NiVCe-Layered Double Hydroxide as Multifunctional Nanomaterials for Energy and Sensor Applications
TL;DR: In this article, multifunctional NiVCe-layered double hydroxide nanoparticles were synthesized by modified sol-gel method, which demonstrated excellent potential for its utilization as electrode materials for hybrid supercapacitor, oxygen evolution reaction (OER) and sensor applications.
Abstract: Multifunctional nanomaterials have been attracting increasing attention as solutions to the existing challenges in energy systems and sensing technologies. In this regards, multifunctional NiVCe-layered double hydroxide (NiVCe-LDH) nanoparticles were synthesized by modified sol-gel method. The analysis of this material demonstrated excellent potential for its utilization as electrode materials for hybrid supercapacitor, oxygen evolution reaction (OER) and sensor applications. The NiVCe-LDH nanoparticles delivered a specific charge of 740 C g-1 at 10 A g-1 and decent rate performance (charge retention of 68.7% at 100 A g−1), showing excellent prospects as electrode material for hybrid energy storage devices. In addition, NiVCe-LDH nanoparticles have also been successfully applied as proof-of-concept for OER, as confirmed by their low Tafel slope of 47 mV dec−1. Finally, trimetallic NiVCe-LDH-based screen-printed electrodes were developed for the sensing of hydrogen peroxide directly in a real complex mouthwash sample, achieving a satisfactory recovery value around 98% employing a fast and simple BIA procedure. These results allow us to predict the great potential of this trimetallic hydroxide for building electrochemical sensors with good perspectives as electroactive material for OER processes and energy storage technologies.
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TL;DR: In this paper , a supramolecular electrocatalyst for Oxygen Evolution Reaction (OER) was synthesized from a central multibridging cobalt tetrapyridylporphyrazine (CoTPyPz) species by attaching four [Ru(bpy)2Cl]+ groups.
Abstract: A new supramolecular electrocatalyst for Oxygen Evolution Reaction (OER) was synthesized from a central multibridging cobalt tetrapyridylporphyrazine (CoTPyPz) species by attaching four [Ru(bpy)2Cl]+ groups. Both CoTPyPz and the tetraruthenated cobalt porphyrazine species, TRuCoTPyPz, form very homogenous molecular films just by dropcasting their methanol solutions onto GCE electrodes. Such films exhibited low overpotentials for O2 evolution, e.g., 560 e 340 mV, respectively, displaying high stability, typically exceeding 15 h. The kinetic parameters obtained from the Tafel plots showed that the peripheral complexes are very important for the electrocatalytic activity. Hyperspectral Raman images taken along the electrochemical process demonstrated that the cobalt center is the primary active catalyst site, but its performance is enhanced by the ruthenium complexes, which act as electron-donating groups, in the supramolecular system.
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TL;DR: In this article , the synthesis of micro- and nanostructures derived from metal-glycerolate, using different preparation processes, as well as the applications of these materials, especially for the preparation of supercapacitors and batteries electrodes, and electrocatalysts for water splitting.
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TL;DR: In this article , it was shown that Ni-based precursor complexes are the primary products of the Tower method reaction, and these precursors undergo transition to layered Ni-glycerolate derivatives upon thermal treatment.
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517 citations
TL;DR: This feature article summarizes the latest developments in the design, preparation and evaluation of LDH materials toward electrochemical energy storage and conversion.
320 citations
TL;DR: The hydrothermal synthesis of porous ultrathin ternary NiFeV layer double hydroxides (LDHs) nanosheets grown on Nickel foam (NF) substrate as a highly efficient electrode toward overall water splitting in alkaline media is reported.
Abstract: Herein, the hydrothermal synthesis of porous ultrathin ternary NiFeV layer double hydroxides (LDHs) nanosheets grown on Nickel foam (NF) substrate as a highly efficient electrode toward overall water splitting in alkaline media is reported. The lateral size of the nanosheets is about a few hundreds of nanometers with the thickness of ≈10 nm. Among all molar ratios investigated, the Ni0.75 Fe0.125 V0.125 -LDHs/NF electrode depicts the optimized performance. It displays an excellent catalytic activity with a modest overpotential of 231 mV for the oxygen evolution reaction (OER) and 125 mV for the hydrogen evolution reaction (HER) in 1.0 m KOH electrolyte. Its exceptional activity is further shown in its small Tafel slope of 39.4 and 62.0 mV dec-1 for OER and HER, respectively. More importantly, remarkable durability and stability are also observed. When used for overall water splitting, the Ni0.75 Fe0.125 V0.125 -LDHs/NF electrodes require a voltage of only 1.591 V to reach 10 mA cm-2 in alkaline solution. These outstanding performances are mainly attributed to the synergistic effect of the ternary metal system that boosts the intrinsic catalytic activity and active surface area. This work explores a promising way to achieve the optimal inexpensive Ni-based hydroxide electrocatalyst for overall water splitting.
268 citations
TL;DR: The combination of the remarkable catalytic ability and the facile normal temperature synthesis conditions endows the Ce-doped LDH nanocomposite as a promising catalyst to expand the field of lanthanide- doped layered materials for efficient water-splitting electrocatalysis with scale-up potential.
Abstract: Developing convenient doping to build highly active oxygen evolution reaction (OER) electrocatalysts is a practical process for solving the energy crisis. Herein, a facile and low-cost in situ self-assembly strategy for preparing a Ce-doped NiFe-LDH nanosheets/nanocarbon (denoted as NiFeCe-LDH/CNT, LDH = layered double hydroxide and CNT = carbon nanotube) hierarchical nanocomposite is established for enhanced OER, in which the novel material provides its overall advantageous structural features, including high intrinsic catalytic activity, rich redox properties, high, flexible coordination number of Ce3+, and strongly coupled interface. Further experimental results indicate that doped Ce into NiFe-LDH/CNT nanoarrays brings about the reinforced specific surface area, electrochemical surface area, lattice defects, and the electron transport between the LDH nanolayered structure and the framework of CNTs. The effective synergy prompts the NiFeCe-LDH/CNT nanocomposite to possess superior OER electrocatalytic ...
241 citations
TL;DR: In this article, the authors developed non-noble metal based hollow hierarchical nanotubes (HHNTs) of CoVP@NiFeV-layered double hydroxides (LDHs) heterostructures as a high-performance electrocatalyst for nitrogen reduction reaction (NRR) under ambient conditions.
Abstract: Electrocatalytical nitrogen reduction reaction (NRR) under ambient conditions provides a promising substitute to the typical Haber−Bosch process that involves high energy and greenhouse gases emission. Herein, we develop non-noble metal based hollow hierarchical nanotubes (HHNTs) of CoVP@NiFeV-layered double hydroxides (LDHs) heterostructures as a high-performance electrocatalyst for NRR, in which the novel 3D hollow hierarchical structure provides highly rich surface active sites for the adsorption and reduction of nitrogen to NH3. Electrochemical measurements for NRR reveal high activity (NH3 rate: 1.6 × 10−6 mol h−1 cm−2), high Faradaic efficiency (13.8%) and excellent selectivity at −0.3 V versus reversible hydrogen electrode (RHE), outperforming other noble metals catalysts for N2 fixation and most of state-of-the-art metal-free NRR electrocatalysts. Furthermore, CoVP@NiFeV-LDHs HHNTs could maintain high selectivity and durability over repeated reaction cycles. Therefore, this work highlights the first example of CoVP@NiFeV-LDHs hierarchical micro/nanostructures, which serve as electrocatalysts towards high-efficiency, pH-universal NRR to ammonia synthesis.
237 citations