Abstract
Highlights
A novel high-entropy metal–organic frameworks (HE-MOFs) electrode for fast sodium-ion storage devices has been realized by introducing five metallic elements.
The platform capacity/voltage of the electrode materials are precisely regulated by the adjustable metal species/content of HE-MOFs.
The sodium-ion capacitors assembled based on high-entropy MOFs electrode exhibit high-power density (20,000 W kg-1) and high-energy density (99.4 Wh kg-1).
Precise regulation of the platform capacity/voltage of electrode materials contributes to the efficient operation of sodium-ion fast-charging devices. However, the design of such electrode materials is still in a blank stage. Herein, based on tunable metal–organic frameworks, we have designed a novel material system—two-dimensional high-entropy metal–organic frameworks (HE-MOFs), which exhibits unique properties in sodium storage and is of vital importance for realizing fast-charging batteries. Furthermore, we have found that the high-entropy effect can regulate the electronic structure, the sodium-ion migration environment, and the sodium-ion storage active sites, thereby meeting the requirements of electrode materials for sodium-ion fast-charging devices. Impressively, the HE-MOFs material still maintains a reversible specific capacity of 89 mAh g−1 at a current density of 20 A g−1. It presents an ideal sodium storage voltage plateau of approximately 0.5 V, and its platform capacity is increased to 122.7 mAh g−1, far superior to that of Mn-MOFs (with no platform capacity). This helps to reduce safety hazards during the fast-charging process and demonstrates its great application value in the fields of fast-charging sodium-ion batteries and capacitors. Our research findings have broken the barriers to the application of non-conductive MOFs as energy storage materials, enhanced the understanding of the regulation of platform capacity and voltage, and paved the way for the realization of high-security sodium-ion fast-charging devices.
You have requested "on-the-fly" machine translation of selected content from our databases. This functionality is provided solely for your convenience and is in no way intended to replace human translation. Show full disclaimer
Neither ProQuest nor its licensors make any representations or warranties with respect to the translations. The translations are automatically generated "AS IS" and "AS AVAILABLE" and are not retained in our systems. PROQUEST AND ITS LICENSORS SPECIFICALLY DISCLAIM ANY AND ALL EXPRESS OR IMPLIED WARRANTIES, INCLUDING WITHOUT LIMITATION, ANY WARRANTIES FOR AVAILABILITY, ACCURACY, TIMELINESS, COMPLETENESS, NON-INFRINGMENT, MERCHANTABILITY OR FITNESS FOR A PARTICULAR PURPOSE. Your use of the translations is subject to all use restrictions contained in your Electronic Products License Agreement and by using the translation functionality you agree to forgo any and all claims against ProQuest or its licensors for your use of the translation functionality and any output derived there from. Hide full disclaimer
Details
1 Central South University, College of Chemistry and Chemical Engineering, Changsha, People’s Republic of China (GRID:grid.216417.7) (ISNI:0000 0001 0379 7164)
2 Central South University, College of Chemistry and Chemical Engineering, Changsha, People’s Republic of China (GRID:grid.216417.7) (ISNI:0000 0001 0379 7164); University College London, Department of Chemistry, London, UK (GRID:grid.83440.3b) (ISNI:0000 0001 2190 1201)
3 Central South University, College of Chemistry and Chemical Engineering, Changsha, People’s Republic of China (GRID:grid.216417.7) (ISNI:0000 0001 0379 7164); University of Oxford, Department of Materials, Oxford, UK (GRID:grid.4991.5) (ISNI:0000 0004 1936 8948)





