Gilded nanoparticles for plasmonically enhanced fluorescence in TiO2:Sm3+ sol-gel films
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Silica-gold core-shell nanoparticles were used for plasmonic enhancement of rare earth fluorescence in sol-gel-derived TiO2:Sm3+ films. Local enhancement of Sm3+ fluorescence in the vicinity of separate gilded nanoparticles was revealed by a combination of dark field microscopy and fluorescence spectroscopy techniques. An intensity enhancement of Sm3+ fluorescence varies from 2.5 to 10 times depending on the used direct (visible) or indirect (ultraviolet) excitations. Analysis of fluorescence lifetimes suggests that the locally stronger fluorescence occurs because of higher plasmon-coupled direct absorption of exciting light by the Sm3+ ions or due to plasmon-assisted non-radiative energy transfer from the excitons of TiO2 host to the rare earth ions.
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KeywordsSilica-gold core-shell nanoparticles Plasmonics Rare-earth fluorescence Metal-enhanced fluorescence
Noble metal nanoparticles are under intense scientific and applied attention because of their unique optical properties . Incident light which is in resonance with the collective electronic oscillations near the surface of metal nanoparticles causes the so-called localized surface plasmon resonance. It results in strong concentration of light energy and electric field in the subwavelength nanoscale region near the particle. The strong local field causes an increase in the efficiency of light absorption, scattering, and fluorescence .
Metal-enhanced fluorescence as a branch of nano-optics was formed on the one hand from the needs of fluorescent sensing of minute amounts of matter [2, 3] and on the other hand from fundamental interest to the control of light energy on the nanoscale and inducing of coherent plasmons with low damping . Effective coupling of plasmons with fluorescent light is actual also for the fluorescent glasses [5, 6] and active optical waveguides . Trivalent rare earth (RE) ions, which are popular due to their efficient narrow-band photostable fluorescence, are of special interest as subjects for plasmonic enhancement. It is because their absorption cross sections as well as radiative decay rate are both very low compared to other emitters, such as dye molecules. There are a few studies suggesting local plasmonic enhancement of RE fluorescence induced by noble metal nanodopant in sol-gel-derived optical materials, such as silica glasses and active fibers in the visible [5, 6] and infrared  spectral ranges. Yet, the preparation of such samples requires specific methods for dispersion of metal particles in the host media, avoiding their aggregation and oxidation, especially for the silver nanoparticles [6, 8]. As far as we know, detected local enhancement of fluorescence intensity in the RE-doped sol-gel materials does not exceed two to three times [5, 6, 7]. Plasmonic resonance in small metal particles (approximately 5 to 20 nm) mainly causes a waste of the incident light energy as heat and do not contribute significantly to fluorescence enhancement. In contrast, plasmonic resonance in bigger nanoparticles (>50 nm) results in a stronger light scattering, which could support fluorescence more essentially in the resonance spectral range . However, the synthesis of such bigger nanoparticles with uniform size is not an easy task.
Hereby, we propose to utilize silica-gold core-shell nanoparticles described earlier by Pham et al.  for the enhancement of RE3+ fluorescence. Relatively big uniform size of silica core approximately 140 nm together with the plasmonic properties of the gold shell provide the necessary conditions for the plasmonically enhanced fluorescence which will be demonstrated in the case of sol-gel-derived TiO2:Sm3+. Used delicate combination of microscopic and spectroscopic techniques allowed investigation of Sm3+ fluorescence in the vicinity of separate gilded nanoparticles and detection of up to 10 times higher local intensity of emitted light.
Silica core nanoparticles were prepared by Stöber method  and functionalized by amino groups providing good covering of the silica core by the gold seeds. Then, joining of the gold seeds and formation of a continuous gold shell around the silica core were realized . Gilded nanoparticles dispersed in water were obtained. Plasmonic light extinction by this dispersion was confirmed by using Jasco V-570 spectrophotometer (Easton, MD, USA). The gilded nanoparticles were redispersed (approximately 0.6 wt.%) in butanol and added into the titanium butoxide precursor containing 2 mol% of samarium salt. This mixture was spin-coated on the glass substrates and annealed at 500°C. Thus, TiO2:Sm3+ films doped with gilded nanoparticles were obtained.
Optical imaging and microluminescence measurements were carried out on a home-assembled setup based on Olympus BX41M microscope (Olympus Corporation, Shinjuku-ku, Japan) combined with Andor iXon electron multiplying charge coupled device (EMCCD) camera (Springvale Business Park, Belfast, UK ) for highly sensitive optical imaging and fiber-coupled Andor SR303i spectrometer with Andor Newton camera for spectral measurements. Colored image of light scattering from bigger sample area was made by digital photocamera attached to an ocular of the microscope because the EMCCD camera used for fluorescence imaging has only black and white mode. Both dark field and fluorescence measurements were carried out by using a side illumination. In the case of dark field imaging, the beam of a bright white light-emitting diode (LED) was used so that the field of view remains dark if no scattering entities were present in the sample. The fluorescence was excited with a 355 nm diode-pumped solid-state (DPSS) laser while the signal was observed though a long-pass filter. In the latter case, the small aperture of the single-mode fiber allowed highly confocal spectral measurements in spite of the wide-field illumination. Alternatively, spectral measurements with point excitation were possible by using 532 nm DPSS laser focused onto the sample through the microscope objective.
