RESUMO
The α-diimine late transition metal catalyst represents a new strategy for the synthesis of atactic polypropylene elastomer. Taking into account the properties of the material, enhancing the molecular weight of polypropylene at an elevated temperature through modifying the catalyst structure, and further increasing the activity of α-diimine catalyst for propylene polymerization, are urgent problems to be solved. In this work, two α-diimine nickel(II) catalysts with multiple hydroxymethyl phenyl substituents were synthesized and used for propylene homopolymerization. The maximum catalytic activity was 5.40 × 105 gPP/molNi·h, and the activity was still maintained above 105 gPP/molNi·h at 50 °C. The large steric hindrance of catalysts inhibited the chain-walking and chain-transfer reactions, resulting in polypropylene with high molecular weights (407~1101 kg/mol) and low 1,3-enchainment content (3.57~16.96%) in toluene. The low tensile strength (0.3~1.0 MPa), high elongation at break (218~403%) and strain recovery properties (S.R. ~50%, 10 tension cycles) of the resulting polypropylenes, as well as the visible light transmittance of approximately 90%, indicate the characteristics of the transparent elastomer.
RESUMO
Electrochemically reversible redox couples that embrace more electron transfer at a higher potential are the eternal target for energy storage batteries. Here, we report a four-electron aqueous zinc-iodine battery by activating the highly reversible I2/I+ couple (1.83 V vs. Zn/Zn2+) in addition to the typical I-/I2 couple (1.29 V). This is achieved by intensive solvation of the aqueous electrolyte to yield ICl inter-halogens and to suspend its hydrolysis. Experimental characterization and modelling reveal that limited water activity and sufficient free chloride ions in the electrolyte are crucial for the four-electron process. The merits of the electrolyte also afford to stabilize Zn anode, leading to a reliable Zn-I2 aqueous battery of 6000 cycles. Owing to high operational voltage and capacity, energy density up to 750 Wh kg-1 based on iodine mass was achieved (15-20 wt% iodine in electrode). It pushes the Zn-I2 battery to a superior level among these available aqueous batteries.
RESUMO
The highly reversible zinc-bromine redox couple has been successfully applied in the zinc-bromine flow batteries; however, non-electroactive pump/pipe/reservoir parts and ion-selective membranes are essential to suppress the bromine diffusion. This work demonstrates a zinc-bromine static (non-flow) battery without these auxiliary parts and utilizing glass fiber separator, which overcomes the high self-discharge rate and low energy efficiency while the advantages of the zinc-bromine chemistry are well preserved. It is achieved by a multifunctional additive, tetrapropylammonium bromide (TPABr), which not only mitigates the bromine cross-diffusion by regulating the fluidic bromine to a condensed solid phase but also provides a favorable interface for zinc electrodeposition toward non-dendritic growth. The proposed zinc-bromine static battery demonstrates a high specific energy of 142 Wh kg-1 with a high energy efficiency up to 94%. By optimizing the porous electrode architecture, the battery shows an ultra-stable cycling life for over 11,000 cycles with controlled self-discharge rate.