Nitrogen-containing mesoporous carbon nanospheres have been prepared through an aqueous self-assembly process with F127 as a template and morphological control agent, and 3-aminophenol as carbon and nitrogen sources.
Nanocarbon-supported Pt nanoparticles (NPs) were prepared and tested for the propane dehydrogenation reaction (PDH). The nanocarbon support is composed of a nanodiamond core and a defective, ultrathin graphene nanoshell (ND@G). The Pt/ND@G catalyst experienced slight deactivation during the 100 h PDH test, while the Pt/Al 2 O 3 catalyst showed severe deactivation after the 20 h PDH test. Pt NPs exhibited superior sintering resistance versus that of the ND@G support. This particular support structure of ND@G allows electrons on the defects to transfer to the Pt NPs, leading to a strong metal−support interaction, which significantly prevents Pt NP sintering and promotes the desorption of electron-rich propylene. This electron transfer mechanism was also confirmed by a CO catalytic oxidation test.
Aqueous zinc ion batteries (ZIBs) have been extensively investigated as a next‐generation energy storage system due to their high safety and low cost. However, the critical issues of irregular dendrite growth and intricate side reactions severely restrict the further industrialization of ZIBs. Here, a strategy to fabricate a semi‐immobilized ionic liquid interface layer is proposed to protect the Zn anode over a wide temperature range from −35 to 60 °C. The immobilized SiO2@cation can form high conjugate racks that can regulate the Zn2+ concentration gradient and self‐polarizing electric field to guarantee uniform nucleation and planar deposition; the free anions of the ILs can weaken the hydrogen bonds of the water to promote rapid Zn2+ desolvation and accelerate ion‐transport kinetics simultaneously. Because of these unique advantages, the cycling performance of the symmetric Zn batteries is greatly enhanced, evidenced by a cycling life of 1800 h at 20 mA cm−2, and a cycle lifespan of 2000 h under a wide temperature window from −35 to 60 °C. The efficiency of this semi‐immobilizing strategy is well demonstrated in various full cells including pouch cells, showing high performance at large current (20 A g−1) and wide temperatures with extra‐long cycles up to 80 000 cycles.
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