脱氢
催化作用
丙烷
金属间化合物
合金
Atom(片上系统)
材料科学
漫反射红外傅里叶变换
纳米结构
X射线光电子能谱
原位
化学工程
化学
光化学
纳米技术
冶金
有机化学
光催化
工程类
嵌入式系统
计算机科学
作者
Yanan Xing,Leilei Kang,Jingyuan Ma,Qike Jiang,Yang Su,Shengxin Zhang,Xiaoyan Xu,Lin Li,Aiqin Wang,Zhi‐Pan Liu,Sicong Ma,Xiao Yan Liu,Tao Zhang
标识
DOI:10.1016/s1872-2067(23)64402-x
摘要
The PtSn/Al2O3 is a prototypical industrial catalyst for propane dehydrogenation (PDH). However, the local structures of the active sites are still inconclusive under the operation conditions. Herein, the evolutions of the Pt-Sn active centers supported on nano-Al2O3 are definitely discerned at the atomic level during PDH reaction. By combining complementary in situ characterizations and theoretical calculations, we demonstrate that a highly productive Sn1Pt single-atom alloy (47.6 molC3H6 gPt–1 h–1) forms after the reduction, and thereby self-assembles to the Pt3Sn intermetallic compound during the reaction, which exhibits a rather stable performance (kd-10~40h: 0.0026 h–1). Intriguingly, the results of in situ diffuse reflectance infrared Fourier-transform spectroscopy further corroborate that the adjacent Pt atoms with terrace sites aggravating the coke deposition can be circumvented through this single-atom alloy mediated reconstruction. Our findings depict an unprecedented evolution process of the active sites of the PtSn/Al2O3, and afford an effectual nanostructure engineering pathway for stable PDH catalysts.
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