloys have become a ubiquitous choice as catalysts for electrochemical hydrogen evolution in alkaline media. However, scarce and expensive Pt remains the key electrocatalyst in acidic electrolytes, making the search for earth-abundant and cheaper alternatives important. Herein, we present a facile and efficient synthetic route towards polycrystalline Co3Mo and Co7Mo6 alloys. The single-phased nature of the alloys is confirmed by X-ray diffraction and electron microscopy. When electrochemically tested, they achieve competitively low overpotentials of 115 mV (Co3Mo) and 160 mV (Co7Mo6) at 10 mA cm−2 in 0.5 M H2SO4, and 120 mV (Co3Mo) and 160 mV (Co7Mo6) at 10 mA cm−2 in 1 M KOH. Both alloys outperform Co and Mo metals, which showed significantly higher overpotentials and lower current densities when tested under identical conditions, confirming the synergistic effect of the alloying. However, the low overpotential in Co3Mo comes at the price of stability. It rapidly becomes inactive when tested under applied potential bias. On the other hand, Co7Mo6 retains the current density over time without evidence of current decay. The findings demonstrate that even in free-standing form and without nanostructuring, polycrystalline bimetallic electrocatalysts could challenge the dominance of Pt in acidic media if ways for improving their stability were found.


2021 ◽  
Vol 11 (5) ◽  
pp. 13019-13030

The extract of Justicia secunda (JS) leaves was investigated as an eco‐friendly corrosion inhibitor of aluminum in 0.5 M HCl using weight loss, electrochemical impedance spectroscopy (EIS), potentiodynamic polarization (PDP), and scanning electron microscopy (SEM) techniques. The inhibitor concentrations used ranged from 50 to 250 ppm at 30, 40, and 50oC. Results show that Justicia secunda acts as a good inhibitor for aluminum. Its efficiency increased with increasing inhibitor concentration but decreased with increasing temperature. Maximum inhibition efficiency as high as 94.3% was found at 30°C for 250 ppm of the inhibitor with the weight loss technique. Tafel polarization results show that the extract acts as a mixed-type inhibitor. The Nyquist plots indicated decreasing double-layer capacitance and increasing charge transfer resistance on increasing JS concentration. The inhibition action occurred through the physical adsorption of the extract on the aluminum surface. The adsorption process was found to follow Langmuir adsorption isotherm. The formation of a protective film on the metal surface was confirmed by scanning electron microscopy.


Author(s):  
V. Dharmalingam ◽  
P. Arockia Sahayaraj ◽  
A. John Amalraj ◽  
R. Shobana ◽  
R. Mohan

The goal of studying corrosion process is to find means of minimizing corrosion or prevent it from occurring. The use of inhibitors is one of the most popular methods for corrosion protection. A protective film has been formed on the surface of the mild steel in a neutral aqueous environment using a synergistic mixture of an eco-friendly inhibitor viz., Potassium Sodium Tartrate (SPT) along with polyacrylic acid (PAA) and Zn2+ ions. The inhibiting effect of SPT, PAA and Zn2+ ions have been investigated by gravimetric studies, Potentiodynamic polarization and electrochemical impedance spectroscopy (EIS). The investigations revealed that SPT acts as an excellent synergist in corrosion inhibition. Optimum concentrations of all the three components of the ternary formulation are established by gravimetric studies. Potentiodynamic polarization studies inferred that this mixture functions as a cathodic inhibitor. EIS studies of the metal/solution interface indicated that the surface film is highly protective against the corrosion of mild steel. Surface characterization techniques (FTIR, SEM, AFM) are also used to ascertain the nature of the protective film. The mechanical aspect of corrosion inhibition is proposed.


Author(s):  
Muddasir Nawaz ◽  
Sehrish Habib ◽  
Adnan Khan ◽  
Abdul Shakoor ◽  
Ramazan Kahraman

The use of organic coating for the metals has been widely being used to protect the surface against corrosion. Polymeric coating incorporated with Nanocontainers loaded with inhibitor and self-healing provides better corrosion resistance. Cellulose microfibers (CMFs) used as smart carriers were synthesized and loaded with dodecylamine (DOC)-inhibitor and polyethyleneimine (PEI)-both inhibitor and self-healing agents. Smart polymeric coatings were developed by mixing CMF/DOC and CMFs/PEI into the epoxy matrix. Reference coatings (that has only CMFs) were also prepared for a compersion. Scanning electron microscope (SEM), X-ray diffraction spectroscopy (XRD), Fourier transform infrared spectroscopy (FTIR) and thermal gravitational analysis (TGA) were used to confirm the loading of DOC and PEI onto the CMFs. UV-vis analysis indicates that the self-release of inhibitor from CMFs is sensitive to pH of the solution and the immersion time. Recovery of controlled surface damage confirms the decent self-healing ability of the prepared smart coatings is due to the efficient release of inhibitor (DOC) and self-healing agent (PEI) in the damaged area leading to the formation of a protective film. Electrochemical impedance spectroscopy (EIS) results demonstrate that corrosion resistance of the smart coating increases with an increase in immersion time which is due to the progressive release of inhibitors from CMFs in response to the pH change. Therefore, smart coatings demonstrate superior properties as compared to the reference coatings. The study reveals the polymeric composite coatings have potential to inhibit the corrosion of steel for oil and gas industry.


