Despite significant research on its electrocatalytic OER activity, the geometric performance of Co O has remained unsatisfactory compared to relatively amorphous Co-based materials. In particular, the activity of Co O prepared through annealing always gets inferior compared to its amorphous precursor. This demands the development of synthetic techniques to prepare Co O with superior activity as the unpredictable crystal structure of the amorphous materials makes it difficult to understand their structure-activity relationships despite higher geometric activity. In this article, we have shown that incorporation of sulfate in pre-annealed materials plays a pivotal role in boosting the OER activity of annealed Co O irrespective of the pre-annealed phase. In contrast to commonly used nitrate or carbonate that leaves the structure upon annealing and renders the resulting Co O with poor activity, sulfate remains in the annealed structure due to its thermal stability and causes a dramatic enhancement in the geometric electrocatalytic OER activity of resulting Co O compared to the pre-annealed phase. This was due to the "pore-alteration ability" and "crystallization hindrance effect" of sulfate ions that significantly alter the microstructure of the resulting Co O during annealing process by dramatically improving the surface area, pore size, and pore volume. Moreover, sulfate incorporation provided structures with considerably higher mesoporosity that is known to be conducive for reactant and product diffusion within the network. The improved textural properties led to better exposure of the catalytic centres to the electrolyte leading to higher geometric OER activity despite identical intrinsic activity of both sulfate free and incorporated Co O as confirmed from their specific activities. Further, the Co O synthesized by annealing sulfate incorporated precursor was found to be rich with oxygen defects that are known to increase the potency of a material towards electrocatalytic OER. The sulfate ions also etched out in the electrolyte during electrocatalysis leading to complete unblocking of the pores thereby helping in sustaining the high geometric OER activity. To our knowledge, this is the first report where the geometric electrocatalytic OER activity of an annealed Co O is significantly better compared to its pre-annealed phase and is in fact comparable to the activity of amorphous Co-hydroxide based compounds.
Download full-text PDF |
Source |
---|---|
http://dx.doi.org/10.1002/asia.202100175 | DOI Listing |
Dalton Trans
January 2025
Department of Chemical Engineering, Integrated Engineering Major, College of Engineering, Kyung Hee University, Yongin, 17104, Republic of Korea.
Oxygen evolution reaction (OER) is a half-reaction that occurs at the anode during water electrolysis, and owing to its slow kinetics, it is the rate-limiting step in the process. Alloying with transition metal and combining with transition metal oxide supports are effective methods for modifying the electronic structure of noble metal catalysts and improving their catalytic properties. In this study, we synthesized IrCu/CoO hybrid nanostructures by attaching IrCu alloy nanoparticles onto CoO nanosheets.
View Article and Find Full Text PDFJ Am Chem Soc
January 2025
School of Photovoltaic and Renewable Energy Engineering, University of New South Wales, Tyree Energy Technologies Building, 229 Anzac Parade, Kensington, NSW 2052, Australia.
An ideal water-splitting electrocatalyst is inexpensive, abundant, highly active, stable, selective, and durable. The anodic oxygen evolution reaction (OER) is the main bottleneck for H production with a complex and not fully resolved mechanism, slow kinetics, and high overpotential. Nickel oxide-based catalysts (NiO) are highly active and cheaper than precious metal catalysts.
View Article and Find Full Text PDFACS Appl Mater Interfaces
January 2025
Key Laboratory of Material Chemistry for Energy Conversion and Storage Ministry of Education, Hubei Key Laboratory of Material Chemistry and Service Failure, School of Chemistry and Chemical Engineering, Huazhong University of Science and Technology (HUST), Wuhan, Hubei 430074, China.
Various sustainable energy conversion techniques like water electrolyzers, fuel cells, and metal-air battery devices are promising to alleviate the issues in fossil fuel consumption. However, their broad employment has been mainly inhibited by the lack of advanced electrocatalysts to accelerate the sluggish kinetics of the three involved half-reactions including oxygen evolution reaction (OER), oxygen reduction reaction (ORR), and hydrogen evolution reaction (HER). Recent advances have witnessed the cucurbit[]uril (CB[])-directed strategy as a prominent tool to develop high performance electrocatalysts with either OER, ORR, or HER activities.
View Article and Find Full Text PDFChem Commun (Camb)
January 2025
Materials Genome Institute of Shanghai University, Shanghai 200444, China.
The development and generation of affordable and highly efficient energy, particularly hydrogen, are one of the best approaches to address the challenges posed by the depletion of non-renewable energy sources. Hydrogen energy, as a green and ecosystem-friendly source with zero carbon emission, can be generated through various methods, including water splitting (HER/OER) either photo- or electrocatalytic reactions. To implement these reactions effectively in practical applications, it is highly desirable to develop extremely efficient and cost-effective catalytic materials that are comparable to contemporary catalysts.
View Article and Find Full Text PDFNanoscale
January 2025
School of Chemistry, Southwest Jiaotong University, Chengdu, Sichuan 610031, China.
Engineering the local electronic structure of single atom catalysts (SACs) still remains challenging. In this study, a Ru-NiS single atom catalyst with a controlled S coordination environment, where Ru single atoms are implanted on a NiS nanoflower consisting of plenty of cross-linked nanosheets, has been developed a facile atom capture strategy. Using Density Functional Theory (DFT) calculations, it has been revealed that the fine-tuned local S coordination environment can optimize the electronic structure of Ru active sites, and reduce the energy barrier of the rate-determining step for the oxygen evolution reaction (OER), thus boosting the electrocatalytic activity, such as a low overpotential of 269 mV at 10 mA cm.
View Article and Find Full Text PDFEnter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!