Selective Excitation on Tip-Enhanced Raman Spectroscopy by Pulse Shaping Femtosecond Laser
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In this paper, we propose a scheme for achieving ultrafast coherent control of the selective excitation among three excited states in stimulated Raman scattering process on a tip-enhanced Raman spectroscopy (TERS). The center frequencies of the pump and Stokes laser pulses are 14,000 cm−1 and 12,500 cm−1, and their spectral bandwidths are both 700 cm−1. By properly modulating the spectral phase distribution and cutting the frequency components, the stimulated Raman transition probabilities of two excited state keep maximal, while the other one can be suppressed to zero. The shaped pump and Stokes pulse irradiate obliquely into the TERS nanostructure containing a single layer molecule. The impulse response in temporal and frequency domain is calculated by using finite-difference time-domain (FDTD) simulation followed by Fourier transform. The frequency components and the relative phase are same with the corresponding input pulses, but the intensities are enhanced by more than 10 times. Compared with the case without the TERS nanostructure, the probability of selective excited Raman transition increases by more than 4 orders of magnitude, and the selective depressed Raman peak keeps at 0.
KeywordsTip-enhanced Raman spectroscopy Single molecule detecting Ultrafast coherent control Pulse shaping
Tip-enhanced Raman spectroscopy (TERS) is a powerful technique resulting in strongly increasing Raman signals from molecules attached to a metallic nanostructure. It is of great significance in many fields such as chemistry, biology, medicine, pharmacology, and environmental science [1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14]. TERS is one of the useful tools for detecting single molecule with high sensitivity and molecular specificity. R. Zhang et al. reported Raman spectral imaging and resolved the inner structure and surface configuration of a single H2TBPP molecule . Dmitry Kurouski et al. compared the nanoscale redox behavior of Nile Blue by electrochemical TERS with conventional cyclic voltammetry . To gain insight into intramolecular coupling, substrate coupling, and dynamic processes, Kyoung-Duck Park et al. used TERS at variable and cryogenic temperatures, to slow and control the motion of a single molecule . Besides, Raman spectroscopy of single molecule was used to study molecular isomerization and its intermediate processes .
How to enhance the signal-noise ratio is a key problem in detecting single molecule by TERS, which is very important in improving the spatial resolution and expanding its applications in the fields of molecular dynamics and controlling [10, 11, 12, 15, 16]. A main method to enhance the signal-noise ratio is the tip fabrication [1, 2, 18]. Recently, R. Zhang et al. demonstrated chemical mapping of a single molecule with a spatial resolution less than 1 nm through the generation of an efficient double-resonance enhancement for both Raman excitation and Raman emission by precisely adjusting the tunneling gap . However, several neighboring Raman peaks were excited simultaneously, which depressed the signal-noise ratio of the TERS spectra.
An effective method for the coherent control of Raman scattering is femtosecond pulse shaping technique, where the laser spectral phase and/or amplitude were modulated to achieve the constructive/destructive interference between different path integral leading to expected/depressed outcomes [19, 20, 21, 22, 23, 24, 25, 26, 27]. This method was widely used in controlling molecular vibration state, rotation state, ionization state, isomerization, and other molecule dynamics. By tailoring the phase of probe pulse, Dan Oron et al. demonstrated a narrow-band coherent anti-Stokes Raman spectroscopy (CARS) signal with a width of less than 15 cm−1, which is an order of magnitude narrower than the signal from a transform limited (TL) pulse . They further eliminated the non-resonant CARS background and selectively excited one of two neighboring Raman levels by shaping both the pump and the Stokes pulses with an appropriate spectral phase function . Selective excitation of CARS by shaping femtosecond laser pulses using adaptive learning algorithms, good signal-to-background ratio, and high sensitivity were realized in many kinds of molecules [21, 22, 23].
