Nikos G. Tsierkezos, Alexandra Karagianni, Eike Felix Reddmann, Uwe Ritter, David E. Sanchez, Mauricio Terrones, Konstantinos V. Kordatos
{"title":"硫氮共掺杂多壁碳纳米管作为电化学同时测定生物分子的传感器","authors":"Nikos G. Tsierkezos, Alexandra Karagianni, Eike Felix Reddmann, Uwe Ritter, David E. Sanchez, Mauricio Terrones, Konstantinos V. Kordatos","doi":"10.1007/s10008-024-06157-1","DOIUrl":null,"url":null,"abstract":"<div><p>Multi-walled carbon nanotubes co-doped with sulfur and nitrogen (S–N-MWCNTs) were produced onto silicon/silicon oxide by means of chemical vapor deposition (CVD) upon decomposition of dimethyl sulfoxide (DMSO) and acetonitrile (ACN) in the presence of ferrocene (FeCp<sub>2</sub>). The synthesized S–N-MWCNTs were characterized by means of scanning electron microscopy (SEM), transmission electron microscopy (TEM) combined with energy dispersive X-ray spectroscopy (EDX), Raman spectroscopy, and electrochemical impedance spectroscopy (EIS). The electrochemical response of S–N-MWCNTs towards oxidation of ascorbic acid (AA), dopamine (DA), uric acid (UA), and glucose (GL) was investigated in phosphate buffer solution (PBS) (pH 7.4) by means of cyclic voltammetry (CV). Strong dependence of electrochemical quality of S–N-MWCNTs on the concentration of decomposed DMSO precursor was observed. Namely, upon increasing the percentage of decayed DMSO from 1.0 up to 2.0% wt., the electrocatalytic activity of S–N-MWCNTs tends to improve. The separations of oxidation waves between AA-DA, DA-UA, and AA-UA reached their maximum values on S–N-MWCNTs-3, fabricated upon decomposition of 2.0% wt. DMSO precursor, permitting their individual and simultaneous electrochemical determination. Strong interference of GL in the analysis of DA was observed, and consequently, simultaneous analysis of AA, DA, and UA can be only carried out in the absence of GL. A great influence of concentration of decomposed DMSO precursor on the sensitivity of S–N-MWCNTs was also observed. Specifically, upon increasing the percentage of decayed DMSO from 1.0 up to 2.0% wt., the sensitivity and detection capability of S–N-MWCNTs towards AA, DA, UA, and GL analytes tend to enhance.</p></div>","PeriodicalId":665,"journal":{"name":"Journal of Solid State Electrochemistry","volume":"29 5","pages":"1945 - 1961"},"PeriodicalIF":2.6000,"publicationDate":"2024-11-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://link.springer.com/content/pdf/10.1007/s10008-024-06157-1.pdf","citationCount":"0","resultStr":"{\"title\":\"Multi‐walled carbon nanotubes co‐doped with sulfur and nitrogen as sensors for the simultaneous electrochemical determination of biomolecules\",\"authors\":\"Nikos G. Tsierkezos, Alexandra Karagianni, Eike Felix Reddmann, Uwe Ritter, David E. Sanchez, Mauricio Terrones, Konstantinos V. Kordatos\",\"doi\":\"10.1007/s10008-024-06157-1\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>Multi-walled carbon nanotubes co-doped with sulfur and nitrogen (S–N-MWCNTs) were produced onto silicon/silicon oxide by means of chemical vapor deposition (CVD) upon decomposition of dimethyl sulfoxide (DMSO) and acetonitrile (ACN) in the presence of ferrocene (FeCp<sub>2</sub>). The synthesized S–N-MWCNTs were characterized by means of scanning electron microscopy (SEM), transmission electron microscopy (TEM) combined with energy dispersive X-ray spectroscopy (EDX), Raman spectroscopy, and electrochemical impedance spectroscopy (EIS). The electrochemical response of S–N-MWCNTs towards oxidation of ascorbic acid (AA), dopamine (DA), uric acid (UA), and glucose (GL) was investigated in phosphate buffer solution (PBS) (pH 7.4) by means of cyclic voltammetry (CV). Strong dependence of electrochemical quality of S–N-MWCNTs on the concentration of decomposed DMSO precursor was observed. Namely, upon increasing the percentage of decayed DMSO from 1.0 up to 2.0% wt., the electrocatalytic activity of S–N-MWCNTs tends to improve. The separations of oxidation waves between AA-DA, DA-UA, and AA-UA reached their maximum values on S–N-MWCNTs-3, fabricated upon decomposition of 2.0% wt. DMSO precursor, permitting their individual and simultaneous electrochemical determination. Strong interference of GL in the analysis of DA was observed, and consequently, simultaneous analysis of AA, DA, and UA can be only carried out in the absence of GL. A great influence of concentration of decomposed DMSO precursor on the sensitivity of S–N-MWCNTs was also observed. 