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Exploring high-activity electrocatalysts for an oxygen reduction reaction (ORR) is of great significance for a variety of renewable energy conversion and storage technologies. Here, ultrafine MoC nanoparticles assembled in N and P-co-doped carbon (MoC@NPC) was developed from ZIF-8 encapsulated molybdenum-based polyoxometalates (PMo) as a highly efficient ORR electrocatalyst and shows excellent performance for zinc-air batteries. The well distribution of the PMo in ZIF-8 results in the formation of ultrafine MoC nanocrystallites encapsulated in a porous carbon matrix after pyrolysis. Significantly, from experimental and theoretical investigations, the highly porous structure, highly dispersed ultrafine MoC and the N and P co-doping in the MoC@NPC lead to the remarkable ORR activity with an onset potential of ∼1.01 V, a half-wave potential of ∼0.90 V and a Tafel slope of 51.7 mV dec at 1600 rpm in 0.1 M KOH. In addition, the MoC@NPC as an ORR catalyst in zinc-air batteries achieved a high power density of 266 mW cm and a high specific capacity of 780.9 mA h g, exceeding that driven by commercial Pt/C. Our results revealed that the porous architecture and ultrafine MoC nanocrystallites of the electrocatalysts could facilitate mass transport and increase the accessibility of active sites, thus optimizing their performances in an ORR. The present study provides some guidelines for the design and synthesis of efficient nanostructured electrocatalysts.
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http://dx.doi.org/10.1039/d1nr07613b | DOI Listing |
J Am Chem Soc
November 2024
State Key Lab of High Performance Ceramics and Superfine Microstructure, Shanghai Institute of Ceramics, Chinese Academy of Sciences, Shanghai 200050, P. R. China.
Pt-based intermetallics are expected to be the highly active catalysts for oxygen reduction reaction (ORR) in proton-exchange membrane fuel cells but still face great challenges in controllable synthesis of interatomically ordered and ultrafine intermetallic nanoparticles. Here, we propose an oxygen vacancy-mediated atomic diffusion strategy by mechanical alloying to reduce the energy barrier of the transition from interatomic disordering to ordering, and to resist interparticulate sintering via strong M-O-C bonding. This synthesis results in a nanosized core/shell structure featuring an interatomically ordered PtM core and a Pt shell of two to three atomic layers in thickness and can be extended to the multicomponent PtM (M = Co, FeCo, FeCoNi, FeCoNiGa) systems.
View Article and Find Full Text PDFACS Appl Mater Interfaces
October 2024
School of Materials Science and Engineering, Lanzhou University of Technology, Lanzhou 730050, People's Republic of China.
Because of the high theoretical energy density of 2600 Wh kg, lithium-sulfur batteries (LSBs) are anticipated to be among the next generation of high-energy-density storage technologies. However, the practical application of LSBs has been severely hampered by the significant shuttle effect and slow redox kinetics of polysulfides (LiPSs). To address the above problems, in this paper, the concept of quantum dots (QDs) was introduced to design and synthesize MoN QD-modified N-doped graphene nanosheets (marked as MoN-QDs@NG), which were used as separator modification materials for LSBs.
View Article and Find Full Text PDFChem Sci
July 2024
Department of Materials Process Engineering, Graduate School of Engineering, Nagoya University Nagoya 464-8603 Japan.
Molybdenum carbide (MoC) has emerged as a promising material for capacitive deionization (CDI), but the poor electrochemical kinetics in conventional MoC owing to the bulk structure and low electric conductivity limit its CDI performance. To address this challenge, herein, we develop a novel strategy to synthesize ultrafine MoC nanocrystals that are embedded within a three-dimensional nitrogen-doped carbon framework (NC/MoC). This synthesis method involves the space-confined pyrolysis of molybdate precursors within metal-organic frameworks (MOFs).
View Article and Find Full Text PDFJ Colloid Interface Sci
August 2024
State Key Laboratory of Heavy Oil Processing, College of Chemistry and Chemical Engineering, China University of Petroleum (East China), Qingdao 266580, PR China. Electronic address:
Accurately regulating ultrafine molybdenum carbide (MoC)-based catalysts is a significant challenge in the rational design of hydrogen evolution reaction (HER) electrocatalysts. Herein, under the guidance of the first principle calculations, we proposed an in-situ polyoxometalate-confined strategy for creating uniformly distributed ultrafine Co-MoC bimetallic nanoparticles in porous carbon nanostars, with the assistance of precisely designed metal-organic framework (MOF). The Co-MoC@C electrocatalyst has a high specific surface area of 969 m·g because of the conductive carbon substrate with abundant mesopores, which makes for exposing more active sites of Co-MoC nanocrystals (∼1.
View Article and Find Full Text PDFChem Commun (Camb)
September 2023
Institute of Functional Nano & Soft Materials (FUNSOM), Soochow University, 199 Ren'ai Road, Suzhou 215123, Jiangsu, China.
Selenium cathodes have attracted much attention because of the high electronic conductivity and energy density. However, the shuttle effect of lithium polyselenides (LiPSes) leads to rapid capacity fading, hindering the practical application of lithium-selenium (Li-Se) batteries. Herein, an ultrafine MoC catalyst has been synthesized and utilized to accelerate the conversion from liquid LiPSes to solid LiSe/LiSe, leading to suppressed shuttle effect and thus improved battery performance.
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