Highly stable Ti3C2Tx (MXene)/Pt nanoparticles-modified glassy carbon electrode for H2O2 and small molecules sensing applications

被引:224
作者
Lorencova, Lenka [1 ]
Bertok, Tomas [1 ]
Filip, Jaroslav [2 ]
Jerigova, Monika [3 ,4 ]
Velic, Dusan [3 ,4 ]
Kasak, Peter [5 ]
Mahmoud, Khaled A. [6 ]
Tkac, Jan [1 ]
机构
[1] Slovak Acad Sci, Inst Chem, Dubravska Cesta 9, Bratislava 84538, Slovakia
[2] Tomas Bata Univ Zlin, Dept Environm Protect Engn, Vavreckova 275, Zlin 76272, Czech Republic
[3] Comenius Univ, Dept Phys Chem, Fac Nat Sci, Bratislava 84215, Slovakia
[4] Int Laser Ctr, Ilkovicova 3, Bratislava 84104, Slovakia
[5] Qatar Univ, Ctr Adv Mat, POB 2713, Doha, Qatar
[6] Hamad Bin Khalifa Univ, QEERI, Qatar Fdn, POB 34110, Doha, Qatar
基金
欧洲研究理事会;
关键词
T-x MXene; H2O2; sensor; Pt nanoparticles; Nafion; Chitosan; Redox stability; PT BIMETALLIC NANOPARTICLES; HYDROGEN-PEROXIDE; ASCORBIC-ACID; ELECTROCHEMICAL DETECTION; PLATINUM NANOPARTICLES; URIC-ACID; GRAPHENE; DOPAMINE; COMPOSITE; BIOSENSOR;
D O I
10.1016/j.snb.2018.02.124
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Electrochemical performance of a 2D Ti3C2Tx (MXene, where T: =0, OH, F) sheets modified with Pt nanoparticles (PtNPs) was investigated. The results showed that Ti3C2Tx/PtNP nanocomposite deposited on the surface of GCE showed much better and stable redox behavior in an anodic potential window as compared to the GCE modified with pristine Ti3C2Tx MXene. For example, the H2O2 sensor of Ti3C2Tx/PtNP on GCE offered LOD of 448 nM with a potential at which reduction starts of-+250 mV (vs. Ag/AgC1) in comparison to values of 883 OA and similar to-160 mV observed for Ti3C2Tx modified GCE. Moreover, the Ti3C2Tx/PtNP sensor could detect small redox molecules such as ascorbic acid (AA), dopamine (DA), uric acid (UA) and acetaminophen (APAP) at a potential higher than similar to+250 mV with high selectivity and LOD down to nM level. We proved that selectivity of detection of such molecules (AA, DA, UA and APAP) could be modulated to high extent using external membranes. (C) 2018 Elsevier B.V. All rights reserved.
引用
收藏
页码:360 / 368
页数:9
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