Design of a MEMS Force Sensor for Quantitative Measurement in the Nano- to Pico-Newton Range

2010 ◽  
Vol 2010 (DPC) ◽  
pp. 001841-001868
Author(s):  
Li-Anne Liew ◽  
John M. Moreland ◽  
Jonathan R. Pratt

We describe the design and fabrication of a MEMS nano- to pico-Newton force sensor with SI traceability. There has been much recent interest in developing instrumentation for the quantitative measurement of forces in the nano- to pico-Newton range. Forces in this range are frequently encountered when investigating mechanical properties of nanomaterials, in nanobiotechnology, and in single-molecule biophysics. Various methods of measuring forces at these levels include using AFM cantilevers, scanning probe microscopy, and nanoindentation. However, such measurements are relative, and in order to obtain precise quantitative measurements, it is necessary to be able to calibrate such sensors in a manner that is traceable to fundamental SI units. One such method of calibration is using an Electrostatic Force Balance (EFB) that has been established at NIST. We thus describe the design and fabrication of a MEMS-based force sensor that may be directly calibrated with the EFB and thus has the potential to measure nano- to pico-Newtons of force with SI traceability. The sensor consists of a silicon rigid arm supported on silicon tethers and which are attached to capacitive electrodes. The bar, tethers and electrodes are made from the device layer of a double side SOI wafer. A glass wafer with patterned metal electrodes is anodically bonded on both the top and bottom of the wafer to form symmetrical capacitive electrodes. An external force moves the silicon arm and the resulting capacitive force gradient of the electrodes is measured with the EFB. The mechanical structure and electrodes are designed for force sensitivity in the nano- to pico-Newton ranges and for operation in UHV to reduce thermomechanical noise. We discuss the design, initial fabrication and testing of this force sensor as a step toward the ultimate goals of quantitative nanomechanical testing of materials, NEMS, and engineered surfaces at the nanoscale.

2004 ◽  
Vol 19 (1) ◽  
pp. 366-379 ◽  
Author(s):  
Jon R. Pratt ◽  
Douglas T. Smith ◽  
David B. Newell ◽  
John A. Kramar ◽  
Eric Whitenton

Recent experiments with the National Institute of Standards and Technology (NIST) Electrostatic Force Balance (EFB) have achieved agreement between an electrostatic force and a gravitational force of 10−5 N to within a few hundred pN/μN. This result suggests that a force derived from measurements of length, capacitance, and voltage provides a viable small force standard consistent with the Système International d’Unités. In this paper, we have measured the force sensitivity of a piezoresistive microcantilever by directly probing the NIST EFB. These measurements were linear and repeatable at a relative standard uncertainty of 0.8%. We then used the calibrated cantilever as a secondary force standard to transfer the unit of force to an optical lever–based sensor mounted in an atomic force microscope. This experiment was perhaps the first ever force calibration of an atomic force microscope to preserve an unbroken traceability chain to appropriate national standards. We estimate the relative standard uncertainty of the force sensitivity at 5%, but caution that a simple model of the contact mechanics suggests errors may arise due to friction.


Author(s):  
Jon R. Pratt ◽  
David B. Newell ◽  
John A. Kramar ◽  
Eric Whitenton

The characterization of material properties and mechanical performance of micro-electromechanical devices often hinges on the accurate measurement of small forces. Calibrated load cells of appropriate size and range are used, but are often not calibrated in a fashion traceable to the International System of Units (SI). Recently, we calibrated a piezoresistive cantilever in terms of SI force sensitivity. Here, we employ this device as a secondary force standard to calibrate another, optical lever based sensor in a force probe instrument, demonstrating an unbroken tracability chain to appropriate national standards.


