Optomechanics and thermometry of cryogenic silica microresonators

Optomechanics and thermometry of cryogenic silica microresonators

Abstract

We present measurements of silica optomechanical resonators, known as bottle resonators, passively cooled in a cryogenic environment. These devices possess a suite of properties that make them advantageous for preparation and measurement in the mechanical ground state, including high mechanical frequency, high optical and mechanical quality factors, and optomechanical sideband resolution. Performing thermometry of the mechanical motion, we find that the optical and mechanical modes demonstrate quantitatively similar laser-induced heating, limiting the lowest average phonon occupation observed to just 1500. Thermalization to the 9 mK thermal bath would facilitate quantum measurements on these promising nanogram-scale mechanical resonators.

I Introduction

Cavity optomechanical systems, consisting of high-quality optical cavities coupled to mechanical resonators, offer a promising route to making precision measurements in both the applied and fundamental science domains Aspelmeyer et al. (2014). In dispersively-coupled systems, the motion of the mechanical resonator shifts the resonance frequency of the optical cavity, which can in turn be observed as periodic changes in the amplitude or phase of light traversing the cavity. Optomechanics thus provides an extremely sensitive readout for micro- and nano-mechanical resonators, enabling their use as exquisite sensors of a variety of phenomena on small scales, including displacement Anetsberger et al. (2010), force Gavartin et al. (2012); Miao et al. (2012); Doolin et al. (2014a), torque Kim et al. (2013); Wu et al. (2014) and acceleration Krause et al. (2012). This readout sensitivity has also motivated fundamental searches for quantum properties of nanomechanical resonators Gangat et al. (2010) at, or near, their vibrational ground state where mechanical motion originates from quantum zero-point fluctuations. The hybrid nature of optomechanical systems additionally makes them desirable for applications in quantum information processing architectures Stannigel et al. (2010), and as a resource for entangled Palomaki et al. (2013), squeezed Safavi-Naeini et al. (2013) or other non-classical states Brkje (2014).

Noise from thermally-driven oscillations of mechanical resonators poses a significant obstacle to performing many of these proposed experiments. Mechanical resonators with frequencies in the kHz to GHz range have thermal occupancies of billions to thousands of phonons at room temperature, which can easily drown out any quantum signature. Reducing this thermal occupation is thus of great importance. The optomechanical interaction can be exploited to actively cool the mechanical mode into or near its ground state Schliesser et al. (2008); Chan et al. (2011); Park and Wang (2009) but a fundamental limit to this process is imposed by the temperature of the mechanical resonator’s bath, necessitating cryogenic pre-cooling Aspelmeyer et al. (2014). Active optomechanical cooling furthermore reduces the quality factor () of the mechanical resonator, decreasing the signal-to-noise ratio at low temperatures Aspelmeyer et al. (2014). For these reasons, we focus on passively cooling our resonators, which additionally facilitates the use of sensitive optomechanical systems for probing low temperature phenomena such as superfluidity Sun et al. (2013); De Lorenzo and Schwab (2014) and superconductivity Geim et al. (1997).

Figure 1: (a) Photograph of a string of bottle resonators along with the tapered fiber for optomechanical measurement. Scale bar is 100 m. (b) Simulation of a whispering gallery mode optical resonance, showing a cross-section of the bottle with the optical field localized along the equator. (c) Representative mechanical spectrum, measured at room temperature. The three most prominent resonances are indicated by the corresponding mechanical mode simulation.

In previous experiments, optomechanical systems have been passively cooled using both helium flow cryostats Park and Wang (2009); Rivière et al. (2013) and dilution refrigerators Palomaki et al. (2013); Meenehan et al. (2014). Our system uses a dilution refrigerator for its lower achievable base temperature and, in contrast to the system presented in Ref. 22, uses the highly-efficient tapered-fiber coupling method Knight et al. (1997); Cai et al. (2000), which is compatible with both bulk and on-chip optomechanical systems MacDonald et al. (2015); Hauer et al. (2014).

