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Photo-Thermal Transfer Function Indicator

Updated 13 January 2026
  • Transfer function-type indicators quantify how modulated optical power absorption in dielectric coatings produces effective mirror displacement via thermo-elastic and thermo-refractive effects.
  • They utilize multilayer thermal diffusion models to detect sign-switching phenomena, enabling micron-scale determination of absorption depth within complex coatings.
  • Applications include precision optical metrology, noise prediction in gravitational-wave detectors, and optomechanical system stabilization.

The transfer function-type indicator, specifically the photo-thermal transfer function, quantifies the relationship between modulated absorbed optical power at the surface of a dielectric mirror and the effective mirror displacement as perceived by an interferometric read-out. Formally, for an incident intensity fluctuation j(ω)j(\omega) [W/m²] at angular frequency ω\omega, the transfer function H(ω)H(\omega) relates this to a displacement δz(ω)\delta z(\omega) such that H(ω)δz(ω)/j(ω)H(\omega) \equiv \delta z(\omega)/j(\omega). This multidimensional quantity integrates the periodic thermal response of a multilayer dielectric mirror and substrates, encompassing thermo-elastic expansion and thermo-refractive optical phase shifts. The functional form and frequency dependence of H(ω)H(\omega) serve as a sensitive diagnostic, notably providing a robust indicator of the absorption depth within complex coatings, and hence play a pivotal role in both precision optical metrology and optomechanical system design (Ballmer, 2014).

1. Mathematical Formulation and Multilayer Thermal Response

The derivation of the photo-thermal transfer function begins with the thermal diffusion equation in each of the k=1Nk=1\dots N dielectric layers and the semi-infinite substrate k=sk=s. In the Fourier domain, the coupled equations involve layer-specific density ρk\rho_k, specific heat CkC_k, and thermal conductivity κk\kappa_k: jk(z,ω)z+iωρkCkTk(z,ω)=0,\frac{\partial j_k(z,\omega)}{\partial z} + i\omega \rho_k C_k T_k(z,\omega) = 0,

jk(z,ω)=κkTk(z,ω)z,j_k(z,\omega) = -\kappa_k \frac{\partial T_k(z,\omega)}{\partial z},

where Tk(z,ω)T_k(z,\omega) is the complex temperature perturbation, and jk(z,ω)j_k(z,\omega) is the (one-dimensional) heat flux. The spatial temperature profile obeys

ξk2Tk(z)=2Tk(z)z2,ξk=iωρkCkκk,\xi_k^2 T_k(z) = \frac{\partial^2 T_k(z)}{\partial z^2}, \qquad \xi_k = \sqrt{\frac{i\omega \rho_k C_k}{\kappa_k}},

yielding general solutions within each layer: Tk(z)=Ake+ξk(zzk)+Bkeξk(zzk),T_k(z) = A_k e^{+\xi_k(z-z_k)} + B_k e^{-\xi_k(z-z_k)}, with AkA_k and BkB_k determined by interface continuity conditions and boundary constraints.

The layer-averaged temperature Tˉk(ω)\bar T_k(\omega) for expansion and refractive-index coupling is

Tˉk(ω)dk=zkdk/2zk+dk/2Tk(z,ω)dz=2ξksinh(ξkdk2)(Ak+Bk).\bar T_k(\omega)d_k = \int_{z_k-d_k/2}^{z_k+d_k/2} T_k(z,\omega)\,dz = \frac{2}{\xi_k}\sinh\left(\frac{\xi_k d_k}{2}\right)(A_k + B_k).

For the substrate,

Tˉs(ω)ds=TR,s(ω)ξs.\bar T_s(\omega)d_s = \frac{T_{R,s}(\omega)}{\xi_s}.

2. Conversion to Effective Displacement: Thermo-Elastic and Thermo-Optic Coupling

Thermal fluctuations in each layer produce mechanical expansion with a constrained expansion coefficient αˉk\bar\alpha_k and modify the coating's optical phase due to refractive-index changes (βk=dnk/dT\beta_k = dn_k/dT). The round-trip optical phase change is: δϕk=4πλ0k(βk+αˉknk)Tk(z)dz,\delta\phi_k = \frac{4\pi}{\lambda_0} \int_k (\,\beta_k + \bar\alpha_k n_k)\,T_k(z)\,dz, with λ0\lambda_0 the probe wavelength, nkn_k the refractive index. The constrained thermal expansion is defined by elastic moduli and Poisson ratios of each layer and the substrate. The overall reflected phase shift δϕc(ω)\delta\phi_c(\omega) is obtained by

δϕc(ω)=k=1N4πλ0[ϕcϕk(βk+αˉknk)+αˉk]Tˉk(ω)dk,\delta\phi_c(\omega) = \sum_{k=1}^N \frac{4\pi}{\lambda_0}\Big[\frac{\partial\phi_c}{\partial\phi_k}(\beta_k+\bar\alpha_k n_k)+\bar\alpha_k\Big]\bar T_k(\omega)d_k,

and the equivalent displacement as read out by the Gaussian beam: δz(ω)=λ04πδϕc(ω).\delta z(\omega) = \frac{\lambda_0}{4\pi} \delta\phi_c(\omega). Thus,

H(ω)=k=1N[ϕcϕk(βk+αˉknk)+αˉk]2ξksinh(ξkdk2)Ak+Bkj(ω),H(\omega) = \sum_{k=1}^N \Big[\frac{\partial\phi_c}{\partial\phi_k}(\beta_k+\bar\alpha_k n_k)+\bar\alpha_k\Big] \frac{2}{\xi_k}\sinh\left(\frac{\xi_k d_k}{2}\right)\frac{A_k+B_k}{j(\omega)},

with all parameters defined as above.

