3D printing has emerged as a highly efficient process for fabricating electrodes in hydrogen evolution through water splitting, whereas metals are the most popular choice of materials in hydrogen evolution reactions (HER) due to their catalytic activity. However, current 3D printing solutions face challenges, including high cost, low surface area, and sub-optimal performance. In this work, we introduce metal-deposited 3D printed pyrolytic carbon (PyC) as a facile and cost-effective HER electrode. We adopt an integrated approach of resin 3D printing, pyrolysis, and electrochemical metal deposition. 3D printing of a resin and its subsequent pyrolysis led to 3D complex architectures of the conductive substrate, facilitating the electrochemical metal deposition and leading to layered 3D metal architecture. Both monolayers of metals (such as copper and nickel) and bi-metallic 3D PyC structures are demonstrated. Each metal layer thickness ranges from 6 to10 µm. The metal coatings, particularly the bi-metallic configurations, result in achieving significantly higher mechanical properties under compressive loading and improved electrical properties due to the synergistic contributions from each metal counterpart. The metalized PyC structures are further demonstrated for HER catalysts, contributing to the development of highly efficient and durable catalyst systems for hydrogen production. Among the materials studied here, Ni@Cu bimetallic 3D PyC electrodes are particularly well-suited, demonstrating a low HER overpotential value of 264 mV (100 mA/cm, KOH (1 M)) with corresponding Tafel slopes of 107 mV/dec, with exceptional stability during a 10 h operation at a high applied current of -50 mA/cm.
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http://dx.doi.org/10.1080/14686996.2024.2421740 | DOI Listing |
Micromachines (Basel)
November 2024
Department of Fiber System Engineering, Yeungnam University, 280 Dehak-Ro, Gyeongsan 38541, Republic of Korea.
The pursuit of efficient and economical catalysts for water splitting, a critical step in hydrogen production, has gained momentum with the increasing demand for sustainable energy. Among the various electrocatalysts developed to date, cobalt oxide (CoO) has emerged as a promising candidate owing to its availability, stability, and catalytic activity. However, intrinsic limitations, including low catalytic activity and poor electrical conductivity, often hinder its effectiveness in electrocatalytic water splitting.
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December 2024
Department of Chemistry, Faculty of Science, Fukuoka University, 8-19-1 Nanakuma, Jonan-ku, Fukuoka 814-0180, Japan.
In this article, we investigate the encapsulation of K[Ni(maleonitriledithiolate)] () within a host molecule, β-cyclodextrin (β-CD), via single-crystal X-ray analysis. An inclusion complex, K{[Ni(maleonitriledithiolate)]@(β-CD)} (), was constructed from and two β-CDs. The anion guest Ni complex included a host cavity, constructed using two β-CDs, and the Ni atom of the anion was located between the two hydrophilic primary rims.
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December 2024
School of Pharmaceutical Sciences, Gannan Medical University, Ganzhou 341000, China.
Photocatalytic hydrogen evolution using inexhaustible clean solar energy is considered as a promising strategy. In order to build an efficient photocatalytic hydrogen production system to satisfy the demands of practical applications, it is of great significance to design photocatalysts that offer high activity, low cost, and high stability. Herein, a series of cheap CdS/Ni(OH) composite photocatalysts were designed and synthesized using the hydrothermal method.
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December 2024
School of Chemistry and Chemical Engineering, Northwestern Polytechnical University, Xi'an 710129, China.
Developing highly efficient and cost-competitive electrocatalysts for the hydrogen evolution reaction (HER), which can be applied to hydrogen production by water splitting, is of great significance in the future of the zero-carbon economy. Here, by means of first-principles calculations, we have scrutinized the HER catalytic capacity of single-atom catalysts (SACs) by embedding transition-metal atoms in the C and Mo vacancies of a tetragonal MoC slab, where the transition-metal atoms refer to Ti, V, Cr, Mn, Fe, Co, Ni and Cu. All the MoC-based SACs exhibit excellent electrical conductivity, which is favorable to charge transfer during HER.
View Article and Find Full Text PDFJ Colloid Interface Sci
January 2025
College of Chemical Engineering, Qingdao University of Science and Technology, Qingdao 266042, China. Electronic address:
Developing efficient and cost-effective rare earth element-based electrocatalysts for water splitting remains a significant challenge. To address this, interface engineering and charge modulation strategies were employed to create a three-dimensional coral-like CeF/MoO heterostructure electrocatalyst, grown in situ on the multistage porous channels of carbonized sugarcane fiber (CSF). Integrating abundant CeF/MoO heterostructure interfaces and numerous oxygen vacancy defects significantly enhanced the catalyst's active sites and molecular activation capabilities.
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