SwePub
Sök i LIBRIS databas

  Utökad sökning

WFRF:(Liu Yujie)
 

Sökning: WFRF:(Liu Yujie) > Voltammetric Ion-Se...

Voltammetric Ion-Selective Electrodes in Thin-Layer Samples : Absolute Detection of Ions Using Ultrathin Membranes

Liu, Yujie, 1995- (författare)
KTH,Kemi
Crespo, Gaston A., 1980- (författare)
KTH,Tillämpad fysikalisk kemi,Univ Catolica San Antonio Murcia, UCAM SENS, UCAM HiTech, Murcia 30107, Spain.
Cuartero, Maria, PhD, 1984- (författare)
KTH,Tillämpad fysikalisk kemi,Univ Catolica San Antonio Murcia, UCAM SENS, UCAM HiTech, Murcia 30107, Spain.
 (creator_code:org_t)
American Chemical Society (ACS), 2024
2024
Engelska.
Ingår i: Analytical Chemistry. - : American Chemical Society (ACS). - 0003-2700 .- 1520-6882. ; 96:3, s. 1147-1155
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
Stäng  
  • Calibration-free sensors are generally understood as analytical tools with no need for calibration apart from the initial one (i.e., after its fabrication). However, an "ideal" and therefore "more restricted" definition of the concept considers that no calibration is necessary at all, with the sensor being capable of directly providing the analyte concentration in the sample. In the electroanalysis field, investigations have been directed to charge-based readouts (i.e., coulometry) that allow for concentration calculation via the Faraday Law: The sample volume must be precisely defined and the absoluteness of the electrochemical process in which the analyte is involved must be ensured (i.e., the analyte in the sample is similar to 100% converted/transported). Herein, we report on the realization of calibration-free coulometric ISEs based on ultrathin ion-selective membranes, which is demonstrated for the detection of potassium ions (K+). In essence, the K+ transfer at the membrane-sample interface is modulated by the oxidation state of the conducting polymer underlying the membrane. The accumulation/release of K+ to/from the membrane is an absolute process owing to the confinement of the sample to a thin-layer domain (thickness of <100 mu m). The capacity of the membrane expressed in charge is fixed to ca. 18 mu C, and this dictates the detection of micromolar levels of K+ present in ca. 5 mu L sample volume. The system is interrogated with cyclic voltammetry to obtain peaks related to the K+ transfer that can be treated charge-wise. The conceptual and technical innovative steps developed here made the calibration-free detection of K+ possible in artificial and real samples with acceptable accuracy (<10% difference compared with the results obtained from a current-based calibration and ion chromatography). The charge-based analysis does not depend on temperature and appeared to be repetitive, reproducible, and reversible in the concentration range from 1 to 37.5 mu M, with an average coulometry efficiency of 96%.

Ämnesord

NATURVETENSKAP  -- Kemi -- Analytisk kemi (hsv//swe)
NATURAL SCIENCES  -- Chemical Sciences -- Analytical Chemistry (hsv//eng)

Publikations- och innehållstyp

ref (ämneskategori)
art (ämneskategori)

Hitta via bibliotek

Till lärosätets databas

Hitta mer i SwePub

Av författaren/redakt...
Liu, Yujie, 1995 ...
Crespo, Gaston A ...
Cuartero, Maria, ...
Om ämnet
NATURVETENSKAP
NATURVETENSKAP
och Kemi
och Analytisk kemi
Artiklar i publikationen
Analytical Chemi ...
Av lärosätet
Kungliga Tekniska Högskolan

Sök utanför SwePub

Kungliga biblioteket hanterar dina personuppgifter i enlighet med EU:s dataskyddsförordning (2018), GDPR. Läs mer om hur det funkar här.
Så här hanterar KB dina uppgifter vid användning av denna tjänst.

 
pil uppåt Stäng

Kopiera och spara länken för att återkomma till aktuell vy