Biomass Production and Carbon Stocks in Poplar-Crop Agroforestry Chronosequence in Subtropical Central China.

Agroforest systems have been widely recognized as an integrated approach to sustainable land use for addressing the climate change problem because of their greater potential to sequester atmospheric CO2 with multiple economic and ecological benefits. However, the nature and extent of the effects of an age-sequence of agroforestry systems on carbon (C) storage remain largely unknown. To reveal the influence of different aged poplar-crop systems on C stocks, we investigated the variation in biomass and C storage under four aged poplar-crop agroforest systems (3-, 9-, 13-, and 17-year-old) in the Henan province of China. The results showed that stand biomass increased with forest age, ranging from 26.9 to 121.6 t/ha in the corresponding four aged poplar-crop systems. The poplar tree biomass accounted for >80% of the total stand biomass in these poplar-crop agroforestry systems, except in the 3-year-old agroforestry system. The average stand productivity peaked in a 9-year-old poplar-crop system (11.8 t/ha/yr), the next was in 13- and 17-year-old agroforestry systems, and the minimum was found in 3-year-old poplar-crop stands (4.8 t/ha/yr). The total C stocks increased, with aging poplar-crop systems ranging from 99.7 to 189.2 t/ha in the studied agroforestry systems. The proportion of C stocks accounted for about 6, 25, and 69% of the total C stocks in the crop, poplar tree, and soil components in all studied agroforestry ecosystems, respectively. Our results suggested that the poplar-crop system, especially in productive and mature stages, is quite an effective agroforestry model to increase the study site's biomass production and C stocks. This study highlighted the importance of agroforestry systems in C storage. It recommended the poplar-crop agroforest ecosystems as a viable option for sustainable production and C mitigation in the central region of China.

Dynamic Liquid Metal Catalysts for Boosted Lithium Polysulfides Redox Reaction.

Designing efficient electrocatalysts with high electroconductivity, strong chemisorption, and superior catalytical efficiency to realize rapid kinetics of the lithium polysulfides (LiPSs) conversion process is crucial for practical lithium-sulfur (Li-S) battery applications. Unfortunately, most current electrocatalysts cannot maintain long-term stability due to the possible failure of catalytic sites. Herein, a novel dynamic electrocatalytic strategy with the liquid metal (i.e., gallium-tin, EGaSn) to facilitate LiPSs redox reaction is reported. The combined theoretical simulations and microstructure experiment analysis reveal that Sn atoms dynamically distributed in the liquid Ga matrix act as the main active catalytic center. Meanwhile, Ga provides a uniquely dynamic environment to maintain the long-term integrity of the catalytic system. With the participation of EGaSn, a tailor-made 2 Ah Li-S pouch cell with a specific energy density of 307.7 Wh kg-1 is realized. This work opens up new opportunities for liquid-phase binary alloys as electrocatalysts for high-specific-energy Li-S batteries.

Inducing rapid polysulfide transformation through enhanced interfacial electronic interaction for lithium-sulfur batteries.

Sluggish dynamics of polysulfide (LiPS) conversion leads to reduced utilization of active sulfur and rapid capacity decay. Introducing catalysts into lithium-sulfur battery systems is a feasible and imperative strategy to tackle this problem. Previous research studies have mainly been focused on selecting new catalysts and design functional structures to improve performance, and ignoring the interaction between catalysts and their carriers. Herein, by simply fabricating a high-efficiency ZnS quantum dot@graphene nanosheet catalyst (ZnS QD@rGO), we utilized enhanced interfacial electronic interaction to accelerate polysulfide conversion for high energy density Li-S batteries. With the smaller size of ZnS, the interfacial electronic interaction becomes more enhanced, which was evidenced by DFT calculations and XPS experiments. After mixing with sulfur, the electrodes achieved a high capacity of 857.8 mA h g-1 at 1 C and a retention of 91.2% after 300 cycles. Also, a sulfur cathode with a high actual capacity of ∼4.0 mA h cm-2 could be obtained, with no obvious capacity decay within 100 cycles. We believe that this strategy represents a new perspective on designing efficient high-load electrodes for Li-S batteries.