Spatiotemporal control of optical fields in plasmonic nanostructures excited by shaped ultrafast laser pulse was studied theoretically [28, 29, 30, 31, 32, 33]. Mark Stockman et al. predicted and theoretically investigated the coherent control of nanoscale localization of ultrafast optical excitation in V-shaped nanostructures by spectral phase modulation, which permits one to coherently control the local light fields to be concentrated at a desired location at certain times [29, 30]. Laser pulse shaping techniques were further used to spatiotemporal control of optical fields in nanoantennas and plasmonic circuits . Using finite-difference time-domain (FDTD) simulations followed by Fourier transformation, the impulse response of a nanostructure in the time and frequency domain was obtained. Ultrafast dynamics of nanoplasmonic dephasing of individual silver nanoparticles and small clusters were studied via accurately delayed femtosecond laser pulses, which provided insight into inhomogeneous and homogeneous broadening mechanisms in nanoplasmonic spectroscopy . The response over a broad spectrum of a snowflake antenna was used, inversely, in femtosecond pulse shaping . Spatiotemporal control of optical fields in plasmonic nanostructures was widely applied in the fields of high-harmonic and single attosecond pulse generation [35, 36], ultrafast coherent surface enhanced Raman scattering [37, 38], and vibrational wave packet motion on single molecules .
In this paper, we introduce a scheme for achieving a precise control of the selective excitation among three excited states in the stimulated Raman scattering process by shaping femtosecond laser pulses. In our model, two excited states are maximally populated, while the other one is suppressed to zero by phase modulating and frequency cutting of the pump and Stokes pulse. The shaped pulses are transformed into time domain by inverse Fourier transform, and the temporal evolution at the probe point of the gap center of TERS structure is calculated by using COMSOL Multiphysics. The temporal, phase, and frequency distributions of the response pulse are calculated and discussed respectively. The theoretical results show that the enhanced and selected Raman scattering is realized simultaneously in the TERS structure by shaping the pump and Stokes femtosecond laser pulses.
TERS Nanostructure and Simulation Method
The finite element method (COMSOL Multiphysics) is employed to calculate the optical properties of the TERS nanostructure. The simulation region is 750 × 750 × 750 nm3. A cubical perfectly matched layer is used to absorb all outgoing radiation and to eliminate the reflections at the domain boundaries. During the numerical simulation, the minimum element size of local adaptive mesh refinement is set as 0.5 nm.
Coherent Control and Selective Excitation of Raman Transitions by Shaping Femtosecond Pulses
Coherent control was intensely studied in the application of selective excitation of Raman scattering by shaping the ultrafast pump and Stokes laser pulses [19, 20, 21, 22, 23, 24, 25, 26, 27]. In the following, we theoretically study how to achieve a high degree selective excitation of two Raman peaks among three excited states.
The TERS spectra of Rhodamine 6G, malachite, porphyrin, and DNA were intensely studied [2, 7, 10, 12, 13, 15, 16, 17, 18, 41, 42, 43]. There are many Raman peaks in the range of 1000–1700 cm−1. In our theoretical model, three Raman peaks of 1600 cm−1, 1520 cm−1, and 1400 cm−1 are studied as representative sample. The center frequencies of the pump and Stokes laser pulses Γp and Γs are set at 14000 cm−1 and 12,500 cm−1, and the FWHM δp and δs are both 700 cm−1. The difference between the center frequencies of the pump and stokes lasers is nearly equal to the average value of three Raman peaks, and the bandwidths are much larger than the differences among the three Raman peaks, which ensure the three Raman modes are all efficiently excited.
Figure 3b shows the temporal distribution of the electric field intensity of the Stokes laser after the modulation. The laser pulse changes from a Gaussian shape into a complex profile with many small peaks caused by the amplitude and phase modulation. The temporal FWHM of the laser intensity elongates to 480 fs with three dumbbell-shaped peaks. The maximum value of the laser intensity is greatly depressed, only 0.023 of the initial Gaussian pulse.
With further increasing π phase step position, the Raman transition pf3 begins to be suppressed, while pf1 and pf2 keep the same value. When π phase step position increases to 13,883.3 cm−1, Raman transitions 1 and 2 are well excited and the probabilities pf1 and pf2 are same as the values for the pump laser being a TL pulse. However, pf3 is suppressed to zero, which is resulted from the destructive interference among different optical pathways in the stimulated Raman transition process.
