Optically modified MNPs coupled with SQDs (super structures) demonstrating tunable emission and enhanced photocatalytic activity are synthesized through homogeneous nucleation of indium chloride, thioacetamide and silver nitrate. Ag nanospheres (1–15 nm) are embedded in the matrix of β-In2S3 quantum dots. Modification of the absorption profile and shift in excitonic binding energy from 3.60 eV to 3.25 eV occurs due to plasmon mediated indirect columbic interaction between the SQDs. Raman spectrum of β-In2S3 (1:1)-Ag Nanohybrids (NHs) shows asymmetric line-shape broadening due to the fano-interaction (electron-phonon interaction) of the triply degenerate F2g mode of SQDs with a continuum of plasmon excitations. The emission spectra of the quantum dots, with significant peak shifting and enhanced intensity, indicates stronger coupling between the SQDs and MNPs. In the proximity of Ag NPs, the defect emission due to IIn (∼708 nm) is completely quenched, and an enhanced blue emission occurs at ∼ 496 nm. Further with increase in pump beam energy, there is a gradual peak maxima shift, spectral distortion, narrowing of emission profile and enhancement in emission intensity, which is attributed to amplified spontaneous emission assisted amplification in the gain media (SQDs). Measurement of photocatalytic efficiency for irradiation of 60 min (400 nm–700 nm) with β-In2S3 (1:1) QDs-Ag NHs as photocatalyst, prompted 100 % degradation while pure β-In2S3 (1:1) QDs as photocatalyst material could attain 98.6 % degradation only after 280 min of irradiation.
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