Introduction

   - Microscopy¶õ? : Microscopes¸¦ »ç¿ëÇÏ¿© ¹°Ã¼ÀÇ morphology¿Í fine structure¸¦ ¿¬±¸Çϴ °Í.

     °íºÐÀÚ ±¸Á¶ÀÇ Å©±â¿Í visibilityµîÀÌ microscopy¸¦ Ȱ¿ëÇÏ¿© È®ÀεȴÙ.

      (ex: ±¸Á¤(spherulites)ÀÇ »çÀÌÁî¿Í ºÐÆ÷µµ ±¤Çбâ¼ú·Î °üÂûµÉ ¼ö ÀÖ´Ù.)

FIg.1 (A) TEM°ú (B) Optical microscopyÀÇ ºñ±³.

 

Lenses in the microscope

     

   - Magnetic lenses :  Glass lenses¿Í À¯»çÇÏ°Ô ±× À§Ä¡¸¦ ¹Ù²Ù±â º¸´Ù power¸¦  º¯È­½ÃÅ´À¸·Î½á Æ÷Ä¿½ÌÀÌ                                    ¸ÂÃçÁö´Â ·»Áî.

 

   - Condenser lens : filament·Î ºÎÅÍ ¹æÃâµÇ´Â ÀԻ籤À» È¿°úÀûÀ¸·Î ¸ðÀ¸´Â ¿ªÇÒÀ» ÇÏ´Â ·»Áî.

 

   - Objective lens : ½ÃÆíÀ» Åë°úÇÏ°í ³­ ÈÄ, »ê¶õµÈ ÀԻ籤À» ¸ðÀ¸´Â ·»Áî.

 

   - Eyepiece lens : ´«¿¡ ½Ç»ó(virtual image)¸¦ Çü¼º½ÃŰ´Â ·»Áî. ±¤ÇÐÇö¹Ì°æÀÇ °æ¿ì                               projector lens°¡ »ç¿ëµÈ´Ù.

 

Optical Microscopy

  

  - Á¤ÀÇ : ºû°ú ¹°Ã¼ ¶Ç´Â ½ÃÆí»çÀÌÀÇ »óÈ£ÀÛ¿ë (interaction)¿¡ ÀÇÇØ »ó(image)ÀÌ ¸¸µé¾îÁö´Â Çö¹Ì°æ.

     

  - Ư¡ : 1) °üÂûµÇ´Â »óÀº 2¹è¿¡¼­ 2000¹èÁ¤µµÀÇ ¹èÀ² ¹üÀ§·Î ½ÃÆíÀÇ ¼¼¹ÐÇÑ Ç¥ÇöÀ» ±¸ÇöÇØ ³¾ ¼ö ÀÖ´Ù.

              2) 0.5ÀÇ resolution ÀÌ °¡´ÉÇÏ¸ç ½ÃÆí¸¶´ÙÀÇ Æ¯¼º°ú objective lens¿Í ºûÀÇ ÆÄÀå¿¡ µû¶ó Á¦ÇѵȴÙ.

              3) ¾ò¾îÁö´Â Á¤º¸´Â º¸Åë °¡½Ã¹°(visible features)ÀÇ ±æÀÌ, ÇüÅ ±×¸®°í »ó´ëÀûÀÎ ¹è¿­(arrangement)µî°ú                   °ü·ÃµÈ °ÍµéÀÌ´Ù. º¹±¼Àý(birefringence)À̳ª ±¼Àý·üÁö¼ö(reflective index)°°Àº »ó¼öÀÇ ÃøÁ¤µµ °¡´ÉÇÏ´Ù.

              4) Çϳª ȤÀº ±× ÀÌ»óÀÇ ±¤¿ø°ú ½ÃÆí¿¡ ±¤¼±À» ¸ÂÃß´Â ¿©·¯ °¡Áö ·»Áî·Î ±¸¼ºµÇ¾î ÀÖÀ¸¸ç »óµéÀº »çÁøÀ̳ª                  video tapeµîÀ¸·Î ±â·ÏµÇ´Â °ÍÀÌ º¸ÅëÀÌ´Ù.

