Choose the Right Instrument for Your Battery Analysis
How To Guide
Published: August 10, 2023
Lithium-ion batteries have revolutionized the way we power our lives. These advanced rechargeable batteries have become integral to countless applications, from portable electronics to electric vehicles and renewable energy storage.
In the dynamic landscape of lithium-ion battery manufacturing, a suite of cutting-edge tools has emerged to facilitate both production and rigorous testing. Choosing the tool that suits your needs best is then vital to advance battery analysis research.
This guide highlights robust and comprehensive testing solutions to unlock the potential of lithium-ion batteries and accelerate battery development.
Download this guide to explore the best instruments for:
- Material testing, thermal analysis and internal structure evaluation
- Organic and inorganic component analysis
- Microanalysis and particle characterization
Guide to Lithium-ion
Battery Solutions
C10G-E092
Guide to Lithium-ion
Battery Solutions
C10G-E092
2 3
Test /
Evaluation
Items
Test /
Evaluation Items
(Detail)
Instrument Application Example
Material
Testing
Compression Test Micro Compression Tester
MCT
Compression test of positive electrode active materials P6
Compression test of solid electrolyte raw materials P7
Tensile Test
Puncture Test
DIC Analysis
AUTOGRAPH Precision
Universal Tester
AG
Tensile test of the separator P8
Tensile strength measurement of the separator P9
Puncture strength measurement of the separator P10
Evaluating the strain characteristics of separators after
puncture damage P11
Thermal
Analysis
Evaluation of
Meltability
Differential Scanning
Calorimeter
DSC
Evaluation of decomposition characteristics and thermal
stability of each component P12
Determination of the melting temperature and
calorimetry of separators P13
Moisture
Measurement
Thermogravimetric Analyzer
TGA
Measurement of moisture content in the electrode active
material P14
Heat Shrinkage
Measurement
Thermomechanical Analyzer
TMA Measurement of the shrinkage of the separator P15
Organic /
Inorganic
Component
Analysis
Component Analysis
Internal Gas
Component Analysis
Estimated Amount
of Internal Gas
Generated
Deterioration
Evaluation
Fourier Transform Infrared
Spectrophotometer FTIR
Comparison of spectra under argon and atmospheric
atmospheres P16
Component analysis of electrolytes and solvents used in
electrolyte solution P17
Ion Chromatograph IC Deterioration evaluation of electrolyte solution P18
Gas Chromatograph/
Single Quadrupole GC-MS
GC/GCMS
Analysis of the solvents used in electrolyte solution and
component analysis of additives P19
Simultaneous analysis of internal gas P20
Confirmation of changes in gas composition due to
deterioration P21
Test /
Evaluation
Items
Test /
Evaluation Items
(Detail)
Instrument Application Example
Internal
Structure
Evaluation
Internal Structure
Observation
Non-Destructive
Inspection
In-situ Observation
(charge / discharge,
stress)
Microfocus X-Ray CT System
SMX
Non-destructive observation of the current collector
and of the lower part of the battery P22
Internal observation of cells that have been charged
and discharged 100 to 1500 times P23
Non-destructive observation of the internal structure
of an exploded Lithium-ion Battery P24
Non-destructive observation of an internal structure before
and after a charge / discharge test P25
Microanalysis
Observation and
Elemental Mapping
Analysis and Chemical
Bonding State Analysis
of Minute Parts
Electron Probe Microanalyzer
EPMA
Observation and elemental analysis of minute parts of
the positive electrode cross section P26
Evaluate the chemical bonding state of the active
material of the positive electrode P27
Observation of Surface
Shape and Evaluation
of Physical Properties
of Minute Parts
In-situ Observation (in
Liquid / Heating)
Scanning Probe Microscope/
Atomic Force Microscope
SPM/AFM
Observation of the surface shape and measurement of
the potential distribution of minute parts of the positive
electrode P28
Surface shape observation and force curve measurement
of the binder in electrolyte solution P30
Particle
Characterization
Particle Size
Measurement
Laser Diffraction Particle Size
Analyzer SALD Particle size measurement of electrode materials P32
Particle Size
Measurement and
Image Analysis
Dynamic Particle Image
Analysis System DIA
Particle size measurement and image analysis of active
materials P33
Table of Contents
(Test / Evaluation Item) Click here for Table of Contents (Unit)
4
5
Material Instrument Application Example Positive Electrode Active Material / Conductive Additive / Binder
Micro Compression Tester
