The first use of a Rh(III) complex as a novel ionophore for thiocyanate-selective polymeric membrane electrodes

The feasibility of a newly synthesized Rh(III) complex, Rh[(trpy)(bpy)Cl](PF₆)₂, as a novel ionophore for the preparation of anion-selective polymeric membrane electrodes was tested. The ionophore exhibited anti-Hofmeister behavior with enhanced potentiometric selectivity toward thiocyanate ion compared to other anions. The influence of some experimental parameters such as membrane composition, nature and amount of plasticizer and additive and concentration of internal solution on the potential response of the SCN⁻ sensor were investigated. The electrode exhibits a Nernstian response for SCN⁻ over a wide concentration range (1.0 × 10⁻⁵ to 1.0 × 10⁻¹ M) with a slope −58.7 ± 0.5 mV per decade and a detection limit of 4.0 × 10⁻⁶ M (0.23 ppm). It could be used in a pH range of 3.0-8.0 and has a fast response time of about 15 s. The proposed sensor was used for the determination of thiocyanate ions in real samples such as urine and saliva of smokers and nonsmokers and, as an indicator electrode, in potentiometric titrations of SCN⁻ ion.     

Photovoltammetric behavior and photoelectrochemical determination of p-phenylenediamine on CdS quantum dots and graphene hybrid film

A photoelectroactive film composed of CdS quantum dots and graphene sheets (GS) was coated on F-doped SnO₂ (FTO) conducting glass for studying the electrochemical response of p-phenylenediamine (PPD) under photoirradiation. The result indicated that the cyclic voltammogram of PPD on CdS–GS hybrid film became sigmoidal in shape after exposed under visible light, due to the photoelectrocatalytic reaction. Such a photovoltammetric response was used to rapidly optimize the photoelectrocatalytic activity of hybrid films composed of different ratios of CdS to GS toward PPD. The influences of scan rate and pH on the photovoltammetric behavior of PPD on CdS–GS film revealed that although the controlled step for electrochemical process was not changed under photoirradiation, more electrons than protons might participate the photoelectrocatalytic process. Furthermore, the photoelectroactive CdS–GS hybrid film was explored for PPD determination based on the photocurrent response of film toward PPD. Under optimal conditions, the photocurrent signal on CdS–GS film was linearly proportional to the concentration of PPD ranging from 1.0 × 10⁻⁷ to 3.0 × 10⁻⁶ mol L⁻¹, with a detection limit (3S/N) of 4.3 × 10⁻⁸ mol L⁻¹. Our work based on CdS–GS hybrid film not only demonstrated a new facile photovoltammetric way to study the photoinduced electron transfer process of PPD, but also developed a sensitive photoelectrochemical strategy for PPD determination.     

A novel nonenzymatic hydrogen peroxide sensor based on multi-wall carbon nanotube/silver nanoparticle nanohybrids modified gold electrode

A novel strategy to fabricate hydrogen peroxide (H₂O₂) sensor was developed based on multi-wall carbon nanotube/silver nanoparticle nanohybrids (MWCNT/Ag nanohybrids) modified gold electrode. The process to synthesize MWCNT/Ag nanohybrids was facile and efficient. In the presence of carboxyl groups functionalized multi-wall carbon nanotubes (MWCNTs), silver nanoparticles (Ag NPs) were in situ generated from AgNO₃ aqueous solution and readily attached to the MWCNTs convex surfaces at room temperature, without any additional reducing reagent or irradiation treatment. The formation of MWCNT/Ag nanohybrids product was observed by transmission electron microscope (TEM), and the electrochemical properties of MWCNT/Ag nanohybrids modified gold electrode were characterized by electrochemical measurements. The results showed that this sensor had a favorable catalytic ability for the reduction of H₂O₂. The resulted sensor could detect H₂O₂ in a linear range of 0.05-17 mM with a detection limit of 5 × 10⁻⁷ M at a signal-to-noise ratio of 3. The sensitivity was calculated as 1.42 μA/mM at a potential of −0.2 V. Additionally, it exhibited good reproducibility, long-term stability and negligible interference of ascorbic acid (AA), uric acid (UA), and acetaminophen (AP).     

