TY - JOUR
T1 - Cyclohexylammonium Hexaisothiocyanatonickelate(II) Dihydrate as a Single-Source Precursor for High Surface Area Nickel Oxide and Sulfide Nanocrystals
AU - Aboud, Mohamed F.Aly
AU - Bintaleb, Abdulmalik M.
AU - Yahia, Hamdi Ben
AU - Albaid, Abdelhamid
AU - Albishi, Sultan
AU - Arasheed, Rasheed
AU - Albinali, Ibrahim
AU - Albaqi, Fahad
AU - Anojaidi, Khalid
AU - Alqahtani, Fahad
AU - Alenad, Asma M.
AU - Taha, Kamal
AU - Bagabas, Abdulaziz
N1 - Publisher Copyright:
© 2022 by the authors. Licensee MDPI, Basel, Switzerland.
PY - 2022/3
Y1 - 2022/3
N2 - Cyclohexylammonium hexaisothiocyanatonickelate(II) dihydrate, (C6 H11 NH3 )4 [Ni(NCS)6 ]·2H2 O, was synthesized, for the first time, by a four-step method in a yield of 95%. The compound was fully characterized by elemental microanalysis, Fourier transform infrared (FTIR), ultraviolet-visible-near infrared (UV-Vis-NIR), and nuclear magnetic resonance (NMR) spectroscopy and thermogravimetry. A single crystal X-ray diffraction (SXRD) gave the monoclinic space group P21 /c with a = 15.8179 (5) Å, b = 10.6222 (3) Å, c = 13.8751 (4) Å, β = 109.362 (1)◦, V = 2199.45 (11) Å3, Z = 2 (T = 293 K) for this novel hybrid organic–inorganic compound. The title compound was employed as a single-source precursor for the synthesis of mesoporous, high surface area nickel oxide (53 Å; 452 m2 /g) and nickel sulfide (46 Å; 220 m2 /g) via pyrolysis under air at 550◦ C or helium atmosphere at 500◦ C, respectively. X-ray powder diffraction (XRPD) demonstrated the nanocrystalline nature of both NiO and NiS with an average crystallite size of 16 and 54 nm, respectively. Scanning electron microscope (SEM) indicated the formation of agglomerated, quasispherical particles of nickel oxide and agglomerated flake-like structures of nickel sulfide. The high surface area, porosity, and nanocrystallinity of both NiO and NiS, obtained via this approach, are promising for a wide spectrum of applications.
AB - Cyclohexylammonium hexaisothiocyanatonickelate(II) dihydrate, (C6 H11 NH3 )4 [Ni(NCS)6 ]·2H2 O, was synthesized, for the first time, by a four-step method in a yield of 95%. The compound was fully characterized by elemental microanalysis, Fourier transform infrared (FTIR), ultraviolet-visible-near infrared (UV-Vis-NIR), and nuclear magnetic resonance (NMR) spectroscopy and thermogravimetry. A single crystal X-ray diffraction (SXRD) gave the monoclinic space group P21 /c with a = 15.8179 (5) Å, b = 10.6222 (3) Å, c = 13.8751 (4) Å, β = 109.362 (1)◦, V = 2199.45 (11) Å3, Z = 2 (T = 293 K) for this novel hybrid organic–inorganic compound. The title compound was employed as a single-source precursor for the synthesis of mesoporous, high surface area nickel oxide (53 Å; 452 m2 /g) and nickel sulfide (46 Å; 220 m2 /g) via pyrolysis under air at 550◦ C or helium atmosphere at 500◦ C, respectively. X-ray powder diffraction (XRPD) demonstrated the nanocrystalline nature of both NiO and NiS with an average crystallite size of 16 and 54 nm, respectively. Scanning electron microscope (SEM) indicated the formation of agglomerated, quasispherical particles of nickel oxide and agglomerated flake-like structures of nickel sulfide. The high surface area, porosity, and nanocrystallinity of both NiO and NiS, obtained via this approach, are promising for a wide spectrum of applications.
KW - Cyclohexylammonium
KW - Hexaisothiocyanatonickelate(II)
KW - Nickel oxide
KW - Nickel sulfide
KW - Pyrolysis
UR - http://www.scopus.com/inward/record.url?scp=85125222025&partnerID=8YFLogxK
U2 - 10.3390/cryst12030315
DO - 10.3390/cryst12030315
M3 - Article
AN - SCOPUS:85125222025
SN - 2073-4352
VL - 12
JO - Crystals
JF - Crystals
IS - 3
M1 - 315
ER -