Zhang Chenghu, Xing Zezhou, Li Ying, Xu Tong, Sun Yinghui, Bai Jie
College of Chemical Engineering, Inner Mongolia University of Technology, Hohhot, 010051, People's Republic of China.
Inner Mongolia Key Laboratory of Green Chemical Engineering, Hohhot, 010051, People's Republic of China.
Nanoscale. 2025 Aug 7;17(31):18229-18239. doi: 10.1039/d5nr01846c.
Bimetallic synergy can competently optimize the electronic structure of active metals and coordinate interaction between metal components, which is a good strategy to effectively enhance the catalytic performance and stability of monometallic catalysts. Herein, we report a CuNi bimetallic catalyst supported on mesoporous zirconia prepared electrospinning technology, which can achieve high catalytic transfer hydrogenation (CTH) performance with excellent cycling stability. The bimetallic synergistic effect on CTH capacity was systematically investigated by precisely regulating the Cu/Ni molar ratio. The optimized CuNi-ZrO catalyst exhibited exceptional performance, achieving 88.9% furfural conversion with 93.6% furfuryl alcohol selectivity in isopropanol at 170 °C for 12 h, accompanied by a notable TOF value of 4.90 h. The electron transfer between Cu and Ni promotes the generation of more Cu/Cu active sites, which effectively enhances the CTH activity of the catalyst. Additionally, the CuNi-ZrO catalyst showed stable performance over 6 cycles with negligible activity decay. Finally, the hydrogen transfer pathway of furfural on the catalyst surface was studied H isotope labeling mass experiments.
双金属协同作用能够有效地优化活性金属的电子结构以及金属组分之间的配位相互作用,这是有效提高单金属催化剂催化性能和稳定性的良好策略。在此,我们报道了一种通过静电纺丝技术制备的负载在介孔氧化锆上的铜镍双金属催化剂,该催化剂能够实现高催化转移氢化(CTH)性能以及出色的循环稳定性。通过精确调节铜/镍摩尔比,系统地研究了双金属对CTH能力的协同效应。优化后的CuNi-ZrO催化剂表现出优异的性能,在170°C的异丙醇中反应12小时,糠醛转化率达到88.9%,糠醇选择性为93.6%,同时具有4.90 h的显著TOF值。铜和镍之间的电子转移促进了更多Cu/Cu活性位点的产生,有效地提高了催化剂的CTH活性。此外,CuNi-ZrO催化剂在6次循环中表现出稳定的性能,活性衰减可忽略不计。最后,通过氢同位素标记质谱实验研究了糠醛在催化剂表面的氢转移途径。