Here, we present measurements of so-called silica bottle resonators Kakarantzas et al. (2001); Pöllinger et al. (2009), shown in Figure 1, which have ellipsoidal shapes and exhibit optical whispering gallery modes (WGM) in the infrared and visible range, a simulation of which is shown in Figure 1(b). They are interesting structures for their high optical quality factors ( up to ) and the tunability of their mode structure Pöllinger et al. (2009). Additionally, these bottle resonators have mechanical breathing modes with frequencies in the 50 to 250 MHz range, Figure 1(c), corresponding to average phonon occupancies of just 3.3 and 0.4, respectively, at a temperature of 9 mK (the base temperature of our dilution refrigerator). The significant modal overlap of the optical and mechanical modes, which are both localized at the equator, leads to a large optomechanical coupling, on the order of GHz/nm. Furthermore, the combination of high optical quality factor and high mechanical frequency places these devices in the sideband-resolved regime, enabling many of the important tools of optomechanics Aspelmeyer et al. (2014).

Ii Experimental Details

We fabricate our bottle resonators by applying tension to each end of a single mode optical fiber while melting it with a CO laser. This process results in a string of resonators, as shown in Figure 1(a), separated from each other by thin stems. By controlling the intensity of the CO laser and the length of the pull time, we create resonators with symmetric shapes and extremely thin supporting stems. This reduces phonon tunnelling through the stems and increases the mechanical quality factor Anetsberger et al. (2008).

Tapered fibers Knight et al. (1997); Cai et al. (2000) are used to couple light into the WGMs of the bottles. These fibers have a small core (on the order of the wavelength of the light) and no cladding, save the medium surrounding the fiber. Our tapers are created by heating an optical fiber with a hydrogen torch and pulling it until a minimum diameter of 1 m is reached Hauer et al. (2014), resulting in a large evanescent field. This allows efficient coupling of light to WGM resonators through frustrated total internal reflection.

We passively cool the taper and bottle resonators using a dilution refrigerator with a base temperature of 9 mK MacDonald et al. (2015). To facilitate taper-resonator coupling at cryogenic temperatures, we have built an optomechanical coupling system within the inner vacuum can (IVC), on the mixing chamber plate, as pictured in Figure 2(a). The bottles are mounted on top of a stack of nanopositioning stages, which allow full three-dimensional control over the position of the resonators. They are thermally anchored to the mixing chamber through a series of oxygen-free high-conductivity copper plates and braids. The taper is epoxied and mounted to a large Invar block, which minimizes the effects of thermal contractions. A homebuilt low-temperature microscope MacDonald et al. (2015) enables real-time in situ imaging of the taper-resonator system with a resolution of 1 m (Figure 2(b)). We inject light from a tunable diode laser housed at room temperature into the tapered fiber and detect the transmitted light with a fast photodetector. The optical and mechanical properties of the bottles can thus be measured from the low- and high-frequency parts of the photodetector voltage, respectively.

Figure 2: (a) Optomechanical coupling apparatus on the mixing chamber stage of our dilution refrigerator. (b) Image of a bottle resonator and tapered fiber taken with the low-temperature microscope. Scale bar is 100 m.

Iii Optical Properties

Characterization of the near-infrared optical modes is performed by scanning a tunable diode laser (1500-1630 nm) with angular frequency across a resonance, resulting in the following expression for the low-frequency part of the transmission (in units of photons per second) through the tapered fiber

(1)

Here is the rate of photons passing through the tapered fiber, for injected laser power and reduced Planck constant . The linewidth of the resonance is given by where is the intrinsic decay rate and is the rate at which photons are exchanged between the bottle and tapered fiber. Our setup allows us to sensitively control the relative strengths of these intrinsic and extrinsic decay rates MacDonald et al. (2015). For the measurements that follow, the resonator is operated in the slightly-undercoupled regime ().

The number of photons inside the cavity,

(2)

is a function of the laser detuning from the cavity resonance, . For the whispering gallery modes in a bottle of radius , the angular optical resonance frequencies are given by

(3)

The integer is a mode label for a particular resonance, is the speed of light in vacuum, is the refractive index of the bottle and is a geometric factor which accounts for the fact that the optical mode is not perfectly confined to the surface of the resonator Carmon et al. (2004).

For relatively low injected optical powers ( nW), the optical resonances can be measured without heating the mixing chamber thermometer and have of 10-10, which are consistent with their room-temperature quality factors. At larger injected powers, light lost from the taper (30%) heats the cryogenic environment MacDonald et al. (2015). Furthermore, the high , and correspondingly long photon lifetime, in the cavity leads to an increased absorption of laser photons in the silica.

Figure 3: (a) Simulated normalized taper transmission (black) and number of intracavity photons (blue) for a linear optical resonance with parameters comparable with those seen in experiment ( MHz, MHz and W). (b) Simulation of a nonlinear resonance, with the same parameters as above and Hz. All real solutions to Equation (5) are plotted in black, while the transmission for a forward (reverse) scan of the laser is plotted in green (red).