Fabrication of a new electrochemiluminescent sensor for fentanyl citrate based on glassy carbon microspheres and ionic liquid composite paste electrode

Due to the high performance of glassy carbon in the aspects of mechanical strength, electrical conductivity and high corrosion resistance, etc., glassy carbon has been widely used in the electrochemistry. A new form of glassy carbon, glassy carbon microsphere, was utilized to couple with ionic liquid in preparing a new electrochemiluminescent platform for Ru(bpy)₃Cl₂. Room temperature ionic liquid has been proposed to be very interesting and efficient pasting binder to replace the non conductive organic binders for the fabrication of composite paste electrode. Attributed to the special characteristics of glassy carbon microspheres and room temperature ionic liquid [N-octylpyridium tetrafluoroborate (OPFP)], this new electrochemiluminescent sensor exhibited excellent electrochemiluminescent performance in Ru(bpy)₃²⁺ solution. We first found that fentanyl citrate could increase the ECL of Ru(bpy)₃²⁺, hence an ECL approach was developed for the determination of fentanyl citrate based on this glassy carbon microspheres based electrochemiluminescent platform with high sensitivity. Under the optimized conditions, the enhanced electrochemiluminescent intensity versus fentanyl citrate concentration was linear in the range of 1.0 × 10⁻⁸ to 1.0 × 10⁻⁴ mol L⁻¹ with a detection limit of 8.5 × 10⁻⁹ mol L⁻¹, and the relative standard deviation for 1.0 × 10⁻⁶ mol L⁻¹ fentanyl citrate was 1.90% (n = 10). This protocol has extended the application scopes of glassy carbon material and promoted the application of glassy carbon microspheres in electroanalysis.     

Electrochemiluminescence from tris(2,2′-bipyridyl)ruthenium(II)-graphene-Nafion modified electrode

An electrochemiluminescence (ECL) sensor based on Ru(bpy)₃²⁺-graphene-Nafion composite film was developed. The graphene sheet was produced by chemical conversion of graphite, and was characterized by atomic force microscopy (AFM), scanning electron microscopy (SEM), and Raman spectroscopy. The introduction of conductive graphene into Nafion not only greatly facilitates the electron transfer of Ru(bpy)₃²⁺, but also dramatically improves the long-term stability of the sensor by inhibiting the migration of Ru(bpy)₃²⁺ into the electrochemically inactive hydrophobic region of Nafion. The ECL sensor gives a good linear range over 1 × 10⁻⁷ to 1 × 10⁻⁴ M with a detection limit of 50 nM towards the determination of tripropylamine (TPA), comparable to that obtained by Nafion-CNT. The ECL sensor keeps over 80% and 85% activity towards 0.1 mM TPA after being stored in air and in 0.1 M pH 7.5 phosphate buffer solution (PBS) for a month, respectively. The long-term stability of the modified electrode is better than electrodes modified with Nafion, Nafion-silica, Nafion-titania, or sol-gel films containing Ru(bpy)₃²⁺. Furthermore, the ECL sensor was successfully applied to the selective and sensitive determination of oxalate in urine samples.     

A novel gaseous pinacolyl alcohol sensor utilizing cataluminescence on alumina nanowires prepared by supercritical fluid drying

A cataluminescence (CTL) sensor using Al₂O₃ nanowires as the sensing material was developed for the determination of trace pinacolyl alcohol in air samples based on the catalytic chemiluminescence (CL) of pinacolyl alcohol on Al₂O₃ nanowires. Eight catalysts were examined and the CL intensity on Al₂O₃ nanowires prepared by supercritical fluid drying was the strongest. This novel CL sensor showed high sensitivity and selectivity to gaseous pinacolyl alcohol at optimal temperature of 340 °C. Quantitative analysis was performed at a wavelength of 460 nm. The linear range of CTL intensity versus concentration of gaseous pinacolyl alcohol was 0.09 × 10⁻⁶ to 2.56 × 10⁻⁶ g mL⁻¹ (r = 0.9983, n = 6) with a detection limit (3σ) of 0.0053 × 10⁻⁶ g mL⁻¹. None or only very low levels of interference were observed while the foreign substances such as water vapor, ethanol, ammonia, chloroform, benzene, nitrogen dioxide, methylbenzene, hydrochloric acid, methanol and butanol were passing through the sensor. The response time of the sensor is less than 100 s, and the sensor had a long lifetime more than 60 h. The sensor would be potentially applied to analysis of the nerve agents such as Soman.     

