Sulfur-doped Co(OH)2 nanosheets with abundant oxygen vacancies for high-performance non-enzymatic glucose sensing

被引:3
|
作者
Zhou, Hai [1 ]
Chen, Xianghua [2 ]
Liu, Yang [1 ]
Fei, Fei [1 ]
Wen, Pushan [1 ]
机构
[1] Zunyi Normal Univ, Dept Chem & Chem Engn, Zunyi 563006, Peoples R China
[2] State Key Lab Adv Chem Power Sources, Zunyi 563006, Peoples R China
基金
中国国家自然科学基金;
关键词
Sulfur; -doping; Oxygen vacancies; Electrochemical; Glucose sensing; ELECTRODE; CO3O4; OXIDE;
D O I
10.1016/j.surfin.2024.103994
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The development of high-performance materials for electrochemical non-enzymatic glucose sensing is crucial for diabetes detection and management. This study presents a facile approach for synthesizing sulfur-doped Co(OH)2 nanosheets with abundant oxygen vacancies, enhancing glucose sensing capabilities. Initially, ultrathin Co(OH)2 nanosheets are synthesized via a dissolution-recrystallization process, facilitated by L-lysine during hydrothermal synthesis. Subsequently, sulfur-doped Co(OH)2 nanosheets with oxygen vacancies (B-S-Co(OH)2) are produced through a two-step modification process using Na2S and NaBH4. The resulting B-S-Co(OH)2 exhibits high specific surface area, numerous oxygen vacancies, and rapid electron transfer, contributing to increased electrochemical activity. Electrochemical measurements, conducted with a glassy carbon rotating disk electrode (RDE), indicate low charge transfer barriers and enhanced redox properties. Consequently, B-S-Co(OH)2 nanosheets demonstrate superior glucose sensing performances, characterized by rapid response, high sensitivity (1.044 mA & sdot;mM-1 & sdot;cm-2), broad linear range (0.01-1.4 mM and 1.6-3.6 mM), low detection limit (2.4 mu M), and excellent long-term stability. This study offers an effective method for modifying the electronic structure and charge transfer properties of Co(OH)2 through surface modification, thereby advancing non-enzymatic glucose sensing capabilities.
引用
收藏
页数:8
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