2015 ◽  
Vol 228 ◽  
pp. 237-241
Author(s):  
Magdalena Popczyk ◽  
B. Łosiewicz

The Ni+MoS2composite coatings were prepared by electrodeposition under galvanostatic conditions from the Ni-plating bath containing suspended MoS2powder (100 mesh). Investigations of hydrogen evolution reaction (HER) were carried out using steady-state polarization measurements and electrochemical impedance spectroscopy (EIS) in 5 M KOH solution on the coatings obtained at 30, 40, and 50°C. It was found that the kinetics of the HER on the Ni+MoS2coatings decreases with the increase in the electrodeposition temperature of the coatings. This effect is attributed to decreasing content of MoS2(from 26.4 to 18.0 wt.%) embedded into the Ni matrix as composite crystalline component having the electrocatalytic properties towards the HER and/or surface development of the coatings. The higher amount of MoS2was embedded, the more porous electrodes containing pear-shape pores on the surface were produced what was detected by EIS.


2018 ◽  
Vol 36 (4) ◽  
pp. 373-384 ◽  
Author(s):  
Rachid Idouhli ◽  
Abdelouahd Oukhrib ◽  
Yassine Koumya ◽  
Abdesselam Abouelfida ◽  
Abdelaziz Benyaich ◽  
...  

AbstractThe inhibition efficiency of Atlas cedar essential oil (ACEO) as a green corrosion inhibitor on steel in 1 m hydrochloric acidic was studied. The effects of temperature and the concentration of the ACEO inhibitor on the inhibition efficiency were studied. Potentiodynamic polarization and electrochemical impedance spectroscopy were used to test the performance of the inhibitor. We found that the inhibition efficiency of ACEO exceeded 88% at 1 g/l at 298 K and increased with increasing concentration. The evaluation of activation and thermodynamic parameters reveals that the organic molecules of cedar essential oil and its fractions act by chemical adsorption on the metal surface. The adsorption of the inhibitor on the surface of steel is in a good agreement with the Langmuir adsorption isotherm. Increasing concentration of the corrosion inhibitor enhances the surface coverage and formation of a protective film.


2021 ◽  
Vol 0 (0) ◽  
Author(s):  
André Weber

Abstract Solid Oxide Cells (SOCs) have gained an increasing interest as electrochemical energy converters due to their high efficiency, fuel flexibility and ability of reversible fuel cell/electrolysis operation. During the development process as well as in quality assurance tests, the performance of single cells and cell stacks is commonly evaluated by means of current/voltage- (CV-) characteristics. Despite of the fact that the measurement of a CV-characteristic seems to be simple compared to more complex, dynamic methods as electrochemical impedance spectroscopy or current interrupt techniques, the resulting performance strongly depends on the test setup and the chosen operating conditions. In this paper, the impact of different single cell testing environments and operating conditions on the CV-characteristic of high performance cells is discussed. The influence of cell size, contacting and current collection, contact pressure, fuel flow rate and composition on the achievable cell performance is presented and limitations arising from the test bed and testing conditions will be pointed out. As today’s high performance cells are capable of delivering current densities of several ampere per cm2 a special emphasis will be laid on single cell testing in this current range.


MRS Advances ◽  
2020 ◽  
Vol 5 (40-41) ◽  
pp. 2129-2137 ◽  
Author(s):  
Wenwen Dou ◽  
Wen Li ◽  
Yuchen Cai ◽  
Mengyao Dong ◽  
Xiaojing Wang ◽  
...  

ABSTRACTTo improve the corrosion resistance and to increase the hardness of copper substrate in marine environment, the Cu-Ni/Ni-P composite coatings were prepared on the copper substrate using the galvanostatic electrolytic deposition method. The deposition current densities were explored to find the optimized deposition conditions for forming the composite coatings. Corrosion resistance properties were analyzed using the polarization curves and electrochemical impedance spectroscopy (EIS). Considering the corrosion resistance and hardness, the −20 mA/cm2 was selected to deposit Cu-Ni coatings on copper substrate and the −30 mA/cm2 was selected to deposit Ni-P coating on the Cu-Ni layer. The Cu-Ni/Ni-P composite coatings not only exhibited superior corrosion resistance compared to single Cu-Ni coating in 3.5 wt.% NaCl solution, but also showed much better mechanical properties than single Cu-Ni coating.


Nanomaterials ◽  
2020 ◽  
Vol 10 (4) ◽  
pp. 791 ◽  
Author(s):  
Sehrish Habib ◽  
Eman Fayyad ◽  
Muddasir Nawaz ◽  
Adnan Khan ◽  
Rana A. Shakoor ◽  
...  

The utilization of self-healing cerium dioxide nanoparticles (CeO2), modified with organic corrosion inhibitors (dodecylamine (DDA) and n-methylthiourea (NMTU)), in epoxy coating is an efficient strategy for enhancing the protection of the epoxy coating and increasing its lifetime. Fourier transform infrared (FTIR) spectroscopy analysis was used to confirm the loading and presence of inhibitors in the nanoparticles. Thermal gravimetric analysis (TGA) measurement studies revealed the amount of 25% and 29.75% w/w for NMTU and DDA in the nanoparticles, respectively. The pH sensitive and self-release behavior of modified CeO2 nanoparticles is confirmed through UV-vis spectroscopy and Zeta potential. It was observed, through scanning electron microscopy (SEM), that a protective layer had been formed on the defect site separating the steel surface from the external environment and healed the artificially created scratch. This protective film played a vital role in the corrosion inhibition of steel by preventing the aggressiveness of Cl− in the solution. Electrochemical impedance spectroscopy (EIS) measurements exhibited the exceptional corrosion inhibition efficiency, reaching 99.8% and 95.7% for the modified coating with DDA and NMTU, respectively, after five days of immersion time.


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