催化作用
葡萄糖酸
化学
选择性
合理设计
纳米颗粒
碳纤维
生物量(生态学)
化学工程
氮气
石墨氮化碳
组合化学
电子转移
协同催化
多相催化
无机化学
氧化还原
分子
作者
Xingyue Qi,Xiaofan Zhang,Junpeng Zhu,Junfeng Du,T. Chen,Jiefei Li,Hu Wei,Jinfang Wu,Haibin Chu
标识
DOI:10.1021/acssuschemeng.5c13068
摘要
Catalytic oxidation of glucose to gluconic acid under ambient conditions represents a pivotal and sustainable route for valorizing biomass-derived platform molecules into value-added chemicals. While Pd-based catalysts demonstrate promising potential in this reaction, their activity and stability still need to be improved for practical use. Herein, we design a series of N-doped glucose-derived carbon sphere-supported Pd (Pd/N-CS) with precisely regulated N species to enhance the catalytic efficiency. The optimized catalyst, rich in graphitic N, exhibits superior catalytic activity and stability, achieving a glucose conversion of 78.6% with nearly 100% gluconic acid selectivity at room temperature and atmospheric pressure. Combined experimental and theoretical analyses reveal that graphitic N not only preserves electron-rich Pd0 species by modulating electron transfer but also promotes the formation of surface OH* species, both of which synergistically enhance glucose oxidation. This work provides deep insights into nitrogen functionality-driven catalysis and offers a rational strategy for designing highly efficient and sustainable catalytic systems for biomass conversion.
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