4. Cantilever Based Sensors



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4. Cantilever Based Sensors

Cantilever based Sensors NCCR Nanoscale Science Universität Basel bi-metallic Heat Source dynamic Resonance frequencyshift static Cantilever Bending Heat Drain Calorimeter Pico-Joule Micro roscale Pico-Gramm Surface Tension Atto-Mol Important: Functionalization of Cantilever Surface.

Cantilever Sensor Principle Detection of Molecular Interactions using Cantilever Arrays Silicon cantilevers are coated with a chemically sensitive layer Selective binding of target molecules leads to bending of the cantilever and changes its resonance frequency Optical beam-deflection allows to measure the tiny deflections. This method allows the sensitive and label-free detection of e.g. DNA, proteines, microorganisms or chemical substances Cantisens Research www.concentris.com Supported by

Cantilever based chemical Nose NCCR Nanoscale Science Universität Basel Principle Quantitative Analysis 1-Propanol 500 600 700 800 900 1000ppm Neuronal Network Analysis 0.01 0-0.01 Toluene Acetone Heptane Water Methanol 2-Propanol 1-Propanol Ethanol Di-Chlormethane -0.05 0 0.05

Magnetic Resonance Force Microscopy: Towards Detection of Single Spins Force sensor with magnetic tip NdFeB d=4µm, f=1231hz Cantilever in collaboration with IBM: Thickness:200-500nm cantilever amplitude [arb. units] 4 3 2 1 0 0.020 0.025 0.030 0.035 0.040 0.045 0.050 b-field [T] Sample: vitreous silica with E-centers Fmin= 3 10-17 N/Hz 1/2 Minimum detectable number of spins = 10 estimated detected spins 500 U. Gysin, P. Ruff, S. Rast, E. Meyer Uni Basel D.W. Lee, M. Despont, IBM

Why SFM with ultrasmall cantilevers? The ideal SFM or AFM would simultaneously and directly map the: NCCR Nanoscale Science University of Basel 1. vertical or force gradients 2. lateral forces or force gradients 3. loss of energy due to vertical mode of oscillation 4. loss of energy due to torsional mode of oscillation 5. tunneling current (as good as an STM) And 1. have an extremely high force sensitivity << 0.1pN 2. allow measurements at a high bandwith 3. be able to position AND keep the tip at an arbitrarily small distance, i.e. have a tip with a controllable compliance Our approach: 1. use sufficiently stiff (>200N/m) 2. operate them at small oscillation amplitudes (< 0.1 A) 3. make them sufficiently small (10-20um) to get the required sensitivity at high bandwiths.

6. Other Members of the SPM Family

Other Members of the SPM Family

Other Members of the SPM Family

5.1. Scanning Near Field Optical Microscopy (SNOM)

5.1.1. Introduction

Das Nahfeldoptische Mikroskop Scanning Near Field Optical Microscope (SNOM, NSOM) NCCR Nanoscale Science Universität Basel Spitze in der Nähe (einige nm) einer Oberfläche kann evaneszentes Feld in ein propagierendes Feld umwandeln: apertureless SNOM Near-field Spitze Surface Detector Reziprozität: Eine lokalisierte (evaneszente) Nahfeldquelle in der Nähe einer Oberfläche führt zur Erzeugung eines propagierenden Feldes: aperture SNOM Tip Near-field Surface Detector

Fabrikation der Apertur NCCR Nanoscale Science Universität Basel Metal Bedampfung und Schatten Effekt: Schlechte Reproduzierbarkeit Apertur ~ 70 nm Parallele Produktion der Spitzen Metalbedampfung Focussed Ion Beam: Gute Reproduzierbarkeit Apertur ~20 nm Einzelspitzen Prozess Teuer F.I.B Th. Huser, Uni Basel

Fabrikation der Apertur NCCR Nanoscale Science Universität Basel Festkörper Elektrolyt Gute Reproduzierbarkeit Apertur < 40 nm Billig Metal abhängig Einzelspitzen Prozess V A. Bouhelier, Uni Basel Cantilever Spitzen AFM Abbilden möglich Apertur < 40 nm Mikrofabriaktion Billig 200 nm Courtesy IMT & CSEM

Kontrolle Spitze-Probe Abstand Shear Force Detection NCCR Nanoscale Science Universität Basel Typische Betriebsparameter Resonanzfrequenz: 33000 Hz Q-Wert: 500 Schwingungsamplitude: 1 nm

Prinzip des SNOM & Betriebsarten Schema NCCR Nanoscale Science Universität Basel Betriebsarten

5.1.2. Imaging a few Examples

SNOM einzelner fluoreszierender Moleküle NCCR Nanoscale Science Universität Basel SNOM Fluorescenz Bild einzelner Moleküle. Jedes Molekül ist eine Punktquelle und erzeugt je nach seiner Orientierung unterschiedliche Bilder der Spitze, z.b. helle Punkte, Ringe, helle Doppelpunkte. N. Van Hulst, Uni Twente

