A relative study on sonochemically synthesized mesoporous WS2 nanorods & hydrothermally synthesized WS2 nanoballs towards electrochemical sensing of psychoactive drug (Clonazepam)

被引:41
作者
Chen, Tse-Wei [1 ,2 ]
Rajaji, Umamaheswari [1 ]
Chen, Shen-Ming [1 ]
Ramalingam, R. Jothi [3 ]
机构
[1] Natl Taipei Univ Technol, Dept Chem Engn & Biotechnol, 1,Sect 3,Chung Hsiao East Rd, Taipei 106, Taiwan
[2] Natl Taipei Univ Technol, Res & Dev Ctr Smart Text Technol, 1,Sect 3,Chung Hsiao East Rd, Taipei 106, Taiwan
[3] King Saud Univ, Coll Sci, Surfactant Res Chair, Dept Chem, Riyadh 11451, Saudi Arabia
关键词
Sonochemical synthesis; Transition metal sulfide; Psychoactive drug; Electrochemical detection; Biological samples; Mesoporous nanorods; HYDROGEN EVOLUTION; MONOLAYER WS2; ACUTE LIVER; NANOCOMPOSITE; NANOSHEETS; MOS2; LITHIUM; HEPATOTOXICITY; EXFOLIATION; PERFORMANCE;
D O I
10.1016/j.ultsonch.2019.02.012
中图分类号
O42 [声学];
学科分类号
070206 ; 082403 ;
摘要
In this paper, mesoporous tungsten sulfide electrocatalyst (MP-WS2) were developed through a facile sonochemical technique (SC) and utilized as an electrocatalyst for the sensitive electrochemical detection of Psychoactive drug. The as-prepared SC-MP-WS2 NRs and HT-WS2 NPs (hydrothermally synthesized) were characterized using XRD, Raman, XPS, FESEM, HRTEM, BET, EDX, and electrochemical analysis, which exposed the formation of WS2 in the form of mesoporous nanorods in shape. Further, the use of the as-developed SC-MPWS2 NRs and HT-WS2 NPs as an electrocatalyst for the detection of clonazepam (CNP). Interestingly, the SC-MPWS2 NRs modified screen-printed carbon electrode (SC-MP-WS2 NRs/SPCE) exhibited an excellent electrocatalytic performance, and enhanced reduction peak current when compared to HT-WS2 NPs with unmodified electrode. Moreover, as-prepared SC-MP-WS2 NRs/SPCE displayed wide linear response range (10-551 mu M), lower detection limit (2.37 nM) and high sensitivity (24.32 mu A mu M(-1)cm(-2)). Furthermore, SC-MP-WS2 NRs/SPCE showed an excellent selectivity even in the existence of potentially co-interfering compounds. The proposed sensor was successfully applied for the determination of CNP in biological and drug samples with acceptable recovery.
引用
收藏
页码:79 / 89
页数:11
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