The practical application of sulfur (S) cathodes in lithium-sulfur (Li-S) batteries is hindered by the shuttling of soluble lithium polysulfides (LiPSs) and sluggish sulfur redox kinetics. Addressing these challenges requires advanced catalytic host materials capable of trapping LiPSs and accelerating Li-S redox reactions. However, single-site catalysts struggle to effectively mediate the complex multi-step and multi-phase sulfur conversion processes. In this study, we present a novel dual-site catalyst, featuring nickel single atoms anchored to nitrogen sites (Ni-N4) within a carbon nitride (NC) matrix and molybdenum carbide (MoC) nanoclusters. Experimental and theoretical analyses reveal that MoC sites efficiently catalyze the reduction of long-chain LiPSs, while Ni-N4 sites drive the reduction of short-chain LiPSs. When incorporated as a coating on the cathode side of a commercial polypropylene (PP) separator, the Ni-MoC-NC catalyst enhances sulfur utilization, suppresses LiPSs shuttling, and facilitates a uniform Li+-ion distribution. Thereby, Li-S batteries demonstrate outstanding performance, including an initial capacity of 1624 mAh g⁻¹ at 0.2C and 1142 mAh g⁻¹ at 1C. At a sulfur loading of 8.3 mg cm⁻² and an electrolyte/sulfur ratio of 6 µL mg⁻¹, the system achieves an initial areal capacity of 9.57 mAh cm⁻² at 0.1C, showcasing significant promise for practical applications.
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http://dx.doi.org/10.1002/anie.202502177 | DOI Listing |
Angew Chem Int Ed Engl
March 2025
Zhengzhou University, School of Chemical Engineering, CHINA.
The practical application of sulfur (S) cathodes in lithium-sulfur (Li-S) batteries is hindered by the shuttling of soluble lithium polysulfides (LiPSs) and sluggish sulfur redox kinetics. Addressing these challenges requires advanced catalytic host materials capable of trapping LiPSs and accelerating Li-S redox reactions. However, single-site catalysts struggle to effectively mediate the complex multi-step and multi-phase sulfur conversion processes.
View Article and Find Full Text PDFJ Colloid Interface Sci
February 2025
College of Materials Science and Engineering, Fuzhou University, Fuzhou 350108 Fujian, China. Electronic address:
The triggering of fast hydrogen spillover through regulating the charge rearrangement of the metal-support serves as a crucial mechanism for decoupling the activity of HER catalysts from the adsorption properties, which not only contributes to enhancing the performance of the catalysts but also facilitates the production of green hydrogen. Herein, we tailor the electronic interaction between two-dimensional (2D) nitrogen-doped MoC (N-MoC) nanosheets and anultra-low content of Pt nanoclusters (1 wt%) to trigger reverse hydrogen spillover and modulate the electronic structure of Pt, thus achieving efficient and stable HER. Compared to Pt/C (0.
View Article and Find Full Text PDFNat Commun
January 2025
State Key Laboratory of Heavy Oil Processing, China University of Petroleum, Qingdao, Shandong, P.R. China.
Pt/α-MoC catalysts exhibit exceptional activity in low-temperature water-gas shift reactions. However, quantitatively identifying and fine-tuning the active sites has remained a significant challenge. In this study, we reveal that fully exposed monolayer Pt nanoclusters on molybdenum carbides demonstrate mass activity that exceeds that of bulk molybdenum carbide catalysts by one to two orders of magnitude at 100-200 °C for low-temperature water-gas shift reactions.
View Article and Find Full Text PDFSci Bull (Beijing)
February 2025
Key Laboratory for Colloid and Interface Chemistry, Ministry of Education, School of Chemistry and Chemical Engineering, Shandong University, Jinan 250100, China. Electronic address:
The challenges posed by the non-conductive nature of iodine, coupled with the easy formation of soluble polyiodides in water, impede its integration with zinc for the development of advanced rechargeable batteries. Here we demonstrate the in-situ loading of molybdenum carbide nanoclusters (MoC) and zinc single atoms (Zn-SA) into porous carbon fibers to invoke electrocatalytic conversion of iodine at the interface. The electronic interactions between MoC and Zn-SA lead to an upshift in the d-band center of Mo relative to the Fermi level, thus promoting the interfacial interactions with iodine species to suppress shuttle effects.
View Article and Find Full Text PDFMikrochim Acta
October 2024
Hunan Provincial Key Laboratory of Micro & Nano Materials Interface Science, College of Chemistry and Chemical Engineering, Central South University, Changsha, 410083, China.
The overexpression of interleukin-17A (IL-17A) is closely associated with the pathogenesis of autoimmune diseases and cancer, rendering precise identification of IL-17A level critical for disease diagnosis and prognosis monitoring. In this study, CsPbBr nanoclusters (NCs) were embedded in CHBrOPb organometallic compound (Pb-MA MOC) via a hot injection approach. Through this way, the issue of CsPbBr NCs susceptible to decomposition in water was solved, and the photocurrent intensity that is generated by CsPbBr was significantly enhanced.
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