Promoting Reversible Redox Kinetics by Separator Architectures Based on CoS2 /HPGC Interlayer as Efficient Polysulfide-Trapping Shield for Li-S Batteries.

Main obstacles from the shuttle effect and slow conversion rate of soluble polysulfide compromise the sulfur utilization and cycling life for lithium sulfur (Li-S) batteries. In pursuit of a practically viable high performance Li-S battery, a separator configuration (CoS2 /HPGC/interlayer) as efficient polysulfide trapping barrier is reported. This configuration endows great advantages, particularly enhanced conductivity, promoted polysulfide trapping capability, accelerated sulfur electrochemistry, when using the functional interlayer for Li-S cells. Attributed to the above merits, such cell shows excellent cyclability, with a capacity of 846 mAh g-1 after 250 cycles corresponding to a high capacity retention of 80.2% at 0.2 C, and 519 mAh g-1 after 500 cycles at 1C (1C = 1675 mA g-1 ). In addition, the optimized separator exhibits a high initial areal capacity of 4.293 mAh cm-2 at 0.1C. Moreover, with CoS2 /HPGC/interlayer, the sulfur cell enables a low self-discharge rate with a very high capacity retention of 97.1%. This work presents a structural engineering of the separator toward suppressing the dissolution of soluble Li2 Sn moieties and simultaneously promoting the sulfur conversion kinetics, thus achieving durable and high capacity Li-S batteries.

Development of a Synergistic Activation Strategy for the Pilot-Scale Construction of Hierarchical Porous Graphitic Carbon for Energy Storage Applications.

Pursuing scalable production of porous carbon with facile and environmentally friendly synthesis methodology is a global goal. Herein, a unique hierarchical porous graphitic carbon (HPGC) with outstanding textural characteristics is achieved by a special synergistic activation mechanism, in which the low-temperature molten state of polymorphisms can induce a high-rate liquid phase porous activation. HPGC with high specific surface area (SSA, ∼2571 m2 g-1) and large pore volume (PV, ∼2.21 cm3 g-1) can be achieved, which also possesses the capability to tune textural characteristics (i.e., SSA, PV, pore size distribution, etc.) within a wide range. Furthermore, the pilot-scale production of HPGC is accomplished, which shows similar textural characteristics to the lab-scale HPGC. Due to the unique structure of HPGC and the capability of the textural control, it can be applicable in a variety of energy storage, energy conversion, and catalysis applications. The applications of pilot-scale HPGC products in supercapacitors and lithium sulfur batteries are highlighted in this work. Furthermore, the synergistic activation strategy can be promoted to other alkali-based carbon activation routes, which can open up new possibilities for the activated carbon production and lead to more widespread industrialized applications of HPGC.

Direct synthesis of pure single-crystalline Magnéli phase Ti8O15 nanowires as conductive carbon-free materials for electrocatalysis.

The Magnéli phase Ti8O15 nanowires (NWs) have been grown directly on a Ti substrate by a facile one-step evaporation-deposition synthesis method under a hydrogen atmosphere. The Ti8O15 NWs exhibit an outstanding electrical conductivity at room temperature. The electrical conductivity of a single Ti8O15 nanowire is 20.6 S cm(-1) at 300 K. Theoretical calculations manifest that the existence of a large number of oxygen vacancies changes the band structure, resulting in the reduction of the electronic resistance. The Magnéli phase Ti8O15 nanowires have been used as conductive carbon-free supports to load Pt nanoparticles for direct methanol oxidation reaction (MOR). The Pt/Ti8O15 NWs show an enhanced activity and extremely high durability compared with commercial Pt/C catalysts.