Introduction

The desired property for an optical tweezer is generally a sharp localisation of light which maximises the optical gradient forces compared to the radiation pressure1,2,3. In free space, it is achieved inside the beam waist of a laser focused by a high numerical aperture microscope objective4. In integrated optics, among the library of photonics structures, the dielectric nanocavities5,6,7,8,9 and the plasmonic nanoantennas10,11 with a strong field localisation are efficient optical traps for single particles, molecules or biological elements. However, these resonant structures provide an optical field distribution set by their design. Thus the resulting optical trap cannot be tuned dynamically. Here, we propose to use coupled cavities which light localisations are addressable by the wavelength5,12,13 to overcome this limitation. In this work, we fabricated different coupled nanobeam cavities on a silicon optofluidic chip and we have explored their properties for tweezing polystyrene particles and micromanipulating them dynamically14. By properly tuning the trapping wavelength with respect to the near-field properties of different coupled cavities15, we first report proof-of-concept demonstrations of particles counting and microscopic motion sensing. Then we demonstrate that coupled cavities are efficient building blocks for the future development of tuneable integrated tweezers devoted to the micromanipulation of the particles.

Results

The silicon nanobeam cavities considered here are photonic crystal Fabry Perot cavities integrated on silicon on insulator waveguide16,17. These one dimensional cavities can be coupled together through their evanescent field on the edge of the silicon waveguide as well as through a central photonic crystal mirror. To provide a robust coupling between the cavities18 but also to minimise the perturbation of the cavity field by the particles to manipulate8, the cavities exhibit moderate quality factor (Q ~ 3,000) for a 0.6 (λ/n)3 volume, where λ is the resonance wavelength and n the cavity refractive index. The silicon photonic chip is then combined to a static microfluidic cell filled by 1 μL volume of green fluorescent polystyrene (PS) 1 μm microspheres solution. As depicted in Fig. 1, the optofluidic cell is mounted onto a fluorescence microscope allowing the observation of the individual particle motion while the cavities are loaded at their resonance wavelength(s). For the experiments shown hereafter, the input power required for optical trapping was only few microwatts which is comparable to the most recent report in this field19. Such a low value is of a prime importance since temperature and flow gradients due to loaded cavities must be minimised on the chip to envisage future optofluidics applications. Here, the local temperature enhancement inside the Fabry Perot cavities was estimated from the resonance wavelength redshift of the loaded cavity compared to the cold cavity at room temperature. For the input powers considered throughout this work, the redshift was measured to almost 50 pm which corresponds to a local heating lower than 1K inside the Fabry Perot cavity according to the thermo-optics coefficient of silicon20,21,22 as well as compared to our earlier works23.

Figure 1
figure 1

Coupled nanobeam cavities integrated inside a microfluidic cell.

A dimer made of two polystyrene microspheres is trapped by the coupled cavities and its orientation is controlled by the wavelength.

Two nanobeam cavities coupled laterally through a 200 nm air slot are studied first. This coupling scheme allows to enhance the local field inside the slot and thus to sense any refractive index change in their proximity12,24. A scanning electron micrograph (SEM) view of the two cavities is shown on Fig. 2 and the 3D electromagnetic calculations of the electric field in water at resonance above the cavities are overlaid. The local field enhancement results from the constructive interference between the modes of each individual cavity12. The nearly perfect matching between the cavities is preliminary checked by Scanning Near-field Optical Microscopy (SNOM) observations available in the Supplementary Section 1 and then the optical trapping experiments are conducted. The nanobeam is loaded at the resonance wavelength while the particles motion above the cavities and the nanobeam transmittance are monitored simultaneously. The nanobeam transmittance is plotted in Fig. 2b and the pictures of the particles motion extracted from Supplementary Movie S1 are shown in Fig. 2c. The experiment shows the successive trapping of two particles. Due to the near-field interactions between the dielectric particles and the field confined inside the slotted structure (the 3D electromagnetic calculations of these interactions are available in the Supplementary Section 1), the resonance wavelength is redshifted by the presence of the particles inside the optical trap25. For this reason, each particle trapping event is associated with a 10% damping of the nanobeam transmittance. This sensitivity to the trapping events is comparable to that one reported for other integrated photonic devices used for optical trapping5,26. However, the sharp field localisation inside the slot12 enables here an enhanced sensitivity to the microscopic motion of the trapped particles. A closer view of the transmittance signal shows small amplitude fluctuations. The latter are directly correlated to the submicrometric motion of the particles inside the trap, as verified by observing Supplementary Movie S1. As a result, the sensitivity shown here enables stored particles counting but also permits to sense their submicrometric motions of the particle inside the trap. As we demonstrated hereafter, we have next considered other coupling schemes between the cavities for controlling these microscopic motions by means of shapeable optical traps.

