Exploring Si-based anode materials with high electrical conductivity and electrode stability is crucial for high-performance lithium-ion batteries (LIBs). Herein, we propose the fabrication of a Si-based composite where Si porous nanospheres (Si p-NSs) are tightly wrapped by Ti 3 C 2 T x (T x stands for the surface groups such as −OH, −F) MXene nanosheets (TNSs) through an interfacial assembly strategy. The TNSs as a conductive and robust tight of the Si p-NSs can effectively improve electron transport and electrode stability, as revealed by substantial characterizations and mechanical simulations. Moreover, the TNSs with rich surface groups enable strong interfacial interactions with the Si p-NS component and a pseudocapacitive behavior, beneficial for fast and stable lithium storage. Consequently, the Si p-NS@TNSs electrode with a high Si content of 85.6% exhibits significantly enhanced battery performance compared with the Si p-NSs electrode such as high reversible capacity (1154 mAh g −1 at 0.2 A g −1 ), long cycling stability (up to 2000 cycles with a 0.026% capacity decay rate per cycle), and excellent rate performances. Notably, the Si p-NS@TNSs electrode-based LIB full cell delivers a high energy uptake of 405 Wh kg −1 , many-times higher than that of the Si p-NSs full cell. This work offers a strategy to develop advanced Si-based anode materials with desirable properties for high-performance LIBs.

The exploration of advanced electrode materials through rational structure/phase design is the key to develop high‐performance rechargeable batteries. Herein, ternary metal phosphorus trisulfides (NiCoPS3) with a bimetallic phase and an extrinsic structure of nanodots combined with nitrogen‐doped graphitized carbon (NC) are developed for lithium‐ion batteries. The designed NiCoPS3/NC holding a nanocube‐like morphology shows a set of structural/compositional advantages as lithium‐ion battery anodes including high electrical conductivity, low ion diffusion barrier, improved theoretical lithium storage capacity, and relieved lithiation stress, which are confirmed by characterizations and density functional theory calculations. As a consequence, the NiCoPS3/NC electrode displays superior comprehensive lithium storage performance, e.g., high reversible capacity (991 mAh g−1 at 0.1 A g−1), excellent cycling stability (up to 1200 cycles at 2 A g−1 and 2000 cycles at 5 A g−1 with respective capacity retention of over or nearly 100%), and good rate capability (58.4% capacity retention after a current change from 0.1 to 5 A g−1), representing the best comprehensive battery performance in MPS3‐based anodes to date.

No abstract

Potassium-ion capacitors (KICs) are promising for sustainable and eco-friendly energy storage technologies, yet their slow reaction kinetics and poor cyclability induced by large K-ion size are a major obstacle toward practical applications. Herein, by employing black phosphorus nanosheets (BPNSs) as a typical high-capacity anode material, we report that BPNS anodes armored with an ultrathin oriented-grown metal–organic-framework (MOF) interphase layer (BPNS@MOF) exhibit regulated potassium storage behavior for high-performance KICs. The MOF interphase layers as protective layer with ordered pores and high chemical/mechanical stability facilitate K ion diffusion and accommodate the volume change of electrode, beneficial for improved reaction kinetics and enhanced cyclability, as evidenced by substantial characterizations, kinetics analysis and DFT calculations. Consequently, the BPNS@MOF electrode as KIC anodes exhibits outstanding cycle performance outperforming most of the reported state-of-art KICs so far.

Effective removal of the organic pollutants from aqueous solution is significative and challenging for environmental sustainability. The high-performance adsorbent materials need to be developed. In this study, oxygen-rich fish-scale-like porous boron nitride (O-PBN) was facilely synthesized only at 900[Formula: see text]C (about 400[Formula: see text]C lower than that of the conventional process) through the molten salt method. The adsorption capacity of the as-prepared O-PBN for Methylene Blue (MB) from water was 422.6 mg/g, resulting from oxidizing groups and B–O bonds induced by oxygen doping as well as fish-scale-like structure composed of the BN nanoflakes. Moreover, the initial removal capacity of O-PBN only lost 7.6% even after 10 adsorption–regeneration cycles due to their strong resistance to oxidation. The unique B–O polar covalent bond, fish-scale-like two-dimensional nanostructure exposing the active adsorption sites to the surface ((002) crystal plane) and high specific surface area of O-PBN are confirmed to be the key factors in significantly enhancing water purification and regeneration performance. Overall, the synthetic method should help to a low-temperature and facile fabrication of O-PBN for effective water cleaning.