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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.
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页数:8
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