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Activation volume and incipient plastic deformation of onlaxially-loaded gold nanowlres at very high strain rates

机译:极高应变速率下单轴加载金纳米粒子的活化体积和初期塑性变形

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摘要

Uniaxial tensile loading is investigated by the molecular dynamic (MD) method on Au nanowires at ultra-high strain rates. The activation volume is used to comprehensively characterize the incipient plastic deformation during this process. For lower strain rates such as 6.287 X 10~8 s~(-1), the moving velocity, V, of the atom planes due to uniaxial loading is two orders of magnitude smaller than the phonon wave propagation speed, V_0, and the coherence between atoms is always maintained with a larger activation volume. In this case, plastic deformation is initiated mainly by collective atomic slipping, and thus only lower flow stress is needed. On the other hand, for higher strain rates such as 6.287 X 10~(10) s~(-1), V is elevated to the same magnitude as V_0, the atom coherence is broken, their individual behavior is dominated by extraordinarily small activation volume, and atom diffusion becomes the main mechanism for plastic deformation. As a result, the yield strength is improved substantially. A higher temperature may weaken this strain-rate-dependent mechanical behavior because of the enhanced atom activity.
机译:通过分子动力学(MD)方法在金纳米线上以超高应变速率研究了单轴拉伸载荷。活化体积用于全面表征此过程中的初期塑性变形。对于较低的应变速率,例如6.287 X 10〜8 s〜(-1),由于单轴载荷而导致的原子平面的移动速度V比声子波的传播速度V_0和相干性小两个数量级。原子之间始终保持较大的活化体积。在这种情况下,塑性变形主要是由集体原子滑动引起的,因此只需要较低的流动应力。另一方面,对于较高的应变速率,例如6.287 X 10〜(10)s〜(-1),V升高到与V_0相同的幅度,原子相干性被破坏,它们的单个行为主要由很小的激活决定原子扩散成为塑性变形的主要机制。结果,屈服强度大大提高。较高的温度可能会由于增强的原子活性而削弱这种依赖于应变率的机械性能。

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