2007 ◽  
Vol 1021 ◽  
Author(s):  
Jon R. Pratt ◽  
John A. Kramar ◽  
Gordon A. Shaw ◽  
Douglas T. Smith ◽  
John M. Moreland

AbstractWe describe the design, fabrication, and calibration testing of a new piezoresistive cantilever force sensor suitable for the force calibration of atomic force microscopes in a range between tens of nanonewtons to hundreds of micronewtons. The sensor is calibrated using the NIST Electrostatic Force Balance (EFB) and functions either as a force reference or stiffness artifact that is traceable to the International System of Units. The cantilever has evenly spaced fiducial marks along its length. We report stiffnesses that vary quadratically with location, from a high of 12.1 N/m at the first fiducial to a low of 0.394 N/m at the last; with force sensitivities that vary linearly, ranging from 18.1 Ù/mN to 106 Ù/mN. We also test the device to transfer the unit of force to an atomic force microscope, finding that force and stiffness based approaches yield independent estimates of the contact force consistent within 2 % of each other.


2020 ◽  
Author(s):  
Nikolas Hundt

Abstract Single-molecule imaging has mostly been restricted to the use of fluorescence labelling as a contrast mechanism due to its superior ability to visualise molecules of interest on top of an overwhelming background of other molecules. Recently, interferometric scattering (iSCAT) microscopy has demonstrated the detection and imaging of single biomolecules based on light scattering without the need for fluorescent labels. Significant improvements in measurement sensitivity combined with a dependence of scattering signal on object size have led to the development of mass photometry, a technique that measures the mass of individual molecules and thereby determines mass distributions of biomolecule samples in solution. The experimental simplicity of mass photometry makes it a powerful tool to analyse biomolecular equilibria quantitatively with low sample consumption within minutes. When used for label-free imaging of reconstituted or cellular systems, the strict size-dependence of the iSCAT signal enables quantitative measurements of processes at size scales reaching from single-molecule observations during complex assembly up to mesoscopic dynamics of cellular components and extracellular protrusions. In this review, I would like to introduce the principles of this emerging imaging technology and discuss examples that show how mass-sensitive iSCAT can be used as a strong complement to other routine techniques in biochemistry.


2020 ◽  
Author(s):  
Achim P. Popp ◽  
Johannes Hettich ◽  
J. Christof M. Gebhardt

Transcription is a vital process activated by transcription factor (TF) binding. The active gene releases a burst of transcripts before turning inactive again. While the basic course of transcription is well understood, it is unclear how binding of a TF affects the frequency, duration and size of a transcriptional burst. We systematically varied the residence time and concentration of a synthetic TF and characterized the transcription of a reporter gene by combining single molecule imaging, single molecule RNA-FISH, live transcript visualisation and analysis with a novel algorithm, Burst Inference from mRNA Distributions (BIRD). For this well-defined system, we found that TF binding solely affected burst frequency and variations in TF residence time had a stronger influence than variations in concentration. This enabled us to device a model of gene transcription, in which TF binding triggers multiple successive steps before the gene transits to the active state and actual mRNA synthesis is decoupled from TF presence. We quantified all transition times of the TF and the gene, including the TF search time and the delay between TF binding and the onset of transcription. Our quantitative measurements and analysis revealed detailed kinetic insight, which may serve as basis for a bottom-up understanding of gene regulation.


Diagnostics ◽  
2020 ◽  
Vol 10 (10) ◽  
pp. 793
Author(s):  
Rooa Sindi ◽  
Yin How Wong ◽  
Chai Hong Yeong ◽  
Zhonghua Sun

Despite the development and implementation of several MRI techniques for breast density assessments, there is no consensus on the optimal protocol in this regard. This study aimed to determine the most appropriate MRI protocols for the quantitative assessment of breast density using a personalized 3D-printed breast model. The breast model was developed using silicone and peanut oils to simulate the MRI related-characteristics of fibroglandular and adipose breast tissues, and then scanned on a 3T MRI system using non-fat-suppressed and fat-suppressed sequences. Breast volume, fibroglandular tissue volume, and percentage of breast density from these imaging sequences were objectively assessed using Analyze 14.0 software. Finally, the repeated-measures analysis of variance (ANOVA) was performed to examine the differences between the quantitative measurements of breast volume, fibroglandular tissue volume, and percentage of breast density with respect to the corresponding sequences. The volume of fibroglandular tissue and the percentage of breast density were significantly higher in the fat-suppressed sequences than in the non-fat-suppressed sequences (p < 0.05); however, the difference in breast volume was not statistically significant (p = 0.529). Further, a fat-suppressed T2-weighted with turbo inversion recovery magnitude (TIRM) imaging sequence was superior to the non-fat- and fat-suppressed T1- and T2-weighted sequences for the quantitative measurement of breast density due to its ability to represent the exact breast tissue compositions. This study shows that the fat-suppressed sequences tended to be more useful than the non-fat-suppressed sequences for the quantitative measurements of the volume of fibroglandular tissue and the percentage of breast density.