MCT Compression test of active materials P6
Differential Scanning Calorimeter
DSC
Evaluation of the decomposition characteristics and
thermal stability of each component P12
Thermogravimetric Analyzer
TGA Measurement of moisture content in the active material P14
Electron Probe Microanalyzer
EPMA
Observation and elemental mapping analysis and
chemical bonding state analysis of minute parts P26
Scanning Probe Microscope / Atomic Force Microscope
SPM/AFM
Observation of the surface shape and measurement of the
potential distribution of minute parts P28
Surface shape observation and force curve
measurement of the binder in electrolyte solution P30
Laser Diffraction Particle Size Analyzer
SALD Particle size measurement of electrode materials P32
Dynamic Particle Image Analysis System
DIA
Particle size measurement and image analysis of
electrode materials P33
Negative Electrode
Active Material / Conductive Additive / Binder
Micro Compression Tester
MCT Compression test of active materials P6
Differential Scanning Calorimeter
DSC
Evaluation of decomposition characteristics and
thermal stability of each component P12
Thermogravimetric Analyzer
TGA Measurement of moisture content in the active material P14
Electron Probe Microanalyzer
EPMA
Observation and elemental mapping analysis and
chemical bonding state analysis of minute parts P26
Scanning Probe Microscope / Atomic Force Microscope
SPM/AFM
Observation of the surface shape and measurement
of the potential distribution of minute parts P28
Surface shape observation and force curve
measurement of the binder in electrolyte solution P30
Laser Diffraction Particle Size Analyzer
SALD Particle size measurement of Electrode Materials P32
Dynamic Particle Image Analysis System
DIA
Particle size measurement and image analysis of
electrode materials P33
Material Instrument Application Example Separator
AUTOGRAPH Precision Universal Tester
AG
Tensile test of the separator P8
Tensile strength measurement of the separator P9
Puncture strength measurement of the separator P10
Evaluating the strain characteristics of separators
after puncture damage P11
Differential Scanning Calorimeter
DSC
Determination of the melting temperature and
calorimetry of separators P13
Thermomechanical Analyzer
TMA Measurement of the shrinkage of the separator P15
Electrolyte Solution
Solvent / Electrolyte / Additive
Fourier Transform Infrared Spectrophotometer
FTIR
Comparison of spectra under argon and atmospheric
atmospheres P16
Component analysis of electrolytes and solvents used
in electrolyte solution P17
Ion Chromatograph
IC Deterioration evaluation of electrolyte solution P18
Gas Chromatograph/
Single Quadrupole GC-MS
GC/GCMS
Analysis of the solvents used in electrolyte solution and
component analysis of additives P19
Solid Electrolyte
Micro Compression Tester
MCT Compression test of solid electrolyte raw materials P7
Electron Probe Microanalyzer
EPMA
Observation and elemental mapping analysis and
chemical bonding state analysis of minute parts P26
Scanning Probe Microscope / Atomic Force Microscope
SPM/AFM
Observation of the surface shape and measurement
of the potential distribution of minute parts P28
Laser Diffraction Particle Size Analyzer
SALD Particle size measurement of electrode materials P32
Battery cell
Module / Internal Gas
Microfocus X-Ray CT System
SMX
Non-destructive observation of the current collector
and of the lower part of the battery P22
Internal observation of cells that have been charged
and discharged 100 to 1500 times P23
Non-destructive observation of the internal structure of
an exploded Lithium-ion Battery P24
Non-destructive observation of the internal structure
before and after a charge / discharge test P25
Gas Chromatograph/
Single Quadrupole GC-MS
GC/GCMS
Simultaneous analysis of internal gas P20
Confirmation of changes in gas composition due
to deterioration P21
Table of Contents (Unit)
Click here for Table of Contents (Test / Evaluation Item)
6 7
index index
Compression test of various materials that construct a Lithium-ion Battery
Test force-displacement graph
• Consideration of conditions for battery packaging and
restraint pressure
• Examination of manufacturing process conditions (change in
strength during heating)
Micro Compression Tester
MCT Series
Inner structural materials of a Lithium-ion Battery are subjected to external force during production processes and to
pressure during use. Therefore, evaluating the strength of each structural material is important to maintain consistent
quality. Below are the results of compression tests performed on Lithium-ion Battery materials using the Micro
Compression Testing Machine.