Material science: Surface plasmon & field enhancement Semiconductors A. Bouhelier, Uni Basel F. Baida, Uni Besancon VCSELs. O. Marti, Uni Ulm

Biology: Shear-force topography and near-field fluorescence from GFP-labeled fibroblast cells. R. Zenobi, ETHZ Topography and florescence images of a growth cone of nerve cells of the hippocampus of a rat. The samples are fluorescence labeled with DIC18 O. Marti, Uni Ulm

5.3. Scanning Ion Conductance Microscopy (SICM)

Scanning Ion Conductance Microscopy (SICM) NCCR Nanoscale Science University of Basel The scanning ion conductance microscope (SICM) uses a micropipette which approaches the surface of a sample immersed in an electrolyte [1]. The ion conductance between the electrode in the solution and the electrode in the pipette is measured. As the pipette approaches the sample surface, the cross-section of the ion path from one electrode to the other is reduced and the conductance decreases. The resolution is essentially given by the size of the aperture. Compared to glass pipette tips, microfabricated probes [2] have the advantage of smaller aperture size and higher stability. Structures of the order of 100nm can be resolved. The distance is controlled by the ionic current. Alternatively, a combination of SICM and SFM can be used [3]. In this case, the pipettes were made of pulled quartz glass tubes, where the front-end portion is bent. The deflection of the pipette can be measured with conventional laser beam deflection method. The microscope can either be operated in contact mode or in tapping mode. In both cases, the ionic current is measured during imaging. However, the resolution in tapping mode on the pores is found to be improved [4]. The main application of SICM is to measure the distribution of ionic currents through the pores in a porous surface.

5.4. Photoemission Microscopy with Scanning Aperature (PEMSA)

Photoemission Microscopy with Scanning Aperature (PEMSA) NCCR Nanoscale Science University of Basel In photoemission microscopy with a scanning aperture (PEMSA) the photoemission of electrons escaping a surface and passing through a small aperture is measured. Using polarized light the circular polarization dependence of this photoemission current can be measured. McClelland and Rettner introduced this method and achieved a resolution of 30nm [1]. Magnetic domains of a Co/Pt film were imaged by the polarization Dependent PEMSA. The magnetic contrast of PEMSA is related to scanning Kerr microscopy. The photons which contribute to the signal must be absorbed very close to the surface. The created photoelectrons have low energies (some electron volts) which limits the mean free path to some nanometers. The apertures used by McClelland et al. were 30-45nm in diameter. The sample was first biased at +1V to suppress photoemission and was approached towards the tip until the tunneling current raised. Then the sample was retracted 30nm and the bias switched to -10V to detect photoemission. With 2mW of light, 100nA photocurrent is generated and 1pA is passed through the 30nm aperture. The photoemission is recorded as the light polarization is alternated. Then the sample is moved to the next position and the cycle is repeated. Since the resolution is approximately given by the mean free path of the photoelectrons and the aperture size, McClelland et al. suggest that the resolution will surpass the SNOM resolution. The potential of PEMSA is not yet fully explored. The energy analysis may provide useful information about the local band structure. Experiments in analogy to ultraviolet photoemission spectroscopy (UPS) or x-ray photoemission spectroscopy (XPS) may be performed, where the local chemistry could be determined with superblateral resolution.

5.5. STM with inverse Photoemission (STMiP)

Photoemission Microscopy with Scanning Aperture (PEMSA) NCCR Nanoscale Science University of Basel In photoemission microscopy with a scanning aperture (PEMSA) the photoemission of electrons escaping a surface and passing through a small aperture is measured. Using polarized light the circular polarization dependence of this photoemission current can be measured. McClelland and Rettner introduced this method and achieved a resolution of 30nm [1]. Magnetic domains of a Co/Pt film were imaged by the polarization Dependent PEMSA. The magnetic contrast of PEMSA is related to scanning Kerr microscopy. The photons which contribute to the signal must be absorbed very close to the surface. The created photoelectrons have low energies (some electron volts) which limits the mean free path to some nanometers. The apertures used by McClelland et al. were 30-45nm in diameter. The sample was first biased at +1V to suppress photoemission and was approached towards the tip until the tunneling current raised. Then the sample was retracted 30nm and the bias switched to -10V to detect photoemission. With 2mW of light, 100nA photocurrent is generated and 1pA is passed through the 30nm aperture. The photoemission is recorded as the light polarization is alternated. Then the sample is moved to the next position and the cycle is repeated. Since the resolution is approximately given by the mean free path of the photoelectrons and the aperture size, McClelland et al. suggest that the resolution will surpass the SNOM resolution. The potential of PEMSA is not yet fully explored. The energy analysis may provide useful information about the local band structure. Experiments in analogy to ultraviolet photoemission spectroscopy (UPS) or x-ray photoemission spectroscopy (XPS) may be performed, where the local chemistry could be determined with superblateral resolution.