材料科学
过电位
电化学
检出限
过氧化氢
纳米技术
电化学气体传感器
化学工程
电极
组合化学
有机化学
物理化学
化学
色谱法
工程类
作者
Xiaoqing Ma,Kanglai Tang,Kang Lu,Chenke Zhang,Wenbing Shi,Wenxi Zhao
标识
DOI:10.1021/acsami.1c11747
摘要
Designing metal sulfides with unique configurations and exploring their electrochemical activities for hydrogen peroxide (H2O2) and hydrazine (N2H4) is challenging and desirable for various fields. Herein, hollow microflower-like CuS@C hybrids were successfully assembled and further exploited as a versatile electrochemical sensing platform for H2O2 reduction and N2H4 oxidation, of which the elaborate strategies make the perfect formation of hollow architecture, providing considerable electrocatalytic sites and fast charge transfer rate, while the appropriate introduction polydopamine-derived carbon skeleton facilitates the electronic conductivity and boosts structural robustness, thus generating wide linear range (0.05–14 and 0.01–10 mM), low detection limit (0.22 μM and 0.07 μM), and a rather low overpotential (−0.15 and −0.05 V) toward H2O2 and N2H4, as well as good selectivity, excellent reproducibility, and admirable long-term stability. It should be highlighted that the operating potentials can compare favorably with those of some reported H2O2 and N2H4 sensors based on noble metals. In addition, good recoveries and acceptable relative standard deviations (RSDs) attained in serum and water samples fully verify the accuracy and anti-interference capability of our proposed sensor systems. These results not only elucidate an effective structural nanoengineering strategy for electroanalytical science but also advance the rational utilization of H2O2 and N2H4 in practicability.
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