Compression Test Results
Sample
Name
Fracture strength
[mN]
Particle size
[µm]
Strength
[MPa]
LiMn2O4 1.67 13.0 7.79
LiCoO2 16.23 13.3 72.75
The force is on the vertical axis, the displacement is on the horizontal axis, and fracture occurs at the inflection point
where the displacement becomes horizontal. The fracture strength of the lithium cobalt oxide LiCoO2 particle was
measured to be 72.75 MPa compared to 7.79 MPa for the lithium manganese oxide, LiMn2O4.
Compression test of positive electrode active
materials
Two types of positive electrode active
materials
Before After
Compression Test Results
Sample
Name
Fracture strength
[mN]
Particle size
[µm]
Strength
[MPa]
A 1.25 1.765 315
B 0.63 4.265 27
By measuring the fracture strength, we can compare the correlation with the ease of molding as an electrolyte.
Comparing particles A and B shows that the fracture strength of particle B is about 1/10 weaker. This indicates that the
particles adhere well to each other during the molding process.
Compression test of solid electrolyte raw
materials
Two types of solid electrolyte raw materials
Purpose Samples
Data
Result
Purpose Samples
Data
Result
Test force-displacement graph
Displacement (μm)
Force (mN)
Displacement (μm)
Force (mN)
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Material Testing
8 9
index index
The separator is installed so that it is in contact with the positive and negative electrodes. Since the temperature rises
during charging, it is necessary to maintain mechanical strength even as the temperature changes. The following shows
an example of measuring how the strength of a separator in the tensile test and the piercing test changes with respect to
temperature changes, and an example of evaluating the strain characteristics after piercing damage.
Tensile Test Results
Specimen Lithium Battery Separator
Specimen Name A B C
Elastic Modulus
(MPa) 902 1856 1376
Tensile Strength
(MPa) 165 118 101
Break Point Strain
(%) 27.6 31.7 29.1
From the measurement results, it can be seen that the separator with high tensile strength is A.
Tensile test of separator Three types of separators
Separator (1) is produced by near uniaxial stretching in the machine direction (MD), and separator (2) is
produced by biaxial stretching at a low stretching ratio. Despite the increase in elongation properties
at 60°C, excellent mechanical strength is maintained.
Tensile strength measurement of a separator
(Condition : 25 °C, 60 °C, and 90 °C)
Two types of separators, prepared in
dumbbell shapes along both the length and
width direction
Purpose Samples
Data
Result
Samples
Purpose
Data
Result
Specimen Lithium Battery Separator
Specimen Name A B C
Thickness
(µm) 20 20 10
Stress-strain graph
Mechanical properties of separator (1) and (2) in the short side and long side directions
Long side: Machine Direction
Short side: Transverse Direction
25 °C 60 °C 90 °C
Sample Tensile strength
(MPa)
Rupture strain
(%)
Tensile strength
(MPa)
Rupture strain
(%)
Tensile strength
(MPa)
Rupture strain
(%)
(1)Short side 36.9 471.4 35.4 898.8 19.3 1044.0
(1)Long side 175.6 26.8 162.5 57.0 129.9 76.7
(2)Short side 78.2 138.5 68.8 347.6 33.8 427.9
(2)Long side 129.5 34.1 118.3 105.3 58.7 367.2
Strength measurement and strain characteristic evaluation of a separator at high temperature
• Various mechanical strength measurements of Lithium-ion Battery
materials
• Evaluation of the piercing strength of a separator packed with high density
• Visualization of strain distribution by DIC analysis
AUTOGRAPH Precision Universal Tester
AGX-V
Stress-strain graph
Separator (1) Separator (2)
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Material Testing
10 11
index index
Strain distribution under tensile load
We evaluated the strain characteristics of a separator after puncture to investigate how a damaged separator may act
under stress.
