Yang Jian, Qiu Zongyang, Zhao Changming, Wei Weichen, Chen Wenxing, Li Zhijun, Qu Yunteng, Dong Juncai, Luo Jun, Li Zhenyu, Wu Yuen
Department of Chemistry, iChEM (Collaborative Innovation Center of Chemistry for Energy Materials), University of Science and Technology of China, Hefei, 230026, China.
Hefei National Laboratory for Physical Sciences at the Microscale, University of Science and Technology of China, Hefei, 230026, China.
Angew Chem Int Ed Engl. 2018 Oct 22;57(43):14095-14100. doi: 10.1002/anie.201808049. Epub 2018 Oct 1.
The arrangement of the active sites on the surface of a catalysts can reduce the problem of mass transfer and enhance the atom economy. Herein, supported Ni metal nanoparticles can be transformed to thermal stable Ni single atoms, mostly located on the surface of the support. Assisted by N-doped carbon with abundant defects, this synthetic process not only transform the nanoparticles to single atoms, but also creates numerous pores to facilitate the contact of dissolved CO and single Ni sites. The proposed mechanism is that the Ni nanoparticles could break surface C-C bonds drill into the carbon matrix, leaving pores on the surface. When Ni nanoparticles are exposed to N-doped carbon, the strong coordination splits Ni atoms from Ni NPs. The Ni atoms are stabilized within the surface of carbon substrate. The continuous loss of atomic Ni species from the NPs would finally result in atomization of Ni NPs. CO electroreduction testing shows that the surface enriched with Ni single atoms delivers better performance than supported Ni NPs and other similar catalysts.
催化剂表面活性位点的排列可以减少传质问题并提高原子经济性。在此,负载型镍金属纳米颗粒可以转化为热稳定的镍单原子,大部分位于载体表面。在具有大量缺陷的氮掺杂碳的辅助下,这种合成过程不仅将纳米颗粒转化为单原子,还产生了许多孔隙,以促进溶解的一氧化碳与单个镍位点的接触。提出的机制是镍纳米颗粒可以打破表面的碳-碳键并钻入碳基质,在表面留下孔隙。当镍纳米颗粒暴露于氮掺杂碳时,强配位作用会使镍原子从镍纳米颗粒中分离出来。镍原子在碳基底表面稳定下来。镍纳米颗粒中原子镍物种的持续损失最终将导致镍纳米颗粒的原子化。一氧化碳电还原测试表明,富含镍单原子的表面比负载型镍纳米颗粒和其他类似催化剂具有更好的性能。