Three-dimensionally multiple protected silicon anode toward ultrahigh areal capacity and stability.

Silicon (Si) is considered as one of the most promising candidates for next-generation lithium-ion battery (LIB) anode due to its high theoretical capacity. However, the drastic volume change of Si anodes during lithiation/delithiation processes leads to rapid capacity fade. Herein, a three-dimensional Si anode with multiple protection strategy is proposed, including citric acid-modification of Si particles (CA@Si), GaInSn ternary liquid metal (LM) addition, and porous copper foam (CF) based electrode. The CA modified supports strong adhesive attraction of Si particles with binder and LM penetration maintains good electrical contact of the composite. The CF substrate constructs a stable hierarchical conductive framework, which could accommodate the volume expansion to retain integrity of the electrode during cycling. As a result, the obtained Si composite anode (CF-LM-CA@Si) demonstrates a discharge capacity of 3.14 mAh cm-2 after 100 cycles at 0.4 A g-1, corresponding to 76.1% capacity retention rate based on the initial discharge capacity and delivers comparable performance in full cells. The present study provides an applicable prototype of high-energy density electrodes for LIBs.

Expired milk powder emulsion-derived carbonaceous framework/Si composite as efficient anode for lithium-ion batteries.

Anodes based on silicon/carbon composites promise their commercial prospects for next-generation lithium ion batteries owing to their merits of high specific capacity, enhanced ionic and electronic conductivity, and excellent compatibility. Herein, a series of carbonaceous framework/Si composites are designed and prepared by rational waste utilization. N, P codoped foam-like porous carbon/Si composites (FPC@Si) and N, P codoped carbon coated Si composites (NPC@Si) are fabricated by utilizing expired milk powder as a carbon source with facile treatment methods. The results indicate that the porous carbon skeleton and carbon shell can improve the conductivity of Si and stabilize the solid electrolyte interfaces to avoid direct contact between active material and electrolyte. Moreover, the influence of drastic volume expansion of Si on the anode can be efficiently alleviated during charge/discharge processes. Therefore, the Si/C composite electrodes present excellent long-term cycling stability and rate capability. The electrochemical performance shows that the reversible capacity of FPC@Si and NPC@Si can be respectively maintained at 587.3 and 731.2 mAh g-1 after 1000 charge/discharge cycles under 400 mA g-1. Most significantly, the optimized Si/C composite electrodes exhibit outstanding performance in the full cell tests, promising them great potential for practical applications. This study not only provides a valuable guidance for recycling of waste resources, but also supports a rational design strategy of advanced composite materials for high-performance energy storage devices.

Inorganic crosslinked supramolecular binder with fast Self-Healing for high performance silicon based anodes in Lithium-Ion batteries.

Capacity retention is one of the key factors affecting the performance of silicon (Si)-based lithium-ion batteries and other energy storage devices. Herein, a three dimension (3D) network self-healing binder (denoted as PVA + LB) consisting of polyvinyl alcohol (PVA) and lithium metaborate (LiBO2) solution is proposed to improve the cycle stability of Si-based lithium-ion batteries. The reversible capacity of the silicon electrode is maintained at 1767.3 mAh g-1 after 180 cycles when employing PVA + LB as the binder, exhibiting excellent cycling stability. In addition, the silicon/carbon (Si/C) anode with the PVA + LB binder presents superior electrochemical performance, achieving a stable cycle life with a capacity retention of 73.7% (858.3 mAh g-1) after 800 cycles at a current density of 1 A g-1. The high viscosity and flexibility, 3D network structure, and self-healing characteristics of the PVA + LB binder are the main reasons to improve the stability of the Si or Si/C contained electrodes. The novel self-healing binder shows great potential in designing the new generation of silicon-based lithium-ion batteries and even electrochemical energy storage devices.

Biomass-derived hierarchical N, P codoped porous 3D-carbon framework@TiO2 hybrids as advanced anode for lithium ion batteries.

Advanced anode materials with high theoretical capacity and rate capability are urgently required for next generation lithium ion batteries (LIBs). In this study, hierarchical N, P codoped porous 3D-carbon framework@TiO2 nanoparticle hybrid (N, PC@TiO2) is synthesized by using pollen as biomass precursor through a facile template assisted sol-gel methode and exhibits hierarchical porous hollow structure with plenty of redox active sites and enhanced specific surface area. Compared with N, P codoped porous micro-carbon sphere framework and TiO2 porous hollow microspheres anodes, the N, PC@TiO2 anode shows superior reversible capacity of 687.3 mAh g-1 at 0.1 A g-1 after 200 cycles and 440.5 mAh g-1 after 1000 cycles at 1 A g-1. The excellent performance can be attributed to the rational hierarchical porous hollow structure and the synergetic contributions from the N, P codoped-carbon and TiO2 components, which enhance Li+ storage capability, accelerate the reaction kinetics and stabilize the electrode structure and interface during charge/discharge process. This study suggests a practical strategy to prepare novel anode material with abundant natural resource and facile synthetic route, and the optimized hybrid anode with outstanding Li+ storage properties provides hopeful application prospect in advanced LIBs and other energy storage devices.