Low-cost and efficient electrocatalysts for overall water splitting are in high demand for a wide range of applications across renewable and clean energy. Here, we report a simple one-step synthesis of a three-dimensional (3D) carbon-coated NiP nanosheet array as bifunctional catalyst for both hydrogen evolution reactions (HER) and oxygen evolution reactions (OER). The nanosheet array possesses low overpotentials, high current densities, and small Tafel slopes in both HER and OER and shows high electrocatalytic activities and long-term stability. The carbon layer with high electric conductivity serves not only as a protective layer to prevent NiP dissolution but also as an active layer to decrease the electrocatalysis overpotential. The nanosheet array has HER outstanding activity in both acid and alkaline media. Its superior performance in OER can be due to the synergistic interaction at the NiP/NiO heterojunction. Furthermore, cell voltage as low as 1.65 V can achieve 10 mA cm current density for full water splitting in an alkaline water electrolyzer, indicating potential application of C@ NiP as bifunctional catalyst for clean and renewable energy utilization.
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http://dx.doi.org/10.1021/acsami.6b10552 | DOI Listing |
Photosynth Res
January 2025
Department of Chemistry, Graduate School of Science and Technology, Proteo-Science Research Center, Ehime University, Bunkyo-cho, Matsuyama, Ehime, 790-8577, Japan.
The active site for water oxidation in photosystem II (PSII) comprises a MnCaO cluster adjacent to a redox-active tyrosine residue (Tyr). During the water-splitting process, the enzyme transitions through five sequential oxidation states (S to S), with O evolution occurring during the STyr· to STyr transition. Chloride also plays a role in this mechanism.
View Article and Find Full Text PDFAngew 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.
View Article and Find Full Text PDFSmall
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.
View Article and Find Full Text PDFSmall
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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