Electrolyte Strategies at Extreme Temperatures for Aqueous Zinc Batteries
Source abstract
Abstract
Abstract The state of aqueous zinc batteries at extreme temperature environment is an important parameter for their widespread application. However, low ionic conductivity and sluggish ionic diffusion at low temperature, and aggravated untoward reactions in the interface of electrode‐electrolyte at high temperature, seriously limit the practical application of zinc‐ion batteries. Currently, numerous zinc‐ion batteries capable of operating within a broad temperature range have been proposed. Herein, the reason of the performance decline at extreme temperature is discussed from the perspective of thermodynamics and dynamics. Then, from the additives/co‐solvents, high concentration salts, hydrogels and other aspects, the main strategies of electrolyte are introduced in detail. Finally, the possible directions to further improve the high and low temperature performance of zinc‐ion batteries are proposed. It is hoped that this review will be helpful to the design and manufacture of wide temperature zinc‐ion battery electrolyte and provide reference for the application of rechargeable zinc‐ion battery in extreme environment.
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Research context
OpenAlex topics: Advanced battery technologies research · Supercapacitor Materials and Fabrication · Electrochemical Analysis and Applications
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Hubei Key Laboratory of Micro-Nanoelectronic Materials and Devices School of Microelectronics Hubei University Wuhan 430062 PR China
Funding
National Natural Science Foundation of China
References (100+)
Show source-provided references
1. Aramendia E. · Nat. Energy · 2024 · 1
2.
3. 10.1038/s41578-024-00657-210.1038/s41578-024-00657-2 ↗
4. 10.1016/j.apenergy.2024.12397410.1016/j.apenergy.2024.123974 ↗
5.
6. Yao R. · E. Science · 2024 · 17 · 3112
7. 10.1016/j.cej.2023.14788910.1016/j.cej.2023.147889 ↗
8.
9. 10.1002/chem.20230321110.1002/chem.202303211 ↗
10. 10.1002/cssc.20240125110.1002/cssc.202401251 ↗
11. 10.1021/acsenergylett.4c0201410.1021/acsenergylett.4c02014 ↗
12.
13. Yao J. · Angew. Chem. Int. Ed. · 2024 · 619
14. Zhang J. · Nano-Micro Lett. · 2024
15.
16. 10.1039/D2EE03793A10.1039/D2EE03793A ↗
17. 10.1038/s41586-022-05281-010.1038/s41586-022-05281-0 ↗
18. 10.1126/sciadv.abn509710.1126/sciadv.abn5097 ↗
19. 10.1038/s41467-021-27755-x10.1038/s41467-021-27755-x ↗
20. Zhang R. · Science · 2024
21.
22. 10.1038/s41467-023-37524-710.1038/s41467-023-37524-7 ↗
23. 10.1038/s41467-023-38384-x10.1038/s41467-023-38384-x ↗
24. 10.1038/s41467-022-28380-y10.1038/s41467-022-28380-y ↗
25. 10.1002/adma.20220823710.1002/adma.202208237 ↗
26. Wu M. · E. Science · 2024 · 17 · 619
27.
28. Geng Y. · Energy Storage Mater. · 2022
29. Zhu J. · Adv. Mater. · 2023
30. 10.1002/aenm.20220206810.1002/aenm.202202068 ↗
31. 10.3390/batteries907038610.3390/batteries9070386 ↗
32. Cui Y. · Materials Futures · 2023
33. Katiyar R. · J. Chem. Phys. · 2024 · 587
34.
35. 10.1016/S0378-7753(99)00472-310.1016/S0378-7753(99)00472-3 ↗
36. 10.1016/j.apenergy.2016.05.15310.1016/j.apenergy.2016.05.153 ↗
37. 10.1016/j.apenergy.2016.10.05910.1016/j.apenergy.2016.10.059 ↗
38.
39. 10.1021/jacs.1c0692310.1021/jacs.1c06923 ↗
40. 10.1016/j.cej.2022.13458910.1016/j.cej.2022.134589 ↗
41. 10.1016/j.etran.2021.10014510.1016/j.etran.2021.100145 ↗
42.
