Hydrogen oxidation reaction (HOR) can effectively convert the hydrogen energy through the hydrogen fuel cells, which plays an increasingly important role in the renewable hydrogen cycle. Nevertheless, when the electrolyte pH changes from acid to base, even with platinum group metal (PGM) catalysts, the HOR kinetics declines with several orders of magnitude. More critically, the pivotal role of reaction intermediates and interfacial environment during intermediate behaviors on alkaline HOR remains controversial. Therefore, exploring the exceptional PGM-based alkaline HOR electrocatalysts and identifying the reaction mechanism are indispensable for promoting the commercial development of hydrogen fuel cells. Consequently, the fundamental understanding of the HOR mechanism is first introduced, with emphases on the adsorption/desorption process of distinct reactive intermediates and the interfacial structure during catalytic process. Subsequently, with the guidance of reaction mechanism, the latest advances in the rational design of advanced PGM-based (Pt, Pd, Ir, Ru, Rh-based) alkaline HOR catalysts are discussed, focusing on the correlation between the intermediate behaviors and the electrocatalytic performance. Finally, given that the challenges standing in the development of the alkaline HOR, the prospect for the rational catalysts design and thorough mechanism investigation towards alkaline HOR are emphatically proposed.
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http://dx.doi.org/10.1002/adma.202414628 | DOI Listing |
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January 2025
National Innovation Platform (Center) for Industry-Education Integration of Energy Storage Technology, Xi'an Jiaotong University, Xi'an, 710049, P. R. China.
As global demand for clean and sustainable energy continues to rise, fuel cell technology has seen rapid advancement. However, the presence of trace impurities like carbon monoxide (CO) and hydrogen sulfide (H₂S) in hydrogen fuel can significantly deactivate the anode by blocking its active sites, leading to reduced performance. Developing electrocatalysts that are resistant to CO and H₂S poisoning has therefore become a critical priority.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
December 2024
State Key Laboratory of Physical Chemistry of Solid Surfaces, College of Chemistry and Chemical Engineering, Xiamen University, Xiamen, 361005, China.
PtRu-based catalysts toward hydrogen oxidation reaction (HOR) suffer from low efficiency, CO poisoning and over-oxidation at high potentials. In this work, an amorphization strategy is adopted for preparation of amorphous SrRuPtOH nanobelts (a-SrRuPtOH NBs). The a-SrRuPtOH NBs has optimized adsorption of intermediates (H and OH), increased number of active sites, highly weakened CO poisoning and enhanced anti-oxidation ability owing to the special amorphous structure.
View Article and Find Full Text PDFACS Appl Mater Interfaces
December 2024
School of Chemistry and Chemical Engineering, Shaanxi Key Laboratory of Chemical Reaction Engineering, Yan'an University, Yan'an, Shaanxi 716000, People Republic of China.
The sluggish anodic hydrogen oxidation reaction (HOR) of the hydroxide exchange membrane fuel cell (HEMFC) is a significant barrier for practical implementation. Herein, we designed a catalyst of MoTiCT MXene-supported Ru-CuO heterojunctions (named as Ru-CuO/MXene). The XPS spectra and the d-band center data of the different amounts of Cu of the Ru-CuO/MXene suggested that there existed a strongly electronic metal-support interaction between the active species and the substrate with MXene as the excellent carrier.
View Article and Find Full Text PDFChemSusChem
December 2024
State Key Laboratory of Pollution Control and Resource Reuse, College of Environmental Science and Engineering, Tongji University, Shanghai Institute of Pollution Control and Ecological Security, Shanghai, 200092, P.R. China.
One important target for anion exchange membrane fuel cells (AEMFCs) is to enable the application of anode non-precious metal hydrogen oxidation reaction (HOR) catalyst. Nickel presents a promising candidate for alkaline HOR; yet, its practical application is hampered by the intrinsically sluggish activity and poor stability. Herein, a series of Ni-based metals (NiMo, NiCo, NiW and Ni) are electrodeposited as model catalysts to systematically explore the alkaline HOR by considering the role of adsorbed hydroxyl (OH).
View Article and Find Full Text PDFACS Appl Mater Interfaces
December 2024
Faculty of Advanced Science and Technology, Kumamoto University, 2-39-1 Kurokami, Chuo-ku, Kumamoto 860-8555, Japan.
The effect of the carbon support─Ketjenblack (C) and Vulcan (C)─on the Ni/C catalyst properties toward alkaline hydrogen oxidation reaction (HOR) was investigated. Both Ni/C and Ni/C presented improved catalytic activity with an increase in Ni particle size; however, Ni/C showed activity significantly higher than that of Ni/C at the same particle size. The reason for the difference in the HOR activity due to the types of carbon support was revealed to be the difference in the 3D structure of Ni nanoparticles determined by metal-support interaction, which is changed by the surface structures of carbon supports.
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