Tuning plasmonic and chemical enhancement for SERS detection on graphene-based Au hybridsElectronic supplementary information (ESI) available: EDX spectrum of GO/Au and rGO/Au in TEM image of Fig. 2 and SEM images of CVD-G nanosheets on SiO2/Si with different Au deposition times were shown in Fig. S1 and S2, respectively, and SERS contrast experiment to exclude the influence of Au deposition method from in situ growth method and sputtering method (with 30 s Au depositing time) (black lines) on S

Various graphene-based Au nanocomposites have been developed as surface-enhanced Raman scattering (SERS) substrates recently. However, efficient use of SERS has been impeded by the difficulty of tuning SERS enhancement effects induced from chemical and plasmonic enhancement by different preparation...

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Hauptverfasser: Liang, Xiu, Liang, BenLiang, Pan, Zhenghui, Lang, Xiufeng, Zhang, Yuegang, Wang, Guangsheng, Yin, Penggang, Guo, Lin
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Sprache:eng
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Zusammenfassung:Various graphene-based Au nanocomposites have been developed as surface-enhanced Raman scattering (SERS) substrates recently. However, efficient use of SERS has been impeded by the difficulty of tuning SERS enhancement effects induced from chemical and plasmonic enhancement by different preparation methods of graphene. Herein, we developed graphene-based Au hybrids through physical sputtering gold NPs on monolayer graphene prepared by chemical vapor deposition (CVD) as a CVD-G/Au hybrid, as well as graphene oxide-gold (GO/Au) and reduced-graphene oxide (rGO/Au) hybrids prepared using the chemical in situ crystallization growth method. Plasmonic and chemical enhancements were tuned effectively by simple methods in these as-prepared graphene-based Au systems. SERS performances of CVD-G/Au, rGO/Au and GO/Au showed a gradually monotonic increasing tendency of enhancement factors (EFs) for adsorbed Rhodamine 6G (R6G) molecules, which show clear dependence on chemical bonds between graphene and Au, indicating that the chemical enhancement can be steadily controlled by chemical groups in a graphene-based Au hybrid system. Most notably, we demonstrate that the optimized GO/Au was able to detect biomolecules of adenine, which displayed high sensitivity with a detection limit of 10 −7 M as well as good reproducibility and uniformity. Three different graphene-based Au hybrids were EM and CM tuned by effective methods as SERS substrates to detect adenine molecules.
ISSN:2040-3364
2040-3372
DOI:10.1039/c5nr06010a