催化作用
材料科学
氢原子
结晶学
对称(几何)
氢
Atom(片上系统)
化学
有机化学
几何学
烷基
计算机科学
嵌入式系统
数学
作者
Haoran Zhang,Feng Wu,Rui Huang,Xiaokang Liu,Zhiwen Zhang,Tao Yao,Yu Zhang,Yuen Wu
标识
DOI:10.1002/adma.202404672
摘要
The performance of single-atom catalysts is greatly influenced by the chemical environment surrounding the central atom. Here, a salt-assisted method is employed to transform the tetrahedral coordination structure of zeolitic imidazolate frameworks - 8 (ZIF-8) into a planar square coordination structure without altering the ligands. During the subsequent carbonization process, concurrent with the evaporation of zinc atoms, the structure of the nitrogen and carbon carriers (NC carriers) undergoes a transition from five-membered rings to six-membered rings to preserve the 2D structure. This transition results in the generation of additional defect sites on the 2D-NC substrates. Hence, the Pt single-atom catalysts with planar square coordination symmetries can be precisely prepared via electrodeposition (denoted as 2D-Pt SAC). The Pt loading of 2D-Pt SAC is 0.49 ± 0.03 µg cm
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