Enhanced detection of high frequency gravitational waves using optically diluted optomechanical filters

Detections of gravitational waves (GW) in the frequency band 35 Hz to 500 Hz have led to the birth of GW astronomy. Expected signals above 500 Hz, such as the quasinormal modes of lower mass black holes and neutron star mergers signatures are currently not detectable due to increasing quantum shot noise at high frequencies. Squeezed vacuum injection has been shown to allow broadband sensitivity improvement, but this technique does not change the slope of the noise at high frequency. It has been shown that white light signal recycling using negative dispersion optomechanical filter cavities with strong optical dilution for thermal noise suppression can in principle allow broadband high frequency sensitivity improvement. Here we present detailed modelling of AlGaAs/GaAs optomechanical filters to identify the available parameter space in which such filters can achieve the low thermal noise required to allow useful sensitivity improvement at high frequency. Material losses, the resolved sideband condition and internal acoustic modes dictate the need for resonators substantially smaller than previously suggested. We identify suitable resonator dimensions and show that a 30 $\mu$m scale cat-flap resonator combined with optical squeezing allows 8 fold improvement of strain sensitivity at 2 kHz compared with Advanced LIGO. This corresponds to a detection volume increase of a factor of 500 for sources in this frequency range

Altering Ligand Fields in Single-Atom Sites through Second-Shell Anion Modulation Boosts the Oxygen Reduction Reaction

Single-atom catalysts based on metal–N4 moieties and anchored on carbon supports (defined as M–N–C) are promising for oxygen reduction reaction (ORR). Among those, M–N–C catalysts with 4d and 5d transition metal (TM4d,5d) centers are much more durable and not susceptible to the undesirable Fenton reaction, especially compared with 3d transition metal based ones. However, the ORR activity of these TM4d,5d–N–C catalysts is still far from satisfactory; thus far, there are few discussions about how to accurately tune the ligand fields of single-atom TM4d,5d sites in order to improve their catalytic properties. Herein, we leverage single-atom Ru–N–C as a model system and report an S-anion coordination strategy to modulate the catalyst’s structure and ORR performance. The S anions are identified to bond with N atoms in the second coordination shell of Ru centers, which allows us to manipulate the electronic configuration of central Ru sites. The S-anion-coordinated Ru–N–C catalyst delivers not only promising ORR activity but also outstanding long-term durability, superior to those of commercial Pt/C and most of the near-term single-atom catalysts. DFT calculations reveal that the high ORR activity is attributed to the lower adsorption energy of ORR intermediates at Ru sites. Metal–air batteries using this catalyst in the cathode side also exhibit fast kinetics and excellent stability

Pt–Fe–Cu Ordered Intermetallics Encapsulated with N‑Doped Carbon as High-Performance Catalysts for Oxygen Reduction Reaction

Ternary platinum (Pt)-based ordered intermetallics represent a group of promising electrocatalysts in energy-conversion applications, because of their multielemental coupling that can potentially boost the activity and durability of the oxygen reduction reaction (ORR). Yet, the achievable catalysis performance is still susceptible to the inevitable transition metal leaching that can hardly be eliminated in an acidic environment. Herein, we report a nitrogen (N)-modified carbon (shell) encapsulated Pt–Fe–Cu ordered intermetallic nanoparticles (core) electrocatalyst for acidic ORR, where the Pt–Fe–Cu core presents a face-centered tetragonal (fct) phase. It is demonstrated that N-doped carbon shells can not only protect Pt–Fe–Cu cores from dissolution, agglomeration, coalescence, and Ostwald ripening but also enable the electronic structure regulation of the central Pt sites through the strong Fe–N coordination. The optimized Pt–Fe–Cu intermetallic with N-doped carbon shells delivers superior ORR activity and is more chemically stable over disordered Pt–Fe–Cu alloy, Pt–Fe–Cu intermetallics without a N-doped carbon shell, and commercial Pt/C, where the achievable ORR mass and specific activities are nearly 5-fold and 4-fold higher than those of commercial Pt/C in the acidic media, respectively

