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Yu-Cheng Chen

Publications and source records attributed to Yu-Cheng Chen.

22 records · Page 2Linked to original sources

Accurate and Efficient Quantum Computations of Molecular Properties Using Daubechies Wavelet Molecular Orbitals: A Benchmark Study against Experimental Data

Although quantum computation (QC) is regarded as a promising numerical method for computational quantum chemistry, current applications of quantum-chemistry calculations on quantum computers are limited to small molecules. This limitation can be ascribed to technical problems in building and manipulating more qubits and the associated complicated operations of quantum gates in a quantum circuit when the size of the molecular system becomes large. As a result, reducing the number of required qubits is necessary to make QC practical. Currently, the minimal STO-3G basis set is commonly used in benchmark studies because it requires the minimum number of spin orbitals. Nonetheless, the accuracy of using STO-3G is generally low and thus cannot provide useful predictions. We propose to adopt Daubechies wavelet functions as an accurate and efficient method for QCs of molecular electronic properties. We demonstrate that a minimal basis set constructed from Daubechies wavelet basis can yield accurate results through a better description of the molecular Hamiltonian, while keeping the number of spin orbitals minimal. With the improved Hamiltonian through Daubechies wavelets, we calculate vibrational frequencies for H$_2$ and LiH using quantum-computing algorithm to show that the results are in excellent agreement with experimental data. As a result, we achieve quantum calculations in which accuracy is comparable with that of the full configuration interaction calculation using the cc-pVDZ basis set, whereas the computational cost is the same as that of a STO-3G calculation. Thus, our work provides a more efficient and accurate representation of the molecular Hamiltonian for efficient QCs of molecular systems, and for the first time demonstrates that predictions in agreement with experimental measurements are possible to be achieved with quantum resources available in near-term quantum computers.

quant-ph↗

Lasing in Self-Assembled Biophotonic Network

Mode competition is conventionally regarded as an unwanted phenomenon that induces instability of laser emission. Here, we experimentally demonstrate that the random dynamics behavior of mode competition provides hidden information of the intracavity topology. We introduced the concept of self-assembled biophotonics networks, where human insulin protein with network topology was sandwiched in a Fabry-Perot (FP) cavity. The optical coupling between insulin fibrils and enables strong mode competition. Thanks to the optical feedback provided by the FP cavity, the interaction between the light and insulin network was enhanced. Subtle changes in the network will cause significant changes in laser mode dynamics. By recording the transverse mode dynamics, we reconstruct a graph that reveals the optical correlation in the insulin network. Our results indicate that the graph represents an intrinsic feature and can sensitivity respond to the stimulus. The unclonable and sensitively responsive property of the biophotonic lasing network can potentially be employed in applications in sensing and information encryption.

physics.optics↗

Tailoring the Chirality of Microlaser with Topological Structured Chiral Droplets

The generation of chiral laser emission offers promising opportunities for modern photonic applications and the study of chiral light-mater interactions. Despite the great process made in recent years, the direct generation of chiral lasers with controllable chirality remains challenging in a microcavity. This study reports a strategy to control the emission chirality of whispering-gallery-mode organic microlasers with topological-structured chiral liquid crystal droplets. The findings suggest that the topological transformations in a microdroplet can induce different optical chirality strength and lasing polarization characteristics. In particular, the role of optical rotatory power was also investigated under linear and circular polarized excitation, where a vast lasing intensity difference between left/right circular polarized excitation was revealed. Theoretical analysis and simulation were carried out to support the significant findings. This study provides a facile tool for manipulating chiral laser emissions in microcavity, giving inspiration for topological-controlled photonics, chiral optical devices, and chiral molecular detection.

physics.optics↗

Chromatin Laser Imaging Reveals Abnormal Nuclear Changes for Early Cancer Detection

We developed and applied rapid scanning laser-emission microscopy to detect abnormal changes in cell nuclei for early diagnosis of cancer and cancer precursors. Regulation of chromatins is essential for genetic development and normal cell functions, while abnormal nuclear changes may lead to many diseases, in particular, cancer. The capability to detect abnormal changes in apparently normal tissues at a stage earlier than tumor development is critical for cancer prevention. Here we report using LEM to analyze colonic tissues from mice at-risk for colon cancer by detecting prepolyp nuclear abnormality. By imaging the lasing emissions from chromatins, we discovered that, despite the absence of observable lesions, polyps, or tumors under stereoscope, high-fat mice exhibited significantly lower lasing thresholds than low-fat mice. The low lasing threshold is, in fact, very similar to that of adenomas and is caused by abnormal cell proliferation and chromatin deregulation that can potentially lead to cancer. Our findings suggest that conventional methods, such as colonoscopy, may be insufficient to reveal hidden or early tumors under development. We envision that this work will provide new insights into LEM for early tumor detection in clinical diagnosis and fundamental biological and biomedical research of chromatin changes at the biomolecular level of cancer development.

q-bio.TO↗