Choosing the Right Accelerating Voltage for SEM (An Introduction for Beginners)

Similar documents
MCR Scanning Electron Microscopy Laboratory Portfolio

SCIENTIFIC INSTRUMENT NEWS. Introduction. Design of the FlexSEM 1000

Scanning Electron Microscopy SEM. Warren Straszheim, PhD MARL, 23 Town Engineering

SECONDARY ELECTRON DETECTION

Scanning Electron Microscopy Laboratory Portfolio

Introduction of New Products

Scanning Electron Microscopy Student Image Portfolio

Scanning Electron Microscopy Laboratory Portfolio

Secondary Electron Detector

ELECTRON MICROSCOPY AN OVERVIEW

Chapter 1. Basic Electron Optics (Lecture 2)

NANO 703-Notes. Chapter 9-The Instrument

Scanning electron microscope

A NEW TECHNIQUE TO RAPIDLY IDENTIFY LOW LEVEL GATE OXIDE LEAKAGE IN FIELD EFFECT SEMICONDUCTORS USING A SCANNING ELECTRON MICROSCOPE.

Scanning electron microscope

Scanning Electron Microscope in Our Facility

Scanning Electron Microscopy Laboratory Portfolio

Functions of the SEM subsystems

Agilent 8700 LDIR Chemical Imaging System. Bringing Clarity and Unprecedented Speed to Chemical Imaging.

Supporting Information

Scanning Electron Microscopy Project Portfolio

Model SU3500 Scanning Electron Microscope

Introduction to Scanning Electron Microscopy

Scanning Electron Microscopy. EMSE-515 F. Ernst

Low Voltage Electron Microscope

DualBeam and FIB capability applied to metals research

Application Note #548 AcuityXR Technology Significantly Enhances Lateral Resolution of White-Light Optical Profilers

Lecture 20: Optical Tools for MEMS Imaging

Material analysis by infrared mapping: A case study using a multilayer

NeoScope. Simple Operation to 40,000. Table Top SEM. Serving Advanced Technology

Agilent Cary 610/620 FTIR microscopes and imaging systems RESOLUTION FOR EVERY APPLICATION

(Refer Slide Time: 00:10)

Evaluating the Performance of a Commercial Silicon Drift Detector for X-ray Microanalysis

MODULE I SCANNING ELECTRON MICROSCOPE (SEM)

FEI Helios NanoLab 600 TEM specimen prep recipe Nicholas G. Rudawski (352) (office) (805) (cell) Last updated: 01/19/17

The microscope is useful in making observations and collecting data in scientific experiments. Microscopy involves three basic concepts:

SCANNING ELECTRON MICROSCOPY By W. C. NIXON (Engineering Laboratory, Cambridge University)

Fabrication of Probes for High Resolution Optical Microscopy

CHAPTER TWO METALLOGRAPHY & MICROSCOPY

Effect of Shot Noise and Secondary Emission Noise in Scanning Electron Microscope Images

MICROSCOPE LAB. Resolving Power How well specimen detail is preserved during the magnifying process.

Supplementary Figure S1. Schematic representation of different functionalities that could be

Read and understand the requirements of this procedure Assist students with installation as needed

Module 4B7: VLSI Design, Technology, and CAD. Scanning Electron Microscopical Examination of CMOS Integrated Circuit

Topics 3b,c Electron Microscopy

5. The Scanning Electron Microscope

Scanning Electron Microscopy

Serial Block Face Imaging

THE STANDARD IN MEASURING

Opto-digital Microscope. DSX Series. DSX Applications. High-resolution Upright scope. High-resolution Inverted scope. Free-angle Wide zoom scope

Low Voltage Electron Microscope. Nanoscale from your benchtop LVEM5. Delong America

Magellan XHR SEM. Discover the world of extreme high resolution scanning electron microscopy

Selective Soldering for Interconnection Technology Used in Enterprise Communication Apparatuses

Chapter 4 Imaging Lecture 17

Dickinson College Department of Geology

INTRODUCTION We believe that every laboratory working in the field of nanotechnology needs an SEM, therefore we would like to introduce to you our IEM

Life Science Chapter 2 Study Guide

1.3. Before loading the holder into the TEM, make sure the X tilt is set to zero and the goniometer locked in place (this will make loading easier).