Observation of Nonlinear Dynamics in an Optical Levitation System

Optical levitation of mechanical oscillators has been suggested as a promising way to decouple the environmental noise and increase the mechanical quality factor. Here, we investigate the dynamics of a free-standing mirror acting as the top reflector of a vertical optical cavity, designed as a testbed for a tripod cavity optical levitation setup. To reach the regime of levitation for a milligram-scale mirror, the optical intensity of the intracavity optical field approaches 3 MW cm$^{-2}$. We identify three distinct optomechanical effects: excitation of acoustic vibrations, expansion due to photothermal absorption, and partial lift-off of the mirror due to radiation pressure force. These effects are intercoupled via the intracavity optical field and induce complex system dynamics inclusive of high-order sideband generation, optical bistability, parametric amplification, and the optical spring effect. We modify the response of the mirror with active feedback control to improve the overall stability of the system

Cancellation of photothermally induced instability in an optical resonator

Optical systems are often subject to parametric instability caused by the delayed response of the optical field to the system dynamics. In some cases, parasitic photothermal effects aggravate the instability by adding new interaction dynamics. This may lead to the possible insurgence or amplification of parametric gain that can further destabilize the system. In this paper, we show that the photothermal properties of an optomechanical cavity can be modified to mitigate or even completely cancel optomechanical instability. By inverting the sign of the photothermal interaction to let it cooperate with radiation pressure, we achieve control of the system dynamics to be fully balanced around a stable equilibrium point. Our study provides a feedback solution for optical control and precise metrological applications, specifically in high-sensitivity resonating systems that are particularly susceptible to parasitic photothermal effects, such as our test case of a macroscopic optical levitation setup. This passive stabilization technique is beneficial for improving system performance limited by photothermal dynamics in broad areas of optics, optomechanics, photonics, and laser technologies

Optical back-action on the photothermal relaxation rate

Photothermal effects can alter the response of an optical cavity, for example, by inducing self-locking behavior or unstable anomalies. The consequences of these effects are often regarded as parasitic and generally cause limited operational performance of the cavity. Despite their importance, however, photothermal parameters are usually hard to characterize precisely. In this work we use an optical cavity strongly coupled to photothermal effects to experimentally observe an optical back-action on the photothermal relaxation rate. This effect, reminiscent of the radiation-pressure-induced optical spring effect in cavity optomechanical systems, uses optical detuning as a fine control to change the photothermal relaxation process. The photothermal relaxation rate of the system can be accordingly modified by more than an order of magnitude. This approach offers an opportunity to obtain precise in-situ estimations of the parameters of the cavity, in a way that is compatible with a wide range of optical resonator platforms. Through this back-action effect we are able to determine the natural photothermal relaxation rate and the effective thermal conductivity of the cavity mirrors with unprecedented resolution

Highly Selective Oxygen Reduction to Hydrogen Peroxide on a Carbon-Supported Single-Atom Pd Electrocatalyst

Selective electrochemical two-electron oxygen reduction is a promising route for renewable and on-site H2O2 generation as an alternative to the anthraquinone process. Herein, we report a high-performance nitrogen-coordinated single-atom Pd electrocatalyst, which is derived from Pd-doped zeolitic imidazolate frameworks (ZIFs) through one-step thermolysis. High-angle annular dark-field scanning transmission electron microscopy (HAADF-STEM) combined with X-ray absorption spectroscopy verifies atomically dispersed Pd atoms on nitrogen-doped carbon (Pd-NC). The single-atom Pd-NC catalyst exhibits excellent electrocatalytic performance for two-electron oxygen reduction to H2O2, which shows ∼95% selectivity toward H2O2 and an unprecedented onset potential of ∼0.8 V versus revisable hydrogen electrode (RHE) in 0.1 M KOH. Density functional theory (DFT) calculations demonstrate that the Pd-N4 catalytic sites thermodynamically prefer *–O bond breaking to O–O bond breaking, corresponding to a high selectivity for H2O2 production. This work provides a deep insight into the understanding of the catalytic process and design of high-performance 2e– ORR catalysts