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Selective Cleavage of α-Olefins to Produce Acetylene and Hydrogen.

Meijia XuZheng-Yang HuXiaoyang LiangYifan ZhuHonghe DingJun HuJinfeng XuZhen ZhuZi-Ang WuXinwei ZhaoWeijun GuoKaiqi NieYifan YeJun-Fa ZhuZhi-Pan LiuXiong ZhouKai Wu
Published in: Journal of the American Chemical Society (2024)
Acetylene production from mixed α-olefins emerges as a potentially green and energy-efficient approach with significant scientific value in the selective cleavage of C-C bonds. On the Pd(100) surface, it is experimentally revealed that C 2 to C 4 α-olefins undergo selective thermal cleavage to form surface acetylene and hydrogen. The high selectivity toward acetylene is attributed to the 4-fold hollow sites which are adept at severing the terminal double bonds in α-olefins to produce acetylene. A challenge arises, however, because acetylene tends to stay at the Pd(100) surface. By using the surface alloying methodology with alien Au, the surface Pd d-band center has been successfully shifted away from the Fermi level to release surface-generated acetylene from α-olefins as a gaseous product. Our study actually provides a technological strategy to economically produce acetylene and hydrogen from α-olefins.
Keyphrases
  • single cell
  • mass spectrometry
  • high resolution
  • metal organic framework