University of Washington Molecular Analysis Facility

How to choose a Scanning Electron Microscope (SEM)

Scanning Electron Microscopy Basics and Applications

JSM 6060 LV SCANNING ELECTRON MICROSCOPE STANDARD OPERATING PROCEDURES

Figure 1. Oil-immersion objectives available for use with the Lionheart FX.

Extending Acoustic Microscopy for Comprehensive Failure Analysis Applications

Quick and simple installation and no maintenance needed. 3 Times More affordable Than a normal SEM. Obtaining results in less than 4 minutes

2014 HTD-E with options

Applications of Optics

Observing Microorganisms through a Microscope LIGHT MICROSCOPY: This type of microscope uses visible light to observe specimens. Compound Light Micros

Recent results from the JEOL JEM-3000F FEGTEM in Oxford

Compare and Contrast. Contrast Methods in Industrial Inspection Microscopy. Application Note. We explain how to

How Microscopes Work By Cindy Grigg

Schottky Emission VP FE-SEM

LOW VOLTAGE BACKSCATTERED ELECTRON IMAGING (< 5 KV) USING FIELD EMISSION SCANNING ELECTRON MICROSCOPY

Development of JEM-2800 High Throughput Electron Microscope

ZEISS EVO SOP. May 2017 ELECTRON OPTICS

SCPA603 Embedding and Sectioning

2.Components of an electron microscope. a) vacuum systems, b) electron guns, c) electron optics, d) detectors. Marco Cantoni 021/

This procedure assumes the user is already familiar with basic operation of the SEM and the MiraTC interface.

contents TABLE OF The SECOM platform Applications - sections Applications - whole cells Features Integrated workflow Automated overlay

SOP for Hitachi S-2150 Scanning Electron Microscope For review purposes only

Scintillation Counters

FRAUNHOFER AND FRESNEL DIFFRACTION IN ONE DIMENSION

S200 Course LECTURE 1 TEM

1. Preliminary sample preparation

SPECIFICATIONS FOR 3M TM PRESTIGE SUN CONTROL WINDOW FILMS

attosnom I: Topography and Force Images NANOSCOPY APPLICATION NOTE M06 RELATED PRODUCTS G

Study on Glow Discharge Plasma Used in Polyester. surface modification

Burton's Microbiology for the Health Sciences

Add CLUE to your SEM. High-efficiency CL signal-collection. Designed for your SEM and application. Maintains original SEM functionality

Microscopy AND Microanalysis MICROSCOPY SOCIETY OF AMERICA 2012

Figure 1 Photograph of a strain gage on a helical wire

1.1. Log on to the TUMI system (you cannot proceed further until this is done).

VISUAL PHYSICS ONLINE DEPTH STUDY: ELECTRON MICROSCOPES

Indian Institute of technology Madras Presents NPTEL NATIONAL PROGRAMME ON TECHNOLOGY ENHANCED LEARNING

ABC Math Student Copy. N. May ABC Math Student Copy. Physics Week 13(Sem. 2) Name. Light Chapter Summary Cont d 2

SCANNING ELECTRON MICROSCOPY AND X-RAY MICROANALYSIS

Measurement of Surface Profile and Layer Cross-section with Wide Field of View and High Precision

Using the Hitachi 3400-N VP-SEM

JEM-F200. Multi-purpose Electron Microscope. Scientific / Metrology Instruments Multi-purpose Electron Microscope

Transcription:

Microscopy101 Choosing the Right Accelerating Voltage for SEM (An Introduction for Beginners) V.M. Dusevich*, J.H. Purk, and J.D. Eick University of Missouri Kansas City, School of Dentistry, 650 E. 25 th St., Kansas City, MO 64108 * dusevichv@umkc.edu Historically, most SEM operators used accelerating voltages that were fairly high, quite often in the range of 15 20 kv. Now progress in electron optics has made low-voltage observations a routine mode of SEM operation. The greatly improved range of utilized accelerating voltages provides the SEM operator with additional flexibility and with additional responsibilities for choosing the right SEM settings for image acquisition. The low-voltage mode of operation is very important in the observation of non-conductive and/or beam sensitive specimens. Because the secondary electron emission coefficient increases as the accelerating voltage decreases, it is possible to find a beam energy where no charging occurs; that is, when the number of electrons (secondary and backscattered) leaving the specimen is equal to the number of incident electrons entering the specimen. This happens for most specimens at accelerating voltages somewhere between 0.4 and 4 kv. Additionally, for beam sensitive specimens, lower electron beam energies (lower kvs) reduce the chance of beam damage. The micrograph of one such specimen is presented in Figure 1a. It is the sticky part of a Post-it Note that has not been sputter-coated. The micrograph was obtained at 300 V accelerating voltage, and the specimen tilt angle was 75º. On this paper substrate (paper fibers are clearly visible) there are hills of glue. The tops of these hills are flattened because they were attached to the adjacent sheet of paper of a Post-it Notes stack. Figure 1b of the Post-it Note after coating with Au-Pd in a sputter coater shows the sensitivity of the glue to coating: hills are no longer flat topped but rounded, indicating that some glue flow did occur during the coating. For this specimen the low-voltage mode (Figure 1a) is the best mode of observation. One of the most obvious consequences of decreased accelerating voltage is reduced interaction volume. The secondary electron signal produced from a smaller sized volume, which is closer to the surface, contains more surface information. Figure 2 represents the images of a brand new steel razor blade wiped with alcohol (that is, prepared for trimming TEM blocks). While at an accelerating voltage of 30 kv the blade looks not too dirty (Figure 2a). At 2 kv it displays a surprising amount of contamination (Figure 2b), which was fully- or semi-transparent in the higher-voltage image. But what if contamination effects are of no interest to the researcher? What voltage should the investigator choose? Not just contamination, but any small details of the surface could be smothered or completely wiped out by a higher accelerating voltage. The micrograph of fractured steel obtained at 2 kv accelerating voltage (Figure 3a) revealed a predominantly cleavage type of fracture, indicating insignificant plasticity during fracture. An important feature of the cleavage fracture is the so-called river pattern, which consists of tiny tear ridges Figure 1. Adhesive on Post-it Notes. (a) uncoated at image at 300 V accelerating voltage, (b) sputter-coated with AuPd and imaged at 5 kv. Bar = 50 µm. that are clearly visible at 2 kv. Raising the accelerating voltage to 15 kv led to the disappearance of many fine details on the fracture surface (Figure 3b) and made the observation of the river pattern much more difficult. However, at 15 kv, dimples formed by the presence of nonmetallic inclusions in the steel (marked with arrows on Figure 3), are emphasized and are more easily identified. Now, if a researcher is looking for dimples, then, perhaps using higher accelerating voltages is not a bad idea at all. Of course, when the goal is the highest possible resolution 48 doi: 10.1017/S1551929509991192 www.microscopy-today.com 2010 January

Put the Knowledge and Experience of an EDS Expert to Work for You...and Change the Way You do Analysis Forever EDAX Introduces the New TEAM Analysis System Smart Features at Your Fingertips: Smart Diagnostics An Environmental Status Panel provides system data, monitors it, and notifies you of operating conditions for your detector, stage, column, and more Smart Acquisition Routine tasks can be automated, allowing you to make the most efficient use of your time Smart Mapping Map your sample immediately and obtain a complete elemental and phase analysis TEAM Up with EDAX for SMART EDS Analysis. Visit our website at www.edax.com/teamsmart or call 1-201-529-4880.

