选择性
催化作用
氢溢流
纳米颗粒
化学
碳纤维
氢
贵金属
金属
光化学
无机化学
材料科学
纳米技术
有机化学
复合数
复合材料
作者
Chunshan Lu,Qianwen Zhu,Xuejie Zhang,Haoke Ji,Yebin Zhou,Hao Wang,Qiangqiang Liu,Juanjuan Nie,Wenfeng Han,Xiao‐Nian Li
标识
DOI:10.1021/acssuschemeng.9b00322
摘要
Achieving high selectivity is one of the major challenges for the noble metal catalysts. A strategy of decoration of Pd nanoparticles by N–S doped carbon quantum dots (N,S-CQDs) to regulate selectivity is proposed. Through adjusting the loading amounts of N,S-CQDs, high selectivity toward catalytic hydrogenation reactions can be obtained. N,S-CQDs facilely adhere to the Pd nanoparticle via surface reactions among C–S/C–N species of N,S-CQDs and C–O species of the carbon support under the catalysis of Pd particles. N loss was detected due to the transformation of some C–N species into nitrogen-containing soluble substances or gas. However, S-containing species, specially −SO2/SO3 species, are turned into C–S–C (thiophene-S), leading to a strong coordination between Pd and S. As a result, a N,S-CQDs-Pd interface is fabricated, in which electrons transfer from Pd to S species and the interface of Pd–S plays a major role in hydrogen spillover and generation of dissociated hydrogen with negative charge. Consequently, Pd@N,S-CQDs suppress the hydrodehalogenation and exhibit superior conversion and selectivity (both 100%) for the selective hydrogenation of various halonitrobenzenes. N,S-CQDs as a nonmetallic promoter of metal catalysts provides a promising strategy for the improvement of selectivity.
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