Rui Gusmão

Black Phosphorus Rediscovered: From Bulk Material to Monolayers

Phosphorus is a nonmetal with several allotropes, from the highly reactive white phosphorus to the thermodynamically stable black phosphorus (BP) with a puckered orthorhombic layered structure. The bulk form of BP was first synthesized in 1914, but received little attention until it was rediscovered in 2014 as a member of the new wave of 2D layered nanomaterials. BP can be exfoliated to a single sheet that acts as a semiconductor with a tunable direct band gap, a high carrier mobility at room temperature, and an in-plane anisotropy. The development of BP applications is hampered by surface degradation, thus efforts to achieve effective BP passivation are ongoing, such as its integration in van der Waals heterostructures. BP has been tested as a novel nanomaterial in batteries, transistors, sensors, and photonics. This Review begins with the origin of the BP story, following the path from a bulk material to modern few/single layers. The physical and chemical properties are summarized, and the state-of-the-art of BP applications highlighted.

Circular Dichroism and Voltammetry, Assisted by Multivariate Curve Resolution, and Mass Spectrometry of the Competitive Metal Binding by Phytochelatin PC5

The competitive binding of Cd(2+) and Pb(2+) by the phytochelatin (γGlu-Cys)5-Gly (PC5) has been examined by several analytical techniques. Positive-mode electrospray ionization mass spectrometry (ESI-MS) is used to determine the stoichiometries of the complexes, while voltammetric and spectroscopic data are analyzed by multivariate curve resolution with alternating least-squares (MCR-ALS) and some recently developed chemometric tools, which allows one to follow the displacement induced by Cd(2+) or Pb(2+) in the binding of Pb(2+) or Cd(2+), respectively, by PC5, and to obtain a complete overview of the processes involved. Differential pulse polarography (DPP) signals of these systems present, besides overlapping peaks due to free metal ion and metal complexes, interference of mercury anodic signals. Circular dichroism (CD) spectroscopy is a useful complementary technique due to the absence of these types of signals and its selective response to different species. A tentative complexation/electrochemical model is proposed for Cd(2+) and Pb(2+) competition toward PC5 complexation. The formation of the previously unreported ternary CdPb(PC5) complex was suggested by DPP and CD spectroscopy experiments and confirmed by ESI-MS.

Pnictogen (As, Sb, Bi) Nanosheets for Electrochemical Applications Are Produced by Shear Exfoliation Using Kitchen Blenders

Layered materials are of high importance because of their anisotropy and as a source of 2D materials. Whilst there is a plethora of multi-elemental 2D materials, the number mono-elemental 2D materials is rather limited. Herein, we demonstrate that aqueous shear exfoliation can be used to obtain As, Sb, and Bi exfoliated nanosheets. Morphological and chemical characterization of the exfoliated materials shows a decrease in thickness, sheet-to-nanosheet scale, and partial oxidation owing to a higher surface area. The electrochemical performance is tested in terms of inherent electrochemistry, electron transfer, and sensing applications as demonstrated with ascorbic acid. Potential energy-related applications are evaluated in the hydrogen evolution reaction (HER), oxygen evolution reaction (OER), and oxygen reduction reaction (ORR), with shear-exfoliated Sb having the best electrochemical performance overall. These findings will have a profound impact on the preparation and application of 2D mono-elemental materials.

Electrochemical survey of the chain length influence in phytochelatins competitive binding by cadmium

Multivariate curve resolution with alternating least squares (MCR-ALS) was applied to voltammetric data obtained in the analysis of the competitive binding of glutathione (GSH) and phytochelatins [(gammaGlu-Cys)(n)-Gly, PC(n), n=2-5] by Cd(2+). The displacements between ligands and chain length influence on the competitive binding of PC(n) toward Cd(2+) were investigated. The analysis of the resulting pure voltammograms and concentration profiles of the resolved components suggests that ligands containing more thiol groups are able to displace the shortest chain ligands from their metal complexes, whereas the opposite does not happen. However, when the length of the chain surpasses that of PC(3), the binding capacity of the molecule still increases (i.e., it can bind more metal ions), but the position and shape of the voltammetric signals practically rest unchanged. This suggests that at this level, the stability of metal binding could depend more on the nature of the binding sites separately than on the quantity of the sites (i.e., the chain length).

