2019
DOI: 10.1016/j.inoche.2019.107469
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Ion diffusion-assisted preparation of Ni3S2/NiO nanocomposites for electrochemical capacitors

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Cited by 15 publications
(7 citation statements)
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“…It should be noted that the synthesis method of Ni 3 S 2 is the same as the CoNi 2 S 4 with some minor modifications. However, the fingerprints of the Ni 3 S 2 are 2217 cm −1 , 2108 cm −1 , 1870 cm −1 , and 618 cm −1 , which have differences with the present spectrum 42 44 . The synthesized nanocomposite has minimal covalent interactions with the H 2 TMP; if the cobalt had any covalent interactions with the porphyrin, some major and sharp peaks at 1099 cm −1 , 920 cm −1 , and also 802 cm −1 should be observed 45 47 .…”
Section: Resultscontrasting
confidence: 70%
“…It should be noted that the synthesis method of Ni 3 S 2 is the same as the CoNi 2 S 4 with some minor modifications. However, the fingerprints of the Ni 3 S 2 are 2217 cm −1 , 2108 cm −1 , 1870 cm −1 , and 618 cm −1 , which have differences with the present spectrum 42 44 . The synthesized nanocomposite has minimal covalent interactions with the H 2 TMP; if the cobalt had any covalent interactions with the porphyrin, some major and sharp peaks at 1099 cm −1 , 920 cm −1 , and also 802 cm −1 should be observed 45 47 .…”
Section: Resultscontrasting
confidence: 70%
“…48-1548), and ZnO (no. 36-1541), respectively. Besides, all the calcined production displayed prominent peaks and an increased peak width in XRD patterns suggesting that the chromate nanoparticles fabricated by the sol–gel approach possessed rather small crystallite sizes. Furthermore, the crystallite sizes of these nanochromates were calculated from their corresponding XRD peak broadening of the most intense diffraction peak (3 1 1) using the Scherrer formula, D = K λ/βcosθ, and the average crystallite sizes of CoCr 2 O 4 , NiCr 2 O 4 , CuCr 2 O 4 , and ZnCr 2 O 4 nanoparticles were determined as 22.0, 23.4, 23.4, and 22.7 nm, respectively.…”
Section: Resultsmentioning
confidence: 96%
“…Based on Figure a, the fingerprint absorption peaks for CoNi 2 S 4 , which are 3450, 1630, 1370, 901  , and 610 cm –1 , match up with the stretching and bending vibrations of the water compartment (O–H) on the surface of the Co (Co–O–H), C–O–C vibrations, N–CS, and CS vibrations of thiourea, respectively, , thus affirming the successful in situ and one-pot synthesis of the nanocomposite along with CoNi 2 S 4 . It should be noted that the synthesis method for Ni 3 S 2 is the same as that of CoNi 2 S 4 with some minor modifications; however, the fingerprints of the Ni 3 S 2 are 2217, 2108, 1870  , and 618 cm –1 , which clearly differ from the present spectrum. By addition of DOX to the synthesized nanocomposite, three new peaks were represented at 810, 1120  , and 1730 cm –1 , which correspond to the stretching bands of DOX on the surface of the carbon-based nanocomposite . It should be noted that the synthesized nanocomposite has not any covalent interactions with the DOX due to the absence of the peaks at around 1099, 920  , and also 802 cm –1 , which are indicative of the covalent bonding between the cobalt or zinc and the DOX structure.…”
Section: Results and Discussionmentioning
confidence: 65%