催化作用
原位
Atom(片上系统)
铂金
纳米技术
密度泛函理论
化学物理
化学
材料科学
计算化学
计算机科学
有机化学
嵌入式系统
标识
DOI:10.1002/anie.202216490
摘要
Qiao and co-workers recently designed and interpreted the construction of high-density Pt single atoms in the Co3 O4 host with inter-site interactions via the Hard-Soft Acid-Base principle and further revealed the dynamic structure evolution process of the single atom sites by a series of in situ/ex situ spectroscopic techniques and theoretical computation.As a new frontier, the rapid development of single-atom catalysts (SACs) in heterogeneous catalysis has attracted extensive attention. However, a fundamental understanding of the dynamic formation process of active metal atom sites is lacking. The rational design of high-performance SACs now becomes possible by explicitly addressing the conundrum of constructing high-density SACs and elucidating the evolution of SACs during the synthesis.
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