Search

Laminated and scale-like Ni/Zn-MOF/ZnO@CC hybrid materials with high orientation are synthesized and exhibit promising electrochemical properties. [Display omitted] Metal-organic frameworks (MOFs) are attracting tremendous research interest because of their rich redox sites and high specific area which are beneficial for the energy storage applications. Nevertheless, the poor conductivity, low mechanical strength and unsatisfactory capacity severely hinder their wide application. Hence, it is of practical significance to design highly efficient and facile strategy to solve these issues. Herein, vertically oriented ZnO nanorod arrays are applied as precursor to synthesize laminated scale-like and highly-oriented Ni/Zn-MOF/ZnO nanocomposite. Owing to the desirable conductivity resulting from the doping nickel ions and the interaction between ZnO and its relative MOF, the fabricated 0.3Ni/Zn-MOF/ZnO@CC electrode exhibits an electrochemical capacitance of 1693 mF cm−2 at 1 mA cm−2. Moreover, the electrochemical capacitance retention of 80.7 % after 2500 cycling numbers is obtained under the constant current density of 10 mA cm−2 and the low internal resistance R s of 0.89 Ω is observed. For practical application, the as-synthesized laminated scale-like Ni/Zn-MOF/ZnO@CC nanocomposite is served as positive electrode to fabricate solid-state asymmetric supercapacitor device. Moreover, a 2.5 V indicator could be powered for 8 min when the prepared supercapacitor units are connected. This work demonstrates the promising potential of the synthesized scale-like Ni/Zn-MOF composites for electrochemical energy storage applications. [ABSTRACT FROM AUTHOR]

Zn metal as a promising anode of aqueous batteries faces severe challenges from dendrite growth and side reactions. Here, tetraphenylporphyrin tetrasulfonic acid (TPPS) is explored as an electrolyte additive for advanced Zn anodes. It is interesting to note that TPPS spontaneously assembles into unique aggregates. As they adsorb on the Zn anode, the aggregates enhance the resistance to electrolyte percolation and dendrite growth compared to single molecules. Meanwhile, TPPS facilitates anion association in the solvation sheath of Zn2+, and boosts the transference number of Zn2+ up to 0.95. Therefore, anion‐related side reactions and anion‐induced electrode overpotentials are reduced accordingly. In this context, the electrolyte containing TPPS exhibits excellent electrochemical performance. Even under a high loading of MnO2 (25 mg cm−2), a limited Zn supply (N/P ratio=1.7), and a lean electrolyte (15 μL mAh−1), the full cells still represent a higher cumulative capacity compared to the reported data. The advantages of this electrolyte are also adapted to other cathode materials. The pouch cells of Zn||NaV3O8 ⋅ 1.5H2O realize a capacity of ~0.35 Ah at 0.4 C under harsh conditions. [ABSTRACT FROM AUTHOR]

Zn metal as a promising anode of aqueous batteries faces severe challenges from dendrite growth and side reactions. Here, tetraphenylporphyrin tetrasulfonic acid (TPPS) is explored as an electrolyte additive for advanced Zn anodes. It is interesting to note that TPPS spontaneously assembles into unique aggregates. As they adsorb on the Zn anode, the aggregates enhance the resistance to electrolyte percolation and dendrite growth compared to single molecules. Meanwhile, TPPS facilitates anion association in the solvation sheath of Zn2+, and boosts the transference number of Zn2+ up to 0.95. Therefore, anion‐related side reactions and anion‐induced electrode overpotentials are reduced accordingly. In this context, the electrolyte containing TPPS exhibits excellent electrochemical performance. Even under a high loading of MnO2 (25 mg cm−2), a limited Zn supply (N/P ratio=1.7), and a lean electrolyte (15 μL mAh−1), the full cells still represent a higher cumulative capacity compared to the reported data. The advantages of this electrolyte are also adapted to other cathode materials. The pouch cells of Zn||NaV3O8 ⋅ 1.5H2O realize a capacity of ~0.35 Ah at 0.4 C under harsh conditions. [ABSTRACT FROM AUTHOR]