材料科学
双金属片
电极
检出限
催化作用
纳米线
电化学
选择性
镍
可逆氢电极
钴
化学工程
过氧化氢
纳米技术
无机化学
工作电极
冶金
化学
色谱法
金属
有机化学
物理化学
工程类
作者
Muhammad Asif Hussain,Amjad Nisar,Lizhi Qian,Shafqat Karim,Maaz Khan,Yanguo Liu,Hongyu Sun,Mashkoor Ahmad
出处
期刊:Nanotechnology
[IOP Publishing]
日期:2021-02-10
卷期号:32 (20): 205501-205501
被引量:20
标识
DOI:10.1088/1361-6528/abe4fb
摘要
Abstract The development of a highly sensitive and selective non-enzymatic electrode catalyst for the detection of a target molecule was remained a great challenge. In this regard, bimetallic nanowires (BMNWs) are considered as promising electrode material for their fascinating physical/chemical properties superior to a single system. In this article, nickel cobalt (Ni x –Co) BMNWs with tunable stoichiometry were prepared by a template assisted electrodeposition method and their catalytic performance was investigated for the detection of hydrogen peroxide (H 2 O 2 ). It has been found that Ni–Co (0.5:1) BMNWs/PC electrode exhibits superior non-enzymatic sensing ability toward H 2 O 2 detection with a high selectivity. The electrode shows fast response within ∼3 s and an excellent reproducible sensitivity of 2211.4 μ AmM −1 cm −2 , which is the best compared to the individual Ni, Co, Ni–Co (0.3:1) BMNWs and previously reported electrodes. In addition, the electrode shows a linear response in the wide concentration range from 0.005 mM to 9 mM, low detection limit of 0.5 μ M (S/N = 3.2) and a relatively long-term storage (50 d). Moreover, the sensor reveals excellent results for H 2 O 2 detection in the real samples. The enhanced sensitivity of the Ni–Co (0.5:1) BMNWs based electrode may be due to the stable structure and synergy of Ni and Co. The results demonstrate that the catalytic activity of the electrode binary catalyst towards H 2 O 2 detection can be improved by adjusting the Ni/Co ratio in BMNWs. The excellent performance of the electrode suggests that Ni–Co BMNWs are promising candidate for the construction of cost-effective electrochemical sensors for medical and industrial applications.
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