Sun Yuxia, Ma Hong, Luo Yang, Zhang Shujing, Gao Jin, Xu Jie
State Key Laboratory of Catalysis, Dalian Institute of Chemical Physics, Chinese Academy of Sciences, Dalian National Laboratory for Clean Energy, Dalian, 116023, P.R. China.
University of Chinese Academy of Sciences, Beijing, 100049, P.R. China.
Chemistry. 2018 Mar 26;24(18):4653-4661. doi: 10.1002/chem.201705824. Epub 2018 Feb 26.
It has long been a challenge for activating O by transition-metal nanocatalysts, which might lose activity due to strong tendency for oxidation. Herein, O could be activated by durable encapsulated cobalt nanoparticles (NPs) with N-doped graphitic carbon shells (Co@N-C), but not by encapsulated cobalt NPs with graphitic carbon, exposed cobalt NPs supported on activated carbon, or N-doped carbon. Electron paramagnetic resonance, real-time in situ FTIR spectroscopy, and mass spectrometry measurements demonstrated the generation of the highly active superoxide radical, O . This unique ability enables Co@N-C to afford an excellent catalytic performance in model aerobic oxidation of monomeric lignin-derived alcohols. Further analysis elucidated that encapsulated cobalt and nitrogen-doped graphitic carbon might contribute to the capacity through influencing the electronic properties of outer layers. Moreover, through isolation by N-doped graphitic carbon shells, the inner metallic cobalt NPs are inaccessible in term of either alcohols or oxygenated products, and a distinctive resistance to leaching and agglomeration has been achieved.
长期以来,利用过渡金属纳米催化剂激活O一直是一项挑战,因为过渡金属纳米催化剂可能会因强烈的氧化倾向而失去活性。在此,O可以被具有N掺杂石墨碳壳的耐用封装钴纳米颗粒(Co@N-C)激活,但不能被具有石墨碳的封装钴纳米颗粒、负载在活性炭上的暴露钴纳米颗粒或N掺杂碳激活。电子顺磁共振、实时原位傅里叶变换红外光谱和质谱测量表明生成了高活性超氧自由基O 。这种独特的能力使Co@N-C在单体木质素衍生醇的模型需氧氧化中具有优异的催化性能。进一步分析表明,封装的钴和氮掺杂石墨碳可能通过影响外层的电子性质来发挥作用。此外,通过N掺杂石墨碳壳的隔离,内部金属钴纳米颗粒无论是对于醇还是氧化产物都是无法接触到的,并且实现了对浸出和团聚的独特抗性。