| Home > Documents in process > SSZ‐13 Zeolite with Isolated Co<sup>2+</sup> Sites as an Efficient and Durable Catalyst System for Non‐Oxidative Ethane Dehydrogenation |
| Journal Article | PUBDB-2026-00193 |
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2026
Wiley-VCH
Weinheim
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Please use a persistent id in citations: doi:10.1002/anie.202519600
Abstract: Non-oxidative dehydrogenation of ethane (EDH) is an attractive method for on-purpose ethene production, but achieving high activity and, especially, durability with catalysts based on earth-abundant metals remains challenging. Herein, we introduce the Co/SSZ-13 system with exclusively divalent cobalt (Co<sup>2+</sup>) ions that meets the above requirements. The use of complementary characterization techniques enabled us to reveal two Co<sup>2+</sup> species: Co<sup>2+</sup>─Z2 located in the six-membered-ring windows and [Co(OH)]<sup>+</sup>─Z in the eight-membered-ring windows, with Z representing a charged zeolite framework site. A quantitative correlation between the rate of ethene formation and the site population establishes Co<sup>2+</sup>─Z2 as the active species. In situ X-ray absorption spectroscopy confirms their structural and electronic stability under high-temperature reaction conditions. The optimized 0.9Co/SSZ-13 (0.9Co) catalyst showed highly durable operation over 200 dehydrogenation/oxidative regeneration cycles at 600–650°C lasting for 150 h with industrially relevant productivity. In this regard, it outperforms almost all previously developed catalysts even those with platinum as an active component. The obtained results uncover the atomic-level origins of EDH activity/durability of the Co/SSZ-13 system and highlight the critical role of metal site location in designing highly active, selective, and durable catalysts for on-purpose ethene production.
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