This absorption generates a local heating of the silica within the optical mode volume, which in turn causes both a change in the bottle dimensions through thermal expansion and a change in the refractive index through the thermo-refractive effect. We can then rewrite Equation (3) with Taylor-expanded expressions for the radius and the refractive index Carmon et al. (2004),

(4)

where is the equilibrium temperature of the glass in the absence of laser heating, is the temperature increase caused by optical absorption, and is the linear thermal expansion coefficient. Although higher-order terms become important under some conditions Arcizet et al. (2009), here we keep only terms to first order in and for simplicity write .

Incorporating the modified into Equation (2), we have

(5)

where the thermo-optical effects have been written into a nonlinear detuning parameter Barclay et al. (2005); Doolin et al. (2014b). This parameter can be thought of as the shift in the optical resonance frequency per intracavity photon, and is related to the parameters in Equation (4) by , under the assumption that the temperature gradient is proportional to the number of intracavity photons. As we will see, the exact constant of proportionality will depend on the resonator’s heat dissipation.

Equation (5) is now a nonlinear function of , giving rise to up to three distinct real solutions for appropriate values of . Experimentally, this is manifest as a bistability and hysteresis in the resonance shape, which is dependent on the scanning direction of the laser Braginsky et al. (1989); Il’chenko and Gorodetskii (1992), as illustrated in Figure 3. As the laser is tuned closer to the optical resonance, more photons are coupled into the cavity, causing a greater shift in the resonance frequency, such that it becomes distorted from the linear shape shown in Figure 3(a).

Figure 4: Transmission measured across a bottle optical resonance with a wavelength of 1516 nm and a temperature of 4.2 K. For similar injected powers, the resonance exhibits different behavior when the bottle is (a) immersed in helium exchange gas and (b) surrounded by vacuum. Fits to the data (black line) yield nonlinear detuning parameters of approximately (a) Hz and (b) Hz.

This nonlinear optical behaviour is observed in our experiments, as shown in Figure 4 for a m bottle. Using the cubic equation to exactly solve Equation (5), we fit our experimental data to extract under various experimental conditions. In particular, we find that injecting a large quantity of helium exchange gas into the IVC at 4.2 K reduces by an order of magnitude ( Hz compared to Hz in vacuum). We furthermore find that at the fridge base temperature ( Hz) is comparable to that at 4.2 K in vacuum.

Although it will not be discussed here, it is worth noting that at intermediate pressures of helium exchange gas, we observe a higher-order thermo-optical nonlinearity. This results in up to five real solutions to a modified form of Equation (5), and presents itself in the experiment as a multistability in the resonance profile. This effect is thought to originate from a reversal of the thermo-refractive effect at low temperatures Arcizet et al. (2009), although the nonlinear temperature dependence of the thermal expansion coefficient White (1975) may also contribute.

Iv Mechanical Properties

The high-frequency part of the taper transmission encodes the mechanical motion of the bottle resonator. We collect this signal by recording a time trace of the high-pass filtered photodetector voltage with a fast analog-to-digital converter. The m bottle studied has several mechanical resonances, with the most prominent being at 55, 85 and 109 MHz, with room temperature quality factors of . At low temperatures, we focus on the lowest-frequency (55 MHz) mode, which has an effective mass ng and optomechanical coupling strength GHz/nm.

It is important to note that, despite significant efforts to thermally anchor the bottle resonators to the base plate of the fridge, the thermometers used to measure the temperature of the mixing chamber will not provide an accurate measure of the mechanical mode temperature. The thermally-insulating nature of silica along with the very thin connections between the bottles prevent efficient conduction of heat, while incident laser light used to measure the mechanics leads to local heating of the resonator. Dynamical back-action effects in the optomechanical interaction can also lead to mode-specific heating or cooling Aspelmeyer et al. (2014) which is not reflected in the temperature of the bulk silica.

To independently determine the temperature, we exploit the thermally-driven motion of the resonator. In this case, the resonator’s spectral response is quantified by its one-sided power spectral density (PSD). For a resonator with effective mass, , at temperature , the displacement PSD is given by Hauer et al. (2013)

(6)

for a sufficiently long measurement time (). Here, is the Boltzmann constant, is the angular frequency of the mechanical resonance and is the Fourier transform of the resonator’s position . It is evident that the amplitude of the displacement PSD () scales linearly with and thus gives a direct measurement of the mode temperature.

