连续可变量子无源光网络

IF 3.5 3区 医学 Q2 CHEMISTRY, MEDICINAL
Adnan A. E. Hajomer, Ivan Derkach, Radim Filip, Ulrik L. Andersen, Vladyslav C. Usenko, Tobias Gehring
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引用次数: 0

摘要

要建立一个可扩展的安全量子网络,一个关键的里程碑是从基本的点对点量子密钥分发(QKD)系统发展到旨在最大化网络容量的固有多用户协议。在这里,我们提出了一种基于连续可变(CV)系统,特别是相干态正交的量子无源光网络(QPON)协议,它能在所有网络用户之间确定性地同时高速生成密钥。我们实施了两种为网络用户分配不同信任度的协议,并在一个有 8 个用户的量子接入网络中实验演示了密钥生成,每个用户的接入链路跨度为 11 千米。根据对用户的信任假设,我们的网络密钥生成总量分别达到了 1.5 和 2.1 Mbits/s(或在有限大小信道估计的情况下分别为 0.4 和 1.0 Mbits/s)。我们的 CV-QPON 协议展示了将网络容量高速扩展到容纳数十个用户的潜力,为建立低成本、高速率、可扩展的安全量子接入网络开辟了新的可能性,是迈向量子互联网的垫脚石。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Continuous-variable quantum passive optical network

Continuous-variable quantum passive optical network

To establish a scalable and secure quantum network, a critical milestone is advancing from basic point-to-point quantum key distribution (QKD) systems to the development of inherently multi-user protocols designed to maximize network capacity. Here, we propose a quantum passive optical network (QPON) protocol based on continuous-variable (CV) systems, particularly the quadrature of the coherent state, which enables deterministic, simultaneous, and high-rate secret key generation among all network users. We implement two protocols with different trust levels assigned to the network users and experimentally demonstrate key generation in a quantum access network with 8 users, each with an 11 km span of access link. Depending on the trust assumptions about the users, we reach 1.5 and 2.1 Mbits/s of total network key generation (or 0.4 and 1.0 Mbits/s with finite-size channels estimation). Demonstrating the potential to expand the network’s capacity to accommodate tens of users at a high rate, our CV-QPON protocols open up new possibilities in establishing low-cost, high-rate, and scalable secure quantum access networks serving as a stepping stone towards a quantum internet.

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来源期刊
ACS Medicinal Chemistry Letters
ACS Medicinal Chemistry Letters CHEMISTRY, MEDICINAL-
CiteScore
7.30
自引率
2.40%
发文量
328
审稿时长
1 months
期刊介绍: ACS Medicinal Chemistry Letters is interested in receiving manuscripts that discuss various aspects of medicinal chemistry. The journal will publish studies that pertain to a broad range of subject matter, including compound design and optimization, biological evaluation, drug delivery, imaging agents, and pharmacology of both small and large bioactive molecules. Specific areas include but are not limited to: Identification, synthesis, and optimization of lead biologically active molecules and drugs (small molecules and biologics) Biological characterization of new molecular entities in the context of drug discovery Computational, cheminformatics, and structural studies for the identification or SAR analysis of bioactive molecules, ligands and their targets, etc. Novel and improved methodologies, including radiation biochemistry, with broad application to medicinal chemistry Discovery technologies for biologically active molecules from both synthetic and natural (plant and other) sources Pharmacokinetic/pharmacodynamic studies that address mechanisms underlying drug disposition and response Pharmacogenetic and pharmacogenomic studies used to enhance drug design and the translation of medicinal chemistry into the clinic Mechanistic drug metabolism and regulation of metabolic enzyme gene expression Chemistry patents relevant to the medicinal chemistry field.
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