 

  - Á¾·ù : simple microscopes, stereo microscopes

 

  - ±¼Àý·üÁö¼öÀÇ ÃøÁ¤ : ±¼Àý·ü Áö¼ö(n)Àº ±¤ÇÐÇö¹Ì°æÀ¸·Î ½±°Ô ÃøÁ¤ÀÌ µÇ¸ç ¾Ë·ÁÁöÁö ¾ÊÀº ¹°ÁúÀ» È®ÀÎÇϴµ¥ À¯¿ë.

 ±¼Àý·ü Áö¼ö°¡ ¾Ë·ÁÁø liquidÀ§¿¡ ÀÔÀÚµéÀ» ¿Ã¸° µÚ, transmissionÀ¸·Î °üÂûÇÑ´Ù.

 transparent ¶Ç´Â translucent ÀÔÀÚ°¡ ¸Å¿ì ³·Àº contrast¸¦ °¡Áú ¶§ liquid´Â  n(liquid)=n(particle)°¡ µÉ ¶§±îÁö ¹Ù²î°Ô µÈ´Ù. ±× º¯È­°¡ n°ªÀ» Áõ°¡½ÃŰ´ÂÁö °¨¼Ò ½ÃŰ´ÂÁö¸¦ °áÁ¤Çϱâ À§Çؼ­ sample¿¡ ºñ½ºµëÇÏ°Ô Á¶¸íÀ» ½ÃŲ´Ù. À̶§ÀÔÀÚ´Â lenses·Î ÀÛ¿ëÇϰí,  n(liquid)<n(particle)ÀÏ ¶§´Â ¼ö·Å·»Áî(converging lenses)·Î ÀÛ¿ëÇÑ´Ù. °áÁ¤ÀÇ ÇÑ ¸é¿¡ ºûÀÌ Á¶»çµÇ¸é Ãà¿¡ µû¶ó ÀüȯµÇ¸ç ±× ¸éÀº ¹à°Ô µÉ °ÍÀÌ´Ù. ÀÌ ¸í¾ÏÀº n(liquid)>n(particle) ÀÏ ¶§ ¹Ý´ë°¡ µÈ´Ù. ¼±ÅÃÀûÀ¸·ÎÀÔÀÚÀÇ sharp boundariesÀÇ axial illuminationÀº edgeºÎ±Ù¿¡ Á¼Àº ºûÀÇ  ¶ì, Áï Becke lineÀ» ºÎ¿©½ÃŲ´Ù. ºûÀº n°ªÀÌ ´õ Å« ¸é¿¡¼­ »ê¶õµÇ¸ç Æ÷Ä¿½º°¡ ÀÔÀÚÀ§¿¡ ÀÖÀ»  ¶§ ±× ¸é¿¡ lineÀÌ ³ªÅ¸³ª¸ç, ÀÔÀÚ ¾Æ·¡ÀÏ ¶§´Â ´Ù¸¥ ¸é¿¡ ³ªÅ¸³­´Ù. Phase contrast´Â n°ªÀÇ Â÷ÀÌ¿¡ ÀÇÇØ contrast¸¦ Áõ°¡½ÃŰ¸ç º¸´Ù Á¤È®ÇÑ °á°ú¸¦ ¾ò°Ô ÇØÁØ´Ù. Transmission¿¡¼­ÀÇ interference contrast´Â optical path length¿Í ½ÃÆí µÎ²²¸¦ ÅëÇÑ Æò±Õ ±¼Àý·ü Áö¼ö°ªÀ» ¾ò°Ô ÇØÁØ´Ù. ƯÈ÷ Becke line ¹æ¹ýÀ» ÅëÇØ¼­´Â Ç¥¸é ±¼Àý·üÁö¼ö°ªÀ» ¾òÀ» ¼ö  ÀÖ´Ù.

