Jiang Xiaoli, Ma Xianhui, Yang Yuanteng, Liu Yang, Liu Yanxia, Zhao Lin, Wang Penglei, Zhang Yagang, Lin Yue, Wei Yen
School of Materials and Energy, University of Electronic Science and Technology of China, Chengdu, 611731, People's Republic of China.
Hefei National Research Center for Physical Sciences at the Microscale, University of Science and Technology of China, Hefei, 230026, People's Republic of China.
Nanomicro Lett. 2024 Aug 22;16(1):275. doi: 10.1007/s40820-024-01493-3.
Electrocatalytic 5-hydroxymethylfurfural oxidation reaction (HMFOR) provides a promising strategy to convert biomass derivative to high-value-added chemicals. Herein, a cascade strategy is proposed to construct Pd-NiCoO electrocatalyst by Pd loading on Ni-doped CoO and for highly active and stable synergistic HMF oxidation. An elevated current density of 800 mA cm can be achieved at 1.5 V, and both Faradaic efficiency and yield of 2,5-furandicarboxylic acid remained close to 100% over 10 consecutive electrolysis. Experimental and theoretical results unveil that the introduction of Pd atoms can modulate the local electronic structure of Ni/Co, which not only balances the competitive adsorption of HMF and OH species, but also promote the active Ni species formation, inducing high indirect oxidation activity. We have also discovered that Ni incorporation facilitates the Co pre-oxidation and electrophilic OH* generation to contribute direct oxidation process. This work provides a new approach to design advanced electrocatalyst for biomass upgrading.
电催化5-羟甲基糠醛氧化反应(HMFOR)为将生物质衍生物转化为高附加值化学品提供了一种很有前景的策略。在此,提出了一种级联策略,通过在镍掺杂的氧化钴上负载钯来构建钯-镍钴氧化物电催化剂,用于高活性和稳定的协同HMF氧化。在1.5 V时可实现800 mA cm的升高电流密度,并且在连续10次电解过程中,2,5-呋喃二甲酸的法拉第效率和产率均保持接近100%。实验和理论结果表明,钯原子的引入可以调节镍/钴的局部电子结构,这不仅平衡了HMF和OH物种的竞争吸附,还促进了活性镍物种的形成,从而诱导出高间接氧化活性。我们还发现,镍的掺入促进了钴的预氧化和亲电OH*的生成,有助于直接氧化过程。这项工作为设计用于生物质升级的先进电催化剂提供了一种新方法。