In this work, well-shaped In(OH)3 hollow microspheres have been successfully prepared via a novel surfactant-free vesicle-template-interface route in the "formamide-resorcinol-water" system, in which spontaneous vesicles were formed under hydrothermal conditions and NH3 from the hydrolysis of formamide acted as the OH- provider. Morphological and structural characterizations indicate that the shells of as-prepared In(OH)3 hollow microspheres were constructed by numerous nanocubes about 80 nm in size. As desired, In2O3 hollow microspheres were obtained from annealing the designed In(OH)3 precursors, and the as-obtained In2O3 hollow microspheres performed well as a gas-sensing material in response to both ethanol and formaldehyde gases and as a photocatalyst for photocatalytic degradation of rhodamine B. The facile preparation method and the improved properties derived from special microstructures are significant in the synthesis and future applications of functional nanomaterials.
Rational design of optimal bifunctional oxygen electrocatalyst with low cost and high activity is greatly desired for realization of rechargeable Zn-air batteries. Herein, we fabricate mesoporous thin-walled CuCoO@C with abundant nitrogen-doped nanotubes via coaxial electrospinning technique. Benefiting from high catalytic activity of ultrasmall CuCoO particles, double active specific surface area of mesoporous nanotubes, and strong coupling with N-doped carbon matrix, the obtained CuCoO@C exhibits outstanding oxygen electrocatalytic activity and stability, in terms of a positive onset potential (0.951 V) for oxygen reduction reaction (ORR) and a low overpotential (327 mV at 10 mA cm) for oxygen evolution reaction (OER). Significantly, when used as cathode catalyst for Zn-air batteries, CuCoO@C also displays a low charge-discharge voltage gap (0.79 V at 10 mA cm) and a long cycling life (up to 160 cycles for 80 h). With desirable architecture and excellent electrocatalytic properties, the CuCoO@C is considered a promising electrocatalyst for Zn-air batteries.
Optical-resolution photoacoustic microscopy (OR-PAM) is becoming a vital tool for studying the microcirculation system in vivo. By increasing the numerical aperture of optical focusing, the lateral resolution of OR-PAM can be improved; however, the depth of focus and thus the imaging range will be sacrificed correspondingly. In this work, we report our development of blind-deconvolution optical-resolution photoacoustic microscopy (BD-PAM) that can provide a lateral resolution ~2-fold finer than that of conventional OR-PAM (3.04 vs. 5.78μm), without physically increasing the system's numerical aperture. The improvement achieved with BD-PAM is demonstrated by imaging graphene nanoparticles and the microvasculature of mice ears in vivo. Our results suggest that BD-PAM may become a valuable tool for many biomedical applications that require both fine spatial resolution and extended depth of focus.
Abstract. We propose an improved version of a synthetic aperture focusing technique (SAFT) based on a delaymultiply-and-sum algorithm for acoustic-resolution photoacoustic microscopy (AR-PAM). In this method, the photoacoustic (PA) signals from multiple scan-lines are combinatorially coupled, multiplied, and then summed. This process can be considered a correlation operation of the PA signals in each scan-line, so the spatial coherent information between the PA signals can be efficiently extracted. By applying this method in conventional AR-PAM, lateral resolution and signal-to-noise ratio in out-of-focus regions are much improved compared with those estimated from the previously developed SAFT, respectively, thereby achieving the extension of the imaging focal region. Our phantom and in vivo imaging experiments prove the validity of our proposed method.
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