43. 10.1016/j.apenergy.2017.12.08610.1016/j.apenergy.2017.12.086 ↗
44. 10.1002/cnl2.16810.1002/cnl2.168 ↗
45.
46. 10.1002/tcr.20220013210.1002/tcr.202200132 ↗
47. 10.1002/adma.20231062310.1002/adma.202310623 ↗
48.
49. 10.1007/s40843-023-2448-010.1007/s40843-023-2448-0 ↗
50. 10.1002/aenm.20200320310.1002/aenm.202003203 ↗
51.
52. 10.1002/aenm.20210093910.1002/aenm.202100939 ↗
53. 10.1016/j.ensm.2024.10384410.1016/j.ensm.2024.103844 ↗
54.
55. 10.1002/adma.20220768210.1002/adma.202207682 ↗
56. 10.1002/adma.20220623910.1002/adma.202206239 ↗
57. Z. Wu J. J. B. Liu Supercapse202400483.
58. 10.1016/j.ensm.2022.06.05210.1016/j.ensm.2022.06.052 ↗
59. 10.1016/j.est.2022.10481110.1016/j.est.2022.104811 ↗
60.
61. 10.1002/adma.20221167310.1002/adma.202211673 ↗
62. 10.1002/smll.20220005510.1002/smll.202200055 ↗
63. 10.1016/j.ensm.2022.07.03210.1016/j.ensm.2022.07.032 ↗
64. 10.1002/batt.20240009510.1002/batt.202400095 ↗
65.
66. 10.1021/acsenergylett.3c0015410.1021/acsenergylett.3c00154 ↗
67. 10.1093/nsr/nwac05110.1093/nsr/nwac051 ↗
68. 10.1002/aenm.20240009010.1002/aenm.202400090 ↗
69.
70. 10.1002/adma.20220713110.1002/adma.202207131 ↗
71. Zheng J. · J. Am. Chem. Soc. · 2024 · 16 · 145
72.
73. 10.1002/aenm.20230146610.1002/aenm.202301466 ↗
74. 10.1016/j.ensm.2021.06.03410.1016/j.ensm.2021.06.034 ↗
75. 10.1002/ange.20230157010.1002/ange.202301570 ↗
76. 10.1021/acs.chemrev.2c0037410.1021/acs.chemrev.2c00374 ↗
77.
78. 10.1016/j.ensm.2022.10.04610.1016/j.ensm.2022.10.046 ↗
79. 10.1002/batt.20210042010.1002/batt.202100420 ↗
80. B. Wang R. Zheng W. Yang C. Hou Q. Zhang K. Li Y. Li H. Wang Available at SSRN 4510401.
81. Xie C. · Sci. Bull. · 2023
82.
83. 10.1016/j.ensm.2021.10.01210.1016/j.ensm.2021.10.012 ↗
84. 10.1016/j.cclet.2022.06.05210.1016/j.cclet.2022.06.052 ↗
85. 10.1021/acsenergylett.1c0271910.1021/acsenergylett.1c02719 ↗
86. X. Shi Y. Zhong Y. Yang J. Zhou X. Cao S. Liang Angew. Chem. Int. Ed. e202414777.
87.
88. 10.1002/adfm.20230079510.1002/adfm.202300795 ↗
89. Ai X. · Cell Rep. Phys. Sci. · 2022 · 3
90. H. Chang Z.-Y. Luo X.-R. Shi X.-X. Caos.-q. J. Liang T Nonferr Metal Soc.2024 34 3358–3371.10.1016/S1003-6326(24)66613-6 ↗
91.
92. Peng H. · J. Zhou, Mater. · 2022 · 5 · 4363
93. 10.1016/j.jpowsour.2024.23490410.1016/j.jpowsour.2024.234904 ↗
94.
95. 10.1016/j.jpowsour.2020.22864910.1016/j.jpowsour.2020.228649 ↗
96. 10.1016/j.cej.2023.14139210.1016/j.cej.2023.141392 ↗
97. 10.1021/jacs.3c0652310.1021/jacs.3c06523 ↗
98.
99. Ren H. · Adv. Mater. · 2022 · 35
100. 10.1039/D2TA08498H10.1039/D2TA08498H ↗