等离子体子
表面等离子共振
胶体金
纳米技术
化学
催化作用
动力学
纳米颗粒
材料科学
基质(水族馆)
光化学
光电子学
有机化学
物理
量子力学
海洋学
地质学
作者
Xuewei Liao,Qiuyang Xu,Hanjun Sun,Wenyuan Liu,Yuming Chen,Xing‐Hua Xia,Chen Wang
标识
DOI:10.1021/acs.jpclett.1c03804
摘要
Among the members of the rapidly growing nanozyme family, plasmonic nanozymes stand out because of their unique localized surface plasmon resonance (LSPR) characteristics and tunable catalytic activity. We prepared a plasmonic nanozyme of Au gold nanoparticles (AuNPs) and Cu metal-organic framework nanosheets (Cu-MOFNs). The Cu-MOFNs have peroxidase-like activity, while AuNPs present unique LSPR characteristics. We found that the as-prepared AuNPs/Cu-MOFNs composite presents 1.6-fold faster reaction kinetics under LSPR excitation compared to that in the dark. Investigations of energy levels, radical capture, and dark-field scattering spectroscopy revealed that LSPR of AuNPs as well as matched energy levels can facilitate efficient hot electron transfer, which could readily cleave the chemical bond of the substrate and accelerate the reaction kinetics. On the basis of these results, we achieved enhanced antibacterial therapy and wound healing using plasmonic AuNPs/Cu-MOFNs. This study spotlights the superiority of plasmonic nanozymes in improving the enzyme-like performance of nanozymes.
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