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. 2015 Feb 8;471(2174):20140792. doi: 10.1098/rspa.2014.0792

Table 5.

Representative methods from the literature for electrochemical precipitation of Ni(OH)2 films onto electrically conducting substrates. Depositions are performed galvanostatically (at constant current), except where noted.

Ni(II) salt and reagents conc. (mol L−1) current density (mA cm−2) deposition time min temp. (°C) substrate product phase comments refs
Ni(NO3)2 0.1 -2.5 10 22 nickel sheet α-Ni(OH)2 product contains NO3 [38]
Ni(NO3)2 0.005 -0.1 60 25 stainless steel sheet (316L) α-Ni(OH)2 product contains NO3 [13]
produces nanoparticles (approx. 5 nm)
Ni(NO3)2 0.005 -2.0 30 40 stainless steel sheet (316L) β-Ni(OH)2 stacking fault disorder and very hydrated [138]
produces nanoparticles (approx. 100 nm)
NiCl2 0.1 -2.5 10 22 nickel sheet α-Ni(OH)2 product contains Cl [38]
NiCl2 0.005 -1.0 a 10 stainless steel sheet (316L) β-Ni(OH)2 stacking fault disorder and very hydrated [139]
produces nanoparticles (less than 5 nm)
NiSO4 0.1 -2.5 2 22 nickel sheet α-Ni(OH)2 very highly disordered material [38]
product contains SO42
NiCl2 0.01 -1.0 12.5 70 graphite sheet β-NixCo1−x(OH)2 x=0.32 [14]
CoCl2 0.02 product contains some α-phase material
NaNO3 0.06
Ni(NO3)2 0.3 -6.25 30 25 nickel sheet α-Ni(OH)2 product is highly disordered [35]
KNO2 0.1 unclear what the role KNO2 or KNO3 serve
KNO3 0.1
NiCl2 0.01 -1.0 12.5 70 graphite sheet α-Ni(OH)2 NaNO3 is used to increase solution conductivity [14]
NaNO3 0.06
Ni(NO3)2 1.8 −0.7 VbSCE titanium sheet α-Ni(OH)2 Mix Brij 56 and aqueous solution, 50% (w/w) [140]
NaNO3 0.075 remove surfactant template at 100°C for 1.5 h
Brij 56 pure hexagonal pore array, dp=2.5 nm, dpp=7.0 nm
Ni(NO3)2 0.01 −1.1 VbAg/AgCl 1–100 s 25 boron-doped diamond nanoparticle size determined by deposition time [141]
(1 s, d=12±3 nm; 15 s, d=39±9 nm)
longer times result in agglomerates

a ‘—’ Indicates experimental details that were not provided.

bDeposition performed potentiostatically (at constant potential).