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Originally posted by xhtangxh at 2010-09-05 20:37:01:
ÒªÖªµÀ£¬XRD¶ÔÑùÆ·ÊÇÓÐÒ»¶¨ÒªÇóµÄ£¬³ýÁ˲âÊÔ¶ÔÏóÐëÊǽᾧÏàÍ⣬¾§Á£´óСҲÊӽᾧÎïÓÐÒ»×îµÍãÐÖµ£¬·ñÔòÊÇÎÞ·¨²úÉúÑÜÉäÏÖÏóµÄ¡£XRD²âÊÔ½á¹û¶Ô½á¾§µ¥ÔªÅÅÁеÄÓÐÐò¶ÈÃô¸Ð£¬¶øXPSÔò¶ÔÔªËØ»¯ºÏ̬¼°Æä·á¶ÈÃô¸Ð¡£µçλÐòÔÚ ...

ÎҵĴ߻¯¼ÁÊÇÔÚ¿ÕÆø·ÕΧÏÂìÑÉյ쬰´ÎÄÏ×½²£¬Ó¦¸Ã500¡æÊÇÏȱä³ÉPdO£¬Ëæ×ÅζȵÄÉý¸ß800¡æ½ø¶ø·Ö½â±ä³ÉPd
4Â¥2010-09-05 20:51:17
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americanyk

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Excellent

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It is fully right. XRD is uesd to characterize the crystall Pd(In the lattice), while XPS can onyl analysis the surface, normally around 1-10 nm. On the surface after high temperature calcination without reduction, it must be composed of Pd and PdO. Here the PdO dominate the surface. If you donot trust waht I have said, I am sure you will get the same answers as I said when you ask the operator of XPS and XRD:
5Â¥2010-09-05 23:29:37
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