Figure 2
figure 2

Trapping and sensing the particles with coupled cavities.

a, Scanning electron micrograph view of the coupled cavities overlaid with the 3D Finite Difference Time Domain calculation of the resonant mode in water. b, Nanobeam transmittance recorded during the trapping experiment. c, Selected snapshots at different instants of the experiment pointed on b, by the arrows extracted from supplementary Movie S1.

Our approach for the trap shaping relies on the coupling engineering between the cavities13 to give rise to an addressable redistribution of the resonant mode. For instance, the two cavities can be coupled to each other through the central photonic crystal mirror. If they are perfectly identical, the coupled structure supports two identical resonant modes delocalised in both cavities. Introducing a nanometrical variation between the length of the two cavities breaks this symmetry18. Depending on the resonant wavelength, a preferential redistribution of the mode inside one or the other cavity occurs. Hence changing the operating wavelength enables to switch the predominant optical trap from one cavity to the other. For a 2 nm difference between the cavity lengths, the 3D FDTD calculations of the two resonant modes in water are overlaid to the SEM view of the fabricated structure in Fig. 3. The transmittance spectrum showing the two resonances is displayed in Fig. 3b and the experimental observation of the corresponding modes by SNOM is provided in Supplementary Section 2.

Figure 3
figure 3

Micro positioning of trapped particles with detuned coupled cavities.

a, Scanning electron micrograph view of the coupled cavities overlaid with the 3D Finite Difference Time Domain calculation of the resonant modes in water. b, Transmittance spectrum of the detuned coupled cavities in water. The two resonance wavelengths are referred as λ1 and λ2. c, Selected snapshots at different times of the experiment extracted from supplementary Movie S2 showing the single particle motion from a cavity to the other actuated by a wavelength change from λ2 to λ1. d, same as c, but with two trapped particles and actuated by a wavelength change from λ1 to λ2.

As shown in Supplementary Movie S2, a single particle as well as two particles trapped together move from a cavity to the other as the resonance wavelength is tuned. The particles move here without being released since they slide inside the same trap which is balanced by the wavelength from one cavity to the other. Figure 3c and 3d show the pictures selected from Supplementary Movie S2 emphasising this experimental observation. The particle average speed inside the trap is measured to 4 μm.s−1 for a single particle and it is reduced to 3 μm.s−1 for two particles due to an increased drag. The linear translation of the trapped particles observed here is triggered by the wavelength changes and may open promising perspectives for the microscopic positioning of particles on predetermined trapping sites. We also believe that an accurate control of the absolute position of the particle between the cavities could be achieved by using a dual wavelengths excitation with balanced intensities.

Another approach for micromanipulation is to use the multiple interferences processes involved between multiple coupled cavities. In this case, the cavities can be switched on and off independently in respect to the symmetry axis of the coupled structure13. For instance, for three cavities coupled through air gaps as shown in Fig. 4, three resonant wavelengths switch on respectively the central cavity only (λ3), the two external ones (λ2) and all together(λ1).

Figure 4
figure 4

Orientation control of a dimer with three coupled cavities.

a, Scanning electron micrograph view of the coupled cavities overlaid with the 3D Finite Difference Time Domain calculation of considered resonant modes λ2 and λ3 in water. c, Transmittance spectrum of the coupled cavities showing the resonant modes λ2 and λ3 in water. d, Selected snapshots at different instants of the experiment extracted from supplementary Movie S3 showing the rotary motion of the dimer triggered by the resonant modes λ2 and λ3.

