Abstract
The effective capture and storage of radiological iodine (129I) remains a strong concern for safe nuclear waste storage and safe nuclear energy. Silver-containing mordenite (MOR) is a longstanding benchmark for iodine capture; however, the molecular level understanding of this process needed to develop more effective iodine getters has remained elusive. Here we probe the structure and distribution of iodine sorbed by silver-containing MOR using differential pair distribution function analysis. While iodine is distributed between α-AgI nanoparticles on the zeolite surface and subnanometer α-AgI clusters within the pores for reduced silver MOR, in the case of unreduced silver-exchanged MOR, iodine is exclusively confined to the pores as subnanometer α-AgI. Consequently, unreduced silver-containing zeolites may offer a more secure route for radioactive iodine capture, with the potential to more effectively trap the iodine for long-term storage.
| Original language | English |
|---|---|
| Pages (from-to) | 8897-8899 |
| Number of pages | 3 |
| Journal | Journal of the American Chemical Society |
| Volume | 132 |
| Issue number | 26 |
| DOIs | |
| State | Published - Jul 7 2010 |
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