催化作用
铂金
异构化
选择性
金属
纳米
吸附
分子
氢
化学
Atom(片上系统)
材料科学
光化学
无机化学
化学物理
化学工程
物理化学
有机化学
工程类
嵌入式系统
复合材料
计算机科学
作者
Tian‐Nan Ye,Zewen Xiao,Jiang Li,Yutong Gong,Hitoshi Abe,Y. Niwa,Masato Sasase,Masaaki Kitano,Hideo Hosono
标识
DOI:10.1038/s41467-019-14216-9
摘要
Abstract Single-atom catalysts (SACs) have attracted significant attention because they exhibit unique catalytic performance due to their ideal structure. However, maintaining atomically dispersed metal under high temperature, while achieving high catalytic activity remains a formidable challenge. In this work, we stabilize single platinum atoms within sub-nanometer surface cavities in well-defined 12CaO·7Al 2 O 3 (C12A7) crystals through theoretical prediction and experimental process. This approach utilizes the interaction of isolated metal anions with the positively charged surface cavities of C12A7, which allows for severe reduction conditions up to 600 °C. The resulting catalyst is stable and highly active toward the selective hydrogenation of nitroarenes with a much higher turnover frequency (up to 25772 h −1 ) than well-studied Pt-based catalysts. The high activity and selectivity result from the formation of stable trapped single Pt atoms, which leads to heterolytic cleavage of hydrogen molecules in a reaction that involves the nitro group being selectively adsorbed on C12A7 surface.
科研通智能强力驱动
Strongly Powered by AbleSci AI