摘要
Fundamental understanding regarding oxygen storage capacity involving how and why an active site can buffer a large number of oxygen atoms in redox processes is vital to the design of advanced oxygen storage materials, while it is challenging because of the complexity of heterogeneous catalysis. Herein, we identified that an eight-atom iridium-aluminum oxide cluster IrAlO6 + can transfer all the oxygen atoms to catalytically oxidize six CO molecules. This finding represents a breakthrough in cluster catalysis where at most three oxygen atoms from a heteronuclear metal oxide cluster can be catalytically involved in CO oxidation. We found that oxygen prefers to be stored on aluminum to form an O3 -• radical in the energetically unfavorable IrAlO6 + isomer and generate the low-coordinated iridium that is pivotal to capturing CO and triggering the catalysis. The powerful electron cycling capability of iridium and the cooperative iridium-aluminum interplay are emphasized to drive the oxygen atom-transfer behavior.
| 源语言 | 英语 |
|---|---|
| 页(从-至) | 7850-7855 |
| 页数 | 6 |
| 期刊 | Journal of Physical Chemistry Letters |
| 卷 | 10 |
| 期 | 24 |
| DOI | |
| 出版状态 | 已出版 - 19 12月 2019 |
| 已对外发布 | 是 |
指纹
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