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The technique of passive daytime radiative cooling (PDRC) is used to cool an object down by simultaneously reflecting sunlight and thermally radiating heat to the cold outer space through the Earths atmospheric window. However, for practical applications, current PDRC materials are facing unprecedented challenges such as complicated and expensive fabrication approaches and performance degradation arising from surface contamination. Here, we develop a scalable paper-based material with excellent self-cleaning and self-cooling capabilities, through air-spraying ethanolic polytetrafluoroethylene (PTFE) microparticles suspensions embedded within the micropores of the paper. The formed superhydrophobic PTFE coating not only protects the paper from water wetting and dust contamination for real-life applications but also reinforces its solar reflectance by sunlight backscattering. The paper fibers, when enhanced with PTFE particles, efficiently reflect sunlight and strongly radiate heat through the atmospheric window, resulting in a sub-ambient cooling performance of 5$^{circ}$C and radiative cooling power of 104 W/m$^2$ under direct solar irradiance of 834 W/m$^2$ and 671 W/m$^2$, respectively. The self-cleaning surface of the cooling paper extends its lifespan and keep its good cooling performance for outdoor applications. Additionally, dyed papers are experimentally studied for broad engineering applications. They can absorb appropriate visible wavelengths to display specific colors and effectively reflect near-infrared lights to reduce solar heating, which synchronously achieves effective radiative cooling and aesthetic varieties in a cost-effective, scalable, and energy-efficient way.
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We demonstrate passive feedback cooling of a mechanical resonator based on radiation pressure forces and assisted by photothermal forces in a high-finesse optical cavity. The resonator is a free-standing high-reflectance micro-mirror (of mass m=400ng and mechanical quality factor Q=10^4) that is used as back-mirror in a detuned Fabry-Perot cavity of optical finesse F=500. We observe an increased damping in the dynamics of the mechanical oscillator by a factor of 30 and a corresponding cooling of the oscillator modes below 10 K starting from room temperature. This effect is an important ingredient for recently proposed schemes to prepare quantum entanglement of macroscopic mechanical oscillators.
The formation of water-in-oil-in-water (W/O/W) double emulsions can be well-controlled through an organized self-emulsification mechanism in the presence of rigid bottlebrush amphiphilic block copolymers. Nanoscale water droplets with well-controlled diameters form ordered spatial arrangements within the micron-scale oil droplets. Upon solvent evaporation, solid microspheres with hexagonal close packed nanopore arrays are obtained resulting in bright structural colors. The reflected color is precisely tunable across the whole visible light range through tailoring contour length of the bottlebrush molecule. In-situ observation of the W/O interface using confocal laser scanning microscopy provides insights into the mechanism of the organized self-emulsification. This work provides a powerful strategy for the fabrication of structural colored materials in an easy and scalable manner.
Discovering and optimizing commercially viable materials for clean energy applications typically takes over a decade. Self-driving laboratories that iteratively design, execute, and learn from material science experiments in a fully autonomous loop present an opportunity to accelerate this research. We report here a modular robotic platform driven by a model-based optimization algorithm capable of autonomously optimizing the optical and electronic properties of thin-film materials by modifying the film composition and processing conditions. We demonstrate this platform by using it to maximize the hole mobility of organic hole transport materials commonly used in perovskite solar cells and consumer electronics. This demonstration highlights the possibilities of using autonomous laboratories to discover organic and inorganic materials relevant to materials sciences and clean energy technologies.
Capabilities of highly sensitive surface-enhanced infrared absorption (SEIRA) spectroscopy are demonstrated by exploiting large-area templates ($cm^2$) based on self-organized (SO) nanorod antennas. We engineered highly dense arrays of gold nanorod antennas featuring polarization-sensitive localized plasmon resonances, tunable over a broadband near- and mid-infrared (IR) spectrum, in overlap with the so-called functional group window. We demonstrate polarization-sensitive SEIRA activity, homogeneous over macroscopic areas and stable in time, by exploiting prototype self-assembled monolayers of IR-active octadecanthiol (ODT) molecules. The strong coupling between the plasmonic excitation and molecular stretching modes gives rise to characteristic Fano resonances in SEIRA. The SO engineering of the active hotspots in the arrays allows us to achieve signal amplitude improved up to 5.7%. This figure is competitive to the response of lithographic nanoantennas and is stable when the optical excitation spot varies from the micro- to macroscale, thus enabling highly sensitive SEIRA spectroscopy with cost-effective nanosensor devices.
Multimode optical fibres are enjoying a renewed attention, boosted by the urgent need to overcome the current capacity crunch of single-mode fibre systems and by recent advances in multimode complex nonlinear optics [1-13]. In this work, we demonstrate that standard multimode fibres can be used as ultrafast all-optical tool for transverse beam manipulation of high power laser pulses. Our experimental data show that the Kerr effect in a graded-index multimode fibre is the driving mechanism for overcoming speckle distortions, leading to a somewhat counter-intuitive effect resulting in a spatially clean output beam robust against fibre bending. Our observations demonstrate that nonlinear beam reshaping into the fundamental mode of a multimode fibre can be achieved even in the absence of a dissipative process such as stimulated scattering (Raman or Brillouin) [14,15].
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