G. T. Burstein
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Research Subjects
G. T. Burstein has a total of 9 co-authors. Here are the top co-authors by number of shared publications:
C Liu
1 shared publicationC. D. A. Brady
1 shared publication- Eric J. Rees
University of Cambridge
1 shared publication I. M. Hutchings
University of Cambridge
1 shared publicationK. Sasaki
1 shared publicationK.R Williams
Department of Materials Science and Metallurgy, University of Cambridge, Pembroke Street, Cambridge CB2 3QZ, UK
1 shared publication
Latest Publications
- 1 January 2008
- Published by The Electrochemical Society in Journal of the Electrochemical Society
- Vol. 155 (5) , B461-B466
Passivation and Electrocatalytic Behavior of an Amorphous Nickel–Carbon Film in Sulfuric Acid
The electrochemical behavior of a sputtered film of carbon and nickel, of approximate stoichiometry , is presented. This film is quite passive in hot sulfuric acid solution. The material also displays considerable electrocatalytic activity toward the hydrogen reaction, both anodically and cathodically. The electrocatalyst is passivated by the carbon component after dissolution of some of the surface nickel. The remaining surface nickel, entrapped by carbon, provides electrocatalytic activity comparable with that of pure polycrystalline nickel.
- 1 January 2008
- Published by The Electrochemical Society in Journal of the Electrochemical Society
- Vol. 155 (5) , B461-B466
Passivation and Electrocatalytic Behavior of an Amorphous Nickel–Carbon Film in Sulfuric Acid
The electrochemical behavior of a sputtered film of carbon and nickel, of approximate stoichiometry , is presented. This film is quite passive in hot sulfuric acid solution. The material also displays considerable electrocatalytic activity toward the hydrogen reaction, both anodically and cathodically. The electrocatalyst is passivated by the carbon component after dissolution of some of the surface nickel. The remaining surface nickel, entrapped by carbon, provides electrocatalytic activity comparable with that of pure polycrystalline nickel.
- 1 January 2005
- Published by Elsevier in Biomaterials
- Vol. 26 (3) , 245-256
The effect of temperature on the nucleation of corrosion pits on titanium in Ringer's physiological solution
- 1 January 2005
- Published by Elsevier in Biomaterials
- Vol. 26 (3) , 245-256
The effect of temperature on the nucleation of corrosion pits on titanium in Ringer's physiological solution
- 29 March 2004
- Published by Elsevier in Journal of Power Sources
- Vol. 128 (1) , 1-12
Characteristics of a direct methanol fuel cell based on a novel electrode assembly using microporous polymer membranes
- 29 March 2004
- Published by Elsevier in Journal of Power Sources
- Vol. 128 (1) , 1-12
Characteristics of a direct methanol fuel cell based on a novel electrode assembly using microporous polymer membranes
- 1 October 2000
- Published by Springer Nature in Nature
- Vol. 407 (6806) , 885-887
Electrochemically induced annealing of stainless-steel surfaces
Modification of the surface properties of metals without affecting their bulk properties is of technological interest in demanding applications where surface stability and hardness are important. When austenitic stainless steel is heavily plastically deformed by grinding or rolling, a martensitic phase transformation occurs that causes significant changes in the bulk and surface mechanical properties of the alloy. This martensitic phase can also be generated in stainless-steel surfaces by cathodic charging, as a consequence of lattice strain generated by absorbed hydrogen. Heat treatment of the steel to temperatures of several hundred degrees can result in loss of the martensitic structure, but this alters the bulk properties of the alloy. Here we show that martensitic structures in stainless steel can be removed by appropriate electrochemical treatment in aqueous solutions at much lower temperature than conventional annealing treatments. This electrochemically induced annealing process allows the hardness of cold-worked stainless steels to be maintained, while eliminating the brittle martensitic phase from the surface. Using this approach, we are able to anneal the surface and near-surface regions of specimens that contain rolling-induced martensite throughout their bulk, as well as those containing surface martensite induced by grinding. Although the origin of the electrochemical annealing process still needs further clarification, we expect that this treatment will lead to further development in enhancing the surface properties of metals.
- 1 October 2000
- Published by Springer Nature in Nature
- Vol. 407 (6806) , 885-887
Electrochemically induced annealing of stainless-steel surfaces
Modification of the surface properties of metals without affecting their bulk properties is of technological interest in demanding applications where surface stability and hardness are important. When austenitic stainless steel is heavily plastically deformed by grinding or rolling, a martensitic phase transformation occurs that causes significant changes in the bulk and surface mechanical properties of the alloy. This martensitic phase can also be generated in stainless-steel surfaces by cathodic charging, as a consequence of lattice strain generated by absorbed hydrogen. Heat treatment of the steel to temperatures of several hundred degrees can result in loss of the martensitic structure, but this alters the bulk properties of the alloy. Here we show that martensitic structures in stainless steel can be removed by appropriate electrochemical treatment in aqueous solutions at much lower temperature than conventional annealing treatments. This electrochemically induced annealing process allows the hardness of cold-worked stainless steels to be maintained, while eliminating the brittle martensitic phase from the surface. Using this approach, we are able to anneal the surface and near-surface regions of specimens that contain rolling-induced martensite throughout their bulk, as well as those containing surface martensite induced by grinding. Although the origin of the electrochemical annealing process still needs further clarification, we expect that this treatment will lead to further development in enhancing the surface properties of metals.