Constructing robust nucleation sites with an ultrafine size in a confined environment is essential toward simultaneously achieving superior utilization, high capacity, and long-term durability in Na metal-based energy storage, yet remains largely unexplored. Here, we report a previously unexplored design of spatially confined atomic Sn in hollow carbon spheres for homogeneous nucleation and dendrite-free growth. The designed architecture maximizes Sn utilization, prevents agglomeration, mitigates volume variation, and allows complete alloying-dealloying with high-affinity Sn as persistent nucleation sites, contrary to conventional spatially exposed large-size ones without dealloying. Thus, conformal deposition is achieved, rendering an exceptional capacity of 16 mAh cm in half-cells and long cycling over 7000 hours in symmetric cells. Moreover, the well-known paradox is surmounted, delivering record-high Na utilization (e.g., 85%) and large capacity (e.g., 8 mAh cm) while maintaining extraordinary durability over 5000 hours, representing an important breakthrough for stabilizing Na anode.
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http://dx.doi.org/10.1126/sciadv.abm7489 | DOI Listing |
J Colloid Interface Sci
December 2024
Collaborative Innovation Center of Sustainable Energy Materials, School of Physical Science and Technology, Guangxi University; Guangxi Key Laboratory of Electrochemical Energy Materials, State Key Laboratory of Featured Metal Materials and Life-cycle Safety for Composite Structures, Nanning 530004, China. Electronic address:
Proton exchange membrane fuel cell (PEMFC) with ultra-low Pt loading is highly desirable but confronts challenges of deficient activity and durability for practical application. Herein, we report a newly integrated catalyst layer based on 3D porous B-doped graphene (3D-PBG) with the atomic layer deposition of Pt (Pt/3D-PBG) for PEMFC, in which highly graphitized 3D-PBG not only provides a robust framework to support Pt but also B dopants further enhances the deposition of Pt and their electronic interaction, resulting in high-performance PEMFC at ultra-low Pt loading. The cell with Pt/3D-PBG at 80.
View Article and Find Full Text PDFACS Appl Mater Interfaces
December 2024
Center for Optoelectronics Engineering Research, School of Physics and Astronomy, Yunnan University, Kunming 650500, China.
Highly efficient single-layer organic light-emitting diodes (OLEDs) are demonstrated by using a pure Mg cathode that is seeded with a small amount of Ag nucleation sites. Bis(4-phenylthieno[3,2-]pyridinato-,C2')(acetylacetonate)iridium(III) (PO-01)-doped devices with three-, two-, and one-region doping configurations exhibit maximum external quantum efficiency (EQE) values of 22.8%, 21.
View Article and Find Full Text PDFACS Appl Mater Interfaces
December 2024
State Key Discipline Laboratory of Wide Band Gap Semiconductor Technology, School of Microelectronics, Xidian University, Xi'an 710071, P. R. China.
Flexibility enhancement is a pressing issue in the current development of advanced lithium-metal battery applications. Many types of organic polymers are inherently flexible, which can form a composite structure enhancing electrode flexibility. However, organic polymers have a negative influence on the plating and stripping of lithium-metal anodes, and the large number of polymers block the pore of the material, reducing the utilization of the active site.
View Article and Find Full Text PDFJACS Au
December 2024
Department of Materials Design Innovation Engineering, Nagoya University, Furo-cho, Chikusa-ku, Nagoya 464-8603, Aichi, Japan.
Controlling the nucleation, growth, and dissolution of Li is crucial for the high cycling stability in rechargeable Li metal batteries. The overpotential for Li nucleation (η) on Li alloys such as Li-Au is generally lower than that on metal current collectors (CCs) with very limited Li solubility like Cu. However, the alloying process of CC and its impact on the Li nucleation kinetics remain unclear.
View Article and Find Full Text PDFJ Phys Chem B
December 2024
State Key Laboratory of Physical Chemistry of Solid Surface, Key Laboratory of Chemical Biology of Fujian Province, Collaborative Innovation Center of Chemistry for Energy Materials (iChEM), Innovation Laboratory for Sciences and Technologies of Energy Materials of Fujian Province (IKKEM), Department of Chemistry, College of Chemistry and Chemical Engineering, Xiamen University, Xiamen 361005, P. R. China.
Nucleation is a critical step that determines the assembly pathway and the structure and functions of the peptide assemblies. However, the dynamic evolution of interactions between nucleating agents and peptides, as well as between peptides themselves during the nucleation process, remains elusive. Herein, we show that the heterogeneous nucleating agent carboxymethylcellulose (CMC) can promote the nucleation of Aβ (KF) peptide.
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