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RSC Advances · 2024 ·Vol. 14 ·期 13 ·8641-8651 · IF 3.9

The microstructure and protective properties of electroplating zinc films on NdFeB from a chloride-free nonaqueous bath

Li Xiaoya,Ma Yongcun,Peng Shusen,Tian lixi

The traditional aqueous electroplating of zinc film causes significant corrosion of NdFeB during the electroplating process, which is accompanied by hydrogen evolution reactions. In this study, electroplating zinc film is carried out from a chloride-free nonaqueous bath using zinc acetate (Zn(OAc)2) as the main salt, sodium acetate (NaOAc) as the conducting salt, and ethylene glycol (EG) as the solvent. The electrochemical properties of the EG bath with Zn(OAc)2 and NaOAc are characterized by means of cyclic voltammetry (CV) and linear sweep voltammetry (LSV) together with a Hull cell test on brass. The results of the experiment show that the Zn(OAc)2 concentration, current density, and temperature significantly impact the deposition behavior of zinc. Moreover, the open circuit potential (OCP) test and scanning electron microscopy (SEM) results demonstrated that the corrosion of NdFeB in the EG bath containing 0.7 M Zn(OAc)2 and NaOAc is effectively inhibited compared to when using the traditional aqueous zinc plating bath. A dense zinc film with a metallic appearance is successfully deposited on the NdFeB surface from the EG bath containing 0.7 M Zn(OAc)2 and NaOAc at 6 mA cm−2 and 60 °C. Comparative experiments demonstrate that the as-deposited Zn film exhibits superior protective performance and exerts less damage to NdFeB compared to the aqueous electroplating film.

研究领域: 材料科学 · 电化学 · 表面工程
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Journal of Energy Chemistry · 2022 · IF 13.599

Host-guest supramolecular interaction behavior at the interface between anode and electrolyte for long life Zn anode

Kai Wu,Fanghua Ning,Jin Yi,Xiaoyu Liu,Jiaqian Qin,Yuyu Liu,Jiujun Zhang

The hydrogen evolution reaction (HER) and dendrite growth associated with Zn anode have become the main bottlenecks for the further development of zinc ion batteries (ZIBs). In this work, the electrochemical activity of H 3 O + is inhibited by the supramolecular host–guest complex composed of H 3 O + as guest and 18-crown-6 as host. The even Zn plating is induced by the host–guest complex electrostatic shielding layer on Zn anode, as detected by in - situ optical microscopy. The lamellar Zn is plated which profits from the improved Zn plating behavior. Density functional theory (DFT) calculation presents the stable structure of complex. The less produced H 2 content is monitored online by a mass spectrometer during Zn plating/stripping, which indicates HER can be hampered by the host–guest behavior. Thus, the ZIBs with long life and high Coulombic efficiency are achieved via introducing 18-crown-6. The proposed host–guest supramolecular interaction is expected to facilitate the furthermore development of Zn batteries.

研究领域: 材料科学 · 电化学
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Journal of the American Chemical Society · 2022 · IF 16.383

Boosting the Kinetics and Stability of Zn Anodes in Aqueous Electrolytes with Supramolecular Cyclodextrin Additives

Kang Zhao,Guilan Fan,Jiuding Liu,Fangming Liu,Jinhan Li,Xunzhu Zhou,Youxuan Ni,Meng Yu,Ying-Ming Zhang,Hui Su,Qinghua Liu,Fangyi Cheng

The hydrophobic internal cavity and hydrophilic external surface of cyclodextrins (CDs) render promising electrochemical applications. Here, we report a comparative and mechanistic study on the use of CD molecules (α-, β-, and γ-CD) as electrolyte additives for rechargeable Zn batteries. The addition of α-CD in aqueous ZnSO4 solution reduces nucleation overpotential and activation energy of Zn plating and suppresses H2 generation. Computational, spectroscopic, and electrochemical studies reveal that α-CD preferentially adsorbs in parallel on the Zn surface via secondary hydroxyl groups, suppressing water-induced side reactions of hydrogen evolution and hydroxide sulfate formation. Additionally, the hydrophilic exterior surface of α-CD with intense electron density simultaneously facilitates Zn2+ deposition and alleviates Zn dendrite formation. A formulated 3 M ZnSO4 + 10 mM α-CD electrolyte enables homogenous Zn plating/stripping (average Coulombic efficiency ∼ 99.90%) at 1 mA cm–2 in Zn|Cu cells and a considerable capacity retention of 84.20% after 800 cycles in Zn|V2O5 full batteries. This study provides insight into the use of supramolecular macrocycles to modulate and enhance the interface stability and kinetics of metallic anodes for aqueous battery chemistry.

研究领域: 材料科学 · 电化学 · 能源存储
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JOURNAL OF COLLOID AND INTERFACE SCIENCE · 2023 · IF 9.9

Artificial bi-functional layers promoting Zn2+ desolvation and homogeneous deposition for reversible zinc metal anodes

Jiahao Chen,Miao He,Anjun Hu,Mengjiao Liu,Chuan Zhao,Bo Zhou,Runjing Li,Zhongfu Yan,Yu Pan,Yining Fan,Jing Liu,Liujun Cao,Jianping Long

Rechargeable aqueous zinc-ion hybrid supercapacitors (ZHSs) are drawing extensive attention because of their cost-effectiveness and diminished safety hazards. Nevertheless, large-scale application of ZHSs has been hindered by the severe side reactions and rampant dendrites growth on the surface of Zn metal anodes. Herein, we propose a three-dimensional organic–inorganic composite frame material as an artificial bi-functional layer coated on the zinc foil, featuring nitrogenous functional groups with zincophilicity (abbreviated as NCFM@Zn). The nitrogen (N) site's strong adsorption capacity and synergistic effect of the sub-nanopore size promote rapid desolvation of zinc ions and reduce side reactions, while also prolonging galvanized nucleation's Sand's time and allowing for even nucleation. Moreover, the uniform distribution of N on the layer results in homogeneous zinc ions flux and supports consistent zinc plating while inhibiting dendrites generation. As a result of this unique artificial bi-functional layer, symmetric Zn cells can survive 2500 h at 2.5 mA cm −2 . High-areal-capacity zinc||activated carbon hybrid supercapacitors also demonstrate 20,000 cycles at high Coulombic efficiency, thus highlighting the utter convenience and potential of this strategy for modifying rechargeable metal hybrid supercapacitor surfaces.

CAS / MDL: 693-98-1
研究领域: 材料科学 · 电化学 · 储能 · 超级电容器
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