In our experiments, we measure this displacement response by Fourier transforming the photodetector voltage, squaring and dividing the result by the measurement bandwidth. The voltage PSD is given by the sum of a detection system-dependent noise floor and the transduction of through the optical cavity and photodetector,

(7)

The transduction of scales with the square of the rate of injected photons, as well as the square of the ratio of the optomechanical coupling strength to the mechanical resonance frequency. All of the detuning dependence of is contained in (see Appendix), a function which describes the transduction of the resonator’s fluctuations in position into fluctuations in first taper transmission and then voltage.

Figure 5: Schematic of the mechanical mode thermometry technique. Modulation of laser light by an electro-optic modulator (EOM) generates optical sidebands on the laser spaced by . The motion of the optomechanical resonator (OMR) imposes additional sidebands, at . Both sets of sidebands are detected by the photodiode (PD), resulting in a high-pass filtered (HPF) spectrum that has two distinct peaks corresponding to the phase modulation (54.5 MHz) and the mechanical motion (55 MHz).

Precise knowledge of the laser detuning, along with the optomechanical coupling strength , injected optical power and the gains of the detection electronics, would allow the extraction of , and hence the temperature, from Equation (7). This is not always experimentally feasible, so we instead indirectly calibrate by injecting an all-optical signal of known energy into the system Gorodetsky et al. (2010). The general procedure for doing so is outlined in Figure 5. An electro-optic modulator (EOM) driven at angular frequency phase modulates the input laser light, generating optical sidebands on the laser at frequencies for integer . If the phase modulation depth, , is small ( for applied voltage and EOM half-wave voltage ), only the first order sidebands () need be considered. If is chosen such that where is the resonance linewidth, the PSD of the photodetector signal becomes (see Appendix)

(8)

where is the spectrum of the applied phase modulation. This spectrum features two distinct peaks, as shown in Figure 5 at and .

If we additionally assume that , such that the response of the detection electronics is flat, then and the phase modulation signal and mechanical motion are transduced similarly through the optical cavity. Although the strength of each peak in depends sensitively on the injected optical power and the laser detuning, this dependence is identical between the two peaks, such that it simply provides an overall scale for the spectrum. In contrast, any change in will affect only the mechanical resonance at through . If the phase modulation conditions are held constant, we can then find the temperature of the mode through the ratio

(9)

where is the integrated area under the phase modulation peak and is the area under the mechanical resonance. For the purpose of these calculations we subtract the detection noise floor, .

Figure 6: (From top to bottom) The low-frequency transmission of light through the tapered fiber traces out the optical resonance profile (top), while information about the mechanical resonance at 55 MHz is contained in the power spectral density of the high-frequency transmission (plotted here on a log scale). From fits to these spectra, we extract the resonance frequency (red), quality factor (green) and temperature (cyan) of the mechanical mode across the optical resonance.

We drive our EOM at MHz and measure at liquid helium temperature (4.2 K), where a copious quantity of exchange gas in the IVC ensures good thermalization of the bottle resonator with the outer helium bath. The result, , fixes the temperature measurement scale. The mechanical mode temperature is thus given by

(10)

Measurements of the bottle resonator made under various experimental conditions at low temperatures are shown in Figure 6. The laser was scanned across the optical resonance and the low- and high-frequency parts of the taper transmission were recorded simultaneously. From left to right, measurements were made at 4.2 K in exchange gas and in vacuum, as well as in vacuum with the fridge operating at its base temperature of 9 mK. In all cases, an injected power of W was used.

As the laser is tuned to the center of the optical resonance, the low-frequency transmission decreases and more photons are coupled into the bottle. There is a corresponding decrease in the mechanical resonance frequency, which is accompanied by an increase in the mode temperature. In exchange gas, the temperature increase is small, on the order of a few kelvin, and the maximum relative frequency shift amounts to approximately . In contrast, when the IVC is evacuated, we see strikingly similar behavior regardless of whether the fridge is operated at 4.2 K or base temperature. In both cases, the temperature increases to approximately 40 K, while the mechanical frequency decreases by . We also observe a significant decrease in , from 1100 to 600, as the laser is tuned to the center of the optical resonance.

Figure 7: (a) Frequency and (b) inverse versus calibrated mode temperature. Lines are guides to the eye and black triangles are data points at 77 K (liquid nitrogen) and 295 K (room temperature) in nitrogen exchange gas.