When the step position scans to 13,926.7 cm−1 and 14,166.7 cm−1, the transition probabilities of pf2 and pf1 are selected suppressed to zero, respectively. Moreover, the transition probability pf3 is larger than the case of TL pump laser by 37% as the step position at 13926.7 cm−1, which is caused by the constructive interference among optical pathways excited by the shaped Stokes laser and pump laser.
The influence of the width of the rectangular π phase modulation on the selection excitation of Raman transition is further studied. The calculation results indicate that if the rectangular π phase modulation width of the Stokes laser, as shown in Fig. 3a, is larger than 80 cm−1, the Raman peak pf3 can be thoroughly depressed, but the other two cannot be depressed to zero. If the modulation width is larger than 120 cm−1, none of the three Raman peaks can be depressed to zero. If the modulation width is less 80 cm−1, all of the three Raman peaks can be depressed to zero. However, as one Raman peak is depressed to zero, the probabilities of the other two become smaller. These results indicate that the pulse shaping shown in Fig. 3 is an effective method to realize selective excitation of two Raman transitions among three ones.
Ultrafast Coherent Control of TERS
When π phase step position of pump pulse is at 13883.3 cm−1, Raman transitions pf1 and pf2 are well excited, while pf3 is depressed to zero. The temporal distribution of the pump and Stokes pulse electric field is shown in Figs. 3 and 4. The impulse response of the TERS structure to the shaped pump and Stokes pulse in temporal and frequency domain are obtained by using FDTD simulation followed by Fourier transform. The simulation time region is set as [0, 10,000] fs, and the interval is 0.1 fs.
In this paper, the stimulated Raman transition is a two-step process: absorbing a photon of pump laser and emitting immediately a photon with same energy of Stokes laser. This is a non-linear interaction of pump and Stokes laser with the molecules. Recently, P. Dawson et al. reported the effects of non-linear response of metal dielectric constant on the tip-enhanced Raman scattering [48, 49, 50]. In the region around the gap of tip-substrate, the light field is greatly enhanced and a Kerr type non-linearity, locally modified dielectric constant is used to study the Raman scattering. This paper focuses on the enhanced selective Raman transition of TERS nanostructure. The effects of the non-linear locally modified dielectric constant of metal on the Raman transition are not enclosed.
In summary, we theoretically demonstrate a scheme for achieving precise control of selective excitation and greatly enhanced Raman transition among three excited states via TERS structure. The frequency components in the middle part of Stokes spectrum are rectangular π phase modulated, and the others are cutoff. By π phase scanning the pump pulses, the stimulated Raman transition probability for one excited state is suppressed to zero, while those for the other two excited states keep at the maximal value.
The shaped pump and Stokes pulse irradiate obliquely into the TERS structure. The impulse responses in temporal and frequency domain are calculated by using FDTD simulation followed by Fourier transform. The results indicate that the frequency components and the relative phase are nearly same with the corresponding input pulses, but the intensities are enhanced by more than ten times. Compared with the case without the TERS nanostructure, the probability of selective excited Raman transition increases by more than 4 orders of magnitude, and the selective depressed Raman peak keeps at 0. The enhanced and selective Raman excitation is realized in the TERS nanostructure simultaneously, which could contribute to the enhancement of the signal-noise ratio for the Raman spectra of single molecule and its application in chemistry, biology, medicine, pharmacology, and environmental science.
This work is supported by the National Natural Science Foundation of China (grant no. 11474097, 11374099, 11274116), the Open Fund of the State Key Laboratory of High Field Laser Physics (Shanghai Institute of Optics and Fine Mechanics), Shandong Provincial Major Science and Technology Special Project (New Emergent Industries) (2015ZDXX0801A03), Shandong Provincial Key Research and Development Project (2017CXGC0810), and Shandong Education Science Plan “Special Subject for Scientific Research of Educational Admission Examination” (ZK1337212B008).
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