The sluggish kinetics of oxygen evolution reaction (OER) and high iridium loading in catalyst coated membrane (CCM) are the key challenges for practical proton exchange membrane water electrolyzer (PEMWE). Herein, we demonstrate high-surface-area nano-metal diborides as promising supports of iridium-based OER nanocatalysts for realizing efficient, low-iridium-loading PEMWE. Nano-metal diborides are prepared by a novel disulphide-to-diboride transition route, in which the entropy contribution to the Gibbs free energy by generation of gaseous sulfur-containing products plays a crucial role. The nano-metal diborides, TaB in particular, are investigated as the support of IrO nanocatalysts, which finally forms a TaO/IrO heterojunction catalytic layer on TaB surface. Multiple advantageous properties are achieved simultaneously by the resulting composite material (denoted as IrO@TaB), including high electrical conductivity, improved iridium mass activity and enhanced corrosion resistance. As a consequence, the IrO@TaB can be used to fabricate the membrane electrode with a low iridium loading of 0.15 mg cm, and to give an excellent catalytic performance (3.06 A cm@2.0 V@80 C) in PEMWE-the one that is usually inaccessible by unsupported Ir-based nanocatalysts and the vast majority of existing supported Ir-based catalysts at such a low iridium loading.
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http://dx.doi.org/10.1038/s41467-023-40912-8 | DOI Listing |
ACS Appl Mater Interfaces
December 2024
State Key Laboratory of Green Chemical Engineering and Industrial Catalysis, School of Chemistry and Molecular Engineering, East China University of Science and Technology, Shanghai 200237, P. R. China.
The sluggish kinetics of the anodic process, known as the oxygen evolution reaction (OER), has posed a significant challenge for the practical application of proton exchange membrane water electrolyzers in industrial settings. This study introduces a high-performance OER catalyst by anchoring iridium oxide nanoparticles (IrO) onto a cobalt oxide (CoO) substrate via a two-step combustion method. The resulting IrO@CoO catalyst demonstrates a significant enhancement in both catalytic activity and stability in acidic environments.
View Article and Find Full Text PDFJ Colloid Interface Sci
December 2024
Department of Energy and Environmental Materials, Suzhou Laboratory, 388 Ruoshui Road, Suzhou, China. Electronic address:
The sluggish kinetics, poor stability, and high iridium loading in acidic oxygen evolution reaction (OER) present significant challenges for proton exchange membrane water electrolyzers (PEMWE). While supported catalysts can enhance the utilization and activity of Ir atoms, they often fail to mitigate the detrimental effects of over-oxidation and dissolution of Ir. Here, we leverage the redox properties of the Mn/Mn couple as electronic modulators to develop a low-iridium, durable electrocatalyst for acidic OER.
View Article and Find Full Text PDFSmall
December 2024
Department of Chemical Sciences, Indian Institute of Science Education and Research, Kolkata, 741246, India.
Transition metal complex-loaded nanosystems (TMCNs) represent a cutting-edge platform for stimuli (light, ultrasound)-responsive cancer therapies. These nanosystems, incorporating metals such as manganese(II), zinc(II), ruthenium(II), rhenium(I), iridium(III), and platinum(IV), significantly enhance the efficacy of light-activated therapies, including photodynamic therapy (PDT) and photothermal therapy (PTT), as well as ultrasound-activated treatments like sonodynamic therapy (SDT). TMCNs based on ruthenium(II), rhenium(I), and iridium(III) improve PDT, while manganese(II) and iridium(III) demonstrate exceptional sonosensitizing properties.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
December 2024
Department of Chemistry and Fujian Provincial Key Laboratory of Chemical Biology, College of Chemistry and Chemical Engineering, Xiamen University, Xiamen, Fujian, 361005, P. R. China.
Reported herein is a convenient and efficient method for one-pot, catalytic reductive amination, as well as the first multi-component tandem reductive amination-functionalization of bench-stable and readily available common carboxylic esters. This method is based on the cationic [Ir(COD)]BArF-catalyzed chemoselective hydrosilylation of esters, followed by one-pot acid-mediated amination and nucleophilic addition. The reaction was conducted under mild conditions at a very low catalyst loading (0.
View Article and Find Full Text PDFAdv Mater
December 2024
Department of Energy, Environmental & Chemical Engineering, Washington University in St. Louis, St. Louis, MO, 63130, USA.
Iridium (Ir) is the most active and durable anode catalyst for the oxygen evolution reaction (OER) for proton exchange membrane water electrolyzers (PEMWEs). However, their large-scale applications are hindered by high costs and scarcity of Ir. Lowering Ir loadings below 1.
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