Boron and Nitrogen Co-Doped Porous Graphene Nanostructures for the Electrochemical Detection of Poisonous Heavy Metal Ions.

Heavy metal poisoning has a life-threatening impact on the human body to aquatic ecosystems. This necessitates designing a convenient green methodology for the fabrication of an electrochemical sensor that can detect heavy metal ions efficiently. In this study, boron (B) and nitrogen (N) co-doped laser-induced porous graphene (LIGBN) nanostructured electrodes were fabricated using a direct laser writing technique. The fabricated electrodes were utilised for the individual and simultaneous electrochemical detection of lead (Pb2+) and cadmium (Cd2+) ions using a square wave voltammetry technique (SWV). The synergistic effect of B and N co-doping results in an improved sensing performance of the electrode with better sensitivity of 0.725 µA/µM for Pb2+ and 0.661 µA/µM for Cd2+ ions, respectively. Moreover, the sensing electrode shows a low limit of detection of 0.21 µM and 0.25 µM for Pb2+ and Cd2+ ions, with wide linear ranges from 8.0 to 80 µM for Pb2+ and Cd2+ ions and high linearity of R2 = 0.99 in case of simultaneous detection. This rapid and facile method of fabricating heteroatom-doped porous graphene opens a new avenue in electrochemical sensing studies to detect various hazardous metal ions.

Low-temperature synthesis of high-entropy amorphous metal oxides (HEOs) for enhanced oxygen evolution performance.

The rational design of multiple metal ions into high-entropy oxide electrode material via a single-step hydrothermal process is applicable to the evolution of oxygen molecules (O2) through simple water electrolysis. Their cost-effectiveness, high performance, and durable nature are the key factors of non-precious high-entropy multiple metal-based electrocatalysts, which can be used as replaceable catalysts instead of precious ones. This article reports a low-temperature synthesis of the cauliflower-type morphology of high-entropy amorphous metal oxides, and their electrochemical performances towards the oxygen evolution reaction (OER) are investigated. The multiple metal ion (Mn2+, Fe3+, Co2+, Ni2+, Cu2+) oxide electrode material shows an acceptable oxygen evolution reaction (OER) with an overpotential of 290 mV at a current density of 10 mA cm-2 and a lower Tafel slope value of 85 mV dec-1, respectively. Moreover, the 20 h durability test with negligible change in overpotential shows the efficacy of the modified electrode material in harsh alkaline media. The observed electrochemical results towards the OER correspond to the amorphous nature of the active material that displayed a cauliflower-type morphology, having a large specific surface area (240 m2 g-1) and providing higher electrochemical active sites as well. Consequently, post-stability characterization studies (such as PXRD, FESEM, TEM, and XPS) provide more information for understanding the post-structural and morphological results of the high-entropy amorphous metal oxide.

Enhanced high rate capability of Li intercalation in planar and edge defect-rich MoS2 nanosheets.

(i) Edge and planar defect-rich and (ii) defect-suppressed MoS2 nanosheets are fabricated by controlled annealing of wet-chemically processed precursors. Wrinkles, folds, bends, and tears lead to the introduction of severe defects in MoS2 nanosheets. These defects are suppressed and highly crystalline MoS2 nanosheets are obtained upon high-temperature annealing. The influence of defects on the electrochemical properties, particularly rate capability and cycling stability, in the Li intercalation regime (1 V to 3 V vs. Li/Li+) and conversion regime (10 mV to 3 V vs. Li/Li+) are investigated. In the intercalation regime, the initial Li intake (x in LixMoS2) for defect-rich nanosheets is larger (x ≈ 1.6) as compared to that in defect-suppressed MoS2 (x ≈ 1.2). Although the reversible initial capacity of all the anodes is nearly the same (x ≈ 0.9) at 0.05C rate, defect-rich MoS2 exhibits high rate capability (>40 mA h g-1 at 40C or 26.8 A g-1). When cycled at 10C (6.7 A g-1) for 1000 cycles, 75% capacity retention is observed. High rate capability can be attributed to the defect-rich nature of MoS2, providing faster access to lithium intercalation by a shortened diffusion length facilitated by Li adsorption at the defect sites. The defect-rich nanosheets exhibit a power density of ∼20% more than that of defect-suppressed nanosheets. For the first time, MoS2/Li cells with a high power density of 10-40 kW kg-1 in the intercalation regime have been realized. In the conversion regime, defect-rich and defect-suppressed MoS2 exhibit initial lithiation capacities of ∼1000 and ∼840 mA h g-1, respectively. Defect-rich MoS2 had a capacity of ∼800 mA h g-1 at 0.1C (67 mA g-1), whereas defect-suppressed MoS2 had a capacity of only ∼80 mA h g-1 at the same current rate. Capacity retention of 78% was observed for defect-rich MoS2 with a reversible capacity of 591 mA h g-1 when cycled at 0.1C (67 mA g-1) for 100 cycles. Despite having a lower energy density in the intercalation regime, the power density of defect-rich MoS2 in the intercalation regime is significantly larger (by three orders of magnitude) as compared to that of defect-suppressed MoS2 in the conversion regime. Defect-rich MoS2 nanosheets are promising for high-rate-capability applications when operated in the intercalation regime.