For a more direct comparison, the mechanical resonance frequency and inverse are plotted versus measured mechanical mode temperature in Figure 7 for a number of injected optical powers. Black triangles indicate measurements taken at 77 K (liquid nitrogen) and 295 K (room temperature), where the bottles were thermalized using nitrogen exchange gas.

V Discussion

Our measurements reveal key information about heat dissipation in the bottle resonators. Despite efforts to thermally anchor the bottles to the base temperature of the fridge, the lowest achieved mode temperature was approximately 4 K, corresponding to an average occupation of just 1500 phonons. This temperature was reached when helium exchange gas was added to the IVC, indicating that the gaseous helium facilitated convection between the resonator and the bath of liquid helium. In vacuum, regardless of whether the fridge was operated at base temperature or liquid helium temperature, the temperature of the bottle was raised upon optomechanical measurements, as shown in Figures 6 and 7. This is evidence of the intrinsically weak thermal connection between the mixing chamber and the silica bottle resonator.

This heating arises as a result of the absorption of laser light into the bulk silica. The degree of nonlinearity in the optical resonances, quantified through the parameter , serves as a measurement of the temperature change generated by the absorbed light. We find that is nearly an order of magnitude larger in vacuum than in exchange gas, since the lack of convection greatly reduces the efficiency with which the bottle can dissipate heat. These results are entirely consistent with measurements of the mechanical frequency shift with temperature. As the laser is scanned across an optical resonance, we find that the mechanical resonance frequency exhibits the same dependence on laser detuning as the taper transmission. We furthermore observe a relative frequency shift in vacuum that is nearly ten times larger than that in exchange gas. Since the optical and mechanical modes occupy nearly the same volume within the bottle structure, heating of the optical modes by laser absorption is reflected equally in the mechanical mode.

Finally, we observe a significant dependence of the mechanical quality factor on temperature, with a shape that is characteristic of phonon-coupling to configurational two-level systems in glass Classen et al. (1994). At high temperatures, thermal activation over a potential barrier allows transitions between the two configurations; as the temperature is lowered, thermal activation ceases and quantum tunneling can occur. At still lower temperatures, quantum tunneling is also forbidden and the mechanical quality factor increases dramatically. From the shape of Figure 7(b), we deduce that our system resides in the region of thermal activation. Lower temperatures would thus allow us to increase the mechanical quality factor far beyond its room temperature value. There is also an increase in the mechanical damping rate when the IVC is filled with exchange gas; we attribute this to interactions with a thin film of liquid helium on the surface of the bottle. This may be in fact be a promising tool to study ultra-thin superfluid films Xu and Crooker (1990) via interactions with the optical and mechanical modes of resonator. We note that the general shapes of both Figure 7(a) and (b) are in agreement with the observations of silica toroid resonators reported in Ref. 31.

Vi Conclusion

We have demonstrated passive cooling of a 64 ng optomechanical resonator down to just 1500 phonons. Further cooling is prevented by the inability to dissipate the heat caused by optical absorption, exacerbated by the high of the silica resonator. The scale of this optical absorption was found to be in excellent agreement with the degree of heating in the mechanical mode. This comparison was enabled by optomechanical mode thermometry, detailed in the Appendix, which is now an important tool for quantum optomechanics. Future experiments will focus on improving the coupling of these sideband-resolved optomechanical resonators to the thermal bath. One possibility to achieve this is to use a local reservoir of helium as a heat link to the 9 mK dilution refrigerator environment, which would reduce optically-induced heating of the resonator Treussart et al. (1998). In particular, it would be intriguing to use liquid helium, which has been shown to provide an excellent thermalization medium for micro-electromechanical systems (MEMS) down to 60 mK Gonzalez et al. (2013). Furthermore, the MEMS in Ref. 42 regain their vacuum mechanical dissipation levels at 100 mK, due to the temperature-dependent phonon occupation in the superfluid state. Successful thermalization of the presented nanogram-scale microresonators to 9 mK would result in average phonon occupancies of , while maintaining the high mechanical and sideband-resolved nature of these optomechanical devices, opening up the door for ground state cooling Chan et al. (2011) and further quantum optomechanical protocols Palomaki et al. (2013). Finally, extension of these cryogenic silica microresonators to doped optical glasses would also enable new quantum technologies, such as photonic memories for quantum cryptographic networks Saglamyurek et al. (2015).

