MoO@aniline-pyrrole (MoO@polymer) spheres as precursors have been used to synthesize unique core-shell nanostructure consisting of molybdenum carbide and molybdenum phosphide composites encapsulated into uniformly dual N, P-doped carbon shells (MoC/MoP@NPC) through a facile two-step strategy. Firstly, porous core-shell N-doped MoC@C (MoC@NC) nanospheres have been synthesized with ultrafine MoC nanoparticles as core and ultrathin NC as shell by a annealing route. Secondly, MoC/MoP@NPC has been obtained maintaining intact spherical-like morphology through a phosphidation reaction in high temperature. The synergistic effect of MoC and MoP may reduce the strong MoH bonding energy of pure MoC and provide a fast hydrogen release process. In addition, the dual N, P-doped carbon matrix as shell can not only improve the electroconductivity of catalysts but also prevent the corrosion of MoC/MoP nanoparticles during the electrocatalytic process. When used as HER cathode in acids, the resulting MoC/MoP@NPC shows excellent catalytic activity and durability, which only needs an overpotential of 160 mV to drive 10 mA cm. Moreover, it also exhibits better HER performance in basic and neutral media with the need for overpotentials of only 169 and 228 mV to achieve 10 mA cm, respectively. This inorganic-organic combination of Mo-based catalysts may open up a new way for water-splitting to produce large-scale hydrogen.
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http://dx.doi.org/10.1016/j.jcis.2017.11.023 | DOI Listing |
J Colloid Interface Sci
January 2025
Hunan Key Laboratory for the Design and Application of Actinide Complexes, College of Chemistry and Chemical Engineering, University of South China, Hengyang, Hunan 421001, China. Electronic address:
Nanoscale Adv
August 2024
Energy Materials Laboratory, Physics Department, School of Sciences & Engineering, The American University in Cairo New Cairo 11835 Egypt
Tuning the surroundings of single-atom catalysts (SACs) has been recognized as a successful approach to enhance their electrocatalytic efficiency. In this study, we utilized density functional theory (DFT) computations to systematically investigate how the coordination environment influences the catalytic performance of individual molybdenum atoms for the nitrogen reduction reaction (NRR) to NH. Upon comparing an extensive array of coordination combinations, Mo-based SACs were found to feature a distinctive N, P-dual coordination.
View Article and Find Full Text PDFACS Nano
May 2024
Energy & Catalysis Center, School of Materials Science & Engineering, Beijing Institute of Technology, Beijing 100081, China.
The ideal interface design between the metal and substrate is crucial in determining the overall performance of the alkyne semihydrogenation reaction. Single-atom alloys (SAAs) with isolated dispersed active centers are ideal media for the study of reaction effects. Herein, a charge-asymmetry "armor" SAA (named PdFe SAA@PC), which consists of a PdFe alloy core and a semiconducting P-doped C (PC) shell, is rationally designed as an ideal catalyst for the selective hydrogenation of alkynes with high efficiency.
View Article and Find Full Text PDFACS Appl Mater Interfaces
April 2024
Department of Chemical Engineering, National Taiwan University, Taipei 10617, Taiwan.
In this work, we demonstrated the synthesis of anions (X = selenium (Se), sulfur (S), and phosphorus (P)) doped cobalt oxytelluride (X-CoOTe) with oxygen and tellurium dual vacancies using hydrothermal methods, followed by selenization, sulfurization, and phosphorization reactions. Especially, the Se-CoOTe-modified nickel foam (Se-CoOTe/NF) electrode delivered a higher specific capacity (752.95 C/g) and an extremely lower charge transfer resistance (0.
View Article and Find Full Text PDFSmall
July 2024
Division of Science Education, Graduate School of Department of Energy Storage/Conversion Engineering, Jeonbuk National University, Jeonju, Jeonbuk, 54896, Republic of Korea.
Fine-tuning nanoscale structures, morphologies, and electronic states are crucial for creating efficient water-splitting electrocatalysts. In this study, a method for electronic structure engineering to enhance overall water splitting in a corrosion-resistant electrocatalyst matrix by integrating Pt, P dual-doped NiMo electrocatalysts onto a TiO nanorod grown on carbon cloth (Pt, P-NiMo-TiO/CC) is introduced. By optimizing platinum and phosphorus concentrations to 1.
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