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Correction: Ultrathin cellulosic gel electrolytes with a gradient hydropenic interface for stable, high-energy and flexible zinc batteries

Jichao Zhaia, Wang Zhaoa, Lei Wang*a, Jianbo Shuaia, Ruwei Chenb, Wenjiao Gea, Yu Zonga, Guanjie He*b and Xiaohui Wang*a
aState Key Laboratory of Pulp and Paper Engineering, School of Light Industry Science and Engineering, South China University of Technology, Guangzhou City, Guangdong Province 510640, China. E-mail: felwang@scut.edu.cn; fewangxh@scut.edu.cn
bDepartment of Chemistry, University College London, 20 Gordon Street, London, WC1H 0AJ, UK. E-mail: g.he@ucl.ac.uk

Received 14th July 2025 , Accepted 14th July 2025

First published on 25th July 2025


Abstract

Correction for ‘Ultrathin cellulosic gel electrolytes with a gradient hydropenic interface for stable, high-energy and flexible zinc batteries’ by Jichao Zhai et al., Energy Environ. Sci., 2025, 18, 4241–4250, https://doi.org/10.1039/D5EE00158G.


The authors would like to express their apologies regarding inaccuracies in the Zn2+ transference numbers (tZn2+) presented in the Results and Fig. S14 and S15 of the original article. Specifically, an incorrect ΔV was applied, which may have led to erroneous Zn2+ deposition, fluctuations in system resistance, and misleading ion transference numbers. However, it is important to note that this issue with the transference number does not alter the core conclusions of the paper. The corrected Fig. S14 and S15 are provided below, and the supplementary information has been updated accordingly.
image file: d5ee90076j-u1.tif

Fig. S14 (a), (c) and (e) Current–time plots of Zn||Zn symmetric cells with different electrolytes after polarization at a constant potential (10 mV) for 1000 s. (b), (d), (f) and (g) the corresponding Nyquist plots before and after polarization tests.

image file: d5ee90076j-u2.tif

Fig. S15 The transference number comparison of different electrolyte systems.

 

In the main text, the claim “As shown in Fig. S14 and S15 (ESI†), the transference number of Zn2+ for DCG (1.13) is significantly higher than that of CG (0.87) and LE (0.84), demonstrating the exceptional Zn2+ transport capability of the gradient DES interface.” should be amended to “As shown in Fig. S14 and S15 (ESI†), the transference number of Zn2+ for DCG (0.81) is significantly higher than that of CG (0.54) and LE (0.47), demonstrating the exceptional Zn2+ transport capability of the gradient DES interface.” to ensure accuracy.

Furthermore, the statement “The transference numbers were measured according to the chronoamperometry (CA) measurement on Zn‖Zn symmetric battery by applying a potential of 150 mV at room temperature.” in the Supplementary Information has been revised to “The transference numbers were measured according to the chronoamperometry (CA) measurement on Zn‖Zn symmetric battery by applying a potential of 10 mV at room temperature.” for consistency.

We also measured the impedance of Zn‖Zn batteries using various electrolytes both before and after polarization. A voltage of 10 mV was applied to test the current–time (It) curves for LE, CG, DCG, and cellulose gels containing 1% DES additive. The obtained values are as follows: IZn0 = 13.5 μA cm−2, IZns = 10.6 μA cm−2, RZn0 = 390 Ω, and RZns = 480 Ω.

The transference number was further evaluated by the following equation (the typical Evans method):1,2

 
image file: d5ee90076j-t1.tif(1)
where ΔV is the applied polarization voltage (10 mV), I0 and R0 are the initial current and resistance, respectively, and Is and Rs are the steady-state current and resistance, respectively. Thereby, the transference number of DCG is estimated as 0.83, with Zn2+ exhibiting a transference number of 0.81. The contribution of the pristine DES to the transference number in the composite electrolyte is negligible.

The Royal Society of Chemistry apologises for these errors and any consequent inconvenience to authors and readers.

References

  1. X. Xiao, X. Ye, Z. Wu, X. Wu, J. Yu, L. Gu and S. Liu, Adv. Mater., 2024, 36, 2408706 CrossRef CAS PubMed.
  2. Z. Yang, Y. Sun, S. Deng, H. Tong, M. Wu, X. Nie, Y. Su, G. He, Y. Zhang, J. Li and G. Chai, Energy Environ. Sci., 2024, 17, 3443–3453 RSC.

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