Vii Acknowledgements

This work was supported by the University of Alberta, Faculty of Science; Alberta Innovates Technology Futures; the Natural Sciences and Engineering Research Council, Canada; the Canada Foundation for Innovation; and the Alfred P. Sloan Foundation.

Viii Appendix: Mechanical Mode Thermometry

viii.1 Solution of the Optomechanical Cavity

The equation of motion for the intracavity optical field in an optical cavity that is coupled to a mechanical resonator with strength is given by Aspelmeyer et al. (2014)

(11)

in a frame rotating at the laser frequency . Here, is the input optical field, normalized such that . The field output by the optical cavity is then

(12)

This system can be solved in the stationary regime (see for example, Ref. 2) but since we intend to inject a time-varying input field, we solve Equation (11) without assuming a stationary state. As in Ref. 15, we assume that can be written as the sum of the solution to the associated homogeneous problem and a particular solution ,

(13)

We further make the assumption that the particular solution can be written as where is a yet-to-be-determined function of time.

We begin by solving for by taking . The resulting differential equation is

(14)

with the solution

(15)

where is an amplitude set by the initial conditions of the problem. We choose the form

(16)

for a damped harmonic oscillator with angular frequency , damping rate , effective mass , and peak amplitude at temperature . Integration yields

(17)

where we have used the high- approximation () to neglect the cosine term.

Substituting Equation (17) into Equation (15), we have

(18)

where we have written

(19)

and used the Jacobi-Anger expression to write

(20)

for small . Here, are the th Bessel functions of the first kind.

We justify this approximation by first noting that for all finite positive times and then rewriting as

(21)

using the vacuum optomechanical coupling rate and the amplitude of the mechanical zero-point fluctuations . Here, is the average phonon occupation of the resonator for . In this form, is absolutely necessary to have , and we must additionally consider the phonon occupation . For optical frequency optomechanical devices, this condition is commonly satisfied, especially at low temperatures where is small. For the bottle resonators used in our experiments, Hz, so and thus as long as (corresponding to a temperature of K).

We now return to Equation (13) to look for the particular solution to Equation (11). We note that

(22)

Given that the homogeneous solution obeys Equation (14), it follows that

(23)

For the mechanical mode thermometry, we phase modulate the input laser light by driving an electro-optic modulator with a sinusoidal signal of the form , where is the drive voltage amplitude, is the drive frequency and is the linewidth of the driving source. This produces an input field of the form

(24)

where we define the phase modulation depth as , given the device-dependent half-wave voltage, . If the phase modulation is weak (), it is sufficient to consider only the first order sidebands at . In this case, we can again use the approximation in Equation (20) to write

(25)

We substitute this result, along with the homogeneous solution of Equation (18), into Equation (23), yielding

(26)

Keeping only terms to first order in the small parameters and , integrating Equation (26) and multiplying by (Equation (18)), we obtain the particular solution

(27)

where we have used the fact that to simplify the final expression. We note that decays much more rapidly than , so we neglect and take .

We now calculate the field output by the cavity by substituting Equations (25) and (27) into Equation (12),

(28)

viii.2 Detection

In our experiments, we use a direct detection scheme where a photodetector sensitive to the intensity of the light outputs a voltage signal proportional to ,

(29)

We have separated the output signal into a part

(30)

which is constant in time, and two high-frequency parts which oscillate at the mechanical resonance frequency,

(31)

and at the modulation frequency,

(32)

respectively. is a function which describes the frequency response of the photodetector and other detection electronics. We assume that it is locally flat, such that for a suitably chosen , we can take . Note that is simply the transmission profile for the optical resonance, as given by Equations (1) and (2) in the main text. For convenience, we have also defined

(33)
(34)

and

(35)

To obtain the power spectral density of the voltage signal, we must first Fourier transform . In our experiment, this is done as part of the software post-processing, but it can also be performed in hardware, using a network or spectrum analyzer, for example. is filtered out by a high-pass filter on our photodetector so we address only the high-frequency part of .

We define the Fourier transform as

(36)

Since the Fourier transform is linear, we apply it to and separately. We begin by substituting the form of given by Equation (19) into Equation (31) and noting that

(37)

Equation (31) then becomes

(38)

with its Fourier transform given by

(39)

Near the mechanical resonance frequency, and

(40)

Similarly, can be rewritten in terms of the original phase modulation signal ,

(41)

Analogous to Equation (40), the Fourier transform of Equation (41) near the modulation frequency is

(42)

where is the Fourier transform of .

