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Jinyang Liang

Publications and source records attributed to Jinyang Liang.

2 recordsLinked to original sources

Increasing Downshifting Luminescence Intensity Through an Extended Active Layer

The near-infrared (NIR) emission of rare-earth doped nanoparticles (RENPs), known as downshifting luminescence, has been extensively investigated in diverse applications from information technology to biomedicine. In promoting brightness and enriching the functionalities of the downshifting luminescence of RENPs, numerous studies have exploited inert shell to protect rare-earth dopants from surface quenchers. However, internal concentration quenching remains an unsolved puzzle when using higher dopant concentrations of rare-earth ions in an attempt to obtain brighter emission. Following a plethora of research involving core-shell structures, the interface has shown to be controllable, ranging from a well-defined, abrupt boundary to an obscure one with cation intermixing. By utilizing this inter-mixed core-shell property for the first time, we design a new architecture to create a homogeneous double-layer core-shell interface to extend the active layer, allowing more luminescent centers without severe concentration quenching. By systematically deploying the crystallinity of the starting core, shell growth dynamics, and dopant concentrations, the downshifting luminescence intensity of new archictecture achieves a 12-fold enhancement surpassing the traditional core-shell structure. These results provide deeper insight into the potential benefits of the intermixed core-shell structure, offering an effective approach to tackling the internal concentration quenching effect for highly boosted NIR optical performance.

cond-mat.mtrl-sci

High-fidelity microsecond-scale cellular imaging using two-axis compressed streak imaging fluorescence microscopy

Compressed streak imaging (CSI) is a computational imaging strategy that can acquire video at over 150 trillion frames per second. Despite this achievement, CSI faces challenges in detecting subtle intensity fluctuations in slow-moving, continuously illuminated objects. This limitation, largely attributable to high streak compression and motion blur, has curtailed the broader adoption of CSI in cellular fluorescence microscopy. To address these issues and expand the utility of CSI, we developed a two-axis compressed streak imaging (TACSI) method that results in significant improvements to the reconstructed video fidelity. TACSI introduces a second scanning axis which shuttles a conjugate image of the object with respect to the coded aperture. The moving image decreases the streak compression ratio and produces a "flash and shutter" phenomenon that reduces coded aperture motion blur, overcoming the limitations of current CSI technologies. This approach is supported with an analytical model describing the TACSI compression ratio, along with simulated and empirical measurements. We demonstrate TACSI's ability to measure rapid variations in cell membrane potentials, previously unattainable with conventional CSI. This method has broad implications for high-speed photography, including visualization of action potentials, muscle contractions, and enzymatic reactions that occur on microsecond and faster timescales using fluorescence microscopy.

physics.optics