HAuCl4 ∙ 3H2O (99.99% (metals basis)), L-cysteine hydrochloride (98%), D-cysteine hydrochloride (98%), L-glutathione (98%+), D-methionine (99%), L-methionine (98 + %), L-cystine dihydrochloride (98%), D-cystine (98%), Cu(NO3)2 trihydrate (98%), Fe(NO3)3 nonahydrate (98%), Co(NO3)2 hexahydrate (99%), Ni(NO3)2 hexahydrate (98%), and KOH (99 + %) were purchased from Alfa Aesar. AgNO3 (>99.9%), HCl (37%), and H2SO4 (75%) were purchased from Roth. Hexadecyl-trimethylammonium bromide (CTAB, >99%), ascorbic acid (AA, >99%), and acetic acid (80%), were purchased from Acros Organics. Hexadecyltrimetryammonium chloride (CTAC, >98.0%), 1-decanol (>98%), L-penicillamine (99%), D-penicillamine (99%), Cd(NO)3 tetrahydrate (99%), Pb(NO3)2 (99%), and ammonium hydroxide (28%–30%) were purchased from Sigma-Aldrich. Milli Q water was used in all experiments. All reagents were used as received without further purification.
Co no3 2 hexahydrate
Manufactured by Thermo Fisher Scientific
Co(NO3)2 hexahydrate is a chemical compound used in various laboratory applications. It is a crystalline solid with a pink or purple color. The compound contains cobalt(II) ions and nitrate ions, and it is commonly used as a source of cobalt ions in chemical reactions and analyses.
Automatically generated - may contain errors
Lab products found in correlation
Hexadecyltrimethylammonium bromide, by Thermo Fisher Scientific (1 mentions)
Ascorbic acid, by Thermo Fisher Scientific (1 mentions)
Acetic acid, by Thermo Fisher Scientific (1 mentions)
Ammonium hydroxide, by Merck Group (1 mentions)
L methionine, by Thermo Fisher Scientific (1 mentions)
L glutathione, by Thermo Fisher Scientific (1 mentions)
Pb no3 2, by Merck Group (1 mentions)
Hydrochloric acid (hcl), by Carl Roth (1 mentions)
L cysteine hydrochloride, by Thermo Fisher Scientific (1 mentions)
Haucl4, by Thermo Fisher Scientific (1 mentions)
Agno3, by Carl Roth (1 mentions)
H2so4, by Carl Roth (1 mentions)
D penicillamine, by Merck Group (1 mentions)
1 decanol, by Merck Group (1 mentions)
D methionine, by Thermo Fisher Scientific (1 mentions)
L penicillamine, by Merck Group (1 mentions)
2 protocols using co no3 2 hexahydrate
1
Synthesis of Metal Nanoparticles
2
Synthesis and Deposition of Co-Bi Catalyst
Check if the same lab product or an alternative is used in the 5 most similar protocols
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The Co-Bi powder was obtained through a modified precipitation
technique.60 (link),61 (link) In a beaker, 291 mg of Co(NO3)2 hexahydrate (Alfa Aesar, >98%) was dissolved
in DIW by sonication. To initiate the precipitation, 5 mL of 0.5 M
NaBH4 aqueous solution was poured in the beaker with fast
stirring. NaBH4 reacted quickly with gas evolution. The
solution was kept stirring for 40 min, and then the precipitate was
rinsed and centrifuged several times with DIW and then ethanol to
remove residues of the reaction solution. Eventually, the powder was
dried from ethanol in a desiccator at 35 °C.
Co-Bi was deposited as catalysts onto the BiVO4 photoanode
surface by drop casting an ethanol dispersion of the powder (0.5 mg/mL)
obtained by 15 min sonication. The catalyst loading was varied by
changing the dropped volume (10, 25, and 50 μL/cm2). After application of the dispersion with a micropipette, ethanol
was evaporated in the desiccator.
technique.60 (link),61 (link) In a beaker, 291 mg of Co(NO3)2 hexahydrate (Alfa Aesar, >98%) was dissolved
in DIW by sonication. To initiate the precipitation, 5 mL of 0.5 M
NaBH4 aqueous solution was poured in the beaker with fast
stirring. NaBH4 reacted quickly with gas evolution. The
solution was kept stirring for 40 min, and then the precipitate was
rinsed and centrifuged several times with DIW and then ethanol to
remove residues of the reaction solution. Eventually, the powder was
dried from ethanol in a desiccator at 35 °C.
Co-Bi was deposited as catalysts onto the BiVO4 photoanode
surface by drop casting an ethanol dispersion of the powder (0.5 mg/mL)
obtained by 15 min sonication. The catalyst loading was varied by
changing the dropped volume (10, 25, and 50 μL/cm2). After application of the dispersion with a micropipette, ethanol
was evaporated in the desiccator.
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