Abstract
Conventional thermal propane dehydrogenation (pDH) faces several notable drawbacks, including high energy requirements, coking-induced catalyst deactivation, and the need for product separation. An electrocatalytic approach, using self-assembled ionic liquid (il)–tin dioxide (SnO2) hollow spheres as the electrocatalyst, enables efficient pDH at ambient temperature. in this process, bromopropane formed in the anolyte from propane reacts with hydroxyl anions from the cathode to yield propene. The propene selectivity exceeds 98%, and the continuous production of high-purity (>99%) propene gas from the anolyte eliminates the need for downstream separation. The il-SnO2 catalyst maintains its activity and selectivity for more than 6000 hours, with a small voltage increase rate of 3.16 microvolts per hour. Mechanistic studies suggest that the il layer enhances propane adsorption and facilitates the carbon-hydrogen bond activation step on adjacent Sn sites. After reaction, the il layer promotes propene desorption and suppresses deep dehydrogenation. Copyright © 2026 the authors, some rights reserved;
| Original language | English |
|---|---|
| Pages (from-to) | 87-92 |
| Number of pages | 6 |
| Journal | Science |
| Volume | 392 |
| Issue number | 6793 |
| Online published | 2 Apr 2026 |
| DOIs | |
| Publication status | Published - 2 Apr 2026 |
Funding
The authors thank the 4W9B station in the Beijing Synchrotron Radiation Facility (BSRF) and the BL10B station in the National Synchrotron Radiation Laboratory (NSRL) for the help with characterizations. The authors also thank G.-W. Lai for the separation of the molecules and the NMR test. Funding: This work was supported by the National Key R&D Program of China (2023YFA1506801); the National Natural Science Foundation of China (22325101 and 223B2902); the Beijing Natural Science Foundation (Z240027); the Global STEM Professorship from the Innovation, Technology and Industry Bureau (ITIB) and Education Bureau (EDB) of Hong Kong.
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