2006 Sixth IEEE Conference on Nanotechnology
DOI: 10.1109/nano.2006.1717097
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Clocking and Cell Placement for QCA

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Cited by 15 publications
(14 citation statements)
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“…Figure 2b shows the structure of the decatriene molecule [8]; this molecule has three real dots represented by three ethylene groups. The two top dots represent the active dots used to encode the binary information (Dot 1 and Dot 2), while the third central one is related to the clock issue [27] (Dot 3). The length of the molecule is l = 0.6 nm.…”
Section: Background: Molecular Qcamentioning
confidence: 99%
“…Figure 2b shows the structure of the decatriene molecule [8]; this molecule has three real dots represented by three ethylene groups. The two top dots represent the active dots used to encode the binary information (Dot 1 and Dot 2), while the third central one is related to the clock issue [27] (Dot 3). The length of the molecule is l = 0.6 nm.…”
Section: Background: Molecular Qcamentioning
confidence: 99%
“…Timing/synchronization in QCA is accomplished by the cascaded clocking of four distinct and periodic phases as shown in Figure 1(c) [19]. In the first (switch) phase, the tunnelling barrier between two dots of a QCA cell starts to rise.…”
Section: Preliminariesmentioning
confidence: 99%
“…Thus, this latching notion employed in quasi-adiabatic switching functions similarly to a clocked multiplexer [20]. We employ zone-based clocking schemes for the quasi-adiabatic switching regions [20,22], avoiding the spatial issues which result when the clocking regions have the same lateral dimension as the QDs themselves.…”
Section: Matrix Multiplier Modelmentioning
confidence: 99%