Wu Taikang, Shi Yingzhang, Wang Zhiwen, Liu Cheng, Bi Jinhong, Yu Yan, Wu Ling
Key Laboratory of Photocatalysis on Energy and Environment, College of Chemistry, Fuzhou University, Fuzhou 350116, P. R. China.
Key Laboratory of Eco-materials Advanced Technology, College of Materials Science and Engineering, Fuzhou University, Fuzhou 350108, P. R. China.
ACS Appl Mater Interfaces. 2021 Dec 29;13(51):61286-61295. doi: 10.1021/acsami.1c20128. Epub 2021 Dec 14.
Creating accessible unsaturated active sites in metal-organic frameworks (MOFs) holds great promise for developing highly efficient catalysts. Herein, ultrathin Ni MOF-74 nanosheets (NMNs) with high-density coordinatively unsaturated Ni centers are prepared as a photocatalyst. The results of in situ ATR-IR, Raman, UV-vis DRS, and XPS suggest that abundant Ni centers can act as the active sites for boosting benzylamine (BA) activation via forming -Ni-NH- coordination intermediates. The generation of coordination intermediates assists the transfer of photo-generated holes to BA molecules for producing BA cation free radicals, better impelling the breaking of N-H bonds and the photooxidation of BA molecules. The photo-generated electrons further activate O molecules to O radicals for triggering the reaction. The experiments reveal that the coordination activation of BA molecules may be a rate-determining step on NMNs rather than the adsorption and activation of O molecules. Moreover, NMNs possess a better ability for the separation of photo-generated carriers in comparison with bulk Ni MOF-74 (NMBs). As a result, NMNs achieve a kinetic rate constant of 0.538 h for the photocatalytic oxidative coupling of BA under visible light, about 50 times higher than that of NMBs (0.0011 h). Finally, a probable synergetic catalytic mechanism with coordination activation and photocatalysis is discussed on a molecular level. This study not only highlights the importance of coordination activation for heterogeneous photocatalysis but also affords an inspiration for building ultrathin MOF nanosheets.
在金属有机框架(MOF)中创建可及的不饱和活性位点对于开发高效催化剂具有巨大潜力。在此,制备了具有高密度配位不饱和镍中心的超薄镍基MOF-74纳米片(NMN)作为光催化剂。原位ATR-IR、拉曼光谱、紫外可见漫反射光谱(UV-vis DRS)和X射线光电子能谱(XPS)结果表明,大量的镍中心可作为活性位点,通过形成-Ni-NH-配位中间体来促进苄胺(BA)的活化。配位中间体的生成有助于光生空穴向BA分子转移以产生BA阳离子自由基,更好地推动N-H键的断裂和BA分子的光氧化。光生电子进一步将O分子活化为O自由基以引发反应。实验表明,BA分子的配位活化可能是NMN上的速率决定步骤,而非O分子的吸附和活化。此外,与块状镍基MOF-74(NMB)相比,NMN具有更好的光生载流子分离能力。结果,NMN在可见光下对BA的光催化氧化偶联反应的动力学速率常数达到0.538 h,约为NMB(0.0011 h)的50倍。最后,在分子水平上讨论了一种可能的配位活化与光催化协同催化机理。这项研究不仅突出了配位活化在多相光催化中的重要性,也为构建超薄MOF纳米片提供了启示。