Key Laboratory of Carbon Materials of Zhejiang Province, College of Chemistry and Materials Engineering, Wenzhou University, Wenzhou 325035, China.
State Key Laboratory of Pulp and Paper Engineering, School of Light Industry and Engineering, South China University of Technology, Guangzhou 510640, China.
J Am Chem Soc. 2023 Jun 14;145(23):12884-12893. doi: 10.1021/jacs.3c04028. Epub 2023 May 30.
Lignin is the most abundant aromatic polymer from the natural and renewable lignocellulosic biomass resource. Developing highly efficient catalysts for lignin depolymerization to produce valuable monophenols with high yield and selectivity remains a desirable but challenging target in this field. Here, we design a synergistic catalyst combining atomically dispersed Mo centers and Al Lewis acid sites on a MgO substrate (MoAl/MgO) for the depolymerization of lignin via the β-aryl ether bond cleavage. A near-theoretical monophenol yield of 46% with an ultrahigh selectivity of 92% for coniferyl and sinapyl methyl ether, as well as good cycling durability, was achieved simultaneously by MoAl/MgO in an inert N atmosphere. First-principles calculations and control catalytic experiments confirmed the synergistic catalysis mechanism between Mo-O single-atom centers and the neighboring Al Lewis acid sites with the participation of a methanol solvent. This study validates the feasibility of designing better-performing catalysts with synergistic multiactive sites for the efficient and selective disassembly of complex renewable biopolymers into highly value-added products with lower cost and greater security.
木质素是自然界中最丰富的芳香族聚合物,来源于可再生的木质纤维素生物质资源。开发高效催化剂,通过β-芳基醚键断裂将木质素解聚为高收率和高选择性的有价值的单酚类化合物,仍然是该领域中一个理想但具有挑战性的目标。在这里,我们设计了一种协同催化剂,将原子分散的 Mo 中心和 Al 路易斯酸位结合在 MgO 载体上(MoAl/MgO),用于通过β-芳基醚键断裂来解聚木质素。在惰性 N2 气氛中,MoAl/MgO 同时实现了近理论的单酚收率 46%,对松柏基和丁香基甲基醚的超高选择性 92%,以及良好的循环稳定性。基于第一性原理的计算和对照催化实验证实了 Mo-O 单原子中心与相邻 Al 路易斯酸位之间的协同催化机制,其中甲醇溶剂参与了反应。这项研究验证了设计具有协同多活性位的更好性能催化剂的可行性,用于高效和选择性地将复杂的可再生生物聚合物解聚为具有更低成本和更高安全性的高附加值产品。