检出限
亚铁氰化物
铁氰化物
铜
牛血清白蛋白
亚铁氰化钾
铁氰化钾
石墨烯
电极
材料科学
选择性
胶体金
电化学气体传感器
电化学
普鲁士蓝
分子印迹聚合物
化学
纳米颗粒
无机化学
纳米技术
色谱法
有机化学
催化作用
物理化学
冶金
作者
Lianming Zhang,Dan Li,Shuhuai Li,Jianping Li,Xionghui Ma,Wei Wang
标识
DOI:10.1016/j.microc.2022.108285
摘要
Despite the promise of ion imprinting technology for the development of electrochemical sensors for heavy metals, improved selectivity and stability are required for practical applications. Herein, a dual recognition strategy based on a protein and an ion-imprinted polymer (IIP) was proposed to develop highly sensitive sensors for copper(II) ions (Cu2+). On Bovine serum albumin (BSA) and graphene oxide (GO)-loaded gold nanoparticles (GO/Au NPs) modify the gold electrode surface, an a Cu2+ IIP was formed on the electrode by electropolymerization. After Cu2+ was removed from IIP, the imprinted holes with a specific recognition ability for Cu2+ were obtained. In the prepared sensor, Cu2+ recognition sites were present in both BSA and the IIP, thus providing a dual recognition strategy for selective Cu2+ detection. Furthermore, owing to the amplification effect of GO/Au NPs, the sensor showed high sensitivity. With potassium ferricyanide/potassium ferrocyanide as a probe, the logarithm of the Cu2+ concentration was proportional to the sensor current response within the range of 1–8000 × 10−14 mol/L, and the detection limit was 1.12 × 10−15 mol/L. Moreover, for Cu2+ detection in actual samples, the sensor exhibited a recovery rate of 93.2–105.6 %.
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