DIC analysis is a method of comparing random patterns on the surface of an object before and after the object is
deformed to determine the amount of pattern movement and measure strain. Using the DIC analysis method, we can
visually see that the area around the damaged area in the center turns red where stress is concentrated and strain is the
largest.
Evaluating the strain characteristics of
separators after puncture damage
Separator after puncture test
Test Force-Displacement Curve
Comparing the results at 25 °C and 60 °C, we can see that the maximum test force is the same, but the maximum
displacement value is higher at 60 °C. Next, comparing the characteristic values at 60 °C and 90 °C, we can see that the
maximum test force decreases at 90 °C, but the maximum displacement is the same. From the above, it can be seen that
the lithium-ion battery separator used in this test has an increase in elongation characteristics but no decrease in strength
at 60 °C.
Puncture strength measurement of a separator
(Under environment of 25 °C, 60 °C, 90 °C)
Separator
Maximum Test Force /
Displacement for Each Temperature
Test Temperature
(°C)
Maximum Test Force
(N)
Maximum
Displacement (mm)
25 3.85 4.45
60 4.07 6.63
90 2.13 6.68
Purpose Samples
Data
Result
Purpose Samples
Data
Result
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Material Testing
Puncture
location
Mark
12 13
index index
DSC Measurement of Electrode Active Materials
DSC Measurement of Separators
In some cases, lithium-ion batteries may generate abnormal heat due to overcharging, which may lead to problems
such as ignition, in the worst case. To ensure the safety of the battery, it is important to evaluate the decomposition
characteristics and thermal stability of each component by DSC during heating.
The upper curve shows the active material after charging. The active material becomes unstable due to charging, and
a large exothermic peak due to decomposition is observed from around 200 °C. The exothermic peak around 290 °C is
thought to be from the electrolyte.
Evaluation of decomposition characteristics
and thermal stability of each component
Charged/Uncharged electrode active
material and electrolyte solution
The endothermic peaks were observed at around 100 °C to 140 °C, which is expected to be the melting point of
polyethylene. When the separator is exposed to high temperature, it shrinks near the melting temperature, which affects
the insulation. For safety reasons, it is necessary to know the temperature at which the separator contracts, and the
measurement of the melting temperature by DSC is an indicator of the contraction temperature.
Determining the melting temperature and
calorimetry of separators
Three types of separators
Purpose Samples
Data
Result
Purpose Samples
Data
Result
Evaluate the decomposition characteristics and thermal stability of battery materials during heating
• Examination of Lithium-ion Battery safety
• Selection of compound for electrode material and selection of
compounding conditions
• Evaluation of physical properties of polymer materials by crystallinity
Differential Scanning Calorimeter
DSC-60 Plus
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Thermal Analysis
14 15
index index
Moisture evaluation during heating of electrode active material Evaluation of shrinkage amount when the separator is heated
TGA Measurement of Electrode Active Materials TMA Measurement of Separators
It is important to control the moisture content in lithium-ion batteries because it affects their lifetime. The moisture
content of a material can be measured using a thermogravimetric analyzer (TGA).
In general, the higher the shrinkage temperature and the smaller the amount of shrinkage, the safer it is. Thermomechanical analysis (TMA) was used to measure mainly the shrinkage of the separator.
A weight loss rate at 200 °C was determined, and the moisture content was 0.033% and 0.214%, respectively. According to the data, the start of shrinkage begins approximately between 80 °C and 100°C. In terms of the amount of
shrinkage, the amount of shrinkage is larger in the MD direction than in the TD direction for both No. 1 and 2 .
