Liu Wei, Sheng Hui, Zhu Liu, Zhang Yiwen, Liu Wenxu, Zhao Yuwei, Li Qian, Peng Yong, Wang Zhongpeng
School of Water Conservancy and Environment, University of Jinan, Jinan 250022, China.
Key Laboratory of Magnetism and Magnetic Materials of the Ministry of Education, School of Physical Science and Technology and Electron Microscopy Centre of Lanzhou University, Lanzhou University, Lanzhou 730000, China.
J Colloid Interface Sci. 2022 Dec;627:53-63. doi: 10.1016/j.jcis.2022.07.007. Epub 2022 Jul 8.
The classical strong metal-support interaction (SMSI) plays a key role in improving thermal stability for supported Au catalysts. However, it always decreases the catalytic activity because of the encapsulation of Au species by support. Herein, we demonstrate that Al is a functional additive which could effectively improve both catalytic activity and sintering resistant property for H pretreated Al doped CeO supported Au (AuCeAl) catalyst at high temperature. The physical characterization and in-situ DRIFTS results provide insight that more oxygen vacancies generated by Al doping could be as preferential adsorption sites for CO molecules when the encapsulation of Au species occurred, which is certificated by an accelerated formation of bicarbonate species. In the meantime, smaller Au nanoparticles with higher dispersion (2.8 nm, 85.63%) is achieved in AuCeAl catalysts, compared with that in CeO supported Au (AuCe) catalysts (5.1 nm, 36.17%). Additionally, the as-prepared AuCeAl catalysts also have superior catalytic performance even after calcination at 800 °C in air.
经典的强金属-载体相互作用(SMSI)在提高负载型Au催化剂的热稳定性方面起着关键作用。然而,由于载体对Au物种的包覆,它总是会降低催化活性。在此,我们证明Al是一种功能性添加剂,它可以有效提高经H预处理的Al掺杂CeO负载型Au(AuCeAl)催化剂在高温下的催化活性和抗烧结性能。物理表征和原位漫反射红外傅里叶变换光谱(DRIFTS)结果表明,当Au物种发生包覆时,Al掺杂产生的更多氧空位可作为CO分子的优先吸附位点,这通过碳酸氢盐物种的加速形成得到了证实。同时,与CeO负载型Au(AuCe)催化剂(5.1 nm,36.17%)相比,AuCeAl催化剂中获得了具有更高分散度(2.8 nm,85.63%)的更小Au纳米颗粒。此外,所制备的AuCeAl催化剂即使在空气中800℃煅烧后也具有优异的催化性能。