Choosing the Right Accelerating Voltage for SEM colonies on a black background (Figure 5); however, 30 kv is an inferior choice for the observation of individual yeast cells. Similarly to the yeast colonies, bone cells (osteocytes) are highlighted in Figure 6a at the accelerating voltage of 15 kv (original magnification 200 ). The sample was a mouse bone embedded in acrylic resin, polished, and slightly etched. Etching removed a thin layer of bone mineral, leaving behind the resin casts of cells and their dendrites (to be precise, they were not exactly cell casts, but casts of the slightly bigger lacunae). Highlighting the cells with the help of the edge effect is useful for cell identification and location, but taking pictures of individual cells at higher magnifications is better done with a minimized edge effect at lower accelerating voltages, such as 5 kv (Figure 6b, original magnification 5000 ). So, the selection of the accelerating voltage for this type of specimen is magnification-dependant: 15 kv for lower magnifications and 5 kv for higher ones (until hollow magnification begins). Of course, SEM is used not only for the study of specimen topography but also for the study of its composition. This is often done with the help of the backscattered electron (BSE) signal, but in many cases it is possible to combine the topographical and compositional information in a single secondary electron picture. Secondary electrons are produced by both incident electrons when they enter the specimen and by BSE when they Figure 2. Steel razor blade wiped with alcohol and imaged at 15 kv (a) and 2 kv (b). Bar = 2 µm. for specific details, then the task becomes very specimen- and microscope-dependant, and the right accelerating voltage should be chosen on a case-by-case basis. The micrograph of a cell culture obtained at 1 kv accelerating voltage (Figure 4a) looks fine, and only a comparison with the micrograph obtained at 4 kv (Figure 4b) shows the drawbacks of the lower-voltage image. The most striking difference is that the 1 kv image could not make a distinction between the cell surface and the substrate surface, displaying them at the same brightness level. When the voltage was increased to 4 kv, the difference between cells and substrate became clearly visible, cell attachments (fine details on cells edges) became far more noticeable, and the obtained micrograph was overall much better suited for cell culture examinations. A further increase in accelerating voltage (15 kv, Figure 4c) did not yield additional improvements. On the contrary, the edge effect, more pronounced at higher voltages, made some image feature edges extra bright, thus decreasing the overall image quality. Thus, for cell culture studies, this procedure provides a method for finding a suitable accelerating voltage for specimen observation. Special imaging needs of a researcher can be met with specific choices of accelerating voltage. For example, when just the shape of a yeast colony is of interest, then the 30 kv accelerating voltage can give rather interesting pictures of specimens with white Figure 3. Steel fracture imaged at 2 kv (a) and 15 kv (b). Bar = 2 µm. 50 www.microscopy-today.com 2010 January

Choosing the Right Accelerating Voltage for SEM Figure 5. Yeast colonies observed at 30 kv. Bar = 200 µm. Figure 4. Cell culture observed at 1 kv (a), 4 kv (b), and 15 kv (c). Bar = 50 µm. leave the specimen. Therefore, the secondary electron signal under the right conditions can carry information about both topography and composition. The micrograph of a fractured dental composite (used for dental restorations) taken at 2 kv accelerating voltage presents nicely detailed surface features (Figure 7a). The dental composite consists of a resin matrix and filler particles, and these materials 2010 January www.microscopy-today.com Figure 6. Mouse bone, resin embedded, polished, and etched. (a) Imaged at original magnification of 200 and 15 kv. Bar = 100 µm. (b) Imaged at original magnification of 5000 and 5 kv. Bar = 5 µm. have significantly different mean atomic numbers. Raising the voltage to 20 kv increases the number of BSEs contributing to the image signal, especially from the filler particles 51

Choosing the Right Accelerating Voltage for SEM Figure 7. Fracture surface of dental composite observed at 2 kv (a) and 20 kv (b). Bar = 2 µm. that have a higher mean atomic number. At 20 kv the filler particles are highlighted (Figure 7b), but the trade-off is a somewhat less sharp image of the surface because of the larger interaction volume. Again, to choose the value of accelerating voltage, the researcher should decide what is more important: fine surface information or additional compositional information. Of course, it is always possible to acquire two images: one at a lower voltage in secondary electrons and one at a higher voltage in BSE [1 3]. References [1] All micrographs presented in this paper were obtained with Field Emission SEM XL30 (FEI, Hillsboro, OR). [2] The authors greatly acknowledge Drs. S. Honigberg and D. Guo for permission to use their specimens in preparation of this paper. [3] This paper was supported in part by USPHS Grant K23-DE016324. 52 www.microscopy-today.com 2010 January