Figure 8: Calculated ratio of to for experimental parameters ( MHz, MHz, MHz and MHz). A variation of less than 3% in this ratio across the optical resonance is shown.

Combining the results of Equations (40) and (42), we calculate the voltage power spectral density,

(43)

which can be reduced to

(44)

if we choose such that . This prevents overlap between the peaks in the spectrum and allows us to neglect the cross terms. The final result is then

(45)

where is the PSD of the phase fluctuations induced by the phase calibration signal. We have defined the transduction coefficient as

(46)

We see that for a choice of the modulation frequency , and the phase modulation signal is transduced nearly identically to the mechanical motion by the optical cavity and photodetector. In actuality, is also dependent on the detuning of the laser, but it can be shown that for , the variation of the ratio of with detuning is negligibly small. For the parameters in our experiment, Figure 8 illustrates that this variation across laser detuning is less than 3% in our experiment.

Although we have focussed on direct detection techniques, this method of calculating the detected PSD applies equally well to other detection schemes, including optical homodyne or heterodyne systems. It can be shown that analogous results, albeit with a different functional dependence on the laser detuning, can be obtained for such systems.

We finally note that we have made no assumptions about the optomechanical system, beyond requiring that , as is true for any system in the standard hierarchy of optomechanics. The only constraints placed on the modulation signal are that it is small () and that its frequency is chosen appropriately, namely that is close enough to that any frequency dependence in the detection electronics can be neglected and far enough that overlap between the two peaks can be ignored. It is additionally beneficial if is chosen close enough to that any detuning-dependence in the ratio can be neglected (as is true in our experiment); however, even if this is not the case, the closed form of allows the for the analytical calculation of this ratio provided that the optical resonance is well-characterized and the laser detuning is known.

