Lian Jiabiao, Subburam Gokila, El-Khodary Sherif A, Zhang Kai, Zou Bobo, Wang Juan, Wang Chuan, Ma Jianmin, Wu Xiaojun
Institute for Energy Research, School of Materials Science and Engineering, Jiangsu University, Zhenjiang 212013, P. R. China.
Key Laboratory of Precision and Intelligent Chemistry, School of Chemistry and Material Sciences, CAS Key Laboratory of Materials for Energy Conversion, and Collaborative Innovation Center of Chemistry for Energy Materials (iChEM), University of Science and Technology of China, Hefei, Anhui 230026, P. R. China.
J Am Chem Soc. 2024 Mar 27;146(12):8110-8119. doi: 10.1021/jacs.3c12051. Epub 2024 Mar 15.
Exploring high-sloping-capacity carbons is of great significance in the development of high-power lithium-ion batteries/capacitors (LIBs/LICs). Herein, an ion-catalyzed self-template method is utilized to synthesize the hydrogen-rich carbon nanoribbon (HCNR), achieving high specific and rate capacity (1144.2/471.8 mAh g at 0.1/2.5 A g). The Li storage mechanism of the HCNR is elucidated by spectroscopic techniques. Intriguingly, the protonated aromatic sp-hybridized carbon (C(sp)-H) can provide additional active sites for Li uptake via reversible rehybridization to sp-C, which is the origin of the high sloping capacity. The presence of this sloping feature suggests a highly capacitance-dominated storage process, characterized by rapid kinetics that facilitates superior rate performance. For practical usage, the HCNR-based LIC device can deliver high energy/power densities of 198.3 Wh kg/17.9 kW kg. This work offers mechanistic insights on the crucial role of aromatic C(sp)-H in boosting Li storage and opens up new avenues to develop such sloping-type carbons for high-performance rechargeable batteries/capacitors.