2020 ◽  
Vol 238 ◽  
pp. 12009
Author(s):  
Walter S. J. Ferreira ◽  
Paulo S. S. dos Santos ◽  
Paulo Caldas ◽  
Pedro A. S. Jorge ◽  
João M. S. Sakamoto

In this work, a long-period fiber grating (LPG) based sensor was evaluated as a sensing device for micro-force measurement, in the order of micro Newtons. It was used an LPG fabricated by arc-inducted technique in a SMF-28 standard optical fiber. The optical fiber was fixed between two clamps with a separation of 150 mm with the middle of the LPG located at the center. Characterizations were performed in terms of temperature, curvature and strain. The grating was then used as a micro-force sensor by means of both curvature and strain, induced by a hung mass in a stretched fiber. Furthermore, the evaluation of a precurvature LPG was performed to assess if an increase of sensitivity is achieved. Micro-force sensitivity achieved with the stretched LPG was 1.41 nm/mN and it was demonstrated that its sensitivity can be enhanced to 5.14 nm/mN with a pre-curvature of 2.2 m–1 applied to the LPG, achieving a spectral resolution of at least 15.6 μN.


Author(s):  
Pezhman A. Hassanpour ◽  
Patricia M. Nieva ◽  
Amir Khajepour

In this paper, a novel sensing mechanism is introduced. This mechanism consists of a clamped-clamped beam and two parallel electrodes. An analytical model of the system, that takes into account the mechanical linear and nonlinear stiffnesses as well as the nonlinear electrostatic force, is developed. The time response of the system to a disturbance is derived while the applied voltage is increasing at a constant rate. It has been shown that the voltage, that destabilize the beam, can be used as a measure of the axial force in the beam. This technique can be used in the development of new type of sensors.


2019 ◽  
Vol 476 (16) ◽  
pp. 2411-2425 ◽  
Author(s):  
Jagadish P. Hazra ◽  
Amin Sagar ◽  
Nisha Arora ◽  
Debadutta Deb ◽  
Simerpreet Kaur ◽  
...  

Abstract Tip-link as force-sensor in hearing conveys the mechanical force originating from sound to ion-channels while maintaining the integrity of the entire sensory assembly in the inner ear. This delicate balance between structure and function of tip-links is regulated by Ca2+-ions present in endolymph. Mutations at the Ca2+-binding sites of tip-links often lead to congenital deafness, sometimes syndromic defects impairing vision along with hearing. Although such mutations are already identified, it is still not clear how the mutants alter the structure-function properties of the force-sensors associated with diseases. With an aim to decipher the differences in force-conveying properties of the force-sensors in molecular details, we identified the conformational variability of mutant and wild-type tip-links at the single-molecule level using FRET at the endolymphatic Ca2+ concentrations and subsequently measured the force-responsive behavior using single-molecule force spectroscopy with an Atomic Force Microscope (AFM). AFM allowed us to mimic the high and wide range of force ramps (103–106 pN s−1) as experienced in the inner ear. We performed in silico network analysis to learn that alterations in the conformations of the mutants interrupt the natural force-propagation paths through the sensors and make the mutant tip-links vulnerable to input forces from sound stimuli. We also demonstrated that a Ca2+ rich environment can restore the force-response of the mutant tip-links which may eventually facilitate the designing of better therapeutic strategies to the hearing loss.


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