化学
生物传感器
纳米材料
催化作用
纳米颗粒
组合化学
电化学
过氧化氢
检出限
纳米技术
氧化还原
安培法
协同催化
石墨烯
超氧化物
活性氧
氧化物
电催化剂
谷胱甘肽
熵(时间箭头)
氧气
过渡金属
作者
Ziyu Yin,Kaylee M. Clark,Hwa-Jin Kwak,Tyler R. Ray
标识
DOI:10.1021/acs.analchem.5c04654
摘要
) detection with a LOD of 2.2 μM and a selective "signal-off" response for glutathione (GSH) quantification (LOD: 0.01 μM) through an inhibitory binding mechanism. Mechanistic studies establish that the versatile catalytic performance originates from the synergistic interplay between M(II)/M(III) redox cycling, superoxide radical generation at oxygen vacancies, and efficient electron transfer. The entropy-stabilized structure maintains 92% of its activity over 20 days without refrigeration. These findings establish multimetallic entropy engineering as a powerful strategy for creating stable, high-performance nanozymes suitable for wearable biosensors and point-of-care diagnostics.
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