Measurement of moisture content in the
active material
Positive/Negative electrode active material Measure the shrinkage of the separator The two directions of the separator
called the MD (machine direction) and TD
(transverse direction)
Purpose Samples Purpose Samples
Data Data
Result Result
• A small amount of water content can be detected
• Evaluation of connectivity by measuring the dehydration process
temperature
• Measurement is possible in the atmosphere of air or nitrogen
• It is possible to measure the amount of shrinkage and shrinkage stress at each
temperature
• Continuous recording of a sample's dimensional changes as temperature
changes or over time in the order of µm
• Tensile measurement, expansion measurement, and needle insertion
measurement are possible with one unit
Thermogravimetric Analyzers
TGA-50 series
Thermomechanical Analyzer
TMA-60
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Thermal Analysis
16 17
index index
Infrared Spectra of EC+DEC (3 : 7) Electrolyte Solution Containing 1M LiPF6
Infrared Spectra of EC+DEC (3 : 7) Electrolyte Solution Containing
1M LiPF6 (red) and EC+DEC (3 : 7) Solution (black)
Difference Spectrum between EC+DEC (3 : 7) Electrolyte Solution
Containing 1M LiPF6 and EC+DEC (3 : 7) Solution
It is desirable to handle and characterize the cell components under an atmosphere not affected by water vapor or
oxygen. The IRSpirit, a compact FTIR, can be installed in a glove box, thus enabling the evaluation of cell components in a
high-purity argon atmosphere with low dew point and low oxygen concentration.
Although the optical properties of argon and air are very different, the left image shows that the infrared spectra
acquired under both atmospheres were almost identical, appearing to be unaffected by the difference in atmosphere.
Note that in the right image, the broad absorption of symmetric and antisymmetric OH-stretching vibrations from water
molecules were observed between 3400 and 3700 cm-1 in the air atmosphere. Meanwhile, the influence was negligible in
the infrared spectrum in the argon atmosphere.
Comparison of spectra under argon and air
atmospheres
EC+DEC (3 : 7) Electrolyte Solution
Containing 1M LiPF6
1M LiPF6 : Lithium Hexafluorophosphate
EC : Ethylene Carbonate
DEC : Diethyl Carbonate
Purpose Samples
Data
Result
The red and black arrows on the left are characteristic absorptions of each component. To clarify the difference between
the two spectra, the red line minus the black line is shown on the right.
In the frequency range of 700 ~ 1000 cm -1, characteristic vibrational modes in which EC or DEC and lithium ions are
solvated are observed. Therefore, it can be assumed that the four absorption lines shown in the right figure are
characteristic absorption lines in which EC or DEC and lithium ions are solvated.
The data shown above was provided by Associate Professor Takashi Ito at Frontier Research Institute for Interdisciplinary
Sciences, Tohoku University. We would like to take this opportunity to express our sincere gratitude. Please also see the
article in FTIR TALK LETTER Vol. 35.
Spectrum comparison in the presence and
absence of LiPF6
EC + DEC (3: 7) Electrolyte Solution
(Containing 1M LiPF6)
EC + DEC (3: 7) Electrolyte Solution
(Not containing 1M LiPF6)
1M LiPF6 : Lithium Hexafluorophosphate
EC : Ethylene Carbonate
DEC : Diethyl Carbonate
Samples
Purpose
Data
Result
*Since IRSpirit can be controlled wirelessly, a sample can be measured while the
FTIR unit is installed in a glove box (custom order required).
Evaluation of electrolyte solution in an inert atmosphere
• Raw material confirmation, foreign matter screening analysis
• Small design allows it to be used in glove boxes and draft
chambers
Fourier Transform Infrared Spectrophotometer
IRSpirit™
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Organic / Inorganic Component Analysis
18 19
index index
Comparison of components between new and deteriorated electrolyte solutions
Lithium hexafluorophosphate is commonly used as the electrolyte solution. It is hydrolyzed by the trace amount of water
contained in the electrolyte solution. Fluoride ions generated by this decomposition affect battery performance, so
analysis of decomposition is important in the quality control process.
