Mesoporous Solid and Yolk–Shell Titania Microspheres as Touchless Colorimetric Sensors with High Responsivity and Ultrashort Response Times

Touchless user interfaces offer an attractive pathway toward hygienic, remote, and interactive control over devices. Exploiting the humidity generated from fingers or human speech is a viable avenue for realizing such technology. Herein, titania microspheres including solid and yolk–shell structures with varying microstructural characteristics were demonstrated as high-performance, ultrafast, and stable optical humidity sensors aimed for touchless control. When water molecules enter the microporous network of the microspheres, the effective refractive index of the microsphere increases, causing a detectable change in the light scattering behavior. The microstructural properties of the microspheres, namely, the pore characteristics, crystallinity, and particle size, were examined in relation to the humidity-sensing performance, establishing optimum structural conditions for realizing humidity-responsive wavelength shifts above 100 nm, near full-scale relative humidity (RH) responsivity, ultrashort response times below 30 ms, and prolonged lifetimes. These optimized microspheres were used to demonstrate a colorimetric touchless sensor that responds to humidity from a finger and a microcontroller-based detector that translates the moisture pattern from human speech to electrical signals in real time. These results provide practical strategies for enabling humidity-based touchless user interfaces

Mesoporous Solid and Yolk–Shell Titania Microspheres as Touchless Colorimetric Sensors with High Responsivity and Ultrashort Response Times

Touchless user interfaces offer an attractive pathway toward hygienic, remote, and interactive control over devices. Exploiting the humidity generated from fingers or human speech is a viable avenue for realizing such technology. Herein, titania microspheres including solid and yolk–shell structures with varying microstructural characteristics were demonstrated as high-performance, ultrafast, and stable optical humidity sensors aimed for touchless control. When water molecules enter the microporous network of the microspheres, the effective refractive index of the microsphere increases, causing a detectable change in the light scattering behavior. The microstructural properties of the microspheres, namely, the pore characteristics, crystallinity, and particle size, were examined in relation to the humidity-sensing performance, establishing optimum structural conditions for realizing humidity-responsive wavelength shifts above 100 nm, near full-scale relative humidity (RH) responsivity, ultrashort response times below 30 ms, and prolonged lifetimes. These optimized microspheres were used to demonstrate a colorimetric touchless sensor that responds to humidity from a finger and a microcontroller-based detector that translates the moisture pattern from human speech to electrical signals in real time. These results provide practical strategies for enabling humidity-based touchless user interfaces

Atomically Thin Holey Two-Dimensional Ru₂P Nanosheets for Enhanced Hydrogen Evolution Electrocatalysis

The defect engineering of low-dimensional nanostructured materials has led to increased scientific efforts owing to their high efficiency concerning high-performance electrocatalysts that play a crucial role in renewable energy technologies. Herein, we report an efficient methodology for fabricating atomically thin, holey metal-phosphide nanosheets with excellent electrocatalyst functionality. Two-dimensional, subnanometer-thick, holey Ru2P nanosheets containing crystal defects were synthesized via the phosphidation of monolayer RuO2 nanosheets. Holey Ru2P nanosheets exhibited superior electrocatalytic activity for the hydrogen evolution reaction (HER) compared to that exhibited by nonholey Ru2P nanoparticles. Further, holey Ru2P nanosheets exhibited overpotentials of 17 and 26 mV in acidic and alkaline electrolytes, respectively. Thus, they are among the best-performing Ru–P-based HER catalysts reported to date. In situ spectroscopic investigations indicated that the holey nanosheet morphology enhanced the accumulation of surface hydrogen through the adsorption of protons and/or water, resulting in an increased contribution of the Volmer–Tafel mechanism toward the exceptional HER activity of these ultrathin electrocatalysts