Practical strategy for arsenic(III) electroanalysis without modifier in natural water: triggered by iron group ions in solution

Significant progress has been made in nanomaterial-modified electrodes for highly efficient electroanalysis of arsenic(III) (As(III)). However, the modifiers prepared using some physical methods may easily fall off, and active sites are not uniform, causing the potential instability of the modified...

Full description

Saved in:
Bibliographic Details
Main Authors: Cai, Xin, Xia, Rui-Ze, Ye, Jia-Jia, Huang, Cong-Cong, Yang, Yuan-Fan, Zhang, Long-Ke, Liang, Bo, Yang, Meng, Lin, Chu-Hong, Li, Pei-Hua, Huang, Xing-Jiu
Other Authors: School of Chemistry, Chemical Engineering and Biotechnology
Format: Article
Language:English
Published: 2023
Subjects:
Online Access:https://hdl.handle.net/10356/170138
Tags: Add Tag
No Tags, Be the first to tag this record!
Institution: Nanyang Technological University
Language: English
id sg-ntu-dr.10356-170138
record_format dspace
spelling sg-ntu-dr.10356-1701382023-08-29T06:39:31Z Practical strategy for arsenic(III) electroanalysis without modifier in natural water: triggered by iron group ions in solution Cai, Xin Xia, Rui-Ze Ye, Jia-Jia Huang, Cong-Cong Yang, Yuan-Fan Zhang, Long-Ke Liang, Bo Yang, Meng Lin, Chu-Hong Li, Pei-Hua Huang, Xing-Jiu School of Chemistry, Chemical Engineering and Biotechnology Science::Chemistry Iron Heavy Metals Significant progress has been made in nanomaterial-modified electrodes for highly efficient electroanalysis of arsenic(III) (As(III)). However, the modifiers prepared using some physical methods may easily fall off, and active sites are not uniform, causing the potential instability of the modified electrode. This work first reports a promising practical strategy without any modifiers via utilizing only soluble Fe3+ as a trigger to detect trace-level As(III) in natural water. This method reaches an actual detection limit of 1 ppb on bare glassy carbon electrodes and a sensitivity of 0.296 μA ppb-1 with excellent stability. Kinetic simulations and experimental evidence confirm the codeposition mechanism that Fe3+ is preferentially deposited as Fe0, which are active sites to adsorb As(III) and H+ on the electrode surface. This facilitates the formation of AsH3, which could further react with Fe2+ to produce more As0 and Fe0. Meanwhile, the produced Fe0 can also accelerate the efficient enrichment of As0. Remarkably, the proposed sensing mechanism is a general rule for the electroanalysis of As(III) that is triggered by iron group ions (Fe2+, Fe3+, Co2+, and Ni2+). The interference analysis of coexisting ions (Cu2+, Zn2+, Al3+, Hg2+, Cd2+, Pb2+, SO42-, NO3-, Cl-, and F-) indicates that only Cu2+, Pb2+, and F- showed inhibitory effects on As(III) due to the competition of active sites. Surprisingly, adding iron power effectively eliminates the interference of Cu2+ in natural water, achieving a higher sensitivity for 1-15 ppb As(III) (0.487 μA ppb-1). This study provides effective solutions to overcome the potential instability of modified electrodes and offers a practical sensing platform for analyzing other heavy-metal anions. This work was supported by the National Key R&D Program of China (2021YFB3201400), the National Natural Science Foundation of China (22206187, 21735005, 21802145, 22174144, 22204166), the Key R&D Program of Anhui Province (202104i07020006 and 202104i07020011), the Anhui Provincial Natural Science Foundation (2208085QB57, 2008085QB79), the China Postdoctoral Innovation Talents Supporting Project (BX2021317), the Postdoctoral Researcher Funding Project of Anhui Province (2021B528), the CASHFIPS Director’s Fund (YZJJ2022QN26, YZJJZX202019, YZJJ202102, YZJJ202302-TS), the Special Foundation of President of the Chinese Academy of Sciences, and the Special Project (SXHZ202003) of Science and Technology Cooperation between Fuyang Municipal People’s Government and Fuyang Normal University. 2023-08-29T06:39:31Z 2023-08-29T06:39:31Z 2023 Journal Article Cai, X., Xia, R., Ye, J., Huang, C., Yang, Y., Zhang, L., Liang, B., Yang, M., Lin, C., Li, P. & Huang, X. (2023). Practical strategy for arsenic(III) electroanalysis without modifier in natural water: triggered by iron group ions in solution. Analytical Chemistry, 95(8), 4104-4112. https://dx.doi.org/10.1021/acs.analchem.2c04935 0003-2700 https://hdl.handle.net/10356/170138 10.1021/acs.analchem.2c04935 36688529 2-s2.0-85147015357 8 95 4104 4112 en Analytical Chemistry © 2023 American Chemical Society. All rights reserved.
