Scaling up electrochemical water splitting is nowadays in high demand for hydrogen economy implementation. Tremendous efforts over the past decade have been focused on exploring alternative catalytic materials, including a variety of earth-abundant transition-metal-based catalysts, to replace traditional noble metals such as Pt, Ir, or Ru. Nevertheless, few efforts have been carried out for (1) scalable catalyst synthesis on current collectors and (2) practical device design toward large-scale H generation. Herein, we designed a modular alkaline water-splitting electrolyzer system with scaled-up metal foam electrodes covered by low-cost NiMo alloy and NiFe oxide for efficient hydrogen evolution and oxygen evolution, respectively. An electrolyte circulation system facilitates the mass transport and thus can further boost the H generation particularly under large currents. As a result, the overall water-splitting performance of one-unit cell with a dimension of 10 × 10 cm under room temperature presents an early onset voltage of 1.54 V and delivered practical currents of 20 and 55 A (9.1 and 25.0 L/h H generation) under 2.2 and 2.9 V without iR compensations, respectively. This demonstration could stimulate new focuses in water splitting toward more practical applications.
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http://dx.doi.org/10.1021/acsami.8b19251 | DOI Listing |
Angew Chem Int Ed Engl
January 2025
Zhejiang University, College of Chemical and Biological Engineering, CHINA.
Electrochemical water splitting is a pivotal technology for storing intermittent electricity from renewable sources into hydrogen fuel. However, its overall energy efficiency is impeded by the sluggish oxygen evolution reaction (OER) at the anode. In the quest to design high-performance anode catalysts for driving the OER under non-acidic conditions, iron (Fe) has emerged as a crucial element.
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January 2025
Hubei Key Laboratory for Precision Synthesis of Small Molecule Pharmaceuticals, Collaborative Innovation Center for Advanced Organic Chemical Materials Co-constructed by the Province and Ministry, Ministry-of-Education Key Laboratory for the Synthesis and Application of Organic Functional Molecules, College of Chemistry and Chemical Engineering, Hubei University, Wuhan, 430062, P. R. China.
Exploring highlyefficient electrocatalysts for overall water splitting is a challenging butnecessary task for development of green and renewable energy. Herein, PtIrFeCoNi high-entropy alloy nanoflowers (HEA NFs) withstrong 3d-5d orbital hybridization were fabricated to achieve highly efficientoverall water splitting at high current density. The PtIrFeCoNi HEA NFs achieved a 57.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
January 2025
Nanjing University of Aeronautics and Astronautics, College of Materials Science and Technology, No. 169 Sheng Tai West Road, Jiangning District, Nanjing, Jiangsu, China, 211106, Nanjing, CHINA.
Transition metal-based catalysts with high efficiency and stability for overall water splitting (OWS) offer significant potential for reducing green hydrogen production costs. Utilizing sputtering deposition technology, we propose a deposition-diffusion strategy to fabricate heterojunction coatings composed of ultrafine FeCoNi-C-N transition metal interstitial solid solution (TMISS) nanocrystals and amorphous nitrided carbon (NC) on the pre-deposited NC micro column arrays. The diffusion of C and N atoms results in the formation of uniformly distributed TMISS nanocrystals, with an average diameter of ~1.
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January 2025
Key Laboratory of Eco-chemical Engineering, International S&T Cooperation Foundation of Eco-chemical Engineering and Green Manufacture, College of Chemistry and Molecular Engineering, Qingdao University of Science and Technology, Qingdao, 266042, P. R. China.
Crafting anisotropically epitaxial p-n heterostructures with Z-scheme charge transmission is a promising avenue toward excellent photocatalytic efficiency, yet the large lattice mismatch and diverse crystal growth habits between components have often arisen as a big challenge to this goal. Here, anisotropically epitaxial p-n heterostructures with 19.8% lattice mismatch are obtained via a dynamics-mediated seeded growth tactic under reaction temperature as low as 60 °C.
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January 2025
Institute of Environmental Research at Greater Bay, Key Laboratory for Water Quality and Conservation of the Pearl River Delta, Ministry of Education, Guangzhou University, Guangzhou, 510006, P. R. China.
Developing efficient, multifunctional electrodes for energy storage and conversion devices is crucial. Herein, lattice strains are reported in the β-phase polymorph of CoMoO within CoMoO@CoO heterostructure via phosphorus doping (P-CoMoO@CoO) and used as a high-performance trifunctional electrode for supercapacitors (SCs), hydrogen evolution reaction (HER), and oxygen evolution reaction (OER) in alkaline electrolytes. A tensile strain of +2.
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