 

Scanning electron microscopy (SEM)

 

Fig.2 SEMÀÇ µµ½Äµµ

   - Á¤ÀÇ : scanning microscopyÀÇ ±âº»ÀûÀΠƯ¡Àº probe°¡ ½ÃÆíÀ» Áö³ª°¡¸ç¸ç scanningÀ» ÇÔÀ¸·Î½á  Á¡´ëÁ¡(ponit by point)À¸·Î »óÀÌ Çü¼ºµÈ´Ù´Â °ÍÀÌ´Ù. À̶§ probe´Â ÀüÀÚºö (electron beam)ÀÌ°í °üÃøµÇ´Â signalÀº TV Å¸ÀÔÀÇ »óÀ¸·Î ³ªÅ¸³ª°Ô µÈ´Ù. Display tube³»ÀÇ ÀüÀÚºöÀº ½ÃÆíÀÇ probe¿Í µ¿½Ã¿¡ ¿òÁ÷ÀδÙ.

 

   - Ư¡ : 1) ¹èÀ²Àº (linear size of the image / size of the region scanned on the specimen)À¸·Î °áÁ¤µÊ. µû¶ó¼­                   ¹èÀ²Àº focus°°Àº »óÀÇ Á¶°Ç¿¡ ¿µÇâ¾øÀÌ ¹Ù²Ü ¼ö ÀÖ´Ù.

               2) ±¤ÇÐÇö¹Ì°æº¸´Ù ´õ ³ôÀº resolutionÀ» °¡Áö¸ç chamber³»ÀÇ ½ÃÆíµµ Å©°í ¼ö mm¿¡¼­ ¼ö inch±îÁö Á÷°æµµ                   °¡´ÉÇÏ´Ù.

               3) sample Áغñ°¡ ÀϹÝÀûÀ¸·Î ¸Å¿ì °£´ÜÇÏ´Ù.

            4) ÀϹÝÀûÀÎ polymerµé°ú °°Àº ºñÀüµµ¼º ¹°ÁúµéÀº ³·Àº °¡¼ÓÀü¾ÐÀ» »ç¿ëÇϰųª Àüµµ ÄÚÆÃÀ» ¿ä±¸ÇÑ´Ù.

             5) »óÀÇ ÇüÅ´ interaction°ú detector, signal processingµî¿¡ ÀÇÁ¸ÇÑ´Ù.

               6) Spatial resolutionÀº signalÀÌ À¯µµµÇ´Â ½ÃÆí ¿µ¿ªÀÇ Å©±â·Î °áÁ¤µÈ´Ù. À̰ÍÀº interaction volume°ú

                  °ü·Ã µÇ¾î ÀÖÀ¸¸ç À̰ÍÀº ½ÃÆí°ú ºöÀÌ ¼­·Î »óÈ£ÀÛ¿ëÇÏ´Â ¿µ¿ªÀ» ÀǹÌÇÑ´Ù.

                  (ex: radiation sensitivity¸¦ »ç¿ëÇÏ¿© PMMA¿¡ 20 keV ÀüÀÚÀÇ interaction volumeÀ» Çü¼º½ÃŰ´Â °æ¿ì¸¦                        »ý°¢ÇØ º¸ÀÚ. ¹°Áú¿¡ ÀüÀÚºöÀ» ³ëÃâ½ÃŲ ÈÄ ¼¼Ã´°ú etchingÀ» ½ÃŰ¸é ¹è(pear)¸ð¾çÀÇ 10m ±íÀÌ·Î                        »ý±ä holeÀÌ ºö°ú »óÈ£ÀÛ¿ëÇÏ´Â PMMA ¿µ¿ªÀ» º¸¿©ÁØ´Ù. ÀüÀÚºö°úÀÇ »óÈ£ÀÛ¿ëÀ» °è»êÇÏ¸é ³ôÀº                        °¡¼ÓÀü¾Ð°ú ½ÃÆíÀÇ ³·Àº ¿øÀÚ¹øÈ£¿¡ ´ëÇØ interaction volumeÀÌ Áõ°¡ÇÏ´Â °ÍÀ» º¸¿©ÁØ´Ù.)

