Geometric Tuning of Single‐Atom FeN4 Sites via Edge‐Generation Enhances Multi‐Enzymatic Properties

材料科学 密度泛函理论 催化作用 GSM演进的增强数据速率 Atom(片上系统) 活动站点 同种类的 化学物理 纳米技术 组合化学 计算化学 化学 生物化学 计算机科学 物理 嵌入式系统 热力学 电信
作者
Kang Kim,Jae Wook Lee,Ok Kyu Park,Jong Seung Kim,Jiheon Kim,Donghyun Lee,Vinod K. Paidi,Euiyeon Jung,Hyeon Seok Lee,Bowon Lee,Chan Woo Lee,Wonjae Ko,Kangjae Lee,Yoon Seok Jung,Changha Lee,Nohyun Lee,Seoin Back,Seung Hong Choi,Taeghwan Hyeon
出处
期刊:Advanced Materials [Wiley]
卷期号:35 (19): e2207666-e2207666 被引量:53
标识
DOI:10.1002/adma.202207666
摘要

Abstract Single‐atom nanozymes (SAzymes) are considered promising alternatives to natural enzymes. The catalytic performance of SAzymes featuring homogeneous, well‐defined active structures can be enhanced through elucidating structure‐activity relationship and tailoring physicochemical properties. However, manipulating enzymatic properties through structural variation is an underdeveloped approach. Herein, the synthesis of edge‐rich Fe single‐atom nanozymes (FeNC‐edge) via an H 2 O 2 ‐mediated edge generation is reported. By controlling the number of edge sites, the peroxidase (POD)‐ and oxidase (OXD)‐like performance is significantly enhanced. The activity enhancement results from the presence of abundant edges, which provide new anchoring sites to mononuclear Fe. Experimental results combined with density functional theory (DFT) calculations reveal that FeN 4 moieties in the edge sites display high electron density of Fe atoms and open N atoms. Finally, it is demonstrated that FeNC‐edge nanozyme effectively inhibits tumor growth both in vitro and in vivo, suggesting that edge‐tailoring is an efficient strategy for developing artificial enzymes as novel catalytic therapeutics.
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