Sammanfattning
The synthesis of high-value fuels and plastics starting from small hydrocarbon molecules plays a central role in the current transition towards renewable energy. However, the detailed mechanisms driving the growth of hydrocarbon chains remain to a large extent unknown. Here we investigated the formation of hydrocarbon chains resulting from acetylene polymerization on a Ni(111) model catalyst surface. Exploiting X-ray photoelectron spectroscopy up to near-ambient pressures, the intermediate species and reaction products have been identified. Complementary in situ scanning tunneling microscopy observations shed light onto the C−C coupling mechanism. While the step edges of the metal catalyst are commonly assumed to be the active sites for the C−C coupling, we showed that the polymerization occurs instead on the flat terraces of the metallic surface.
Originalspråk | engelska |
---|---|
Artikelnummer | e202213295 |
Tidskrift | Angewandte Chemie - International Edition |
Volym | 62 |
Nummer | 1 |
Tidigt onlinedatum | 2022 |
DOI | |
Status | Published - 2023 jan. 2 |
Bibliografisk information
Publisher Copyright:© 2022 The Authors. Angewandte Chemie International Edition published by Wiley-VCH GmbH.
Ämnesklassifikation (UKÄ)
- Fysikalisk kemi