Single atom catalysts for triiodide adsorption and fast conversion to boost the performance of aqueous zinc-iodine batteries

Fuhua Yang (Co-first Author), Jun Long (Co-first Author), Jodie A. Yuwono (Co-first Author), Huifang Fei, Yameng Fan, Peng Li, Jinshuo Zou, Junnan Hao, Sailin Liu, Gemeng Liang, Yanqiu Lyu, Xiaobo Zheng, Shiyong Zhao*, Kenneth Davey, Zaiping Guo*

*Corresponding author for this work

Research output: Journal Publications and ReviewsRGC 21 - Publication in refereed journalpeer-review

139 Citations (Scopus)

Abstract

Zinc-iodine (Zn-I2) batteries are promising for energy storage because of their low cost, environmental friendliness, and attractive energy density. However, triiodide dissolution and poor conversion kinetics hinder their application. Herein, we demonstrated that the ‘shuttle effect’ in Zn-I2 batteries can be suppressed via single atom catalyst (SAC) cathodes because of efficient catalytic activity in I2/I3/I reactions and their ability to adsorb I3. Based on DFT computations, an I poisoning mechanism was proposed for SAC selection to suppress the shuttle effect in Zn-I2 batteries. I formation and desorption are crucial to maintaining the catalytic and adsorption role of metallic elements. SACu favours the reduction of I2 to I and exhibits a low energy barrier to release I from the surface, thus allowing more rapid conversion kinetics, while at the same time suppressing the shuttle effect of I3 in Zn-I2 batteries. In contrast, without sufficient energy, the final product of I will remain adsorbed at the metal site of SAFe, SAMn, SAV, and SATi, thus killing the catalytic activity of SACs to facilitate the iodine reduction reaction (IRR). To confirm practicality, single-atom Cu-embedded nitrogen-doped Ketjen black (SACu@NKB), together with SACo@NKB and NKB, were synthesized and electrochemically assessed. The as-prepared SACu@NKB outperformed the SACo@NKB and NKB cathodes in terms of reversible capacity and cycle life. In addition, a rate-limiting step in these redox reactions was identified, and overpotential was estimated, and these were found to be dependent on the d-band centre of SACs. A lower d-band centre can be associated with more optimal catalytic performance in SACs. This work reveals that the superior cycle life of Zn-I2 batteries is underpinned by the catalytic and adsorption role of metallic catalysts, and we report an in-depth understanding of how this boosts the performance of Zn-I2 batteries, with implications for future long-life battery design. © 2023 The Royal Society of Chemistry.
Original languageEnglish
Pages (from-to)4630-4640
JournalEnergy and Environmental Science
Volume16
Issue number10
Online published5 Sept 2023
DOIs
Publication statusPublished - 1 Oct 2023
Externally publishedYes

Funding

Financial support is gratefully acknowledged from the Australian Research Council (ARC) (FL210100050, LP160101629, DP210101486, DP200101862, and LE180100141) and the National Natural Science Foundation of China (No. 52102276). J. A. Y. acknowledges the assistance of high-performance computing resources and services from the National Computational Infrastructure (NCI) Australia that is supported by the Australian Government through the Adapter Q4 and NCMAS scheme. Part of this work was carried out at the wiggler XAS beamline (12-ID), Australian Synchrotron (awarded beamtime: M18566). The authors thank Shao-Jian Zhang for helpful discussion, and Dr Alberto Varzi for providing laboratory facilities for revision.

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