The development of lithium-sulfur batteries (LSBs) is hindered by the solubility of polysulfide intermediates. Herein, we synthesized oxygen-doped MoS on a highly conductive CNT as a cathode material for LSBs. The spaced oxygen dopants on the catalyst surface enable Li polysulfide chains to adsorb parallel to the catalyst surface. This configuration restricts solubility and accelerates the conversion of soluble Li polysulfides to insoluble LiS. Therefore, the Mo(S-O)/CNT cathode demonstrates an impressive discharge capacity (1410.4 mAh g at 0.2 C and 880.3 mAh g at 2 C) along with exceptional cycle stability, retaining 62.7% capacity after 100 cycles at 0.2 C and showing a low decay rate of 0.094% per cycle over 400 cycles at 2 C in LSBs. This work will inspire further research on the deanchoring design of LiS from negatively charged polar dopants in catalysts as well as studies on the synchronization of catalysis with the anchoring-deanchoring process.
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http://dx.doi.org/10.1021/acs.nanolett.4c05857 | DOI Listing |
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March 2025
Multidisciplinary Platform of Advanced Engineering, Department of Chemical Engineering, School of Engineering, Monash University Malaysia, Jalan Lagoon Selatan, Bandar Sunway, Selangor, 47500, Malaysia.
The design of highly efficient photocatalysts to photoreduce nitrogen (N) to ammonia (NH) under mild conditions is extremely challenging. In this work, various molar ratio of molybdenum (Mo) is incorporated into BiOCl via a hydrothermal process. The resulting Mo-doped BiOCl exhibits remarkable solar-driven activity for N photo fixation without any scavengers or sacrificial agents.
View Article and Find Full Text PDFAdv Mater
March 2025
Key Laboratory of Light Energy Conversion Materials of Hunan Province College, College of Chemistry and Chemical Engineering, Hunan Normal University, Changsha, Hunan, 410081, China.
Iridium-based electrocatalysts are commonly regarded as the sole stable operating acidic oxygen evolution reaction (OER) catalysts in proton-exchange membrane water electrolysis (PEMWE), but the linear scaling relationship (LSR) of multiple reaction intermediates binding inhibits the enhancement of its activity. Herein, the compressive strain and oxygen vacancy effect exists in iridium dioxide (IrO)-based catalyst by a doping engineering strategy for efficient acidic OER activity. In situ synchrotron characterizations elucidate that compressive strain can enhance Ir─O covalency and reduce the Ir─Ir bond distance, and oxygen vacancy (O) as an electronic regulator causes rapid adsorption of water molecules on the Ir and adjacent Ov (Ir─O) pair site to be coupled directly into O─O intermediates.
View Article and Find Full Text PDFInorg Chem
March 2025
Research Center for X-ray Science & Department of Physics, Tamkang University, Tamsui 251301, Taiwan.
Metal-supported cerium dioxide catalysts are widely used in industrial processes. This study investigates copper-cerium dioxide (Cu-CeO) as a promising catalyst for CO oxidation, noted for its cost-effectiveness and low activation temperature. However, the reaction mechanism remains unclear.
View Article and Find Full Text PDFJ Phys Chem Lett
March 2025
Graduate School of System Informatics, Kobe University, 1-1 Rokkodai-cho, Nada-ku, Kobe 657-8501, Japan.
Perovskite SrTiO (STO) is a widely used semiconductor photocatalyst whose photocatalytic activity is significantly influenced by cation doping. In this work, we explore effective divalent dopants to improve the photocatalytic performance of water splitting through both theoretical and experimental approaches. First-principles calculations suggest that divalent Mg and Zn are promising dopants replacing Ti sites of STO to help mitigate charge recombination processes associated with defect levels caused by oxygen vacancies.
View Article and Find Full Text PDFAdv Sci (Weinh)
March 2025
Ultrasound Department of the Second Affiliated Hospital of Chongqing Medical University, Chongqing Key Laboratory of Ultrasound Molecular Imaging, Chongqing, 400010, P. R. China.
Piezocatalyst-enabled sonopiezoelectric therapy offers noninvasive treatment with high spatiotemporal selectivity, yet existing piezocatalysts are limited by suboptimal efficacy, cancer cell resistance to oxidative stress, and biosafety concerns. Here, hafnia (HfO), one of the only few FDA-approved inorganic nanomaterials for clinical trials, is identified as a promising piezocatalyst with high translational potential for sonopiezoelectric and enzymatic PANoptosis-boosted nanocatalytic therapy. Specifically, engineered transition metal-substituted HfO nanocatalysts are synthesized to optimize piezoelectric and enzyme-mimicking activities.
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