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Multi‐walled carbon nanotubes co‐doped with sulfur and nitrogen as sensors for the simultaneous electrochemical determination of biomolecules
Multi-walled carbon nanotubes co-doped with sulfur and nitrogen (S–N-MWCNTs) were produced onto silicon/silicon oxide by means of chemical vapor deposition (CVD) upon decomposition of dimethyl sulfoxide (DMSO) and acetonitrile (ACN) in the presence of ferrocene (FeCp2). The synthesized S–N-MWCNTs were characterized by means of scanning electron microscopy (SEM), transmission electron microscopy (TEM) combined with energy dispersive X-ray spectroscopy (EDX), Raman spectroscopy, and electrochemical impedance spectroscopy (EIS). The electrochemical response of S–N-MWCNTs towards oxidation of ascorbic acid (AA), dopamine (DA), uric acid (UA), and glucose (GL) was investigated in phosphate buffer solution (PBS) (pH 7.4) by means of cyclic voltammetry (CV). Strong dependence of electrochemical quality of S–N-MWCNTs on the concentration of decomposed DMSO precursor was observed. Namely, upon increasing the percentage of decayed DMSO from 1.0 up to 2.0% wt., the electrocatalytic activity of S–N-MWCNTs tends to improve. The separations of oxidation waves between AA-DA, DA-UA, and AA-UA reached their maximum values on S–N-MWCNTs-3, fabricated upon decomposition of 2.0% wt. DMSO precursor, permitting their individual and simultaneous electrochemical determination. Strong interference of GL in the analysis of DA was observed, and consequently, simultaneous analysis of AA, DA, and UA can be only carried out in the absence of GL. A great influence of concentration of decomposed DMSO precursor on the sensitivity of S–N-MWCNTs was also observed. Specifically, upon increasing the percentage of decayed DMSO from 1.0 up to 2.0% wt., the sensitivity and detection capability of S–N-MWCNTs towards AA, DA, UA, and GL analytes tend to enhance.
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The Journal of Solid State Electrochemistry is devoted to all aspects of solid-state chemistry and solid-state physics in electrochemistry.
The Journal of Solid State Electrochemistry publishes papers on all aspects of electrochemistry of solid compounds, including experimental and theoretical, basic and applied work. It equally publishes papers on the thermodynamics and kinetics of electrochemical reactions if at least one actively participating phase is solid. Also of interest are articles on the transport of ions and electrons in solids whenever these processes are relevant to electrochemical reactions and on the use of solid-state electrochemical reactions in the analysis of solids and their surfaces.
The journal covers solid-state electrochemistry and focusses on the following fields: mechanisms of solid-state electrochemical reactions, semiconductor electrochemistry, electrochemical batteries, accumulators and fuel cells, electrochemical mineral leaching, galvanic metal plating, electrochemical potential memory devices, solid-state electrochemical sensors, ion and electron transport in solid materials and polymers, electrocatalysis, photoelectrochemistry, corrosion of solid materials, solid-state electroanalysis, electrochemical machining of materials, electrochromism and electrochromic devices, new electrochemical solid-state synthesis.
The Journal of Solid State Electrochemistry makes the professional in research and industry aware of this swift progress and its importance for future developments and success in the above-mentioned fields.
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