In Situ Construction of Organic–Inorganic Hybrid Interfacial Films via Electrolyte Additive for Advanced Aqueous Zinc-Ion Batteries

Aqueous zinc ion batteries have garnered widespread attention due to their high safety, cost-effectiveness, and environmental friendliness. However, hydrogen precipitation, byproduct aggregation, and dendrite growth at zinc anode as well as material degradation of the cathode severely impede further practical development. Here, we construct organic–inorganic hybrid interfacial films on electrodes by employing trifluoroacetamide (CNF) as an additive. The interfacial films homogenize zinc deposition, inhibit the byproducts’ aggregation as well as hydrogen evolution on the anode, and enhance cathode morphological integrity upon cycling. The cycle life of Zn||Zn cells is significantly extended at a high current density. Meanwhile, a Coulombic efficiency of 99.9% is achieved at 10 mA cm–2 after 4000 cycles for Zn||Cu cell. The Zn||Na2V6O16·3H2O full cells after 12000 cycles present 145 and 99 mAh g–1 at 5 and 20 A g–1, respectively. Therefore, the efficient and convenient strategy of introducing an electrolyte additive provides a reliable solution to issues at the interfaces for other secondary battery systems.

Authors

Institutions

Publication Details

Journal
ACS Energy Letters
Published
2025-03-12
DOI
https://doi.org/10.1021/acsenergylett.4c02684
Citations
21
Primary Topic
Advanced battery technologies research
Type
article
Field-Weighted Citation Impact
15.34

Funders

Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

In Situ Construction of Organic–Inorganic Hybrid Interfacial Films via Electrolyte Additive for Advanced Aqueous Zinc-Ion Batteries

Xue Chen, Yu Jia, Ying Bai, Kai Zhang et al.
21 citations
ACS Energy Letters
Advanced battery technologies research
15.34
article

In Situ Construction of Organic–Inorganic Hybrid Interfacial Films via Electrolyte Additive for Advanced Aqueous Zinc-Ion Batteries

Xue Chen, Yu Jia, Ying Bai, Kai Zhang, Kai Wang, Jiasen Shen, Peng Lv, Shijia Li, Yibing Zhang, Jingwen Zhao
article en
21 citations

Abstract

Aqueous zinc ion batteries have garnered widespread attention due to their high safety, cost-effectiveness, and environmental friendliness. However, hydrogen precipitation, byproduct aggregation, and dendrite growth at zinc anode as well as material degradation of the cathode severely impede further practical development. Here, we construct organic–inorganic hybrid interfacial films on electrodes by employing trifluoroacetamide (CNF) as an additive. The interfacial films homogenize zinc deposition, inhibit the byproducts’ aggregation as well as hydrogen evolution on the anode, and enhance cathode morphological integrity upon cycling. The cycle life of Zn||Zn cells is significantly extended at a high current density. Meanwhile, a Coulombic efficiency of 99.9% is achieved at 10 mA cm–2 after 4000 cycles for Zn||Cu cell. The Zn||Na2V6O16·3H2O full cells after 12000 cycles present 145 and 99 mAh g–1 at 5 and 20 A g–1, respectively. Therefore, the efficient and convenient strategy of introducing an electrolyte additive provides a reliable solution to issues at the interfaces for other secondary battery systems.

ACS Energy LettersVol. 10(4)
Henan University (CN), Center for Theoretical Physics (PL), Joint Research Center (ES)
National Natural Science Foundation of China, China Scholarship Council, Science and Technology Innovation Talents in Universities of Henan Province
Openalex Percentile: Top 1%
Advanced battery technologies research
15.34
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.