The electrolyte solution in a Lithium-ion Battery is composed of organic solvent (mainly carbonate-based), electrolyte and
additives. It is important to evaluate the electrolyte solution and the deterioration state of the electrolyte solution due to
charging and discharging. GCMS is useful for the analysis of those constituents.
A peak was not detected in the new electrolyte solution (New), but only in the deteriorated electrolyte solution (Degraded
Product).
Dimethyl carbonate, ethyl methyl carbonate, and ethylene carbonate, which are used as solvents, were identified from
library search results. Vinylene carbonate, which was used as an additive, was also identified.
Evaluation of Lithium Hexafluorophosphate
Decomposition in Electrolyte Solution
Solvents used in electrolyte solution and
component analysis of additives
Electrolyte Solution
(New, deteriorated: accelerated deterioration test)
Electrolyte Solution
Purpose Samples Purpose Samples
Result Result
Chromatogram of Electrolyte Solution (New) Chromatogram of Electrolyte Solution (Degraded Product)
Data Data
• Evaluation of products generated by decomposition of
electrolyte
• Shorten analysis time by utilizing a column switching system
• Evaluation of reaction products generated by deterioration
• Qualitative analysis of unknown components that cannot be
identified only by retention time information
Ion Chromatograph
HIC-ESP
Single Quadrupole GC-MS
GCMS-QP™2020 NX
Qualitative analysis of solvents and trace additives used in electrolyte solutions
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Organic / Inorganic Component Analysis
20 21
index index
Component analysis of internally generated gas and deterioration evaluation due to charging and discharging
It is necessary to analyze the internally generated gas when conducting a deterioration evaluation of a Lithium-ion
Battery. We will introduce an example of simultaneous analysis of internal gas using a system equipped with the unique
BID detector. It eliminates the need for carrier gas switching and the combined use of multiple devices, which was
required in the past, and enables easier and faster measurement.
The GC-BID enables simultaneous analysis of inorganic gas components (H2, O2, N2, CO, CO2) and lower hydrocarbon
components (CH4, C2H4, C2H6, C3H6, C3H8) in the battery.
Simultaneous analysis of internal gas Internal gas
Purpose Samples
Result
Simultaneous analysis of internal gas
Data
Changes in the composition of internal gas due to deterioration
As the capacity retention rate decreases, the ratio of hydrogen decreases and the ratio of hydrocarbon increases.
Confirmation of changes in gas composition
due to deterioration
Internal gas obtained from four batteries
with different capacity retention rates
Purpose Samples
Data
Result
• BID (Barrier-discharge Ionization Detector) is more sensitive than
TCD, and can deal with objects that cannot be detected by FID
• Detect inorganic gases and hydrocarbons simultaneously
• Qualitative analysis when combined with GCMS
Gas Chromatograph
Nexis™ GC-2030
Component Concentration
Ratio (%)
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Organic / Inorganic Component Analysis
22 23
index index
Non-destructive observation of internal structures and deterioration evaluation after charging and discharging
The X-ray CT device can observe the internal structure non-destructively. Therefore, it is used for analysis of defective
products, comparison of non-defective products / defective products, comparison before and after charging / discharging,
and observation of internal structures in cycle tests. In many cases, it is used for finished battery products. It is also used
for observing the three-dimensional structure of minute parts such as electrodes.
The green frame is the positive electrode current collector, the red frame is the negative electrode current collector, and
the blue frame is the X-ray CT image of the lower part of the battery. You can see in detail how the negative electrode is
bent.
Non-destructive observation of the current
collector and of the lower part of the battery
Large Lithium-ion Battery for a vehicle.
W114mm×D48mm×H184mm
Purpose Samples
Result
The X-ray CT image of a large Lithium-ion Battery for a vehicle
Data
Cross-sectional image of a Lithium-ion Battery in a charge-discharge cycle test (100 ~ 1500 times)
This data shows results from repeatedly charging and discharging the Lithium-ion Battery and scanning at 100 times, 500
times, 1000 times, and 1500 times. Because X-ray CT can observe the inside non-destructively, it is not necessary to prepare
a lot of samples for a cycle test. Therefore, it is possible to track the state changes over time for the same sample.
