Shengxian Shao, Xiaolong Liu, Junqi Pei, Ting Tan, Xiao Chen, Qiang Zheng, Qing Feng, Bohua WANG, Chengqian Cui, Kun Wang, Caoyu Yang, Pengfei An, Wenxing Chen, Jing Zhang, Bin Liu, Zhiyong Tang, Guodong Li
Platinum (Pt) nanoparticles favor the hydrogenation of CO 2 to CO, presenting a significant challenge for value-added methanol synthesis. Herein we report a sulfonic acid group docking strategy for the gram-scale synthesis of monodispersed Pt clusters within the cavities of double sulfonated zirconium terephthalate UiO-66. The resulting catalyst enables the efficient hydrogenation of CO 2 to methanol, achieving nearly 100% methanol selectivity at 60 °C and sustaining stable performance for 500 h of continuous operation. Computational and experimental investigations reveal that sulfonic acid groups facilitate the modulation of the electronic structures of adjacent Pt clusters and defective zirconium sites, thereby promoting the adsorption and activation of H 2 and CO 2 . Consequently, the interfaces between Pt edges and defective zirconium sites efficiently promote the hydrogenation of CO 2 to methanol at low temperatures. Our developed sulfonic acid group docking strategy can be extended to synthesize a wide range of highly active and stable metal clusters in porous supports, opening new possibilities for important catalytic applications.