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1.
Appl Opt ; 63(4): 1079-1086, 2024 Feb 01.
Artículo en Inglés | MEDLINE | ID: mdl-38437406

RESUMEN

A two-dimensional signal constellation scheme for binary uniform memoryless source transmission in optical fiber channels is studied in this paper. In geometric shaping (GS), optimization algorithms are usually used to change the overall position of constellation points while maintaining the probability of constellation points unchanged. Different optimization functions are used to allocate the position of constellation symbols, thereby improving constellation performance. A 16 quadrature amplitude modulation (QAM) optical signal generation scheme based on weighted optimal Euclidean distance is proposed in this paper. In order to obtain the best constellation diagram and increase the shaping gain, the weighted optimal Euclidean distance that can minimize the bit error rate (BER) over multiple iterative optimizations is used as the objective function. On the one hand, the proposed 16QAM optical signal generation scheme based on weighted optimal Euclidean distance always outperforms the uniform square 16QAM and the uniform circle 16QAM schemes in the back to back (BTB) transmission. On the other hand, after analyzing the simulation demonstration in a 50GBaud coherent optical communication system over 3000 km, results demonstrate that the optical signal to noise ratio (OSNR) performance of this system is better than that of the uniform square 16QAM and the uniform circle 16QAM, which is improved by 0.52 dB and 0.85 dB, respectively. In addition, the proposed 16QAM system increases the transmission distance by 989 km and 741 km, respectively, compared to the other two systems. The performance confirms that the proposed novel 16QAM scheme, to the best of our knowledge, can effectively improve the reliability and transmission distance. Therefore, the proposed scheme has a certain development prospect in the future long-distance transmission of high-speed optical fiber communication.

2.
Opt Express ; 31(26): 42961-42975, 2023 Dec 18.
Artículo en Inglés | MEDLINE | ID: mdl-38178401

RESUMEN

A double key (DK) real-time update and hybrid five-dimensional (5-D) hyperchaotic deoxyribonucleic acid (DNA) dynamic encryption scheme is proposed, which can ensure the security in the orthogonal frequency division multiplexing passive optical network (OFDM-PON). Chaotic sequences for DNA dynamic encryption are produced using a four-dimensional (4-D) hyperchaotic Lü system and a one-dimensional (1-D) logistic map. In this scheme, the DK consists of an external key set, which is stored locally, and an internal key, which is associated with the plaintext and external key. In addition, a pilot cluster is used as the carrier of key transmission and key embedding is achieved by converting key to phase information of the pilot. To verify the feasibility of the scheme, a simulation validation is performed on a 46.5Gb/s 16 quadrature amplitude modulation (QAM) coherent OFDM-PON system transmitted over an 80 km transmission distance. The results show that the proposed scheme can improve the security performance of OFDM-PON at a low OSNR cost of 0.3 dB and the key space is expanded to (8.514 × 10102)S. When the correlation redundancy (CR) G⩾7, the 0 bit error rate (BER) of key can be achieved and the key can be updated and distributed in real-time without occupying additional secure channels.

3.
Inorg Chem ; 60(9): 6463-6471, 2021 May 03.
Artículo en Inglés | MEDLINE | ID: mdl-33856787

RESUMEN

99Tc is one of the most abundant radiotoxic isotopes in used nuclear fuel with a high fission yield and a long half-life. Effective removal of pertechnetate (TcO4-) from an aqueous solution is important for nuclear waste separation and remediation. Herein, we report a series of facilely obtained benzene-linked guanidiniums that could precipitate TcO4- and its nonradioactive surrogate ReO4- from a high-concentration acidic solution through self-assembly crystallization. The resulting perrhenate and pertechnetate solids exhibit exceptionally low aqueous solubility. The benzene-linked guanidiniums hold one of the highest TcO4- removal capacities (1279 mg g-1) among previously reported materials and possess a removal percentage of 59% for ReO4- in the presence of Cl- over 50 times. The crystallization mechanism was clearly illustrated by the single-crystal structures and density functional theory calculations, indicating that TcO4- is captured through a charge-assisted hydrogen bonding interaction and stabilized by π-π stacking layers. In addition, the removal process is easily recycled and no toxic organic reagents are introduced. This work provides a green approach to preliminarily separate TcO4- from high-level nuclear wastes.

4.
Chemistry ; 27(18): 5632-5637, 2021 Mar 26.
Artículo en Inglés | MEDLINE | ID: mdl-33506531

RESUMEN

As one of most problematic radionuclides, technetium-99, mainly in the form of anionic pertechnetate (TcO4 - ), exhibits high environmental mobility, long half-life, and radioactive hazard. Due to low charge density and high hydrophobicity for this tetrahedral anion, it is extremely difficult to recognize it in water. Seeking efficient and selective recognition method for TcO4 - is still a big challenge. Herein, a new water-stable cationic metal-organic framework (ZJU-X8) was reported, bearing tetraphenylethylene pyrimidine-based aggregation-induced emission (AIE) ligands and attainable silver sites for TcO4 - detection. ZJU-X8 underwent an obvious spectroscopic change from brilliant blue to flavovirens and exhibited splendid selectivity towards TcO4 - . This uncommon fluorescent recognition mechanism was well elucidated by batch sorption experiments and DFT calculations. It was found that only TcO4 - could enter into the body of ZJU-X8 through anion exchange whereas other competing anions were excluded outside. Subsequently, after interaction between TcO4 - and silver ions, the electron polarizations from pyrimidine rings to Ag+ cations significantly lowered the energy level of the π* orbital and thus reduced the π-π* energy gap, resulting in a red-shift in the fluorescent spectra.

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