A novel nonenzymatic sensor based on LaNi0.6Co0.4O3 modified electrode for hydrogen peroxide and glucose

In this paper, LaNi_0.6Co_0.4O₃ (LNC) nanoparticles were synthesized by the sol–gel method, and the structure and morphology of LNC nanoparticles were characterized by X-ray diffraction spectrum, scanning electron microscopy and transmitting electron microscopy. And then, LNC was used to modify carbon paste electrode (CPE) without any adhesive to fabricate hydrogen peroxide and glucose sensor, and the results demonstrated that LNC exhibited strong electrocatalytical activity by cyclic voltammetry and amperometry. In H₂O₂ determination, linear response was obtained in the concentration range of 10 nM–100 μM with a detection limit of 1.0 nM. In glucose determination, there was the linear region of 0.05–200 μM with a detection limit of 8.0 nM. Compared with other reports, the proposed sensor also displayed high sensitivity toward H₂O₂ (1812.84 μA mM⁻¹ cm⁻²) and glucose (643.0 μA mM⁻¹ cm⁻²). Moreover, this prepared sensor was applied to detect glucose in blood serum and hydrogen peroxide in toothpaste samples with satisfied results, indicating its possibility in practical application.     

A novel amperometric sensor for the detection of difenidol hydrochloride based on the modification of Ru(bpy)3 on a glassy carbon electrode

An amperometric sensor for the detection of difenidol, a tertiary amine-containing analyte, was proposed. Ruthenium(II) tris(bipyridine)/multi-walled carbon nanotubes/Nafion composite film was suggested to modify the glassy carbon electrode. The modified electrode was shown to be an excellent amperometric sensor for the detection of difenidol hydrochloride. The linear range is from 1.0 × 10⁻⁶ to 3.3 × 10⁻⁵ M with a correlation coefficient of 0.998. The limit of detection was 5 × 10⁻⁷ M, which was obtained through experimental determination based on a signal-to-noise ratio of three. The sensor was employed to the determination of the active ingredients in the tablets containing difenidol hydrochloride.     

3D nanostructured Ni(OH)2 microspheres as an efficient immobilization matrix of Ru(bpy)3 for high-performance electrochemiluminescence sensor

The electrochemistry and electrochemiluminescence (ECL) of novel three-dimensional nanostructured Ru(bpy)₃²⁺/Ni(OH)₂ microspheres were investigated for the first time. The negatively charged porous Ni(OH)₂ microspheres composed of Ni(OH)₂ nanowires were specifically designed to interact with Ru(bpy)₃²⁺. The large surface area and porous structure of Ni(OH)₂ microspheres enhance loading of Ru(bpy)₃²⁺ and mass transport of the model analyte, tripropylamine (TPA). Excellent ECL performance of the presented sensor was achieved including good stability and wide linear range from 7.7 × 10⁻¹⁰ to 3.8 × 10⁻³ M with the detection limit of 2.6 × 10⁻¹⁰ M to TPA.     

Application of 2-mercaptobenzothiazole self-assembled monolayer on polycrystalline gold electrode as a nanosensor for determination of Ag(I)

Fabrication and application of a voltammetric sensor based on gold 2-mercaptobenzothiazole self-assembled monolayer (Au-MBT SAM) for determination of silver ion is described. Preliminary experiments were performed to characterize the monolayer. The surface pK_a determined for the MBT monolayer is 7.0. This value was obtained by impedimetric titration of the monolayer in the presence of Fe(CN)₆^3−/4− as a redox probe. The extent of surface coverage was evaluated as 1.52 × 10⁻⁹ mol cm⁻² based on charged consumed for reductive desorption of the monolayer in the 0.50 M NaOH solution. Then the sensor was used for determination of Ag(I) by square wave voltammetry. The parameters affecting the sensor response, such as pH and supporting electrolyte, were optimized. A dynamic calibration curve with two linear parts was obtained in the concentration ranges of 5 × 10⁻⁸-8 × 10⁻⁷ and 1 × 10⁻⁶-1 × 10⁻⁵ M of Ag(I). The detection limit adopted from cathodic striping square wave voltammetry was as 1 × 10⁻⁸ M for n = 7. Furthermore, the effect of potential interfering ions on the determination of Ag(I) was studied, and an appropriate method was used for the elimination of this effect.     