3. Frequency Response and Sign-Switching Phenomena

The frequency dependence of H(ω)H(\omega) is driven by the relative scale of the thermal diffusion length ddiff=κ/(ρCω)d_\mathrm{diff} = \sqrt{\kappa/(\rho C \omega)} and coating thickness dcoatd_\mathrm{coat}. At low frequencies ddiffdcoatd_\mathrm{diff} \gg d_\mathrm{coat}, the system approaches the single-layer (substrate) limit,

Hsub(ω)=αˉiωρC,H_\mathrm{sub}(\omega) = \frac{\bar\alpha}{i\omega\rho C},

characterized by 1/ω1/\omega amplitude roll-off and 90-90^\circ phase lag. At intermediate frequencies (ddiffdcoatd_\mathrm{diff}\sim d_\mathrm{coat}), the top layers dominate, leading to a bump in H(ω)|H(\omega)| and a phase rotation across +90+90^\circ, marking a sign change in H(ω)H(\omega). At very high frequencies (ddiffdcoatd_\mathrm{diff}\ll d_\mathrm{coat}), only nanometric-scale layers contribute, with H(ω)H(\omega) rolling off as 1/ω1/\sqrt{\omega} and phase tending to +90+90^\circ. For Advanced LIGO Ta2_2O5_5:SiO2_2 coatings (dcoat5μd_\mathrm{coat}\sim 5\,\mum), the critical frequency is fcoat105f_\mathrm{coat} \sim 10^5 Hz.

4. Transfer Function as an Absorption-Depth Indicator

The magnitude and zero-crossing behavior of H(ω)H(\omega) at high frequencies uniquely diagnose the localization of optical absorption. If absorption is concentrated at the front surface, the negative ϕcϕk\frac{\partial\phi_c}{\partial\phi_k} of the first quarter-wave layer yields a distinctive positive amplitude bump and a sharp sign flip near fcoatf_\mathrm{coat}. If the absorption is distributed deeper (e.g., at an interface), the bump diminishes or vanishes, and the sign-crossing shifts upward or disappears. When absorption follows the optical power penetration profile (indicative of bulk absorption), the high-frequency features interpolate between these extremes. Experimentally, a modulated heating beam (e.g., acousto-optic modulator) and interferometric read-out enable measurement of δz(ω)\delta z(\omega), and fitting the observed H(ω)H(\omega) yields the effective absorption depth with micron-scale precision.

5. Implementation and Experimental Requirements

Precise realization of the transfer function-based absorption-depth indicator involves:

  • A modulation source for heating at frequencies up to 2fcoat2f_\mathrm{coat} (200\sim 200 kHz for LIGO coatings, $1$ MHz for AlGaAs).
  • An interferometric read-out of δz\delta z with sub-fm/Hz\sqrt{\text{Hz}} sensitivity from DC to MHz.
  • Calibrated incident heating intensity j(ω)j(\omega) via controlled modulator drive.
  • A comprehensive multilayer thermal model for H(ω)H(\omega) using known dielectric layer design and material constants.
  • Parameter fitting of measured H|H| and arg(H)(H) to model families (surface, interface, and bulk absorption) to extract absorption depth.

6. Applications in Precision Measurement, Noise Prediction, and Optomechanics

These transfer function indicators underpin several advanced applications:

  • In optomechanical stabilization ("optical spring"), the 1/ω1/\omega substrate effect adds a 90-90^\circ phase lag, causing destabilization above resonance. If the resonance frequency is high enough to cross +90+90^\circ phase (sign flip), photothermal feedback shifts to positive damping, permitting passive cavity self-locking.
  • Thermo-optic noise predictions in coatings require the full H(ω)H(\omega) formalism above \sim10 kHz; using coating-averaged models for ωωcoat\omega \ll \omega_\mathrm{coat} is insufficient, and high-frequency corrections can reach $10$–100%100\% above 100 kHz.
  • Alx_xGa1x_{1-x}As crystalline coatings (with high κ\kappa and tailored layer counts) leverage near-total cancellation between thermo-elastic and thermo-refractive noise, but high-frequency deviations dominate residual noise, as predicted by the detailed H(ω)H(\omega) heat flow model.

7. Summary and Significance

The photo-thermal transfer function H(ω)H(\omega) acts as both a predictive model for photothermal noise and a quantitative probe of optical absorption location in precision dielectric coatings. Its high-frequency amplitude and sign dynamics provide a robust, micron-scale indicator for distinguishing absorption sources (coating-internal vs. surface contamination). This utility extends to critical tasks in gravitational-wave detector mirror characterization, optomechanical system stabilization, and the design of next-generation, low-noise crystalline coatings (Ballmer, 2014).

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