| Literature DB >> 34883378 |
Yixuan Xia1, Yong Zhao2, Fengxiang Ai1, Yinhui Yi1, Tingting Liu1, Huiyu Lin3, Gangbing Zhu4.
Abstract
The present electrochemical stripping analysis (ESA) for multiple heavy metal ions (HMI) generally requires an electrodeposition process at a very low potential below -1.0 V, which inevitably makes the sensing procedures more complex, inefficient and power-wasting. Meanwhile, the emerging MXenes rising-star materials have been studied in various fields recently. While there are only few reports focusing on the heteroatom doping of MXenes, especially no doping-MXenes for electroanalysis. Based on these issues, a novel multifunctional heteroatoms-doped MXenes nanomaterial, N and P co-doped Ti3C2Tx MXenes nanoribbons (N,P-Ti3C2TxR), was prepared herein for the first time, and then N,P-Ti3C2TxR was used as electrode material to propose an electrodeposition-free ESA strategy for multiple HMI (Cu2+, Hg2+). Owing to the unique spontaneous adsorption and reducing capacities of N,P-Ti3C2TxR towards Cu2+ and Hg2+ coupled with the excellent sensing performances, Cu2+ and Hg2+ can undergo self-reduction to be preconcentrated on N,P-Ti3C2TxR surface with the form of Cu0 and Hg0, thus a simple and ultrasensitive electrodeposition-free ESA platform was developed successfully for the simultaneous detection of Cu2+and Hg2+. This work opened a new pathway for the detection for multiple HMI and the preparation/application of heteroatoms doping MXenes.Entities:
Keywords: Electrochemical sensing; Electrodeposition-free; Heavy metal ions; MXenes; Self-reduction
Year: 2021 PMID: 34883378 DOI: 10.1016/j.jhazmat.2021.127974
Source DB: PubMed Journal: J Hazard Mater ISSN: 0304-3894 Impact factor: 10.588