Internal observation of cells that have been
charged and discharged 100 to 1500 times
Small-capacity Lithium-ion Battery that has
been charged / discharged
Purpose Samples
Data
Result
• Non-destructive internal observation is possible
• Data can be confirmed immediately after shooting by high-speed
calculation
• Confirmation of detailed parts with a high-resolution detector
Microfocus X-Ray CT System
inspeXio™ SMX™-225CT series
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Internal Structure Evaluation
24 25
index index
セル内部構造の非破壊観察および充放電後の劣化評価
The cross-sectional image of an 18650 type Lithium-ion Battery before and after a charge / discharge test is shown. As
shown in the red circles, you can see a deformation near the center of the battery due to expansion and contraction of
the inside caused by charging and discharging.
Even if the battery has no problem in appearance, it’s possible to observe any internal deformations using X-ray CT.
Non-destructive observation of an internal
structure before and after a charge /
discharge test
An 18650 type Lithium-ion Battery
You can see that the inside is greatly deformed by the explosion. With X-ray CT, it is possible to observe the condition
without destroying it, so it is possible to exactly confirm what kind of deformation has occurred from a load test.
Non-destructive observation of the internal
structure of an exploded Lithium-ion Battery
An 18650 type Lithium-ion Battery that was
overcharged, heated, and exploded
Purpose Samples
Data
Result
Purpose Samples
Result
Cross-sectional image
inspeXio™ SMX™-225CT FPD HR Plus
with attached charge / discharge system
Cross-sectional image of 18650 type Lithium-ion Battery before and after a charge / discharge test
3D image (movie)
Data
Charge / discharge instrument
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Internal Structure Evaluation
26 27
index index
Observation of minute parts of the positive electrode, elemental analysis and chemical bond state analysis
A positive electrode has a structure in which a mixture of the active material, binder, and conductive additive are coated
on a collector made of aluminum foil. Evaluation of the distribution of these components is important to improve cell
performance and quality control, and when conducting failure analysis.
Above data is the result of a mapping analysis of the positive electrode cross section. Not only coarse particles with sizes of several
μm, but also fine particles with sizes of less than 1 μm, the condition of boundaries and the element distribution can be observed.
Observation and elemental analysis of minute
parts of a positive electrode's cross section
Positive electrode active material
Purpose Samples
Result
Element mapping analysis of the cross section of a positive electrode
Data
State analysis of the positive electrode surface Spectrum of Mn on Positive Electrode Surface and
Enlarged View of Peak Tops
The difference shown in the spectrum is due to a peak shift between the initial state and the charged state. EPMA can
detect changes in the state of chemical bonds aimed at small parts.
Evaluate the chemical bonding state of the
active material of a positive electrode
Comparison of initial state and charged state
Purpose Samples
Data
Result
Samples were provided by the National Institute of Advanced Industrial Science and Technology
Samples were provided by the National Institute of Advanced Industrial Science and Technology
• Both high sensitivity and high spatial resolution are
achieved due to excellent electron probe characteristics
• Chemical bond state analysis of minute parts is possible
• Wide area mapping by stage scan
Electron Probe Microanalyzer
EPMA™-8050G
Initilal State Charged State
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Microanalysis
28 29
index index
Observation of the shape of minute areas of battery material and measurement of conductive distribution
Positive and negative electrodes contain active materials, conductive aids, and binders. In order to improve the
conductivity between the active materials, a conductive aid is added, and each is bound and held by a binder.
Evaluating how these elements are distributed in the positive electrode and how conductive paths are formed helps
improve the performance of Lithium-ion Batteries. We observed the surface shape and current distribution by measuring
the minute amount of current flowing through the conductive cantilever while applying a voltage to the positive
electrode.
We observed the surface shape and current distribution by measuring a minute amount of current flowing through the
conductive cantilever while applying a voltage to the positive electrode. From the topography image, it is not possible
to determine where conductive aids, active materials, and binders are. However, in the current image, you can see the
three areas of red, yellow-green, and blue in order of conductivity. It can be estimated that the red areas are conductive
additives, the yellow-green areas are active materials, and the blue areas are binders.
