Dendrite-free zinc metal anodes enabled by electrolyte additive for high-performing aqueous zinc-ion batteries.

Rechargeable aqueous zinc (Zn)-ion batteries are regarded as a suitable candidate for large-scale energy storage due to their high safety and the natural abundance of Zn. However, the Zn anode in the aqueous electrolyte faces the challenges of corrosion, passivation, hydrogen evolution reaction, and the growth of severe Zn dendrites. These problems severely affect the performance and service life of aqueous Zn ion batteries, making it difficult to achieve their large-scale commercial applications. In this work, the sodium bicarbonate (NaHCO3) additive was introduced into the zinc sulfate (ZnSO4) electrolyte to inhibit the growth of Zn dendrites by promoting uniform deposition of Zn ions on the (002) crystal surface. This treatment presented a significant increase in the intensity ratio of (002) to (100) from an initial value of 11.14 to 15.31 after 40 cycles of plating/stripping. The Zn//Zn symmetrical cell showed a longer cycle life (over 124 h at 1.0 mA cm-2) than the symmetrical cell without NaHCO3. Additionally, the high capacity retention rate was increased by 20% for Zn//MnO2 full cells. This finding is expected to be beneficial for a range of research studies that use inorganic additives to inhibit Zn dendrites and parasitic reactions in electrochemical and energy storage applications.

Multishelled NiO/NiCo2O4 hollow microspheres derived from bimetal-organic frameworks as high-performance sensing material for acetone detection.

Recently, tremendous research interest was stimulated to obtain advanced function materials with hierarchical structure and tailored chemical composition from metal-organic frameworks (MOFs) based precursors. Herein, Bimetal-organic frameworks of Ni-Co-BTC solid microspheres synthesized through hydrothermal method were acted as template to induce multishelled NiO/NiCo2O4 hollow microspheres by annealing treatment. When evaluated as gas sensing material, the optimal hybrid of NiO/NiCo2O4 (the molar ration of NiCo=1.5) multishelled hollow microspheres endowed a high sensitivity (17.86) to 100 ppm acetone with rapid response/recovery time (11/13 s) under low working temperature (160 °C) and the low detection limit reached 25 ppb. The enhanced mechanism was originated from the following aspects: the multishelled hollow architecture provided efficient diffusion path for gas molecules and sufficient active site for gas sensing reaction; the nanoscale p-p heterojunction created at NiO and NiCo2O4 nanoparticles interface amplified the resistance variation by tuning the potential barrier; the potent combination of the "chemical catalytic" effect of NiO and the "electrical catalytic" effect of NiCo2O4 improved the selective acetone detection.