institution Nanyang Technological University
building NTU Library
continent Asia
country Singapore
Singapore
content_provider NTU Library
collection DR-NTU
language English
topic Science::Chemistry
Iron
Heavy Metals
spellingShingle Science::Chemistry
Iron
Heavy Metals
Cai, Xin
Xia, Rui-Ze
Ye, Jia-Jia
Huang, Cong-Cong
Yang, Yuan-Fan
Zhang, Long-Ke
Liang, Bo
Yang, Meng
Lin, Chu-Hong
Li, Pei-Hua
Huang, Xing-Jiu
Practical strategy for arsenic(III) electroanalysis without modifier in natural water: triggered by iron group ions in solution
description Significant progress has been made in nanomaterial-modified electrodes for highly efficient electroanalysis of arsenic(III) (As(III)). However, the modifiers prepared using some physical methods may easily fall off, and active sites are not uniform, causing the potential instability of the modified electrode. This work first reports a promising practical strategy without any modifiers via utilizing only soluble Fe3+ as a trigger to detect trace-level As(III) in natural water. This method reaches an actual detection limit of 1 ppb on bare glassy carbon electrodes and a sensitivity of 0.296 μA ppb-1 with excellent stability. Kinetic simulations and experimental evidence confirm the codeposition mechanism that Fe3+ is preferentially deposited as Fe0, which are active sites to adsorb As(III) and H+ on the electrode surface. This facilitates the formation of AsH3, which could further react with Fe2+ to produce more As0 and Fe0. Meanwhile, the produced Fe0 can also accelerate the efficient enrichment of As0. Remarkably, the proposed sensing mechanism is a general rule for the electroanalysis of As(III) that is triggered by iron group ions (Fe2+, Fe3+, Co2+, and Ni2+). The interference analysis of coexisting ions (Cu2+, Zn2+, Al3+, Hg2+, Cd2+, Pb2+, SO42-, NO3-, Cl-, and F-) indicates that only Cu2+, Pb2+, and F- showed inhibitory effects on As(III) due to the competition of active sites. Surprisingly, adding iron power effectively eliminates the interference of Cu2+ in natural water, achieving a higher sensitivity for 1-15 ppb As(III) (0.487 μA ppb-1). This study provides effective solutions to overcome the potential instability of modified electrodes and offers a practical sensing platform for analyzing other heavy-metal anions.
author2 School of Chemistry, Chemical Engineering and Biotechnology
author_facet School of Chemistry, Chemical Engineering and Biotechnology
Cai, Xin
Xia, Rui-Ze
Ye, Jia-Jia
Huang, Cong-Cong
Yang, Yuan-Fan
Zhang, Long-Ke
Liang, Bo
Yang, Meng
Lin, Chu-Hong
Li, Pei-Hua
Huang, Xing-Jiu
format Article
author Cai, Xin
Xia, Rui-Ze
Ye, Jia-Jia
Huang, Cong-Cong
Yang, Yuan-Fan
Zhang, Long-Ke
Liang, Bo
Yang, Meng
Lin, Chu-Hong
Li, Pei-Hua
Huang, Xing-Jiu
author_sort Cai, Xin
title Practical strategy for arsenic(III) electroanalysis without modifier in natural water: triggered by iron group ions in solution
title_short Practical strategy for arsenic(III) electroanalysis without modifier in natural water: triggered by iron group ions in solution
title_full Practical strategy for arsenic(III) electroanalysis without modifier in natural water: triggered by iron group ions in solution
title_fullStr Practical strategy for arsenic(III) electroanalysis without modifier in natural water: triggered by iron group ions in solution
title_full_unstemmed Practical strategy for arsenic(III) electroanalysis without modifier in natural water: triggered by iron group ions in solution
title_sort practical strategy for arsenic(iii) electroanalysis without modifier in natural water: triggered by iron group ions in solution
publishDate 2023
url https://hdl.handle.net/10356/170138
_version_ 1779156661282275328