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Electrodeposition of NiCo alloy from methansulfonate electrolyte. The role of the electrolyte pH in the anomalous codeposition of nickel and cobalt

The kinetic characteristics of the electrochemical codeposition of nickel and cobalt from a methanesulfonate electrolyte have been investigated. An analysis of the partial voltammograms of the nickel and cobalt deposition into the alloy showed that the potentials of the metal deposition into the all...

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Published in:Surface & coatings technology 2020-04, Vol.387, p.1-8, Article 125542
Main Authors: Sknar, Yu.E., Sknar, I.V., Savchuk, O.O., Danilov, F.I.
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description The kinetic characteristics of the electrochemical codeposition of nickel and cobalt from a methanesulfonate electrolyte have been investigated. An analysis of the partial voltammograms of the nickel and cobalt deposition into the alloy showed that the potentials of the metal deposition into the alloy are significantly shifted in a positive direction compared to the deposition of the pure metals. This effect is more pronounced in the case of cobalt, and is the cause of the anomalous codeposition of nickel and cobalt. In the presence of the H3BO3 as a buffering agent in the electrolyte, the electroreduction of nickel(II) and cobalt(II) ions is inhibited; this reveals a significant role of the near-electrode pH in the kinetics of these reactions. The thermodynamic and kinetic aspects of the NiCo alloy electrodeposition were considered. It has been found that the kinetic factor is the determining factor responsible for the anomalous codeposition of nickel and cobalt. It has been shown that an adequate explanation of the observed regularities is possible using a concept that assumes equally accessible electroreduction of alloy components at the catalytic centers formed during the adsorption of their hydroxo complexes on the electrode surface. Based on the proposed mechanism, a kinetic model has been developed that correctly describes the features of nickel and cobalt codeposition. It has been found that the microhardness and internal stresses of NiCo electrolytic alloys obtained from methanesulfonate electrolytes are higher than those of coatings deposited from sulfate electrolytes. This is due to the difference in the degree of distortion of their crystal lattices. The low buffering properties of methanesulfonate electrolytes in comparison with sulfate electrolytes cause the formation of a greater number of hydroxide compounds in the near-electrode layer, which are incorporated into the cathode deposit and affect its structure. [Display omitted] •The NiCo alloy was electrodeposited from a methanesulfonate electrolyte.•The characteristics of electrodeposition of NiCo alloy coatings have been investigated.•The relation between composition, microstructure and properties of NiCo alloy was investigated.
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In the presence of the H3BO3 as a buffering agent in the electrolyte, the electroreduction of nickel(II) and cobalt(II) ions is inhibited; this reveals a significant role of the near-electrode pH in the kinetics of these reactions. The thermodynamic and kinetic aspects of the NiCo alloy electrodeposition were considered. It has been found that the kinetic factor is the determining factor responsible for the anomalous codeposition of nickel and cobalt. It has been shown that an adequate explanation of the observed regularities is possible using a concept that assumes equally accessible electroreduction of alloy components at the catalytic centers formed during the adsorption of their hydroxo complexes on the electrode surface. Based on the proposed mechanism, a kinetic model has been developed that correctly describes the features of nickel and cobalt codeposition. It has been found that the microhardness and internal stresses of NiCo electrolytic alloys obtained from methanesulfonate electrolytes are higher than those of coatings deposited from sulfate electrolytes. This is due to the difference in the degree of distortion of their crystal lattices. The low buffering properties of methanesulfonate electrolytes in comparison with sulfate electrolytes cause the formation of a greater number of hydroxide compounds in the near-electrode layer, which are incorporated into the cathode deposit and affect its structure. [Display omitted] •The NiCo alloy was electrodeposited from a methanesulfonate electrolyte.•The characteristics of electrodeposition of NiCo alloy coatings have been investigated.•The relation between composition, microstructure and properties of NiCo alloy was investigated.</description><identifier>ISSN: 0257-8972</identifier><identifier>EISSN: 1879-3347</identifier><identifier>DOI: 10.1016/j.surfcoat.2020.125542</identifier><language>eng</language><publisher>Lausanne: Elsevier B.V</publisher><subject>Alloys ; Anomalous codeposition ; Buffers ; Cobalt base alloys ; Codeposition ; Crystal lattices ; Electrodeposition ; Electrodes ; Electrolytes ; Electrowinning ; Intermetallic compounds ; Methanesulfonate electrolyte ; Microhardness ; Ni[sbnd]Co alloy ; Nickel ; Physical-mechanical properties ; Reaction kinetics ; Residual stress ; Еlectrodeposition</subject><ispartof>Surface &amp; coatings technology, 2020-04, Vol.387, p.1-8, Article 125542</ispartof><rights>2020 Elsevier B.V.</rights><rights>Copyright Elsevier BV Apr 15, 2020</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><orcidid>0000-0002-1188-3684</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids></links><search><creatorcontrib>Sknar, Yu.E.</creatorcontrib><creatorcontrib>Sknar, I.V.