A Holistic Additive Protocol Steers Dendrite‐Free Zn(101) Orientational Electrodeposition

Author:

Su Yiwen1,Xu Liang2,Sun Yingjie3,Guo Wenyi1,Yang Xianzhong4,Zou Yuhan1,Ding Meng5,Zhang Qihui1,Qiao Changpeng1,Dou Shixue4,Cheng Tao2,Sun Jingyu16ORCID

Affiliation:

1. College of Energy Soochow Institute for Energy and Materials Innovations Jiangsu Provincial Key Laboratory for Advanced Carbon Materials and Wearable Energy Technologies Soochow University Suzhou 215006 P. R. China

2. Institute of Functional Nano and Soft Materials Soochow University Suzhou 215123 P. R. China

3. Key Laboratory of Photoelectric Control on Surface and Interface of Hebei Province College of Science Hebei University of Science and Technology Shijiazhuang 050018 P. R. China

4. Institute of Energy Materials Science University of Shanghai for Science and Technology Shanghai 200093 P. R. China

5. Department of Chemistry Xi'an Jiaotong‐Liverpool University Suzhou 215123 P. R. China

6. Beijing Graphene Institute Beijing 100095 P. R. China

Abstract

AbstractOrientation guidance has shown its cutting edges in electrodeposition modulation to promote Zn anode stability toward commercialized standards. Nevertheless, large‐scale orientational deposition is handicapped by the competition between Zn‐ion reduction and mass transfer. Herein, a holistic electrolyte additive protocol is put forward via incorporating bio‐derived dextrin molecules into a zinc sulfate electrolyte bath. Electrochemical tests in combination with molecular dynamics simulations demonstrate the alleviation of concentration polarization throughout accelerating Zn2+ diffusion and retarding their reduction. The predominant (101) texture on inert current collectors (i.e., Cu, Ti, and stainless steel) and (101)/(002) textures on Zn foils afford homogeneous electrical field distribution, which is contributed by the work difference to form the 2D nucleus and the adsorption of dextrin molecules, respectively. Consequently, the symmetric cell harvests a longevous cycling lifespan of over 4000 h at 0.5 mA cm−2/0.5 mAh cm−2 while the Zn@Cu electrode sustains for 240 h at a high depth of discharge of 40%.

Funder

National Natural Science Foundation of China

Science Fund for Distinguished Young Scholars of Jiangsu Province

Publisher

Wiley

Subject

Biomaterials,Biotechnology,General Materials Science,General Chemistry

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