Characterization of Standard Cells for Intra-Cell Mismatch Variations

S. Sundareswaran, J. Abraham, A. Ardelea, R. Panda
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引用次数: 24

Abstract

With the adoption of statistical timing across industry, there is a need to characterize all gates/cells in a digital library for delay variations (referred to as, statistical characterization). Statistical characterization need to be performed efficiently with acceptable accuracy as a function of several process and environment parameter variations. In this paper, we propose an approach to consider intra-cell process mismatch variations to characterize a cell's delay and output transition time (output slew) variations. A straightforward approach to address this problem is to model these mismatch variations by characterizing for each device fluctuation separately. However, the runtime complexity for such characterization becomes of the order of number of devices in the cell and the number of simulations required can easily become infeasible. We analyze the fluctuations in switching and non-switching devices and their impact on delay variations. Using these properties of the devices, we propose a clustering approach to characterize for cell's delay variations due to intra-cell mismatch variations. The proposed approach results in as much as 12X runtime improvements with acceptable accuracy, compared with Monte Carlo simulations. We show that this approach ensures an upper-bound on the results while keeping the number of simulations for each cell independent of the number of devices.
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细胞内错配变异标准细胞的表征
随着整个行业采用统计时序,需要对数字库中所有门/单元的延迟变化进行表征(称为统计表征)。统计表征需要以可接受的精度作为几个过程和环境参数变化的函数有效地执行。在本文中,我们提出了一种考虑细胞内过程不匹配变化的方法来表征细胞的延迟和输出转换时间(输出转换)变化。解决这一问题的一个直接方法是通过分别描述每个器件波动来对这些不匹配变化进行建模。然而,这种表征的运行时复杂性变成了单元中设备数量的顺序,并且所需的模拟数量很容易变得不可行的。我们分析了开关和非开关器件的波动及其对延迟变化的影响。利用这些器件的特性,我们提出了一种聚类方法来表征由于细胞内不匹配变化引起的细胞延迟变化。与蒙特卡罗模拟相比,所提出的方法可以在可接受的精度下提高多达12倍的运行时间。我们表明,这种方法确保了结果的上限,同时保持每个单元的模拟次数独立于设备的数量。
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