Fluorescent lifetimes were measured by multichannel analyzer P7882 (FAST ComTec, München, Germany) connected to the photomultiplier. Also, we have determined fluorescence lifetimes in the time-gating luminescence mode (TGL) using an imaging attachment (LIFA-X, Lambert Instruments, Roden, The Netherlands) consisting of a signal generator, multi-LED excitation source with a 3-W LED (532 nm) and an intensified charge coupled device (CCD) Li2CAM-X with GEN-III GaAs photocathode. The CCD was mounted on the side port of an iMIC inverted digital fluorescence microscope (Till Photonics GmbH, Gräfelfing, Germany) through a TuCam adapter with × 2 magnification (Andor Technology). Multi-LED was fiber-coupled to the epicondenser of iMIC. The filter cube comprised of a BrightLine HC 520/35 nm (Semrock, Rochester, NY, USA) exciter, a Zt 532 rdcxt dichroic (Chroma, Bellows Falls, VT, USA) and ET 605/70 M nm (Chroma) emitter. Photons were collected with × 4 UPLSAPO objective (Olympus, Shinjuku-ku, Japan). Camera binning of 4 × 4 was used. In TGL mode, the delay time between excitation pulses (for 10 μs) trigger off and camera gain trigger on (for 10 μs) was varied in the interval between 0.6 and 275 μs at cycle frequency of 3 kHz. Full camera exposure time per image was 300 ms. Obtained image data analysis was performed using Lambert instrument fluorescence lifetime imaging microscope (Li-FLIM v1.2.22) software.
Results and discussion
Plasmonic enhancement of fluorescence is usually explained either by enhancement of light absorption or enhancement of radiative decay rate . In the case of TiO2, at least two different RE excitation mechanisms must be distinguished. First mechanism is realized when the absorption of ultraviolet light causes intrinsic excitations in TiO2 host, such as self-trapped or impurity-trapped excitons. These excitons can non-radiatively transfer energy to the fluorescent impurity. The effective cross section of such indirect Sm3+ excitation is several orders of magnitude higher than direct absorption cross section 10−21 to 10−20 cm2 of Sm3+ ions for the visible light . But ultraviolet light cannot efficiently excite plasmon in the gilded nanoparticles due to the lack of resonance. So, the reasons for the enhancement of Sm3+ fluorescence are either plasmonic enhancement of radiative decay rate or plasmonically assisted energy transfer from the excitons to the Sm3+ ions.
Lifetimes of fluorescence for the TiO 2 :Sm 3+ film doped with gilded nanoparticles, λ exc = 355 nm
Place on the sample
Bright spot 1
Bright spot 2
Bright spot 3
Spot 1 on the background
Spot 2 on the background
Fluorescence lifetimes at 532 nm excitation were measured in the time-gated mode on a FLIM in the spectral range of 580 to 660 nm. Obtained fluorescence decay is also multiexponential because different Sm3+ centers situate in TiO2 environment with different local surroundings. Numerical values of the lifetimes are similar to those presented in Table 1. Because of the insignificant changes in the lifetimes of Sm3+ fluorescence, we suppose that the detected 2.5 times enhancement in the intensity of fluorescence could be caused mainly by plasmon-enhanced direct absorption of exciting light by Sm3+ ions near the gilded nanoparticles.
Silica-gold core-shell nanoparticles were synthesized and successfully adjusted for the incorporation into TiO2:Sm3+ films. Prospective capabilities of these particles for the local plasmonic enhancement of rare earth fluorescence are demonstrated. Detected locally strong Sm3+ fluorescence is connected more with local increase in light absorption and energy transfer than with changes in radiative decay rates since fluorescent lifetimes are not changed significantly. Detected enhancement of fluorescence can be based both on the plasmonic enhancement of direct light absorption by Sm3+ ions and on profitable plasmonic support of energy transfer from exciton to rare earth ions in the case of the indirect excitation. As a next step, variation of dielectric core and noble metal shell sizes can be used for the spectral tuning of the plasmon resonance and estimation of its impact on the plasmon-enhanced fluorescence.
This work was supported by ESF project Nr. 2013/0202/1DP/184.108.40.206.0/13/APIA/VIAA/010 and EU through the ERDF (Centre of Excellence ‘Mesosystems: Theory and Applications’, TK114). The work was also partly supported by COST Action MP1303 and ETF grant 9007, Estonian Nanotechnology Competence Centre (EU29996), ERDF ‘TRIBOFILM’ 3.2.1101.12-0028, ‘IRGLASS’ 3.2.1101.12-0027, ‘Nano-Com’ 3.2.1101.12-0010, Estonian Research Council (SF0180032s12 and IUT 20-17), and European Union through the European Regional Development Fund (TK114 and 30020) and partially by the Nanotwinning project FP7-INCO-2011-6 and Marie Curie ILSES project no. 612620.
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