...
首页> 外文期刊>Journal of Catalysis >In situ high-pressure high-temperature scanning tunneling microscopy of a Co(0001) Fischer–Tropsch model catalyst
【24h】

In situ high-pressure high-temperature scanning tunneling microscopy of a Co(0001) Fischer–Tropsch model catalyst

机译:Co(0001)Fischer-Tropsch模型催化剂的原位高压高温扫描隧道显微镜

获取原文
获取原文并翻译 | 示例
           

摘要

The Fischer–Tropsch synthesis of hydrocarbons from carbon monoxide and hydrogen over cobalt catalysts is expected to become the key method for the future production of liquid fuels. Despite decades of research on the reaction mechanism, the state of the surface of the operating catalyst is still uncertain. Using in situ high-temperature high-pressure scanning tunneling microscopy, we have investigated the Fischer–Tropsch reaction over a Co(0001) single crystal model catalyst in the methanation limit. Atomically resolved images show that the surface does not transform into an oxide or carbide, but remains metallic under reaction conditions. The data are consistent with a mobile layer of reversibly adsorbed particles on the surface. The surface morphology under reaction conditions is unchanged from the surface in ultra-high vacuum. Widespread assumptions about a surface restructuring that seemed to explain the activity of cobalt-based Fischer–Tropsch catalysts are not confirmed.
机译:通过钴催化剂由一氧化碳和氢进行费-托合成烃的方法有望成为未来生产液体燃料的关键方法。尽管对反应机理进行了数十年的研究,但操作催化剂表面的状态仍不确定。使用原位高温高压扫描隧道显微镜,我们研究了在甲烷化极限条件下在Co(0001)单晶模型催化剂上的Fischer-Tropsch反应。原子分辨图像显示该表面不会转变为氧化物或碳化物,但在反应条件下仍保持金属性。数据与表面上可逆吸附颗粒的移动层一致。在超高真空下,反应条件下的表面形态与表面没有变化。关于表面重整的普遍假设似乎可以解释钴基费-托催化剂的活性,但尚未得到证实。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号