Non-noble metal-based hydrogenation catalysts have limited practical applications because they exhibit low activity, require harsh reaction conditions, and are unstable in air. To overcome these limitations, herein we propose the alloying of non-noble metal nanoparticles with phosphorus as a promising strategy for developing smart catalysts that exhibit both excellent activity and air stability. We synthesized a novel nickel phosphide nanoalloy (nano-Ni P) with coordinatively unsaturated Ni active sites. Unlike conventional air-unstable non-noble metal catalysts, nano-Ni P retained its metallic nature in air, and exhibited a high activity for the hydrogenation of various substrates with polar functional groups, such as aldehydes, ketones, nitriles, and nitroarenes to the desired products in excellent yields in water. Furthermore, the used nano-Ni P catalyst was easy to handle in air and could be reused without pretreatment, providing a simple and clean catalyst system for general hydrogenation reactions.
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http://dx.doi.org/10.1002/chem.202005037 | DOI Listing |
J Colloid Interface Sci
December 2024
State Key Laboratory of Reliability and Intelligence of Electrical Equipment, Hebei University of Technology, Tianjin 300401, PR China; Engineering Research Center of Ministry of Education for Intelligent Rehabilitation Device and Detection Technology, Hebei University of Technology, Tianjin 300401, PR China; Hebei Key Laboratory of Smart Sensing and Human-Robot Interaction, Hebei University of Technology, Tianjin 300401, PR China; School of Mechanical Engineering, Hebei University of Technology, 5340 Xiping Road, Beichen District, Tianjin 300401, PR China. Electronic address:
Transition-metal-loaded carbon-based electrocatalysts are promising alternatives to conventional precious metal electrocatalysts for the oxygen reduction reaction (ORR) and oxygen evolution reaction (OER) in high-performance zinc-air batteries. However, efficiently doping transition-metal single atoms onto carbon-based frameworks is a significant challenge. Herein, an improved template-sacrificing method combining a two-step carbonization process is proposed to fabricate Cu/Co diatomic sites coanchored on a three-dimensional nitrogen-doped carbon-based framework.
View Article and Find Full Text PDFSmall
December 2024
Department of Chemical Engineering, National Cheng Kung University, Tainan City, 70101, Taiwan.
Development of high-performance and inexpensive electrocatalysts for oxygen evolution reaction (OER) at neutral pH is important for direct seawater splitting and organic electrosynthesis but remains challenging due to the sluggish OER kinetics and diverse side reactions inherent to the constituents of working electrolytes. Herein, we report on a P:NiFe electrode, containing P-doped NiFe alloy, as an excellent electrocatalyst for hydrogen evolution reaction (HER) and OER pre-catalyst for efficient OER in both seawater and organic electrolyte for adiponitrile (ADN) electrosynthesis at neutral pH. Fe and P species modulate the coordination environment of nickel sites, which enables the simultaneous formation of OER-active nickel species and FePO passivation layer, thus transforming HER-active P:NiFe to OER-active a-P:NiFe.
View Article and Find Full Text PDFChempluschem
December 2024
Qinghai University, Mechanical Engineering, Qinghai,China, 810016, Qinghai province, CHINA.
Due to the high catalytic activity and stability for oxygen reduction reaction, N-coordinated Fe-Cu dual-metal doped carbon material (FeCu-N-C) is considered to be one of the promising electrode materials for metal-air battery and fuel cells. Herein, FeCu-N-C dual-metal catalysts was synthesized by an adsorption-calcination strategy. The prepared FeCu-N-C exhibited high activity and stability both in alkaline and acidic media.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
December 2024
Chinese Academy of Sciences Dalian Institute of Chemical Physics, State Key Laboratory of Catalysis, CHINA.
Photocatalytic nitrogen (N2) fixation over semiconductors has always suffered from poor conversion efficiency owing to weak N2 adsorption and the difficulty of N≡N triple bond dissociation. Herein, a Co single-atom catalyst (SAC) model with a C-defect-evoked CoP4 distorted configuration was fabricated using a selective phosphidation strategy, wherein P-doping and C defects co-regulate the local electronic structure of Co sites. Comprehensive experiments and theoretical calculations revealed that the distorted CoP4 configuration caused a strong charge redistribution between the Co atoms and adjacent C atoms, minimizing their electronegativity difference.
View Article and Find Full Text PDFAdv Mater
December 2024
Beijing Key Laboratory of Theory and Technology for Advanced Batteries Materials, School of Materials Science and Engineering, Peking University, Beijing, 100871, China.
Developing sufficiently effective non-precious metal catalysts for large-current-density hydrogen production is highly significant but challenging, especially in low-voltage hydrogen production systems. Here, we innovatively report high-entropy alloy nanoflower array (HEANFA) electrodes with optimizable reaction pathways for hydrazine oxidation-assisted hydrogen production at industrial-grade current densities. Atomic-resolution structural analyses confirm the single-phase solid-solution structure of HEANFA.
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