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用于电子可控微致动器的材料。

Materials for electronically controllable microactuators.

作者信息

Reynolds Michael F, Miskin Marc Z

机构信息

Department of Electrical and Systems Engineering, University of Pennsylvania, Philadelphia, USA.

出版信息

MRS Bull. 2024;49(2):107-114. doi: 10.1557/s43577-024-00665-1. Epub 2024 Feb 21.

Abstract

ABSTRACT

Electronically controllable actuators have shrunk to remarkably small dimensions, thanks to recent advances in materials science. Currently, multiple classes of actuators can operate at the micron scale, be patterned using lithographic techniques, and be driven by complementary metal oxide semiconductor (CMOS)-compatible voltages, enabling new technologies, including digitally controlled micro-cilia, cell-sized origami structures, and autonomous microrobots controlled by onboard semiconductor electronics. This field is poised to grow, as many of these actuator technologies are the firsts of their kind and much of the underlying design space remains unexplored. To help map the current state of the art and set goals for the future, here, we overview existing work and examine how key figures of merit for actuation at the microscale, including force output, response time, power consumption, efficiency, and durability are fundamentally intertwined. In doing so, we find performance limits and tradeoffs for different classes of microactuators based on the coupling mechanism between electrical energy, chemical energy, and mechanical work. These limits both point to future goals for actuator development and signal promising applications for these actuators in sophisticated electronically integrated microrobotic systems.

摘要

摘要

得益于材料科学的最新进展,电子可控致动器已缩小到非常小的尺寸。目前,多种类型的致动器可以在微米尺度上运行,通过光刻技术进行图案化,并由互补金属氧化物半导体(CMOS)兼容电压驱动,从而催生了包括数控微纤毛、细胞大小的折纸结构以及由机载半导体电子设备控制的自主微型机器人在内的新技术。随着许多此类致动器技术尚属首次出现且许多潜在设计空间仍未被探索,该领域有望发展壮大。为了帮助梳理当前的技术水平并设定未来目标,在此,我们概述现有工作,并研究微尺度下驱动的关键性能指标,包括力输出、响应时间、功耗、效率和耐久性是如何从根本上相互交织的。在此过程中,我们基于电能、化学能和机械功之间的耦合机制,找出了不同类型微致动器的性能限制和权衡取舍。这些限制既为致动器的未来发展指明了目标,也为这些致动器在复杂的电子集成微型机器人系统中的应用前景提供了信号。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7533/10907459/10fa5e2c715d/43577_2024_665_Fig1_HTML.jpg

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