The SNOM observations of these three modes are provided in Supplementary Section 3. The two modes in water at λ2 and λ3 displayed on the SEM view of the fabricated structure in Fig. 4a also provide an additional degree of freedom to control the orientation of an anisotropic assembly of trapped particles. To illustrate this, we manipulated a dimer made of two trapped particles. As shown on the pictures of Fig. 4c, a dimer trapped at λ3 is confined and orientated along the central cavity. The dimer orientation is then changed by tuning the wavelength of the laser to λ2. As shown on Supplementary Movie S3, a counter clockwise 90° rotation of the dimer is observed. Then tuning the laser to λ3 enforces a new rotation of the dimer. Remarkably, the rotation is once again observed counter clockwise which gives rise to a global rotary motion. In more detail, from the experimental observations, we determined the angular speed (ω) between two orthogonal orientations. From λ3 to λ2, ω2–3 equals to 0.84 rad.s−1 while from λ2 to λ3, ω3–2 = 1.39 rad.s−1. These differences correspond to the different optical torques associated to the two optical traps. However, the main limitation for the rotary motion remains the switching time between the operating wavelengths. For proof-of-concepts demonstrations, the switch was made manually which results in the sequential motion observed in Supplementary Movie S3 but this could be greatly enhanced by means of an optical switch. A proper control of the switch according to the particle angular speed could permit to achieve a continuous rotary motion. An accurate control of the absolute orientation of the dimer could also be achieved by using a dual wavelengths excitation with balanced intensities. Applying this micromanipulation technique to other types of anisotropic particles, for instance to nanowires or metallic dimers, could permit a dynamical control of their orientation for applications in surface enhanced Raman spectroscopy (SERS) as well as any other optical technique which is polarization sensitive.

Discussion

In summary, by properly engineering the near-field coupling between photonic crystal cavities on a silicon optofluidic chip, we manage to configure a predetermined set of optical forces distributions addressable individually by the wavelength. Different functionalities such as trapping, counting, moving and rotating particles are built by taking benefit from the versatility of the coupling geometry between the cavities. Compared to the existing tweezers integrated on a silicon chip27,28, the near-field coupling between the cavities provides here an additional degree of freedom to address by the wavelength optical traps with different shapes. This capability opens innovative ways for all optical control of microparticle and bio-object micromanipulation in nanoscale science without a free space optical tweezing system.

Despite the small number of coupled cavities considered in this work, the near-field coupling give rise to significantly different optofluidic functions relying on optical gradient forces. A step forward will consist in increasing the number of coupled cavities into a complex photonic array merging the different coupling schemes and thus enabling the manipulation of trapped particles at a larger scale. In this case, new optical strategies with multiple operating wavelengths will be required to achieve a simultaneous and parallel control of the trapped particles.

At last, the reported proof-of-concepts experiments were carried out with purely dielectric particles. However, the near-field interactions with micro and nano sized objects not only depends on the electromagnetic field distribution but also on their intrinsic properties such as their size, their geometry, or their dielectric and magnetic constants. Different behaviours are thus expected for these different objects inside the optical traps. Once the prerequisite analysis on individual species will be conducted, the manipulation of heterogeneous trapped particles could be envisaged in a near future. As shown for dielectric spheres29, this could permit for instance the development of an all integrated light templating technique for building heterogeneous materials.

Methods

The photonics structures are fabricated using the standard microelectronics techniques. We used a 100 keV electron beam to lithography the structure and then we etched the processed 200 mm SOI wafer with a chloride induced coupled plasma machine. The optical characterisations of the samples were made on typical optical end-fire coupling bench experiments. The microfluidics cells used on the photonics samples are made with a spincoated polydimethylsiloxane layer patterned with a rectangular aperture allowing a 1 μL volume of colloidal solution in the cell. This PDMS layer is deposited and bonded on the photonic sample with oxygen plasma. The cell is firstly filled with colloidal solution and sealed by a microscope thin cover slip glass. The photonics structures are visualised with a vision column and a microscope objective arranged around a homemade bright field and fluorescence vision set-up. The nanocavities are lightened through a lensed fiber with a Tunics tunable laser TE polarized source with a 150 nm wide near-infrared spectral range. For the trapping experiment we add in an erbium doped fiber amplifier with output power of 200 mW in the C and L telecommunication bands. The optical signal is collected with a microscope objective and detected with an InGaAs photodiode. The effective power injected inside the waveguide is measured to few microwatts at the output. The detector is linked to a high bandwidth oscilloscope through a current amplifier. A user interface synchronises the camera image recording (over the photonics structures) with the optical signal monitoring.