Transition metal phosphides are a new class of materials that have attracted enormous attention as a potential electrode for supercapacitors (SCs) compared to metal oxides/hydroxides and metal sulfides due to their strong redox-active behaviour, good electrical conductivity, layered structure, low cost, and high chemical and thermal stability. Recently, several efforts have been made to develop nickel phosphides (NiP) (NPs) for high-performance SCs. The electrochemical properties of NPs can be easily tuned by several innovative approaches, such as heteroatom doping, defect engineering, and developing a hollow architecture. The prospects of NPs as a positive electrode in hybrid SCs are summarized to understand the material's practical relevance. Finally, the challenges and perspectives are provided for the development of high-performance NPs for SCs. The thorough elucidation of the structure-property-performance relationship offers a guide for developing NP-based next-generation energy-storage devices.
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http://dx.doi.org/10.1039/d2nr05139g | DOI Listing |
J Colloid Interface Sci
December 2024
Key Laboratory of Synthetic and Natural Functional Molecule of the Ministry of Education, College of Chemistry and Materials Science, Northwest University, Xi'an 710127, China; Shaanxi Key Laboratory for Carbon Neutral Technology, Northwest University, Xi'an 710127, China. Electronic address:
The rational design of highly efficient and cost-effective oxygen evolution reaction (OER) electrocatalysts is crucial for hydrogen production through electrocatalytic water splitting. Although the crystalline/amorphous heterostructure shows great potential in enhancing OER activity, its fabrication presents significantly greater challenges compared to that of crystalline/crystalline heterostructures. Herein, a microwave irradiation strategy is developed to construct reduced graphene oxide supported crystalline NiP/amorphous FePO heterostructure (NiP/FePO/RGO) as an efficient OER electrocatalyst.
View Article and Find Full Text PDFJ Colloid Interface Sci
December 2024
Key Laboratory of Green Utilization of Critical Non-metallic Mineral Resources of Ministry of Education, Wuhan University of Technology, Wuhan, Hubei 430073, China; School of Resources and Environmental Engineering, Wuhan University of Technology, Wuhan, Hubei 430073, China. Electronic address:
J Colloid Interface Sci
December 2024
Guangxi Key Laboratory of Low Carbon Energy Materials, School of Chemistry and Pharmaceutical Sciences, Guangxi Normal University, Guilin 541004, China. Electronic address:
J Am Chem Soc
December 2024
College of Materials, Institute of Artificial Intelligence, State Key Laboratory of Physical Chemistry of Solid Surfaces, College of Chemistry and Chemical Engineering, iChEM, Fujian Key Laboratory of Advanced Materials, College of Energy, Xiamen University, Xiamen 361005, China.
Nickel-iron-based catalysts are recognized for their high efficiency in the oxygen evolution reaction (OER) under alkaline conditions, yet the underlying mechanisms that drive their superior performance remain unclear. Herein, we revealed the molecular OER mechanism and the structure-intermediate-performance relationship of OER on a phosphorus-doped nickel-iron nanocatalyst (NiFeP). NiFeP exhibited exceptional activity and stability with an overpotential of only 210 mV at 10 mA cm in 1 M KOH and a cell voltage of 1.
View Article and Find Full Text PDFJ Colloid Interface Sci
December 2024
School of Chemistry & Chemical Engineering, Guangxi University, Guangxi Key Laboratory of Electrochemical Energy Materials, Nanning 530004, China. Electronic address:
Developing efficient non-noble metal dual-functional electrocatalysts for overall water splitting is essential for the production of green hydrogen. Given the significant advantages of self-supporting electrodes, regulating the growth of self-supporting nanoarrays on a conductive substrate is conducive to improving the electrocatalytic activity. In this work, aligned cobalt phosphide (CoP) nanowire arrays grown on borate-modified Ni foam substrate (CoP/R-NF) were utilized as a bifunctional electrocatalyst for both hydrogen evolution reactions (HER) and oxygen evolution reactions (OER) in alkaline solution.
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