Surface-chemistry-driven actuation in nanoporous gold

Surface-chemistry-driven actuation in nanoporous gold
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DOI:
10.1038/nmat2335
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发表时间:
2009-01-01
期刊:
影响因子:
41.2
通讯作者:
Hamza, A. V.
Hamza, A. V.
中科院分区:
材料科学1区
文献类型:
--
作者:
Biener, J.;Wittstock, A.;Hamza, A. V.

文献摘要

被引文献

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虽然生物系统中的致动完全由化学能驱动,但这一概念尚未在人造致动器技术中实现,因为这些技术首先依赖于发热或发电(1)。在这里,我们证明了表面化学驱动的驱动可以在高表面积材料中实现,如纳米多孔金。例如,通过将纳米孔Au交替暴露于臭氧和一氧化碳中,我们获得了百分之零点几的可逆应变幅度。这种效应可以用吸附物引起的表面应力变化来解释(2),并且可以用来将化学能直接转化为机械响应,从而为表面化学驱动的执行器和传感器技术打开了大门。
Although actuation in biological systems is exclusively powered by chemical energy, this concept has not been realized in man-made actuator technologies, as these rely on generating heat or electricity first(1). Here, we demonstrate that surface-chemistry-driven actuation can be realized in high-surface-area materials such as nanoporous gold. For example, we achieve reversible strain amplitudes of the order of a few tenths of a per cent by alternating exposure of nanoporous Au to ozone and carbon monoxide. The effect can be explained by adsorbate-induced changes of the surface stress(2), and can be used to convert chemical energy directly into a mechanical response, thus opening the door to surface-chemistry-driven actuator and sensor technologies.