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Design of Efficient Full Adder in Quantum-Dot Cellular Automata

Further downscaling of CMOS technology becomes challenging as it faces limitation of feature size reduction. Quantum-dot cellular automata (QCA), a potential alternative to CMOS, promises efficient digital design at nanoscale. Investigations on the reduction of QCA primitives (majority gates and inv...

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Detalles Bibliográficos
Autores principales: Sen, Bibhash, Rajoria, Ayush, Sikdar, Biplab K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3690264/
https://www.ncbi.nlm.nih.gov/pubmed/23844385
http://dx.doi.org/10.1155/2013/250802
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author Sen, Bibhash
Rajoria, Ayush
Sikdar, Biplab K.
author_facet Sen, Bibhash
Rajoria, Ayush
Sikdar, Biplab K.
author_sort Sen, Bibhash
collection PubMed
description Further downscaling of CMOS technology becomes challenging as it faces limitation of feature size reduction. Quantum-dot cellular automata (QCA), a potential alternative to CMOS, promises efficient digital design at nanoscale. Investigations on the reduction of QCA primitives (majority gates and inverters) for various adders are limited, and very few designs exist for reference. As a result, design of adders under QCA framework is gaining its importance in recent research. This work targets developing multi-layered full adder architecture in QCA framework based on five-input majority gate proposed here. A minimum clock zone (2 clock) with high compaction (0.01 μm(2)) for a full adder around QCA is achieved. Further, the usefulness of such design is established with the synthesis of high-level logic. Experimental results illustrate the significant improvements in design level in terms of circuit area, cell count, and clock compared to that of conventional design approaches.
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spelling pubmed-36902642013-07-09 Design of Efficient Full Adder in Quantum-Dot Cellular Automata Sen, Bibhash Rajoria, Ayush Sikdar, Biplab K. ScientificWorldJournal Research Article Further downscaling of CMOS technology becomes challenging as it faces limitation of feature size reduction. Quantum-dot cellular automata (QCA), a potential alternative to CMOS, promises efficient digital design at nanoscale. Investigations on the reduction of QCA primitives (majority gates and inverters) for various adders are limited, and very few designs exist for reference. As a result, design of adders under QCA framework is gaining its importance in recent research. This work targets developing multi-layered full adder architecture in QCA framework based on five-input majority gate proposed here. A minimum clock zone (2 clock) with high compaction (0.01 μm(2)) for a full adder around QCA is achieved. Further, the usefulness of such design is established with the synthesis of high-level logic. Experimental results illustrate the significant improvements in design level in terms of circuit area, cell count, and clock compared to that of conventional design approaches. Hindawi Publishing Corporation 2013-06-05 /pmc/articles/PMC3690264/ /pubmed/23844385 http://dx.doi.org/10.1155/2013/250802 Text en Copyright © 2013 Bibhash Sen et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Sen, Bibhash
Rajoria, Ayush
Sikdar, Biplab K.
Design of Efficient Full Adder in Quantum-Dot Cellular Automata
title Design of Efficient Full Adder in Quantum-Dot Cellular Automata
title_full Design of Efficient Full Adder in Quantum-Dot Cellular Automata
title_fullStr Design of Efficient Full Adder in Quantum-Dot Cellular Automata
title_full_unstemmed Design of Efficient Full Adder in Quantum-Dot Cellular Automata
title_short Design of Efficient Full Adder in Quantum-Dot Cellular Automata
title_sort design of efficient full adder in quantum-dot cellular automata
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3690264/
https://www.ncbi.nlm.nih.gov/pubmed/23844385
http://dx.doi.org/10.1155/2013/250802
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