SEOUL, South Korea , June 13, 2022 /PRNewswire/ — Concerns about rising atmospheric carbon dioxide levels and global warming have made it an environmental imperative to replace fossil fuels with cleaner and more sustainable alternatives. In this regard, hydrogen, a clean energy source, has emerged as an excellent potential candidate.
Among the several methods available for hydrogen generation, splitting water using electricity in presence of a catalyst, or "electrocatalytic water splitting," as it is called, is the cleanest. Unfortunately, the process requires expensive and rare noble metal catalysts, such as platinum, to maintain a reasonable efficiency. This, in turn, has limited its large-scale industrial applications.
A relatively inexpensive option is transition metal-based catalysts, such as oxides, sulfides, hydroxides of cobalt, nickel, iron etc. However, there is a catch: the electrocatalytic water splitting consists of two half-reactions, namely the hydrogen evolution reaction (HER) and the oxygen evolution reaction (OER). In OER, water molecules are oxidized to form oxygen and positive hydrogen ions at the anode (positively charged electrode). The hydrogen ions then move across the electrolyte to the cathode (the negatively charged electrode), where they are reduced to produce hydrogen (HER). It turns out that most transition metal-based catalysts reported so far can only catalyze either HER or OER. This makes for a complicated configuration and a higher overall cost.
Against this backdrop, researchers from Chung-Ang University in Korea developed, in a new study, a novel heterostructured catalyst consisting of hollow cobalt sulfide (CoSx) and nickel-iron (NiFe) layered double hydroxide (LDH) nanosheets that simultaneously boosts both the half-reactions. This paper was made available online on 15 March 2022 and was published in Volume 18 Issue 16 of the journal Small on 16 April 2022.
"A reasonable strategy for fabricating highly efficient catalysts for water splitting is to elaborately integrate OER-active NiFe LDH and HER-active catalysts into a heterostructure," explains Assistant Professor Seung-Keun Park, who headed the study. "Given their high surface area and open structure, hollow HER catalysts are believed to be ideal for this job. It turns out that metal – organic frameworks (MOFs) are an efficient precursor for fabricating hollow structures. However, an MOF-based hollow catalyst with NiFe LDH has not be reported so far."
Accordingly, the researchers electrochemically deposited NiFe LDH nanosheets in a controlled manner on the surface of hollow CoSx nanoarrays supported on nickel foam. "The integration of an active HER catalyst, CoSx and an OER catalyst, NiFe LDH, guarantees a superior bifunctional catalytic activity," says Dr. Park.
And indeed, the catalyst was able to consistently deliver a high current density of 1000 mA cm-2 in both half-reactions at low cell voltages, suggesting its feasibility for industrial scale water-splitting applications. The researchers attributed this to the presence of ample active sites on the catalyst heterostructure, which enabled electrolyte penetration and gas release during the reactions. Additionally, an electrolyzer based on this catalyst demonstrated a high current density of 300 mA cm-2 at a low cell voltage and a durability of 100 hours in overall water splitting.
"The enhanced electrocatalytic properties of our catalyst is likely due to its unique hierarchical heterostructure and the synergy between its components. We believe that our work will take us one step closer towards realizing a zero emission society," says an optimistic Dr. Park.
And we hope we are not far!
Reference
DOI: https://doi.org/10.1002/smll.202200586
Title of original paper: Metal–Organic Framework-Derived Hollow CoSx Nanoarray Coupled with NiFe Layered Double Hydroxides as Efficient Bifunctional Electrocatalyst for Overall Water Splitting
Journal: Small
About Chung-Ang University
Website: https://neweng.cau.ac.kr/index.do
Contact:
Seong-Kee Shin
02-820-6614
338425@email4pr.com
SOURCE Chung-Ang University