</creatorcontrib><creatorcontrib>Savchuk, O.O.</creatorcontrib><creatorcontrib>Danilov, F.I.</creatorcontrib><title>Electrodeposition of NiCo alloy from methansulfonate electrolyte. The role of the electrolyte pH in the anomalous codeposition of nickel and cobalt</title><title>Surface &amp; coatings technology</title><description>The kinetic characteristics of the electrochemical codeposition of nickel and cobalt from a methanesulfonate electrolyte have been investigated. An analysis of the partial voltammograms of the nickel and cobalt deposition into the alloy showed that the potentials of the metal deposition into the alloy are significantly shifted in a positive direction compared to the deposition of the pure metals. This effect is more pronounced in the case of cobalt, and is the cause of the anomalous codeposition of nickel and cobalt. In the presence of the H3BO3 as a buffering agent in the electrolyte, the electroreduction of nickel(II) and cobalt(II) ions is inhibited; this reveals a significant role of the near-electrode pH in the kinetics of these reactions. The thermodynamic and kinetic aspects of the NiCo alloy electrodeposition were considered. It has been found that the kinetic factor is the determining factor responsible for the anomalous codeposition of nickel and cobalt. It has been shown that an adequate explanation of the observed regularities is possible using a concept that assumes equally accessible electroreduction of alloy components at the catalytic centers formed during the adsorption of their hydroxo complexes on the electrode surface. Based on the proposed mechanism, a kinetic model has been developed that correctly describes the features of nickel and cobalt codeposition. It has been found that the microhardness and internal stresses of NiCo electrolytic alloys obtained from methanesulfonate electrolytes are higher than those of coatings deposited from sulfate electrolytes. This is due to the difference in the degree of distortion of their crystal lattices. The low buffering properties of methanesulfonate electrolytes in comparison with sulfate electrolytes cause the formation of a greater number of hydroxide compounds in the near-electrode layer, which are incorporated into the cathode deposit and affect its structure. 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The role of the electrolyte pH in the anomalous codeposition of nickel and cobalt</atitle><jtitle>Surface &amp; coatings technology</jtitle><date>2020-04-15</date><risdate>2020</risdate><volume>387</volume><spage>1</spage><epage>8</epage><pages>1-8</pages><artnum>125542</artnum><issn>0257-8972</issn><eissn>1879-3347</eissn><abstract>The kinetic characteristics of the electrochemical codeposition of nickel and cobalt from a methanesulfonate electrolyte have been investigated. An analysis of the partial voltammograms of the nickel and cobalt deposition into the alloy showed that the potentials of the metal deposition into the alloy are significantly shifted in a positive direction compared to the deposition of the pure metals. This effect is more pronounced in the case of cobalt, and is the cause of the anomalous codeposition of nickel and cobalt. In the presence of the H3BO3 as a buffering agent in the electrolyte, the electroreduction of nickel(II) and cobalt(II) ions is inhibited; this reveals a significant role of the near-electrode pH in the kinetics of these reactions. The thermodynamic and kinetic aspects of the NiCo alloy electrodeposition were considered. It has been found that the kinetic factor is the determining factor responsible for the anomalous codeposition of nickel and cobalt. It has been shown that an adequate explanation of the observed regularities is possible using a concept that assumes equally accessible electroreduction of alloy components at the catalytic centers formed during the adsorption of their hydroxo complexes on the electrode surface. Based on the proposed mechanism, a kinetic model has been developed that correctly describes the features of nickel and cobalt codeposition. It has been found that the microhardness and internal stresses of NiCo electrolytic alloys obtained from methanesulfonate electrolytes are higher than those of coatings deposited from sulfate electrolytes. This is due to the difference in the degree of distortion of their crystal lattices. The low buffering properties of methanesulfonate electrolytes in comparison with sulfate electrolytes cause the formation of a greater number of hydroxide compounds in the near-electrode layer, which are incorporated into the cathode deposit and affect its structure. [Display omitted] •The NiCo alloy was electrodeposited from a methanesulfonate electrolyte.•The characteristics of electrodeposition of NiCo alloy coatings have been investigated.•The relation between composition, microstructure and properties of NiCo alloy was investigated.</abstract><cop>Lausanne</cop><pub>Elsevier B.V</pub><doi>10.1016/j.surfcoat.2020.125542</doi><tpages>8</tpages><orcidid>https://orcid.org/0000-0002-1188-3684</orcidid></addata></record>
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source ScienceDirect Freedom Collection 2022-2024
subjects Alloys
Anomalous codeposition
Buffers
Cobalt base alloys
Codeposition
Crystal lattices
Electrodeposition
Electrodes
Electrolytes
Electrowinning
Intermetallic compounds
Methanesulfonate electrolyte
Microhardness
Ni[sbnd]Co alloy
Nickel
Physical-mechanical properties
Reaction kinetics
Residual stress
Еlectrodeposition
title Electrodeposition of NiCo alloy from methansulfonate electrolyte. The role of the electrolyte pH in the anomalous codeposition of nickel and cobalt
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