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利用离子反应的 ISI 缓解调制方案用于分子通信。

ISI-mitigating modulation scheme using ion reaction for molecular communications.

机构信息

State Key Laboratory of Integrated Services Networks, Xidian University, Xi'an, 710071, People's Republic of China.

School of Computer Science, Shaanxi Normal University, Xi'an 710119, People's Republic of China.

出版信息

IET Nanobiotechnol. 2019 Sep;13(7):674-681. doi: 10.1049/iet-nbt.2018.5272.

Abstract

Here, according to the type-based modulation technique, the authors develop a novel modulation scheme by utilising ion collision and reaction to mitigate inter-symbol interference (ISI) in diffusive molecular communication (MC) systems. Two types of ions are employed as messenger molecules that cause a chemical reaction in the medium. According to the residual molecules and chemical reaction, the proposed modulation scheme adaptively adjusts the number of emitted molecules, thereby guaranteeing that the number of molecules that arrived at the receiver remains at a stable level. The authors evaluate the performance of the proposed scheme by comparing it with the conventional binary molecule shift keying (BMoSK), BMoSK with power adjustment (BMoSK-PA), and ideal BMoSK (without ISI) modulation techniques via diffusion. Numerical results show that the bit error probability and channel capacity of the proposed modulation scheme are much closer to the ideal BMoSK modulation scheme compared to the conventional BMoSK and the BMoSK-PA modulation schemes.

摘要

在此,根据基于类型的调制技术,作者利用离子碰撞和反应开发了一种新颖的调制方案,以减轻扩散分子通信(MC)系统中的符号间干扰(ISI)。两种类型的离子被用作信使分子,它们在介质中引起化学反应。根据残留分子和化学反应,所提出的调制方案自适应地调整发射分子的数量,从而保证到达接收器的分子数量保持在稳定水平。作者通过扩散将所提出的方案与传统的二进制分子移位键控(BMoSK)、具有功率调整的 BMoSK(BMoSK-PA)和理想的 BMoSK(无 ISI)调制技术进行比较,评估了所提出方案的性能。数值结果表明,与传统的 BMoSK 和 BMoSK-PA 调制方案相比,所提出的调制方案的误比特率和信道容量更接近理想的 BMoSK 调制方案。

相似文献

4
D-MoSK Modulation in Molecular Communications.分子通信中的D - MoSK调制
IEEE Trans Nanobioscience. 2015 Sep;14(6):680-3. doi: 10.1109/TNB.2015.2436409.

本文引用的文献

5
D-MoSK Modulation in Molecular Communications.分子通信中的D - MoSK调制
IEEE Trans Nanobioscience. 2015 Sep;14(6):680-3. doi: 10.1109/TNB.2015.2436409.

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