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Detailed explanation of the seven parameters of the optical microscope

Nov 23, 2022

Detailed explanation of the seven parameters of the optical microscope


In microscopic inspection, people always hope to have a clear and bright ideal image, which requires the optical technical parameters of the microscope to meet certain standards, and requires that when using it, it must be coordinated according to the purpose of microscopic inspection and the actual situation The relationship between the parameters. Only in this way can we give full play to the proper performance of the microscope and obtain satisfactory microscopic inspection results.


The optical technical parameters of the microscope include: numerical aperture, resolution, magnification, depth of focus, width of field of view, poor coverage, working distance, etc. These parameters are not always as high as possible, and they are mutually restrictive. When using them, the relationship between the parameters should be coordinated according to the purpose of the microscope inspection and the actual situation, but the resolution should prevail.


1. Numerical aperture

The numerical aperture is abbreviated as NA, and the numerical aperture is the main technical parameter of the objective lens and the condenser lens, and is an important symbol to judge the performance of the two (especially for the objective lens). The size of its numerical value is respectively marked on the casing of the objective lens and condenser lens.

Numerical aperture (NA) is the product of the refractive index (n) of the medium between the front lens of the objective lens and the object to be inspected and the sine of the half of the aperture angle (u). The formula is as follows: NA=nsinu/2

Aperture angle, also known as "mirror mouth angle", is the angle formed by the object point on the optical axis of the objective lens and the effective diameter of the front lens of the objective lens. The larger the aperture angle, the larger the light flux entering the objective lens, which is proportional to the effective diameter of the objective lens and inversely proportional to the distance of the focal point.

When observing with a microscope, if you want to increase the NA value, the aperture angle cannot be increased. The only way is to increase the refractive index n value of the medium. Based on this principle, water immersion objective lenses and oil immersion objective lenses are produced. Because the refractive index n value of the medium is greater than 1, the NA value can be greater than 1.

The maximum value of the numerical aperture is 1.4, which has reached the limit both theoretically and technically. At present, bromonaphthalene with a high refractive index is used as a medium. The refractive index of bromonaphthalene is 1.66, so the NA value can be greater than 1.4.

It must be pointed out here that in order to give full play to the role of the numerical aperture of the objective lens, the NA value of the condenser lens should be equal to or slightly greater than the NA value of the objective lens during observation.

Numerical aperture is closely related to other technical parameters, and it almost determines and influences other technical parameters. It is proportional to the resolution, proportional to the magnification, and inversely proportional to the depth of focus. As the NA value increases, the width of the field of view and the working distance will decrease accordingly.


2. Resolution

The resolution of the microscope refers to the minimum distance between two object points that can be clearly distinguished by the microscope, also known as "discrimination rate". Its calculation formula is σ=λ/NA

In the formula, σ is the minimum resolution distance; λ is the wavelength of light; NA is the numerical aperture of the objective lens. The resolution of the visible objective lens is determined by two factors: the NA value of the objective lens and the wavelength of the illumination source. The larger the NA value, the shorter the wavelength of the illumination light, and the smaller the σ value, the higher the resolution.

To improve the resolution, that is, reduce the σ value, the following measures can be taken

(1) Reduce the wavelength λ value and use a short-wavelength light source.

(2) Increase the medium n value to increase the NA value (NA=nsinu/2).

(3) Increase the aperture angle u value to increase the NA value.

(4) Increase the contrast between light and dark.


3. Magnification and effective magnification

Due to the double magnification of the objective lens and the eyepiece, the total magnification Γ of the microscope should be the product of the objective lens magnification β and the eyepiece magnification Γ1:

Γ=βΓ1

Obviously, compared with the magnifying glass, the microscope can have a much higher magnification, and the magnification of the microscope can be easily changed by exchanging objective lenses and eyepieces with different magnifications.

The magnification is also an important parameter of the microscope, but one cannot blindly believe that the higher the magnification, the better. The limit of microscope magnification is the effective magnification.

Resolution and magnification are two different but mutually related concepts. Relational formula: 500NA<Γ<1000NA

When the numerical aperture of the selected objective lens is not large enough, that is, the resolution is not high enough, the microscope cannot distinguish the fine structure of the object. At this time, even if the magnification is excessively increased, the obtained image can only be an image with a large outline but unclear details. , called the invalid magnification. Conversely, if the resolution meets the requirements but the magnification is insufficient, the microscope has the ability to resolve, but the image is still too small to be clearly seen by human eyes. Therefore, in order to give full play to the resolving power of the microscope, the numerical aperture should be reasonably matched with the total magnification of the microscope.


4. Depth of focus

Depth of focus is the abbreviation of depth of focus, that is, when using a microscope, when the focus is on a certain object, not only all points on the plane of this point can be seen clearly, but also within a certain thickness above and below the plane, To be clear, the thickness of this clear part is the depth of focus. If the depth of focus is large, you can see the entire layer of the object under inspection, while if the depth of focus is small, you can only see a thin layer of the object under inspection. The depth of focus has the following relationship with other technical parameters:

(1) The depth of focus is inversely proportional to the total magnification and the numerical aperture of the objective lens.

(2) The larger the depth of focus, the lower the resolution.

Due to the large depth of field of the low magnification objective lens, it is difficult to take pictures with the low magnification objective lens. This will be described in more detail in photomicrographs.


5. Field of view diameter (FieldOfView)

When observing a microscope, the bright circular area seen is called the field of view, and its size is determined by the field diaphragm in the eyepiece.

The diameter of the field of view is also called the width of the field of view, which refers to the actual range of the inspected object that can be accommodated in the circular field of view seen under the microscope. The larger the diameter of the field of view, the easier it is to observe.

There is a formula F=FN/β

In the formula, F: field diameter, FN: field number (FieldNumber, abbreviated as FN, marked on the outside of the eyepiece barrel), β: objective lens magnification.

It can be seen from the formula:

(1) The diameter of the field of view is proportional to the number of fields of view.

(2) Increasing the multiple of the objective lens reduces the diameter of the field of view. Therefore, if you can see the whole picture of the inspected object under the low power lens, and change to a high power objective lens, you can only see a small part of the inspected object.


6. Poor coverage

The optical system of the microscope also includes the cover glass. Due to the non-standard thickness of the cover glass, the optical path of the light after entering the air from the cover glass is changed, resulting in a phase difference, which is poor coverage. The generation of poor coverage affects the sound quality of the microscope.

According to international regulations, the standard thickness of the cover glass is 0.17mm, and the allowable range is 0.16-0.18mm. The phase difference of this thickness range has been taken into account in the manufacture of the objective lens. The 0.17 marked on the objective lens housing indicates the thickness of the cover glass required by the objective lens.


7. Working distance WD

The working distance is also called the object distance, which refers to the distance from the surface of the front lens of the objective lens to the object to be inspected. During microscope inspection, the object to be inspected should be between one and two times the focal length of the objective lens. Therefore, it and the focal length are two concepts. What is usually called focusing is actually adjusting the working distance.

When the numerical aperture of the objective lens is constant, the aperture angle is larger when the working distance is shorter.

A high-power objective lens with a large numerical aperture has a small working distance.


1.digital microscope

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