Disposable biosensor based on cathodic electrochemiluminescence of tris(2,2-bipyridine)ruthenium(II) for uric acid determination

A new method for uric acid (UA) determination based on the quenching of the cathodic ECL of the tris(2,2-bipyridine)ruthenium(II)–uricase system is described. The biosensor is based on a double-layer design containing first tris(2,2-bipyridine)ruthenium(II) (Ru(bpy)₃²⁺) electrochemically immobilized on graphite screen-printed cells and uricase in chitosan as a second layer. The uric acid biosensing is based on the ECL quenching produced by uric acid over the cathodic ECL caused by immobilized Ru(bpy)₃²⁺ in the presence of uricase. The use of a −1.1 V pulse for 1 s with a dwelling time of 10 s makes it possible to estimate the initial enzymatic rate, which is used as the analytical signal. The Stern–Volmer type calibration function shows a dynamic range from 1.0 × 10⁻⁵ to 1.0 × 10⁻³ M with a limit of detection of 3.1 × 10⁻⁶ M and an accuracy of 13.6% (1.0 × 10⁻⁴ M, n = 5) as relative standard deviation. Satisfactory results were obtained for urine samples, creating an affordable alternative for uric acid determination.     

Ultrasensitive fluorometric determination of hydrogen peroxide and glucose by using multiferroic BiFeO3 nanoparticles as a catalyst

BiFeO₃ magnetic nanoparticles (BFO MNPs) are used as a catalyst to develop an ultrasensitive method for the determination of H₂O₂. It is found that BFO MNPs can catalyze the decomposition of H₂O₂ to produce OH radicals, which in turn oxidize the weakly fluorescent benzoic acid to a strongly fluorescent hydroxylated product with a maximum emission at 405 nm. This makes it possible to sensitively quantify traces of H₂O₂. Under optimized conditions, the fluorescence intensity is observed to be well linearly correlated with H₂O₂ concentration from 2.0 × 10⁻⁸ to 2.0 × 10⁻⁵ mol L⁻¹ with a detection limit of 4.5 × 10⁻⁹ mol L⁻¹ (S/N = 3). In addition, a selective method for glucose determination is developed by using both glucose oxidase and BFO MNPs, which has a linear range for glucose concentration from 1.0 × 10⁻⁶ to 1.0 × 10⁻⁴ mol L⁻¹ with a detection limit of 5.0 × 10⁻⁷ mol L⁻¹. These new methods have been successfully applied for the determination of H₂O₂ in rainwater and glucose in human serum samples.     

Multi-walled carbon nanotubes and Ru(bpy)3/nano-Au nano-sphere as efficient matrixes for a novel solid-state electrochemiluminescence sensor

An effective method for immobilization of Ru(bpy)₃²⁺ on glassy carbon electrode surface (GCE) is developed for the preparation of a novel electrochemiluminescence sensor. First of all, the positively charged Ru(bpy)₃²⁺ is modified on the surface of negatively charged gold nanoparticles (nano-Au) via the electrostatic interactions to obtain the Ru(bpy)₃²⁺/nano-Au nano-sphere (abbreviate as Ru-AuNPs). Subsequently, the large amount of Ru-AuNPs are immobilized on the multi-wall carbon nanotubes (MWCNTs)-Nafion homogeneous composite coated GCE by dual interaction: firstly, the Nafion, a kind of typical cation-exchange membrane, can absorb the Ru-AuNPs as the enrichment of cation Ru(bpy)₃²⁺ on the Ru-AuNPs surface; secondly, the employment of carboxylic MWCNTs in the Nafion film can also chemosorb the Ru(bpy)₃²⁺ cation on the Ru-AuNPs surface to increase the carrier content. At the same time, the experiment confirms that the enhancement of the ECL intensity on the sensor is attributed to following reasons. One hand, the employment of MWCNTs in the Nafion film enlarged the electro-active surface areas to benefit the contact between the signal probe on the composite film and coreactant used as reinforcing agent. On the other hand, the nano-materials of MWCNTs and nano-Au also improve the conductivity of the assembled film to increase the quantity of excited state of Ru(bpy)₃²⁺ in the unit time under the electrochemical condition and finally cause better properties in luminescence. In the experiment, the influence of the coreactant tripropylamine (TPA) on proposed ECL sensor is investigated. The logarithm of ECL intensity is proportional to the logarithm of TPA concentration on the range of 4 × 10⁻¹⁰ M to 2.8 × 10⁻⁶ M and 2.8 × 10⁻⁶ M to 0.71 × 10⁻³ M. After optimizing these conditions, the ECL sensor with TPA as coreactant is employed to detect a kind of alkaloid medicine, Matrine, for evaluating the practical application in the medicine analysis. The present sensor with TPA as coreactant shows the good response to the medicine concentration of the Matrine from 2.0 × 10⁻⁶ M to 6.0 × 10⁻³ M, which is used to detect the Matrine concentration in the Matrine injection.     

