Role of Br- on the Formation of a Bismuth Nanodendrite Structure and Its Use as an Electrochemical Sensor for Heavy Metal Detectionopen access
- Authors
- Anh, Nguyen Hoang; Duy, Pham Khac; Yen, Pham Thi Hai; Hung, Le Quoc; Phong, Pham Hong; Ha, Vu Thi Thu; Chung, Hoeil
- Issue Date
- Jun-2020
- Publisher
- ESG
- Citation
- INTERNATIONAL JOURNAL OF ELECTROCHEMICAL SCIENCE, v.15, no.6, pp.5373 - 5384
- Indexed
- SCIE
SCOPUS
- Journal Title
- INTERNATIONAL JOURNAL OF ELECTROCHEMICAL SCIENCE
- Volume
- 15
- Number
- 6
- Start Page
- 5373
- End Page
- 5384
- URI
- https://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/145656
- DOI
- 10.20964/2020.06.45
- ISSN
- 1452-3981
- Abstract
- Bismuth nanodendrites (BiNDs) were fabricated by simple, one-step electrodeposition of Bi and employed for simultaneous detection of Cd2+ and Pb2+ in water samples. To construct reliable BiNDs on a glassy carbon electrode (BiND@GCE) without agglomeration and structural imperfections, Br- was used as a co-reagent to prohibit agglomeration of Bi. The simultaneously generated hydrogen bubbles from H-2 evolution at the surface during Bi deposition could largely cover potential nucleation sites and subsequently suppress the fast agglomeration of Bi. Britton-Robinson buffer, which allowed the formation of BiPO4 on the surface, was used to ensure the stability of the BiNDs during the electrochemical scans. When BiND@GCE was used to measure Cd2+ and Pb2+ concentrations in aqueous standard samples (concentration range: 2-270 ppb), the achieved limits of detection (LODs) were 0.09 (Cd2+) and 0.05 (Pb2+) ppb. Next, when real field samples obtained from the river and sea were analyzed with BiND@GCE and the subsequent results were compared with those obtained using inductively coupled plasma mass spectrometry, the measurements were accurate, with a recovery range of 89.9-99.3%. Overall, BiNDs represent a versatile electrochemical sensing material, especially for on-site water analysis, with low cost and no serious concern of environmental contamination.
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