12 research outputs found

    Quantum frequency conversion and single-photon detection with lithium niobate nanophotonic chips

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    In the past few years, the lithium niobate on insulator (LNOI) platform has revolutionized lithium niobate materials, and a series of quantum photonic chips based on LNOI have shown unprecedented performances. Quantum frequency conversion (QFC) photonic chips, which enable quantum state preservation during frequency tuning, are crucial in quantum technology. In this work, we demonstrate a low-noise QFC process on an LNOI nanophotonic platform designed to connect telecom and near-visible bands with sum-frequency generation by long-wavelength pumping. An internal conversion efficiency of 73% and an on-chip noise count rate of 900 counts per second (cps) are achieved. Moreover, the on-chip preservation of quantum statistical properties is verified, showing that the QFC chip is promising for extensive applications of LNOI integrated circuits in quantum information. Based on the QFC chip, we construct an upconversion single-photon detector with the sum-frequency output spectrally filtered and detected by a silicon single-photon avalanche photodiode, demonstrating the feasibility of an upconversion single-photon detector on-chip with a detection efficiency of 8.7% and a noise count rate of 300 cps. The realization of a low-noise QFC device paves the way for practical chip-scale QFC-based quantum systems in heterogeneous configurations.Comment: 8pages, 6 figures, 1 tabl

    Metabolomic profiling of Wilson disease, an inherited disorder of copper metabolism, and diseases with similar symptoms but normal copper metabolism

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    Abstract Background Wilson’s disease (WD) is a hereditary disorder that results in the accumulation of copper. The pathogenic mechanism is not well understood, and diagnosing the disease can be challenging, as it shares similarities with more prevalent conditions. To explore the metabolomic features of WD and differentiate it from other diseases related to copper metabolism, we conducted targeted and untargeted metabolomic profiling using ultra-high-performance liquid chromatography-tandem mass spectrometry (UPLC-MS/MS) and liquid chromatography-tandem mass spectrometry (LC-MS). We compared the metabolomic profiles of two subgroups of WD patients, namely hepatic WD (H-WD) and neurological WD (N-WD), H-WD patients and liver cirrhosis patients (who exhibit similar symptoms but have normal copper levels), and N-WD patients and Parkinson’s disease patients (who exhibit similar symptoms but have normal copper levels). Results Our pairwise comparisons revealed distinct metabolomic profiles for male and female WD patients, H-WD and N-WD patients, N-WD and Parkinson’s disease patients, and H-WD and liver cirrhosis patients. We then employed logistic regression analysis, receiver operating characteristic (ROC) analysis, and model construction to identify candidate diagnostic biomarkers that differentiate H-WD from liver cirrhosis and N-WD from Parkinson’s disease. Based on the spatial distribution of data obtained via PLS-DA analysis, we discovered variations in hydrophilic metabolites (aminoacyl-tRNA biosynthesis; alanine, aspartate, and glutamate metabolism; phenylalanine metabolism; arginine biosynthesis; and nicotinate and nicotinamide) and lipophilic metabolites (TG(triglyceride) (16:0_16:1_22:6), TG (16:0_16:0_22:6), and TG (16:0_16:1_22:5)) between H-WD and N-WD. Moreover, WD patients display metabolic traits that distinguish it from comparable conditions (liver cirrhosis and Parkinson’s disease). Conclusions Our analysis reveals significant variations in the levels of metabolites in critical metabolic pathways and numerous lipids in WD.ROC analysis indicates that three metabolites may be considered as candidate biomarkers for diagnosing WD
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