Enhanced electrochemical sensing of polyphenols by an oxygen-mediated surface

We report a straightforward heat treatment in air of commercial screen-printed carbon electrodes (SPCE) at different temperatures and times (ht-SPCE) that produces considerable electrocatalytic effects. The active area and the presence of oxygen groups on the ht-SPCE surface increased upon thermal treatment, more than doubling and by 20%, respectively. The increase of oxygen-containing carbon surface groups results in strong interactions and substantial improvement in Faradaic currents, up to a 10 fold increase in the voltammetric response of relevant polyphenols (hydroquinone, catechol, pyrogallol and dopamine). Moreover, ht-SPCE displayed higher selectivity towards the oxidation of polyphenol mixtures than the untreated SPCE. Finally, good linear ranges were obtained by voltammetric determination of dopamine with detection and quantification limits 5 times lower than the values obtained for the untreated SPCE. The versatility of oxidation by air makes this activation procedure very attractive and easy to implement, which can be further used for numerous applications in the (bio)sensor field.

Competitive binding of cadmium by plant thiols: an electrochemical study assisted by multivariate curve resolution

AbstractMultivariate curve resolution with alternating least squares (MCR-ALS) has been applied to voltammetric data obtained from analysis of the competitive binding of cysteine (Cys) and cysteine–glycine (Cys-Gly) by Cd(II) as a first approach towards mixtures of phytochelatins and related compounds in natural media. From different starting points, the possibilities of formation of mixed complexes and/or displacements between ligands are investigated. Analysis of the resulting unitary voltammograms and concentration profiles of the resolved components by MCR-ALS suggests that the strongest ligand (Cys-Gly) is able to displace the weakest (Cys) from its metal complexes, whereas this does not happen in the opposite direction. On the other hand, no evidence of Cd mixed-ligand complexes was found. FigureDifferential pulse polarograms measured in the independent titrations of 1 × 10-5 mol L-1 Cys, 1 × 10-5 mol L-1 Cys-Gly, and a mixture of Cys-Gly (0.5 × 10-5 mol L-1) and Cys (1 × 10-5 mol L-1) with Cd2+, at TRIS-HNO3 buffer (0.1 mol L-1 and PH 7.5) in the presence of 0.1 mol L-1 KNO3

Electrochemical Fluorographane: Hybrid Electrocatalysis of Biomarkers, Hydrogen Evolution, and Oxygen Reduction

Fluorographane (C1 Hx F1-x+δ )n is a new member of the graphene family that exhibits hydrophobicity and a large band gap that is tunable based on the level of fluorination. Herein, sensing and energy applications of fluorographane are reported. The results reveal that the carbon-to-fluoride ratio of fluorographane has a great impact on the electrochemical performance of the materials. Lowered oxidation potentials for ascorbic and uric acids, in addition to a catalytic effect for hydroquinone and dopamine redox processes, are obtained with a high fluoride content. Moreover, fluorographane, together with residual copper- and nickel-based doping, acted as a hybrid electrocatalyst to promote hydrogen evolution and oxygen reduction reactions with considerably lower onset potentials than those of graphane (starting material), which makes this a promising material for a broad range of applications.

Determination of complex formation constants by phase sensitive alternating current polarography: Cadmium-polymethacrylic acid and cadmium-polygalacturonic acid.

The use of phase sensitive alternating current polarography (ACP) for the evaluation of complex formation constants of systems where electrodic adsorption is present has been proposed. The applicability of the technique implies the previous selection of the phase angle where contribution of capacitive current is minimized. This is made using Multivariate Curve Resolution by Alternating Least Squares (MCR-ALS) in the analysis of ACP measurements at different phase angles. The method is checked by the study of the complexation of Cd by polymethacrylic (PMA) and polygalacturonic (PGA) acids, and the optimal phase angles have been ca. -10 degrees for Cd-PMA and ca. -15 degrees for Cd-PGA systems. The goodness of phase sensitive ACP has been demonstrated comparing the determined complex formation constants with those obtained by reverse pulse polarography, a technique that minimizes the electrode adsorption effects on the measured currents.

Chemometric analysis of voltammetric data on metal ion binding by selenocystine.

The behavior of selenocystine (SeCyst) alone or in the presence of various metal ions (Bi(3+), Cd(2+), Co(2+), Cu(2+), Cr(3+), Ni(2+), Pb(2+), and Zn(2+)) was studied using differential pulse voltammetry (DPV) over a wide pH range. Voltammetric data matrices were analyzed using chemometric tools recently developed for nonlinear data: pHfit and Gaussian Peak Adjustment (GPA). Under the experimental conditions tested, no evidence was found for the formation of metal complexes with Bi(3+), Cu(2+), Cr(3+), and Pb(2+). In contrast, SeCyst formed electroinactive complexes with Co(2+) and Ni(2+) and kinetically inert but electroactive complexes with Cd(2+) and Zn(2+). Titrations with Cd(2+), Co(2+), Ni(2+), and Zn(2+) produced data that were reasonably consistent with the formation of stable 1:1 M(SeCyst) complexes.