Santiago Fajardo

Dr. Santiago Fajardo

Department of Surface Engineering, Corrosion and Durability, National Centre for Metallurgical Research CENIM-CSIC, 28040 Madrid, Spain
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Research Focus & Metrics

Academic Career Length

19Years (2008-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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1 August 2017 in Progress in Materials Science
Verified
Journal Article
Open access
MEM. Esmaily
M. Esmaily
JSJ.E. Svensson
J.E. Svensson
Santiago FajardoSantiago Fajardo
Santiago Fajardo
NBNick Birbilis
Nick Birbilis
GFG.S. Frankel
G.S. Frankel
LJL.G. Johansson
L.G. Johansson

1 May 2015 in Electrochimica Acta
Verified
Journal Article
Closed access
Santiago FajardoSantiago Fajardo
Santiago Fajardo
GFG.S. Frankel
G.S. Frankel


1 July 2019 in Corrosion Science
Verified
Journal Article
Closed access
Santiago FajardoSantiago Fajardo
Santiago Fajardo
ILI. Llorente
I. Llorente
JJJosé A. Jimenez
José A. Jimenez
JBJ.M. Bastidas
J.M. Bastidas
DBD.M. Bastidas
D.M. Bastidas

1 September 2016 in Electrochimica Acta
Verified
Journal Article
Closed access
Santiago FajardoSantiago Fajardo
Santiago Fajardo
CGC.F. Glover
C.F. Glover
GWG. Williams
G. Williams
GFG.S. Frankel
G.S. Frankel

28 May 2015 in Faraday Discussions
Verified
Journal Article
Closed access
PDF file
GFG. S. Frankel
G. S. Frankel
Santiago FajardoSantiago Fajardo
Santiago Fajardo
BLB. M. Lynch
B. M. Lynch
The increase in the rate of hydrogen evolution (HE) on dissolving Mg surfaces with increasing anodic current density or potential, which is sometimes called the negative difference effect, has been the topic of much discussion in recent years. A review of the very recent contributions to this subject is given in this paper. Increased catalytic activity of the corrosion product layer, either from the accumulated impurities or from the Mg oxy-hydroxide itself, is shown to have a minor influence on the anodic HE observed on dissolving Mg at high anodic current densities and potentials. Al exhibits similar characteristics during anodic polarization in concentrated HCl, although the anodic HE rate on Al is less than on Mg. Possible mechanisms for the anodic hydrogen are provided and implications in the area of intergranular corrosion and environmental cracking are discussed.