Qiu Meijia, Sun Peng, Cui Guofeng, Mai Wenjie
Key Laboratory for Polymeric Composite & Functional Materials of Ministry of Education, School of Chemistry, Key Laboratory of Low-carbon Chemistry & Energy Conservation of Guangdong Province, Sun Yat-sen University, Guangzhou 510275, People's Republic of China.
Siyuan Laboratory, Guangdong Provincial Engineering Technology Research Center of Vacuum Coating Technologies and New Energy Materials, Guangzhou Key Laboratory of Vacuum Coating Technologies and New Energy Materials, Department of Physics, Jinan University, Guangdong 510632, People's Republic of China.
ACS Appl Mater Interfaces. 2022 Sep 14;14(36):40951-40958. doi: 10.1021/acsami.2c10517. Epub 2022 Aug 29.
Zn batteries are considered the new-generation candidate for large-scale energy storage systems, taking both safety and environmental problems into account. They are still restricted by unexpected dendrite/byproducts occurring on the Zn anodes. We hereby screen a powerful polymer type additive, hyaluronic acid (HA), to regulate the typical ZnSO electrolyte for obtaining dendrite-free Zn ion batteries. The intrinsically chaotropic property of the HA molecule can efficiently destruct the original hydrogen-bonds from HO-HO, thus restricting the common parasitic reactions derived from the large amount of active water molecules. Simultaneously, the abundant functional groups along the long chain from HA additives can construct an effective tunnel for transferring Zn smoothly, enabling an obviously improved Zn ion transference number of 0.62. Owning to the above intriguing mechanism for regulating the solvation structure of electrolyte systems, the HA additives can greatly increase the cycling life of Zn-Zn symmetric cells to 2200 and 800 h under the conditions of 1 mA cm/1 mAh cm and 5 mA cm/5 mAh cm, respectively. Modified performance for both Zn-Ti and Zn-MnO can all be realized by this valid additive, elucidating it can be potentially utilized in large-scale Zn based aqueous energy storage devices.