催化作用
扫描透射电子显微镜
氮化碳
材料科学
Atom(片上系统)
色散(光学)
吸收(声学)
氢原子
光催化
纳米技术
结晶学
化学
氮化物
碳纤维
透射电子显微镜
有机化学
光学
复合数
物理
图层(电子)
烷基
复合材料
嵌入式系统
计算机科学
作者
Xun‐Heng Jiang,Longshuai Zhang,Haiyan Liu,Daishe Wu,Feiyao Wu,Lei Tian,Lingling Liu,Jian‐Ping Zou,Shenglian Luo,Bing‐Bing Chen
标识
DOI:10.1002/anie.202011495
摘要
Abstract Single atom catalysts (SACs) with the maximized metal atom efficiency have sparked great attention. However, it is challenging to obtain SACs with high metal loading, high catalytic activity, and good stability. Herein, we demonstrate a new strategy to develop a highly active and stable Ag single atom in carbon nitride (Ag‐N 2 C 2 /CN) catalyst with a unique coordination. The Ag atomic dispersion and Ag‐N 2 C 2 configuration have been identified by aberration‐correction high‐angle‐annular‐dark‐field scanning transmission electron microscopy (AC‐HAADF‐STEM) and extended X‐ray absorption. Experiments and DFT calculations further verify that Ag‐N 2 C 2 can reduce the H 2 evolution barrier, expand the light absorption range, and improve the charge transfer of CN. As a result, the Ag‐N 2 C 2 /CN catalyst exhibits much better H 2 evolution activity than the N‐coordinated Ag single atom in CN (Ag‐N 4 /CN), and is even superior to the Pt nanoparticle‐loaded CN (Pt NP /CN). This work provides a new idea for the design and synthesis of SACs with novel configurations and excellent catalytic activity and durability.
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