Conversion-type transition-metal phosphide anode materials with high theoretical capacity usually suffer from low-rate capability and severe capacity decay, which are mainly caused by their inferior electronic conductivities and large volumetric variations together with the poor reversibility of discharge product (LiP), impeding their practical applications. Herein, guided by density functional theory calculations, these obstacles are simultaneously mitigated by confining amorphous FeP nanoparticles into ultrathin 3D interconnected P-doped porous carbon nanosheets (denoted as FeP@CNs) a facile approach, forming an intriguing 3D flake-CNs-like configuration. As an anode for lithium-ion batteries (LIBs), the resulting FeP@CNs electrode not only reaches a high reversible capacity (837 mA h g after 300 cycles at 0.2 A g) and an exceptional rate capability (403 mA h g at 16 A g) but also exhibits extraordinary durability (2500 cycles, 563 mA h g at 4 A g, 98% capacity retention). By combining DFT calculations, transmission electron microscopy, and a suite of microscopic and spectroscopic techniques, we show that the superior performances of FeP@CNs anode originate from its prominent structural and compositional merits, which render fast electron/ion-transport kinetics and abundant active sites (amorphous FeP nanoparticles and structural defects in P-doped CNs) for charge storage, promote the reversibility of conversion reactions, and buffer the volume variations while preventing pulverization/aggregation of FeP during cycling, thus enabling a high rate and highly durable lithium storage. Furthermore, a full cell composed of the prelithiated FeP@CNs anode and commercial LiFePO cathode exhibits impressive rate performance while maintaining superior cycling stability. This work fundamentally and experimentally presents a facile and effective structural engineering strategy for markedly improving the performance of conversion-type anodes for advanced LIBs.
Download full-text PDF |
Source |
---|---|
http://dx.doi.org/10.1021/acsnano.9b08575 | DOI Listing |
Sci Total Environ
December 2024
Australian Rivers Institute and School of Environment and Science, Griffith University, Nathan Campus, 4111, Queensland, Australia.
Iron-bound organic carbon (Fe-OC) is a main pathway for the long-term maintenance of soil organic carbon (SOC), but research on its mechanism is still relatively weak. We investigated the coupling relationships among iron (Fe), carbon (C) and Fe-reducing bacteria (FeRB) in the soil of a reclaimed paddy field in comparison with natural Phragmites australis wetland in the Minjiang River estuary in southeastern China. The results showed that conversion of P.
View Article and Find Full Text PDFJ Environ Manage
October 2024
State Key Laboratory of Efficient Utilization of Arid and Semi-arid Arable Land in Northern China/Key Laboratory of Arable Land Quality Monitoring and Evaluation, Ministry of Agriculture and Rural Affairs/Institute of Agricultural Resources and Regional Planning, Chinese Academy of Agricultural Sciences, Beijing, 100081, China. Electronic address:
Active iron oxides, especially poorly crystalline forms, benefit soil organic carbon (SOC) accumulation via directly bounding and indirectly promoting aggregation. However, it remains unclear on the impacts of active iron oxides on SOC accumulation in paddy and upland soils under long-term fertilization regimes. Here, we attempted to clarify the underlying mechanisms of amorphous (Fe) and organically complexed (Fe) iron oxides mediating SOC accumulation in paddy and upland soils based on two long-term fertilization experiments (both including no fertilization [CK]; chemical nitrogen, phosphorus and potassium [NPK] and NPK plus manure [NPKM] treatments).
View Article and Find Full Text PDFSci Total Environ
November 2024
Biochar Engineering & Technology Research Center of Liaoning Province, Key Laboratory of Biochar and Soil Improvement, Ministry of Agriculture and Rural Affairs, Agronomy College, Shenyang Agricultural University, Shenyang 110866, China. Electronic address:
Soil organic carbon (SOC) and iron/aluminum (Fe/Al) oxides are key cementing agents in driving soil aggregate formation, yet their direct effects and interactions on aggregate under long-term rice straw cyclic utilization (LSCU) in cold regions are still unclear. We compared chemical fertilizer (CF) with LSCU strategy: rice-straw (RS), biochar (RB), and biochar-based fertilizer (BF). We showed that the increase of macroaggregate (2-0.
View Article and Find Full Text PDFACS Appl Mater Interfaces
January 2024
Key Laboratory of Applied Chemistry, Yanshan University, Qinhuangdao 066004, China.
Potassium-ion batteries (PIBs) have become the desirable alternatives for lithium-ion batteries (LIBs) originating from abundant reserves and appropriate redox potential, while the considerable radius size of K leading to poor reaction kinetics and huge volume expansion limits the practical application of PIBs. Hybridization of transition-metal phosphides and carbon substrates can effectively optimize the obstacles of poor conductivity, sluggish kinetics, and huge volume variation. Thus, the peapod-like structural MP@BNCNTs (M = Fe, Co, and Ni) composites as anode materials for PIBs were synthesized through a facile strategy.
View Article and Find Full Text PDFAdv Sci (Weinh)
November 2023
Key Laboratory for Liquid-Solid Structural Evolution and Processing of Materials (Ministry of Education), School of Materials Science and Engineering, Shandong University, Jinan, 250061, China.
Metallic glass, with its unique disordered atomic structure and high density of low-coordination sites, is regarded as the most competitive new catalyst for environmental catalysis. However, the efficiency and stability of metallic glass catalysts are often affected by their atomic configuration. Thus, the design and regulation of the nanoscale structure of metallic glasses to improve their catalytic efficiency and stability remains a challenge.
View Article and Find Full Text PDFEnter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!