School of Material and Chemical Engineering, Zhengzhou University of Light Industry, Zhengzhou 450001, P. R. China.
Henan Provincial Key Laboratory of Surface and Interface Science, Zhengzhou University of Light Industry, Zhengzhou 450001, P. R. China.
Nanoscale. 2023 Mar 2;15(9):4612-4619. doi: 10.1039/d2nr05831f.
Developing Cr-free and non-noble metal catalysts with high activity, selectivity and durability for chemoselective hydrogenation of furfural to furfuryl alcohol is highly desirable yet challenging. In this study, we design a hollow mesoporous Co-N-C@mSiO nanostructure derived from ZIF-67 the encapsulation-pyrolysis strategy. The Co-N-C@mSiO catalyst exhibits excellent catalytic performance in the furfural hydrogenation towards furfuryl alcohol with good stability, and is much better than the Co-N-C catalyst originating from plain ZIF-67 and other reported transition metal catalysts. Characterization methods and control experiments show that Co-N species rather than Co metal should be catalytically active sites for the above reaction. The enhanced performance is associated with abundant Co-N active sites, good mass transport, and the SiO shell protection. This work provides a novel and facile strategy for preparing highly efficient non-precious metal catalysts to replace Cr-based and noble metal catalysts for furfural hydrogenation.
开发具有高活性、选择性和耐久性的无铬和非贵金属催化剂,用于糠醛的选择性加氢制备糠醇,这是一项非常有意义但具有挑战性的工作。在本研究中,我们采用 ZIF-67 模板的封装-热解策略设计了一种中空介孔 Co-N-C@mSiO 纳米结构。Co-N-C@mSiO 催化剂在糠醛加氢制备糠醇反应中表现出优异的催化性能和良好的稳定性,优于由普通 ZIF-67 和其他报道的过渡金属催化剂衍生的 Co-N-C 催化剂。表征方法和控制实验表明,Co-N 物种而非 Co 金属应该是上述反应的催化活性中心。性能的提高与丰富的 Co-N 活性位、良好的质量传递和 SiO2 壳保护有关。这项工作为制备高效非贵金属催化剂提供了一种新的简便策略,以替代 Cr 基和贵金属催化剂用于糠醛的加氢反应。