                7) ½ÃÆíÀ¸·ÎºÎÅÍÀÇ Áß¿äÇÑ signal¿¡´Â backscattered electrons°ú 2Â÷ÀüÀÚ¿Í x-rayµîÀÌ ÀÖ´Ù.                    backscattered electronsÀº sample³»ÀÇ ÇÙ¿¡ ÀÇÇØ elasticÇÏ°Ô »ê¶õµÇ¸ç Ç¥¸éÀ¸·ÎºÎÅÍ ¹ß»ýÇÑ´Ù.                   2Â÷ÀüÀÚ´Â ³·Àº ¿¡³ÊÁö, Áï 50eVÀÌÇÏ¿¡¼­ ½ÃÆíÀ¸·ÎºÎÅÍ ¹æÃâµÈ´Ù. ¸¸¾à ºöÀÌ tilted surface ¶Ç´Â edge¿¡                   Àû¿ëµÈ´Ù¸é º¸´Ù ¸¹Àº 2Â÷ÀüÀÚ°¡ ½ÃÆí¿¡¼­ ¹æÃâµÈ´Ù. ¸¸¾à ºöÀÌ Ç¥¸éÀÇ ±¼°îÁø ºÎºÐÀ̳ª holeºÎºÐ¿¡                   Á¶»çµÇ¸é Ç¥¸é ±ÙóÀÇ interaction volumeÀÌ Àû¾îÁ®¼­ ¹ß»ýµÇ´Â 2Â÷ÀüÀÚ ¼öµµ Àû°Ô µÈ´Ù. 1Â÷ºö¿¡ ÀÇÇØ                   ¸¸µé¾îÁö´Â 2Â÷ÀüÀÚ´Â high resolution topographic images¸¦ Á¦°øÇÑ´Ù. ÀÌ 2Â÷ÀüÀÚ¿¡ ÀÇÇÑ imaging                   (SEI: secondary electron imaging)Àº signal formation°ú collectionÀÇ È¿À²¼º ¶§¹®¿¡ SEM¿¡ Æø³Ð°Ô                   ÀÌ¿ëµÈ´Ù.

               8) PMMA¿Í °°Àº polymerµéÀº ¸Å¿ì beam sensitiveÇϸç rastered area·Î ºÎÅÍÀÇ 'picture frame                      constrast'Àº Áú·® ¼Õ½Ç¿¡ ÀÇÇØ ÈçÇÏ°Ô ³ªÅ¸³­´Ù. ¹Ý°áÁ¤¼º °íºÐÀÚµéÀº ÀüÀÚºöÀÇ ³ëÃâ¿¡ ÀÇÇØ ±×                      °áÁ¤¼ºÀ» ÀÒ°í ½ÃÆíÀÇ morphology¸¦ º¯È­½Ãų ¼ö ÀÖ´Ù. ³·Àº °¡¼ÓÀü¾ÐÀº charging effects¿Í beam                      penetration°ú beam damage¸¦ °¨¼Ò ½ÃŲ´Ù.

Fig. 3 (A) °íü ½ÃÆí°ú ÀÔ»çµÈ ÀüÀÚºöÀÇ »óÈ£ÀÛ¿ë (B) Carbon³»ÀÇ electron path¸¦ °è»êÇÏ¿© (A)ÀÇ Á¤È®ÇÑ °æ°è¿Í À±°ûÀ» È®ÀÎ ÇÒ ¼ö ÀÖ´Ù.

 

    - Optimization ¹æ¹ý : stable specimens¿¡ ´ëÇÑ SEM operationÀÇ ÃÖÀûÈ­¿¡ °í·ÁÇØ¾ß µÉ Áß¿äÇÑ ¸î°¡Áö´Â noise¿Í                                   depth of field¿Í resolutionÀÌ´Ù. ÀÌ·± º¯¼öµéÀº beam voltage, beam current, final aperture                                   size¿Í working distanceµî¿¡ ÀÇÇØ ´Þ¶óÁö¸ç, ÃÖ´ë resolutionÀÇ Á¶°ÇÀº

         1) high accelerating voltage       

       2) ªÀº working distance¿Í ÀÛÀº final aperture·Î ¾ò¾îÁö´Â small probe

       3) ³·Àº noise¿¡ ÃÖÀûÀÎ high beam current

       4) probe size°¡ ÀÛ°í ³·Àº Àü·ùÀÏ ¶§´Â ±ä ³ëÃâ½Ã°£ÀÌ ÇÊ¿ä.