In situ formation of p–n junction: A novel principle for photoelectrochemical sensor and its application for mercury(II) ion detection

The discovery and development of photoelectrochemical sensors with novel principles are of great significance to realize sensitive and low-cost detection. In this paper, a new photoelectrochemial sensor based on the in situ formation of p–n junction was designed and used for the accurate determination of mercury(II) ions. Cysteine-capped ZnS quantum dots (QDs) was assembled on the surface of indium tin oxide (ITO) electrode based on the electrostatic interaction between Poly(diallyldimethylammonium chloride) (PDDA) and Cys-capped ZnS QDs. The in situ formation of HgS, a p-type semiconductor, on the surface of ZnS facilitated the charge carrier transport and promoted electron-hole separation, triggered an obviously enhanced anodic photocurrent of Cys-capped ZnS QDs. The formation of p–n junction was confirmed by P–N conductive type discriminator measurements and current–voltage (I–V) curves. The photoelectrochemical method was used for the sensing of trace mercuric (II) ions with a linear concentration of 0.01 to 10.0 µM and a detection limit of 4.6 × 10⁻⁹ mol/L. It is expected that the present study can serve as a foundation to the application of p–n heterojunction to photoelectrochemical sensors and it might be easily extended to more exciting sensing systems by photoelectrochemistry.     

Simultaneous capillary electrophoretic determination of Sc(III) and Y(III) based on the complex-formation with a lacunary Keggin-type [PW11O39] complex

Trace amounts of Sc(III) and Y(III) can react with [PW₁₁O₃₉]⁷⁻ to form the ternary Keggin-type complexes: [P(Sc^IIIW₁₁)O₄₀]⁶⁻ and [P(Y^IIIW₁₁)O₄₀]⁶⁻ having high molar absorptivities in the UV region. Since the rate of the complex-formation was very rapid and the kinetically stable ternary anions migrated in the capillary with different electrophoretic mobilities, the complex-formation reaction was applied to the simultaneous CE determination of Sc(III) and Y(III) with direct UV detection at 250 nm. For both Sc(III) and Y(III), the pre-column method provided linear calibration curves in the range of 2 × 10⁻⁷ to 1 × 10⁻⁵ M; the respective detection limits were 1 × 10⁻⁷ M (the signal-to-noise ratio = 3). The proposed method was successfully applied to the determination of Sc(III) and Y(III) in river water.     

Visible light photoelectrochemical sensor for ultrasensitive determination of dopamine based on synergistic effect of graphene quantum dots and TiO2 nanoparticles

We have demonstrated a facile approach for fabricating graphene quantum dots–TiO₂ (GQDs–TiO₂) nanocomposites by a simple physical adsorption method. Compared with pure GQDs and TiO₂ nanoparticles (NPs), the as-prepared GQDs–TiO₂ nanocomposites showed enhanced photoelectrochemical (PEC) signal under visible-light irradiation. The photocurrent of GQDs–TiO₂/GCE was nearly 30-fold and 12-fold enhancement than that of GQDs/GCE and TiO₂/GCE, respectively, which was attributed to the synergistic amplification between TiO₂ NPs and GQDs. More interestingly, the photocurrent of GQDs–TiO₂ nanocomposites was selectively sensitized by dopamine (DA), and enhanced with the increasing of DA concentration. Further, a new PEC methodology for ultrasensitive determination of DA was developed, which showed linearly enhanced photocurrent by increasing the DA concentration from 0.02 to 105 μM with a detection limit of 6.7 nM (S/N = 3) under optimized conditions. This strategy opens up a new avenue for the application of GQDs-based nanocomposites in the field of PEC sensing and monitoring.     

Prussian Blue electrodeposited on MWNTs-PANI hybrid composites for H2O2 detection

A Prussian Blue (PB)/polyaniline (PANI)/multi-walled carbon nanotubes (MWNTs) composite film was fabricated by step-by-step electrodeposition on glassy carbon electrode (GCE). The electrode prepared exhibits enhanced electrocatalytic behavior and good stability for detection of H₂O₂ at an applied potential of 0.0 V. The effects of MWNTs thickness, electrodeposition time of PANI and rotating rate on the current response of the composite modified electrode toward H₂O₂ were optimized to obtain the maximal sensitivity. A linear range from 8 × 10⁻⁹ to 5 × 10⁻⁶ M for H₂O₂ detection has been observed at the PB/PANI/MWNTs modified GCE with a correlation coefficient of 0.997. The detection limit is 5 × 10⁻⁹ M on signal-to-noise ratio of 3. To the best of our knowledge, this is the lowest detection limit for H₂O₂ detection. The electrode also shows high sensitivity (526.43 μA μM⁻¹ cm⁻²) for H₂O₂ detection which is more than three orders of magnitude higher than the reported.     

