脱氢
催化作用
丙烷
硼
煅烧
选择性
化学
活动站点
无机化学
魔角纺纱
氮化硼
丙烯
拉曼光谱
光化学
有机化学
核磁共振波谱
物理
光学
作者
Huan Yan,Selim Alayoǧlu,Weiqiang Wu,Yongbo Zhang,Eric Weitz,Peter C. Stair,Justin M. Notestein
标识
DOI:10.1021/acscatal.1c02168
摘要
Oxidative dehydrogenation of propane (ODHP) to propylene could have a significant impact on the production of this critical chemical intermediate, if appropriate catalysts can be discovered. Recently, heterogeneous catalysts based on boron (oxides and nitrides) have been demonstrated to be promising for ODHP, but their active sites have not been conclusively identified. Here, we report that the deposition of differently sized boronic acids into the micropores of silica supports results in different distributions of surface borate species after calcination. These materials, in turn, display a wide range of rates in ODHP but similar selectivity, suggesting that they differ only in the numbers of active sites. Features identified by in situ Raman, IR, and magic-angle-spinning 11B solid-state NMR spectroscopies are compared to catalyst activity. This correlation identifies the S2 borate species, a hydroxylated nonring boron, as the likely active site and provides a target for directed syntheses of future catalysts.
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