2020
DOI: 10.1016/j.arabjc.2019.05.004
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Water soluble gold-polyaniline nanocomposite: A substrate for surface enhanced Raman scattering and catalyst for dye degradation

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Cited by 31 publications
(19 citation statements)
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“…The FT-IR spectra of ONPG powder and Au@PGlyco NPs prepared using different concentrations of ONPG are shown in Figure a. The relatively strong signals at 3400, 1035, and 1066 cm –1 in the FT-IR spectra of Au@PGlyco NPs were attributed to the −OH stretching, C–O stretching, and C–OH bending from the galactose structure, respectively . The binding energy of C 1s appeared at 286.5 eV, which was assigned to the sugar-based fingerprints of the C–O–C and C–OH structures based on X-ray photoelectron spectroscopy (XPS) (Figure S3b).…”
Section: Resultsmentioning
confidence: 99%
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“…The FT-IR spectra of ONPG powder and Au@PGlyco NPs prepared using different concentrations of ONPG are shown in Figure a. The relatively strong signals at 3400, 1035, and 1066 cm –1 in the FT-IR spectra of Au@PGlyco NPs were attributed to the −OH stretching, C–O stretching, and C–OH bending from the galactose structure, respectively . The binding energy of C 1s appeared at 286.5 eV, which was assigned to the sugar-based fingerprints of the C–O–C and C–OH structures based on X-ray photoelectron spectroscopy (XPS) (Figure S3b).…”
Section: Resultsmentioning
confidence: 99%
“…The relatively strong signals at 3400, 1035, and 1066 cm −1 in the FT-IR spectra of Au@PGlyco NPs were attributed to the −OH stretching, C−O stretching, and C−OH bending from the galactose structure, respectively. 39 The binding energy of C 1s appeared at 286.5 eV, which was assigned to the sugar-based fingerprints of the C−O−C and C−OH structures 40 based on X-ray photoelectron spectroscopy (XPS) (Figure S3b). Notably, the intensities of specific peaks at 1525 cm −1 (ν asym ) and 1378 cm −1 (ν sym ), which were attributed to the NO 2 group, 41 were dramatically decreased upon the formation of the Au@PGlyco NPs (Figure 2a).…”
Section: Resultsmentioning
confidence: 99%
“…In case of pristine PANI, the peak appeared at 332 and 631 nm are owing to the π-π* and n-π* transitions of the benzenoid and quinoid structures, respectively that con rms the emeraldine salt form of the PANI [34]. In case of the Au@PANI nanocomposite, the incorporation of AuNPs into the PANI matrix exhibited the shifting of the peak position to the higher wavelength region that con rms the successful encapsulation of the AuNPs by means of the PANI molecular chains [35]. The f-SWNTs and f-MWNTs decorated PANI matrix show the shifting of the absorption peak towards the higher wavelength region that indicates the formation of f-SWNTs@PANI and f-MWNTs@PANI nanocomposites [36].…”
Section: Uv-vis Analysismentioning
confidence: 87%
“…Furthermore, a small peak observed at 815 cm -1 is ascribed to the out of plane bending vibration of C-H bond [19,34,35,[49][50][51][52]. The Au@PANI nanocomposite exhibits all the absorption peaks of the neat PANI matrix with a slightly shifting of the band positions, which con rms the development of the interphase interactions between the AuNPs and PANI matrix due to the a nity of the AuNPs for the nitrogen atoms present in the backbone chain of the PANI matrix [35,53]. Both binary and ternary PANI nanocomposites exhibit all the absorption peaks of the PANI matrix with the shifting of the peak positions of the -OH, C = C, and C-H bonds that pronounces higher absorption intensity as compare to the virgin PANI.…”
Section: Uv-vis Analysismentioning
confidence: 99%
“…The (PAni-Mn) Nano catalyst was used for the first time in Kabachnik-Field Reaction for α-Aminophosphonates synthesis. During the last decade, Polyaniline had great importance in the catalytic field [20][21] . The doping of the polyanilinewith metal increases the catalytical activity 22 .…”
Section: Introductionmentioning
confidence: 99%