双金属片
石墨烯
循环伏安法
X射线光电子能谱
氧化物
材料科学
电化学
高分辨率透射电子显微镜
介电谱
金属
纳米技术
电极
透射电子显微镜
分析化学(期刊)
化学工程
化学
有机化学
物理化学
冶金
工程类
作者
Nahid Rezvani Jalal,Tayyebeh Madrakian,Abbas Afkhami,Mazaher Ahmadi
标识
DOI:10.1021/acsanm.2c02237
摘要
Metal–organic frameworks (MOFs) have previously been researched for electrochemical sensor development. MOFs are commonly stated to have low conductivity, and improving their conductivity remains a significant challenge. We described the preparation of an electrochemical sensor depending on the in situ growth of NiCo-BTC bimetallic MOFs, as model bimetallic MOFs, on a glassy carbon electrode modified with conductive nitrogen-doped graphene oxide nanoribbons (NiCo-BTC MOFs/N-GONRs/GCE). The proposed NiCo-BTC MOFs/N-GONRs/GCE was characterized using X-ray photoelectron spectroscopy (XPS), transmission electron microscopy (TEM), high-resolution TEM (HRTEM), field emission scanning electron microscopy (FESEM), Fourier transform infrared (FT-IR), X-ray diffraction (XRD), electrochemical impedance spectroscopy (EIS), cyclic voltammetry (CV), and Raman spectroscopy. The square-wave voltammetry response of NiCo-BTC MOFs/N-GONRs/GCE to doxorubicin (DOX) is significantly greater than that of NiCo-BTC MOFs/GCE due to the synergic effect between N-GONRs and NiCo-BTC MOFs. The NiCo-BTC MOFs on the modified electrode act as active materials for sensing DOX. The calibration curve for DOX at the NiCo-BTC MOFs/N-GONRs/GCE showed two linear dynamic ranges, 0.01–1.0 and 1.0–80 μmol L–1, with a detection limit of 0.006 μmol L–1 (or 6 nmol L–1), which is less than the DOX concentration in human plasma samples (i.e., 77.2 ± 10.5 nmol L–1). Here, a modified electrode was designed using the large surface area of bimetallic MOFs and conductivity of N-GONRs for the electrochemical sensing of DOX. The current procedure offers a viable solution to the poor conductivity of bimetallic MOFs. Finally, the observed result shows that the proposed NiCo-BTC MOFs/GCE is promising for determining DOX in real samples of human urine and serum.
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