       ¶ÇÇÑ ÃÖ´ëÀÇ depth of field(=focus³»¿¡ ÀÖ´Â ½ÃÆíÀÇ µÎ²² ȤÀº ±íÀÌ)¸¦ À§ÇÑ Á¶°ÇÀº

         1) long working distance

       2) small final aperture size

       3) large probe size

       µîÀÌ´Ù.

    - Operation : SEM¿¡¼­´Â µÎ²¨¿î ±Ý¼ÓÄÚÆÃ°ú ¸Å¿ì ³·Àº °¡¼ÓÀü¾ÐÀÌ polymer¿¡ µµ´ÞÇÏ´ÂÀüÀÚÀÇ ´ëºÎºÐÀ»                         ¸·À» ¼ö ÀÖ´Ù. µÎ²¨¿î ÄÚÆÃ°ú ³·Àº beam voltage´Â SEM imageÀÇ resolutionÀ» ³·Ãß°Ô µÈ´Ù. ¸¸ÀÏ                         5~10kVÀÇ ÀüÀÚ°¡ »ç¿ëµÇ°í À̵éÀÌ polymer¸¦ °üÅëÇÑ´Ù¸é shapeÀÇ fine scale change°¡ ÀϾ°Ô                         µÈ´Ù. SEM¿¡¼­ damage¸¦ ÃÖ¼ÒÈ­Çϰí imagingÀ» Çâ»ó½Ãų ¼ö ÀÖ´Â Á¶°ÇÀº

 

                                           1) ³·Àº °¡¼ÓÀü¾Ð

                                    2) ³·Àº beam current

                                    3) large probe size

                                    4) ³ÐÀº ¿µ¿ª¿¡ ´ëÇÑ ³·Àº ¹èÀ²

                                    5) ªÀº ³ëÃ⠽ð£

                                    6) ³ëÃâ»çÀÌÀÇ beam blanking

                                   

Transmission electron microscopy (TEM)

 

      - Á¤ÀÇ : ½ÃÆíÀÌ ÀüÀÚºö¿¡ ÀÇÇØ illuminateµÇ´Â light microscope¿Í À¯»çÇÑ ÀüÀÚ ±¤ÇÐ Àåºñ.

 

      - Ư¡ :  1) Air scatters electrons ¶§¹®¿¡ Á¶ÀÛÀ» ÇØ¾ß ÇÑ´Ù.   

                   2) ÀüÀÚÀÇ ÂªÀº ÆÄÀå ¶§¹®¿¡ high resolutionÀÌ °¡´É.

                   3) Image contrast´Â ÀüÀÚ »ê¶õ (electron scattering)¿¡ ±âÀÎÇÑ´Ù. ½ÃÆí³»ÀÇ ÀüÀÚºöÀÇ Èí¼ö´Â ÈçÄ¡                      ¾ÈÁö¸¸ ±¤°¢¿¡¼­ÀÇ ÀüÀÚ»ê¶õÀº bright field¿¡¼­ »ó¿¡ ¿µÇâÀ» ¹ÌÄ¡Áö ¾ÊÀ¸¸ç Èí¼öµÇ´Â °ÍÀ¸·Î °üÂûµÈ´Ù.                      ±ÔÄ¢ÀûÀÎ ¶Ç´Â °áÁ¤¼ºÀÎ ¹°Áú¿¡¼­ ÀÌ ÀüÀÚ »ê¶õÀº diffraction constrast¸¦ ºÎ¿©ÇÏ¸ç °áÁ¤ ¹èÇâ¿¡ °­ÇÏ°Ô                      ¿µÇâÀ» ¹ÌÄ£´Ù. amorphous materialÀÇ mass thickness contrast result¿¡¼­, image brightness´Â                      local mass thickness (thickness X density)¿¡ ÀÇÁ¸ÇÑ´Ù.

