Li Zhijun, Dong Xiuli, Zhang Mingyang, Leng Leipeng, Chen Wenxing, Horton J Hugh, Wang Jun, Li Zhijun, Wu Wei
Joint International Research Laboratory of Advanced Chemical Catalytic Materials & Surface Science, College of Chemistry and Chemical Engineering, Northeast Petroleum University, Daqing 163318, PR China.
Beijing Key Laboratory of Construction Tailorable Advanced Functional Materials and Green Applications, School of Materials Science and Engineering, Beijing Institute of Technology, Beijing 100081, PR China.
ACS Appl Mater Interfaces. 2020 Dec 23;12(51):57569-57577. doi: 10.1021/acsami.0c17009. Epub 2020 Dec 9.
Single-atom catalysis represents a new frontier that integrates the merits of homogeneous and heterogeneous catalysis to afford exceptional atom efficiency, activity, and selectivity for a range of catalytic systems. Herein we describe a simple defect engineering strategy to construct an atomically dispersed palladium catalyst (Pd, 0 < δ < 2) by anchoring the palladium atoms on oxygen vacancies created in CeO nanorods. This was confirmed by spherical aberration correction electron microscopy and extended X-ray absorption fine structure measurement. The as-prepared catalyst showed exceptional catalytic performance in the hydrogenation of styrene (99% conversion, TOF of 2410 h), cinnamaldehyde (99% conversion, 99% selectivity, TOF of 968 h), as well as oxidation of triethoxysilane (99% conversion, 79 selectivity, TOF of 10 000 h). This single-atom palladium catalyst can be reused at least five times with negligible activity decay. The palladium atoms retained their dispersion on the support at the atomic level after thermal stability testing in Ar at 773 K. Most importantly, this synthetic method can be scaled up while maintaining catalytic performance. We anticipate that this method will expedite access to single-atom catalysts with high activity and excellent resistance to sintering, significantly impacting the performance of this class of catalysts.
单原子催化代表了一个新的前沿领域,它融合了均相催化和多相催化的优点,为一系列催化体系提供了卓越的原子效率、活性和选择性。在此,我们描述了一种简单的缺陷工程策略,通过将钯原子锚定在CeO纳米棒中产生的氧空位上,构建一种原子分散的钯催化剂(Pd,0 < δ < 2)。这通过球差校正电子显微镜和扩展X射线吸收精细结构测量得到证实。所制备的催化剂在苯乙烯加氢(转化率99%,TOF为2410 h⁻¹)、肉桂醛加氢(转化率99%,选择性99%,TOF为968 h⁻¹)以及三乙氧基硅烷氧化(转化率99%,选择性79%,TOF为10000 h⁻¹)反应中表现出卓越的催化性能。这种单原子钯催化剂可以重复使用至少五次,活性衰减可忽略不计。在773 K的氩气中进行热稳定性测试后,钯原子在载体上保持了原子级别的分散。最重要的是,这种合成方法可以扩大规模同时保持催化性能。我们预计这种方法将加快获得具有高活性和优异抗烧结性能的单原子催化剂,对这类催化剂的性能产生重大影响。