Abstract
The average reactivity of a catalytic surface was appreciably enhanced through spatio-temporally variable operation. Computer steering of a focused laser beam allowed the realization of controlled temperature profiles and their interaction with intrinsic system (reaction/transport) time and space scales. Real-time monitoring of the product concentration then enabled the exploration/implementation of strategies towards optimizing the overall reaction rate. The ability to dictate reaction conditions in space and time, whether in open or in closed loop [1-3] [Science 292 (2001) 1357; Nature 361 (1993) 240; Science 294 (2001) 134], opens new directions for reaction control (e.g., of activity and selectivity in more complex reaction networks) through the combination of chemistry and systems theory.
| Original language | English (US) |
|---|---|
| Pages (from-to) | 407-412 |
| Number of pages | 6 |
| Journal | Chemical Physics Letters |
| Volume | 358 |
| Issue number | 5-6 |
| DOIs | |
| State | Published - Jun 7 2002 |
All Science Journal Classification (ASJC) codes
- General Physics and Astronomy
- Physical and Theoretical Chemistry
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