This data compares EPMA and SPM data within the same area. EPMA evaluates the distribution of elements whereas SPM
evaluates the distribution of shape and conductivity.
By analyzing the state of materials from multiple instruments, it is possible to evaluate the uneven distribution and
isolated state of a battery's material components, which can help with quality improvement and product development.
Evaluation of element distribution and
conductivity distribution in the same field of
view
Positive electrode sheet of the NCM
(lithium nickel manganese cobalt oxide)
Result
Samples
Purpose
Data
Result
Observation of surface shape and
measurement of potential distribution of
minute parts of a positive electrode
Positive electrode sheet of the NCM
(lithium nickel manganese cobalt oxide)
Purpose Samples
Data
Applied Voltage : -2.7V
Topography Image Current Image
(Low Contrast)
Current Image
(High Contrast)
• Observation near the interface and grasp of physical properties
• Confirmation of the conductivity of minute parts
• Observation of minute parts and evaluation of physical
properties are possible the air atmosphere
Scanning Probe Microscope
SPM-Nanoa™
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Microanalysis
30 31
index index
各種部材の微小領域の形状観察および導電性分布測定
The deflection of the cantilever was measured when the probe was pushed into the sample by about 15 nm, and a
force curve was obtained. Point B on the force curve indicates the start of the depression, and point A indicates a 15 nm
depression from point B. The amount of binder deformation can be obtained from the difference between the amount
of indentation and the amount of deflection from point B to point A. From the data obtained, the amount of binder
deformation indicates that (2) is the least rigid and (3) is the most rigid.
It was confirmed that the flat binders (2) and (3) were uniformly gelled in the electrolyte.
SPM enables observation of an electrolyte in a real-world environment!
Result
Result
Data
Data
Surface shape observation in electrolyte
solution
Force curve measurement in electrolyte
solution
Binder for negative electrode Binder for negative electrode
Samples Samples
Purpose Purpose
Sample Provision:Komaba Lab of Tokyo University of Science
Protuberant
Flat
Flat
(1)
(3)
(2)
Sample Provision:Komaba Lab of Tokyo University of Science
(1) (2) (3)
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Microanalysis
32 33
index index
Carbon black particle size and dispersion / aggregation evaluation
The grain size and grain size distribution of carbon black have a great influence on an electrode's characteristics and the
quality and yield of the final product. For proper evaluation, it is important to know the dispersion / aggregation state
of the target sample. SALD-2300 realizes highly sensitive measurement of scattered light, and can perform highly reliable
measurement even with weak scattered light from primary particles after dispersion processing.
It can be seen that by the homogenizer dispersion treatment, aggregates of about 10 μm are dispersed in the fine
particles in the submicron region.
Particle size distribution measurement of
particles with different dispersed states
Carbon black particle
Purpose Samples
Result
Measurement of dispersed solvent
Data
Particle size distribution measurement and shape confirmation of active material particles
DIA can detect trace amounts of coarse particles. By detecting coarse particles in the positive electrode material powder, it
is possible to prevent deterioration of Lithium-ion Battery performance and improve safety.
Coarse particles in powder used for a positive electrode can lead to performance issues and degradation of the material.
These particles can be detected and distinguished either through the image analysis window or a plot based on specific
parameters. This allows the quality of the powdered raw material to be easily verified.
Detection of coarse particles contained in
positive electrode material
Positive electrode material powder
Purpose Samples
Result
Data
• Black samples that easily absorb light can be detected
• Analysis while maintaining the state of slurry
• Monitoring of aggregation and dispersion status
• Abnormal particles (foreign matter, agglomeration) are
detected
• Acquire images of individual particles and check the shape
• Detect trends and abnormal values by statistical analysis
Laser Diffraction Particle Size Analyzer
SALD-2300
Dynamic Particle Image Analysis System
iSpect™ DIA-10
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Particle Characterization
Guide to Lithium-ion Battery Solutions
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