Direct electrocatalytic oxidation of nitric oxide and reduction of hydrogen peroxide based on α-Fe2O3 nanoparticles-chitosan composite

α-Fe₂O₃ nanoparticles prepared using a simple solution-combusting method have been dispersed in chitosan (CH) solution to fabricate nanocomposite film on glass carbon electrode (GCE). The as-prepared α-Fe₂O₃ nanoparticles were characterized by powder X-ray diffraction (XRD), scanning electron microscopy (SEM). The nanocomposite film exhibits high electrocatalytic oxidation for nitric oxide (NO) and reduction for hydrogen peroxide (H₂O₂). The electrocatalytic oxidation peak is observed at +0.82 V (vs. Ag/AgCl) and controlled by diffusion process. The electrocatalytic reduction peak is observed at −0.45 V (vs. Ag/AgCl) and controlled by diffusion process. This α-Fe₂O₃-CH/GCE nanocomposite bioelectrode has response time of 5 s, linearity as 5.0 × 10⁻⁷ to 15.0 × 10⁻⁶ M of NO with a detection limit of 8.0 × 10⁻⁸ M and a sensitivity of −283.6 μA/mM. This α-Fe₂O₃-CH/GCE nanocomposite bioelectrode was further utilized in detection of H₂O₂ with a detection limit of 4.0 × 10⁻⁷ M, linearity as 1.0 × 10⁻⁶ to 44.0 × 10⁻⁶ M and with a sensitivity of 21.62 μA/mM. The shelf life of this bioelectrode is about 6 weeks under room temperature conditions.     

Fluorometric method for the determination of hydrogen peroxide and glucose with Fe3O4 as catalyst

In this paper, we utilized the instinct peroxidase-like property of Fe₃O₄ magnetic nanoparticles (MNPs) to establish a new fluorometric method for determination of hydrogen peroxide and glucose. In the presence of Fe₃O₄ MNPs as peroxidase mimetic catalyst, H₂O₂ was decomposed into radical that could quench the fluorescence of CdTe QDs more efficiently and rapidly. Then the oxidization of glucose by glucose oxidase was coupled with the fluorescence quenching of CdTe QDs by H₂O₂ producer with Fe₃O₄ MNPs catalyst, which can be used to detect glucose. Under the optimal reaction conditions, a linear correlation was established between fluorescence intensity ratio I₀/I and concentration of H₂O₂ from 1.8 × 10⁻⁷ to 9 × 10⁻⁴ mol/L with a detection limit of 1.8 × 10⁻⁸ mol/L. And a linear correlation was established between fluorescence intensity ratio I₀/I and concentration of glucose from 1.6 × 10⁻⁶ to 1.6 × 10⁻⁴ mol/L with a detection limit of 1.0 × 10⁻⁶ mol/L. The proposed method was applied to the determination of glucose in human serum samples with satisfactory results.     

Highly selective and sensitive monohydrogen phosphate membrane sensor based on molybdenum acetylacetonate

In this work, a highly selective and sensitive monohydrogen phosphate membrane sensor based on a molybdenum bis(2-hydroxyanil) acetylacetonate complex (MAA) is reported. The sensor shows a linear dynamic range between 1.0 × 10⁻¹ and 1.0 × 10⁻⁷ M, with a nice Nernstian behavior (−29.5 ± 0.3 mV decade⁻¹) in pH of 8.2. The detection limit of the electrode is 6.0 × 10⁻⁸ M (∼6 ppb). The best performance was obtained with a membrane composition of 32% poly(vinyl chloride), 58% benzyl acetate, 2% hexadecyltrimethylammonium bromide and 8% MAA. The sensor possesses the advantages of short response time, low detection limit and especially, very good selectivity towards a large number of organic and inorganic anions including salicylate, citrate, tartarate, acetate, oxalate, fluoride, chloride, bromide, iodide, sulfite, sulfate, nitrate, nitrite, cyanide, thiocyanate, perchlorate, metavanadate, and bicarbonate ions. The electrode can be used for at least 10 weeks without any considerable divergence in its slope and detection limit. It was used as an indicator electrode in potentiometric titration of monohydrogenphosphate ion with barium chloride. The proposed sensor was successfully applied to direct determination of monohydrogenphosphate in two fertilizer samples (NPK).