过电位
石墨烯
X射线吸收光谱法
材料科学
氧化物
电化学
密度泛函理论
催化作用
纳米孔
透射电子显微镜
Atom(片上系统)
扫描透射电子显微镜
吸收光谱法
结晶学
纳米技术
电极
冶金
化学
计算化学
有机化学
计算机科学
物理化学
物理
量子力学
嵌入式系统
作者
Yi Cheng,Shiyong Zhao,Haobo Li,Shuai He,Jean‐Pierre Veder,Bernt Johannessen,Jianping Xiao,Shanfu Lu,Jian Pan,Mattew F. Chisholm,Shize Yang,Chang Liu,Jingguang G. Chen,San Ping Jiang
标识
DOI:10.1016/j.apcatb.2018.10.046
摘要
Supported single atom catalysts (SACs), emerging as a new class of catalytic materials, have been attracting increasing interests. Here we developed a Ni SAC on microwave exfoliated graphene oxide (Ni-N-MEGO) to achieve single atom loading of ∼6.9 wt%, significantly higher than previously reported SACs. The atomically dispersed Ni atoms, stabilized by coordination with nitrogen, were found to be predominantly anchored along the edges of nanopores ( < 6 nm) using a combination of X-ray absorption spectroscopy (XAS) and aberration-corrected scanning transmission electron microscopy (AC-STEM). The Ni-N-MEGO exhibits an onset overpotential of 0.18 V, and a current density of 53.6 mA mg−1 at overpotential of 0.59 V for CO2 reduction reaction (CO2RR), representing one of the best non-precious metal SACs reported so far in the literature. Density functional theory (DFT) calculations suggest that the electrochemical CO2-to-CO conversion occurs more readily on the edge-anchored unsaturated nitrogen coordinated Ni single atoms that lead to enhanced activity toward CO2RR.
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