References

  1. M. Aspelmeyer, T. J. Kippenberg, and F. Marquardt, Reviews of Modern Physics 86, 1391 (2014).
  2. G. Anetsberger, E. Gavartin, O. Arcizet, Q. P. Unterreithmeier, E. M. Weig, M. L. Gorodetsky, J. P. Kotthaus, and T. J. Kippenberg, Physical Review A 82, 061804(R) (2010).
  3. E. Gavartin, P. Verlot, and T. J. Kippenberg, Nature Nanotechnology 7, 509 (2012).
  4. H. Miao, K. Srinivasan, and V. Aksyuk, New Journal of Physics 14, 075015 (2012).
  5. C. Doolin, P. H. Kim, B. D. Hauer, A. J. R. MacDonald, and J. P. Davis, New Journal of Physics 16, 035001 (2014a).
  6. P. H. Kim, C. Doolin, B. D. Hauer, A. J. R. MacDonald, M. R. Freeman, P. E. Barclay, and J. P. Davis, Applied Physics Letters 102, 053102 (2013).
  7. M. Wu, A. C. Hryciw, C. Healey, D. P. Lake, H. Jayakumar, M. R. Freeman, J. P. Davis, and P. E. Barclay, Physical Review X 4, 021052 (2014).
  8. A. G. Krause, M. Winger, T. D. Blasius, Q. Lin, and O. Painter, Nature Photonics 6, 768 (2012).
  9. A. A. Gangat, T. M. Stace, and G. J. Milburn, New Journal of Physics 13, 043024 (2010).
  10. K. Stannigel, P. Rabl, A. S. Srensen, P. Zoller, and M. D. Lukin, Physical Review Letters 105, 220501 (2010).
  11. T. A. Palomaki, J. D. Teufel, R. W. Simmonds, and K. W. Lehnert, Science 342, 710 (2013).
  12. A. H. Safavi-Naeini, S. Gröblacher, J. T. Hill, J. Chan, M. Aspelmeyer, and O. Painter, Nature 500, 185 (2013).
  13. K. Brkje, Physical Review A 90, 023806 (2014).
  14. A. Schliesser, R. Rivière, G. Anetsberger, O. Arcizet, and T. J. Kippenberg, Nature Physics 4, 415 (2008).
  15. J. Chan, T. P. Mayer Alegre, A. H. Safavi-Naeini, J. T. Hill, A. Krause, S. Gröblacher, M. Aspelmeyer, and O. Painter, Nature 478, 89 (2011).
  16. Y.-S. Park and H. Wang, Nature Physics 5, 489 (2009).
  17. X. Sun, X. Zhang, C. Schuck, and H. X. Tang, Scientific Reports 3, 1436 (2013).
  18. L. A. De Lorenzo and K. C. Schwab, New Journal of Physics 16, 113020 (2014).
  19. A. K. Geim, I. V. Grigorieva, S. V. Dubonos, J. G. S. Lok, J. C. Maan, A. E. Filippov, and F. M. Peeters, Nature 390, 259 (1997).
  20. R. Rivière, O. Arcizet, A. Schliesser, and T. J. Kippenberg, Review of Scientific Instruments 84, 043108 (2013).
  21. S. M. Meenehan, J. D. Cohen, S. Gröblacher, J. T. Hill, A. H. Safavi-Naeini, M. Aspelmeyer, and O. Painter, Physical Review A 90, 011803(R) (2014).
  22. J. C. Knight, G. Cheung, F. Jacques, and T. A. Birks, Optics Letters 22, 1129 (1997).
  23. M. Cai, O. Painter, and K. J. Vahala, Physical Review Letters 85, 74 (2000).
  24. A. J. R. MacDonald, G. G. Popowich, B. D. Hauer, P. H. Kim, A. Fredrick, X. Rojas, P. Doolin, and J. P. Davis, Review of Scientific Instruments 86, 013107 (2015).
  25. B. D. Hauer, P. H. Kim, C. Doolin, A. J. R. MacDonald, H. Ramp, and J. P. Davis, EPJ Techniques and Instrumentation 1:4 (2014).
  26. G. Kakarantzas, T. E. Dimmick, T. A. Birks, R. Le Roux, and P. S. J. Russell, Optics Letters 26, 1137 (2001).
  27. M. Pöllinger, D. O’Shea, F. Warken, and A. Rauschenbeutel, Physical Review Letters 103, 053901 (2009).
  28. G. Anetsberger, R. Rivière, A. Schliesser, O. Arcizet, and T. J. Kippenberg, Nature Photonics 2, 627 (2008).
  29. T. Carmon, L. Yang, and K. J. Vahala, Optics Express 12, 4742 (2004).
  30. O. Arcizet, R. Rivière, A. Schliesser, G. Anetsberger, and T. Kippenberg, Physical Review A 80, 021803(R) (2009).
  31. P. E. Barclay, K. Srinivasan, and O. Painter, Optics Express 13, 801 (2005).
  32. C. Doolin, B. D. Hauer, P. H. Kim, A. J. R. MacDonald, H. Ramp, and J. P. Davis, Physical Review A 89, 053838 (2014b).
  33. V. B. Braginsky, M. L. Gorodetsky, and V. S. Ilchenko, Physics Letters A 137, 8 (1989).
  34. V. S. Il’chenko and M. L. Gorodetskii, Laser Physics 2, 1004 (1992).
  35. G. K. White, Physical Review Letters 34, 204 (1975).
  36. B. D. Hauer, C. Doolin, K. S. D. Beach, and J. P. Davis, Annals of Physics 339, 181 (2013).
  37. M. L. Gorodetsky, A. Schliesser, G. Anetsberger, S. Deleglise, and T. J. Kippenberg, Optics Express 18, 23236 (2010).
  38. J. Classen, C. Enss, C. Bechinger, G. Weiss, and S. Hunklinger, Annalen der Physik 3, 315 (1994).
  39. J. Xu and B. C. Crooker, Physical Review Letters 65, 3005 (1990).
  40. F. Treussart, V. S. Ilchenko, J.-F. Roch, J. Hare, V. Lefèvre-Seguin, J.-M. Raimond, and S. Haroche, European Physcal Journal D 1, 235 (1998).
  41. M. Gonzalez, P. Zheng, B. H. Moon, E. Garcell, Y. Lee, and H. B. Chan, Journal of Low Temperature Physics 171, 200 (2013).
  42. E. Saglamyurek, J. Jin, V. B. Verma, M. D. Shaw, F. Marsili, S. W. Nam, D. Oblak, and W. Tittel, Nature Photonics 9, 83 (2015).
121587
This is a comment super asjknd jkasnjk adsnkj
Upvote
Downvote
Edit
-  
Unpublish
""
The feedback must be of minumum 40 characters
The feedback must be of minumum 40 characters
Submit
Cancel
Comments 0
Request answer
""
The feedback must be of minumum 40 characters
Add comment
Cancel
Loading ...