                   4) Contrast´Â ³·Àº °¡¼ÓÀü¾Ð°ú ÀÛÀº objective aperture diameters¿¡¼­ ´õ Å©´Ù. ¸¸ÀÏ »ê¶õµÈ ÀüÀÚ°¡                      »ó¿¡ ¿µÇâÀ» ¹ÌÄ¡Áö ¾Ê´Â´Ù¸é phase contrast¿¡ ±âÀÎÇÑ ¿µÇâÀ» ¹ÌÄ¡°Ô µÉ °ÍÀÌ´Ù.

                   5) polymer´Â ´ëü·Î ³·Àº ¿øÀÚ¹øÈ£¸¦ °¡Áö°í »ê¶õµÇ´Â ÀüÀÚ°¡ ¾àÇØ¼­ TEM¿¡¼­ÀÇ contrast´Â ÁÁÁö                       ¸øÇÏ´Ù.  À̵é(polymer)Àº ³ôÀº beam sensitivity¸¦ °¡Áö¸ç radiation damage´Â °áÁ¤ÀÇ ±ÔÄ¢¼ºÀÇ                       ÆÄ±«¸¦ ¾ß±â½ÃŲ´Ù. °¡¼ÓÀü¾ÐÀ» ³ôÀÌ°í ½ÃÆíÀ» cooling½Ã۸é contrast¸¦ ³ôÀÌ´Â ¹æ¹ýÀÌ µÇ¼­ »óȲÀ»                       ÁÁ°Ô ¸¸µé ¼ö ÀÖ´Ù.

       - Opearation 

                   1) low dos methods : TEM¿¡¼­ noiseÀÇ ¹ß»ýÀº ÁÖµÈ ¹®Á¦°¡ µÇ¸ç µû¶ó¼­ image¸¦ Çü¼º½Ã۱â À§ÇØ ¸ðµç                      °¡´ÉÇÑ ÀüÀÚ¸¦ »ç¿ëÇÏ´Â °ÍÀÌ Áß¿äÇÏ´Ù. ÀÌ·¸°Ô Çϱâ À§ÇØ low dos method¸¦ »ç¿ëÇÑ´Ù. À̹ۿ¡                      »ó±âÇØ¾ßµÉ ¸î°¡Áö¸¦ µç´Ù¸é

                         * »óÀÌ ±â·ÏµÉ ¶§¸¦ Á¦¿ÜÇÏ°ï »óÀÌ µÇ´Â ¿µ¿ª¿¡ beamÀ» °íÁ¤Ç϶ó.

                         * specimen dose¿Í ±â·Ï¸ÅüÀÇ sensitivity¿Í ¹èÀ²À» match½ÃÄѶó.

                    2) ÀÌ·ÐÀûÀÎ ÇѰ踦 ³Ñ¾î¼­ ÃÖÀûÀÇ imaging conditionÀ» ¾ò±â À§Çؼ­´Â ´ÙÀ½ ³×°¡Áö ¿ä¼Ò¸¦ ½ÉµµÀÖ°Ô                        ³íÀÇ ÇÒ Çʿ䰡 ÀÖ´Ù.

                         * noise ratio¿¡ ´ëÇØ ¿ä±¸µÇ´Â signal

                         * ½ÃÆíÀÌ ÃëÇÒ ¼ö ÀÖ´Â ÃÖ´ë Á¶»ç·®

                         * image contrast

                         * »óÀ» Çü¼º½ÃŰ´Â ÀÔ»çÀüÀÚÀÇ ºÐÀ²

                     3) Image processingÀº original image¿¡ À־ noiseºñ¿¡ ´ëÇÑ signalÀ» °¨¼Ò ½Ãų ¼ö ÀÖ´Ù.

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