Liu Qiaoxi, Xu Wenjie, Huang Hao, Shou Hongwei, Low Jingxiang, Dai Yitao, Gong Wanbing, Li Youyou, Duan Delong, Zhang Wenqing, Jiang Yawen, Zhang Guikai, Cao Dengfeng, Wei Kecheng, Long Ran, Chen Shuangming, Song Li, Xiong Yujie
Hefei National Research Center for Physical Sciences at the Microscale, Key Laboratory of Precision and Intelligent Chemistry, School of Chemistry and Materials Science, School of Nuclear Science and Technology, National Synchrotron Radiation Laboratory, University of Science and Technology of China, Hefei, Anhui, 230026, China.
Suzhou Institute for Advanced Research, University of Science and Technology of China, Suzhou, Jiangsu, 215123, China.
Nat Commun. 2024 Mar 22;15(1):2562. doi: 10.1038/s41467-024-46923-3.
Hydrogen spillover widely occurs in a variety of hydrogen-involved chemical and physical processes. Recently, metal-organic frameworks have been extensively explored for their integration with noble metals toward various hydrogen-related applications, however, the hydrogen spillover in metal/MOF composite structures remains largely elusive given the challenges of collecting direct evidence due to system complexity. Here we show an elaborate strategy of modular signal amplification to decouple the behavior of hydrogen spillover in each functional regime, enabling spectroscopic visualization for interfacial dynamic processes. Remarkably, we successfully depict a full picture for dynamic replenishment of surface hydrogen atoms under interfacial hydrogen spillover by quick-scanning extended X-ray absorption fine structure, in situ surface-enhanced Raman spectroscopy and ab initio molecular dynamics calculation. With interfacial hydrogen spillover, Pd/ZIF-8 catalyst shows unique alkyne semihydrogenation activity and selectivity for alkynes molecules. The methodology demonstrated in this study also provides a basis for further exploration of interfacial species migration.
氢溢流广泛存在于各种涉及氢的化学和物理过程中。近年来,金属有机框架因其与贵金属结合用于各种氢相关应用而受到广泛研究,然而,由于系统复杂性导致收集直接证据面临挑战,金属/金属有机框架复合结构中的氢溢流现象在很大程度上仍不为人所知。在此,我们展示了一种精心设计的模块化信号放大策略,以解耦每个功能区域中氢溢流的行为,从而实现对界面动态过程的光谱可视化。值得注意的是,我们通过快速扫描扩展X射线吸收精细结构、原位表面增强拉曼光谱和从头算分子动力学计算,成功描绘了界面氢溢流作用下表面氢原子动态补充的全貌。在界面氢溢流作用下,钯/沸石咪唑酯骨架材料-8催化剂对炔烃分子表现出独特的炔烃半加氢活性和选择性。本研究中展示的方法也为进一步探索界面物种迁移提供了基础。