In this study, a widely used colloid of Creighton AgNPs (ORI, 1-100 nm, mostly <= 40 nm, similar to 10 mu g mL(-1)) was rapidly manipulated via tangential flow filtration (TFF) for highly reproducible surface-enhanced (resonance) Raman spectroscopy (SE(R)RS) experiments down to the single-molecule (SM) level. The quasi-spherical AgNPs were size-selected, purified, and concentrated in two TFF fractions of a cutoff diameter of similar to 40 nm: AgNP <= 40 (similar to 900 mu g mL(-1)) and AgNP >= 40 (similar to 100 mu g mL(-1)). The SE(R)S-based sensing capabilities of the two TFF fractions were then tested under pre-resonance (632.8 nm) and resonance (532.1 nm) excitation conditions for rhodamine 6G (R6G, 10(-6)-10(-15) M). Both TFF isolates, AgNP <= 40 and AgNP >= 40, were more effective in adsorbing the R6G analyte (>= 91%) than the original colloid (>= 78%) at submonolayer coverages. Furthermore, the surface enhancement factors (SEF) of the two TFF fractions were markedly superior to those of ORI under all excitation conditions. SERS at 632.8 nm: only AgNP >= 40 enabled the detection of R6G at 10(-9) M and produced the largest SEF (2.1 x 10(6)). SE(R)RS and SM-SERRS at 532.1 nm: AgNP >= 40 gave rise to the largest SEF values (2.5 x 10(10)) corresponding to the SM regime down to 10(-15) M of R6G. Nevertheless, AgNP <= 40 compensated for the size-dependence of the electromagnetic enhancements by an increase in the silver concentration, which led to SEF values comparable to those of AgNP >= 40 through additional resonance enhancements. TFF resulted into a similar to 100-fold increase (AgNP <= 40) in the number of negatively charged AgNPs that were available to electrostatically bridge R6G cations and form SERRS "hot-spots" (AgNP-R6G-AgNP) within the focal volume. Evidently, the interplay between AgNP size, AgNP concentration, and excitation wavelength governs the SE(R)RS enhancements. This study demonstrated that TFF can facilitate the ecofriendly isolation of spherical AgNPs of controlled morphological and plasmonic properties for further enhancing their sensing capabilities as SE(R)RS substrates.
机构:
Beijing Univ Technol, Inst Laser Engn, Beijing 100124, Peoples R ChinaBeijing Univ Technol, Inst Laser Engn, Beijing 100124, Peoples R China
Guo, Wei
Wu, Jian
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Beijing Univ Technol, Inst Laser Engn, Beijing 100124, Peoples R ChinaBeijing Univ Technol, Inst Laser Engn, Beijing 100124, Peoples R China
Wu, Jian
Wang, Chunyan
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Chinese Astronaut Sci Researching & Training Ctr, State Key Lab Space Med Fundamentals & Applicat, Beijing 100094, Peoples R ChinaBeijing Univ Technol, Inst Laser Engn, Beijing 100124, Peoples R China
Wang, Chunyan
Zhang, Tian
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Beijing Univ Technol, Inst Laser Engn, Beijing 100124, Peoples R ChinaBeijing Univ Technol, Inst Laser Engn, Beijing 100124, Peoples R China
Zhang, Tian
Chen, Tao
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Beijing Univ Technol, Inst Laser Engn, Beijing 100124, Peoples R ChinaBeijing Univ Technol, Inst Laser Engn, Beijing 100124, Peoples R China
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KBSI, Taejon 305806, South KoreaKBSI, Taejon 305806, South Korea
Bae, Doo Ri
Chang, Sung-Jin
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KBSI, Taejon 305806, South KoreaKBSI, Taejon 305806, South Korea
Chang, Sung-Jin
Huh, Yun Suk
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KBSI, Taejon 305806, South KoreaKBSI, Taejon 305806, South Korea
Huh, Yun Suk
Han, Young-Kyu
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KBSI, Taejon 305806, South Korea
Dongguk Univ Seoul, Dept Energy & Mat Engn, Seoul 100715, South KoreaKBSI, Taejon 305806, South Korea
Han, Young-Kyu
Lee, You-Jin
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Sungkyunkwan Univ, Dept Polymer Sci & Engn, Suwon 440746, South Korea
Chungnam Natl Univ, Ctr Res Facil, Taejon 305764, South KoreaKBSI, Taejon 305806, South Korea
Lee, You-Jin
Yi, Gi-Ra
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Sungkyunkwan Univ, Dept Polymer Sci & Engn, Suwon 440746, South KoreaKBSI, Taejon 305806, South Korea
Yi, Gi-Ra
Kim, Soohyun
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KBSI, Taejon 305806, South KoreaKBSI, Taejon 305806, South Korea
Kim, Soohyun
Lee, Gaehang
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KBSI, Taejon 305806, South KoreaKBSI, Taejon 305806, South Korea