Two-step water electrolysis has been proposed to tackle the ticklish H/O mixture problems in conventional alkaline water electrolysis recently. However, low buffering capacity of pure nickel hydroxide electrode as redox mediator limited practical application of two-step water electrolysis system. A high-capacity redox mediator (RM) is urgently needed to permit consecutive operation of two-step cycles and high-efficiency hydrogen evolution. Consequently, a high mass-loading cobalt-doped nickel hydroxide/active carbon cloth (NiCo-LDH/ACC) RM is synthesized via a facile electrochemical method. The proper Co doping can apparently enhance the conductivity and simultaneously remain the high-capacity of the electrode. Density functional theory results further confirms more negative values in redox potential of NiCo-LDH/ACC than Ni(OH)/ACC on account of the charge redistribution induced by Co doping, which can prevent the parasitic O evolution on RM electrode during decoupled H evolution step. As a result, the NiCo-LDH/ACC combined the superiorities of high-capacity Ni(OH)/ACC and high-conductivity Co(OH)/ACC, and the NiCo-LDH/ACC with 4:1 ratio of Ni to Co presented a large specific capacitance of 33.52F/cm for reversible charge-discharge and high buffering capacity with two-step H/O evolution duration of 1740 s at 10 mA/cm. The necessary input voltage (2.00 V) of the whole water electrolysis was broken into two smaller ones, 1.41 and 0.38 V, for H and O production, respectively. NiCo-LDH/ACC provided a favorable electrode material for the practical application of two-step water electrolysis system.
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http://dx.doi.org/10.1016/j.jcis.2023.06.102 | DOI Listing |
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January 2025
Department of Chemistry, Nanoscience Center, University of Jyväskylä, P.O. Box 35, Jyväskylä, FI-40014, Finland.
Designing cost-effective electrocatalysts with fast reaction kinetics and high stability is an outstanding challenge in green hydrogen generation through overall water splitting (OWS). Layered double hydroxide (LDH) heterostructure materials are promising candidates to catalyze both oxygen evolution reaction (OER) and hydrogen evolution reaction (HER), the two OWS half-cell reactions. This work develops a facile hydrothermal route to synthesiz hierarchical heterostructure MoS@NiFeCo-LDH and MoS@NiFeCo-Mo(doped)-LDH electrocatalysts, which exhibit extremely good OER and HER performance as witnessed by their low IR-corrected overpotentials of 156 and 61 mV with at a current density of 10 mA cm under light assistance.
View Article and Find Full Text PDFNatl Sci Rev
February 2025
Key Laboratory of Precision and Intelligent Chemistry, School of Chemistry and Materials Science, University of Science and Technology of China, Hefei 230026, China.
Ion exchange membranes (IEMs) enable fast and selective ion transport and the partition of electrode reactions, playing an important role in the fields of precise ion separation, renewable energy storage and conversion, and clean energy production. Traditional IEMs form ion channels at the nanometer-scale via the assembly of flexible polymeric chains, which are trapped in the permeability/conductivity and selectivity trade-off dilemma due to a high swelling propensity. New-generation IEMs have shown great potential to break this intrinsic limitation by using microporous framework channels for ion transport under a confinement regime.
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January 2025
Department of Chemistry, School of Natural Sciences, National University of Sciences and Technology, H-12, Islamabad 44000, Pakistan.
Implementing a hydrogen economy on an industrial scale poses challenges, particularly in developing cost-effective and stable catalysts for water electrolysis. This study explores the catalytic potential of selenium nanoparticles (Se-NPs) synthesized via a simple chemical bath deposition method for electrochemical and photoelectrochemical (PEC) water splitting. The successful fabrication of Se-NPs on fluorine-doped tin oxide (FTO) electrodes has been confirmed using a wide range of analytical tools like X-ray diffraction, energy-dispersive X-ray spectroscopy, and scanning electron microscopy.
View Article and Find Full Text PDFJ Colloid Interface Sci
January 2025
School of Chemistry and Chemical Engineering/State Key Laboratory Incubation Base for Green Processing of Chemical Engineering, Shihezi University, Shihezi 832003 China. Electronic address:
Two-dimensional metal-organic framework (2D MOF) materials have significant development prospects in the technology of urea-assisted water electrolysis for hydrogen production. However, the poor conductivity, low mass permeability, and stability have limited their development in electrocatalysis. Here, CoFe-BDC is synthesized using layered double hydroxides (LDH) as the template.
View Article and Find Full Text PDFNat Commun
January 2025
Wuhan National Laboratory for Optoelectronics, School of Optoelectronic Science and Engineering, Huazhong University of Science and Technology, Wuhan, PR China.
Active and stable electrocatalysts are essential for hydrogen production from alkaline water electrolysis. However, precisely controlling the interaction between electrocatalysts and reaction intermediates (HO*, H*, and *OH) remains challenging. Here, we demonstrate an yttrium-doped NiMo-MoO heterogenous electrocatalyst that efficiently promotes water dissociation and accelerates the intermediate adsorption/desorption dynamics in alkaline electrolytes.
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