Zhang Kai, Wang Ning, Meng Yali, Zhang Tianjun, Zhao Pu, Sun Qiming, Yu Jihong
Innovation Center for Chemical Science, College of Chemistry, Chemical Engineering and Materials Science, Soochow University Suzhou 215123 P. R. China
Institute of Sustainable Energy and Resources, College of Chemistry and Chemical Engineering, Qingdao University Qingdao 266071 P. R. China
Chem Sci. 2023 Nov 30;15(1):379-388. doi: 10.1039/d3sc05851d. eCollection 2023 Dec 20.
Atomically dispersed metal catalysts with excellent activity and stability are highly desired in heterogeneous catalysis. Herein, we synthesized zeolite-encaged Pd-based pseudo-single atoms a facile and energy-efficient ligand-protected direct H reduction method. C-corrected scanning transmission electron microscopy, extended X-ray absorption, and pair distribution function measurements reveal that the metal species are close to atomic-level dispersion and completely confined within the intersectional channels of silicalite-1 (S-1) zeolite with the MFI framework. The Pd@S-1-H exhibits excellent activity and stability in methane combustion reactions with a complete combustion temperature of 390 °C, and no deactivation is observed even after 100 h on stream. The optimized bimetallic 0.8Pd0.2Ni(OH)@S-1-H catalyst exhibits an excellent H generation rate from FA decomposition without any additives, affording a superhigh turnover frequency up to 9308 h at 333 K, which represents the top activity among all of the best heterogeneous catalysts under similar conditions. Significantly, zeolite-encaged metal catalysts are first used for Cr(vi) reduction coupled with formic acid (FA) dehydrogenation and show a superhigh turnover number of 2980 mol(CrO) mol(Pd) at 323 K, surpassing all of the previously reported catalysts. This work demonstrates that zeolite-encaged pseudo-single atom catalysts are promising in efficient hydrogen storage and pollutant disposal applications.
在多相催化中,人们非常渴望具有优异活性和稳定性的原子级分散金属催化剂。在此,我们通过一种简便且节能的配体保护直接氢还原法合成了沸石包裹的钯基准单原子。经C校正的扫描透射电子显微镜、扩展X射线吸收和对分布函数测量表明,金属物种接近原子级分散,并且完全限制在具有MFI骨架的硅沸石-1(S-1)沸石的交叉通道内。Pd@S-1-H在甲烷燃烧反应中表现出优异的活性和稳定性,完全燃烧温度为390℃,即使在连续运行100小时后也未观察到失活。优化后的双金属0.8Pd0.2Ni(OH)@S-1-H催化剂在无任何添加剂的情况下,从甲酸(FA)分解中表现出优异的产氢速率,在333K时提供高达9308 h⁻¹的超高周转频率,这代表了在类似条件下所有最佳多相催化剂中的最高活性。值得注意的是,沸石包裹的金属催化剂首次用于与甲酸(FA)脱氢偶联的Cr(Ⅵ)还原,并且在323K时显示出2980 mol(CrO)/mol(Pd)的超高周转数,超过了所有先前报道的催化剂。这项工作表明,沸石包裹的准单原子催化剂在高效储氢和污染物处理应用中具有广阔前景。