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Constructing strong interfacial interactions between the carbon coating layer and the MnO anode is highly desirable for enhancing its structural stability and electronic conductivity. Herein, an aminated graphite/MnO composite (MnO@300NG) with a strong Mn-N-C heterointerface has been designed via coupling hydrothermal self-assembly with a calcination strategy. This stable structure can fully expose more Li-ion storage active sites and accelerate the charge transfer rate and Li-ion diffusion kinetics. As a result, the MnO@300NG anode delivers a high specific capacity of 920.50 and 515.63 mAh/g at 0.1 and 4.0 A/g, respectively, with 56.02% capacity retention rate, showing a superior rate performance. After 1000 cycles, the capacity retention rate is as high as 94.33%, significantly larger than that of MnO@0NG (62.15%), showing excellent cycling stability. In addition, the MnO@300NG//LFP full cell assembled by the MnO@300NG anode and LiFePO cathode delivers a high average specific capacity of 172.40 and 104.10 mAh/g at 0.1 and 5.0 C, corresponding to 60.38% capacity retention rate, delivering an outstanding rate performance. Moreover, the full cell has a maximal energy density of 356.50 Wh/kg coupled with a 98.10% capacity retention rate for 100 cycles. Therefore, this work will provide substantial guidance for rationally designing a high-performance MnO-based anode in a lithium-ion battery.
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http://dx.doi.org/10.1021/acsami.5c11127 | DOI Listing |
ACS Appl Mater Interfaces
September 2025
School of Materials and Energy, Guangdong University of Technology, Guangzhou 510006, China.
The development of anode materials for lithium-ion batteries must meet the demands for high safety, high energy density, and fast-charging performance. TiNbO is notable for its high theoretical specific capacity, low structural strain, and exceptional fast-charging capability, attributed to its Wadsley-Roth crystal structure. However, its inherently poor conductivity has hindered its practical application.
View Article and Find Full Text PDFJ Am Chem Soc
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Department of Chemistry, Zhejiang University, Hangzhou 310027, China.
Narrow electrochemical windows and high reactivity of aqueous solutions remain critical bottlenecks for the practical application of aqueous batteries. However, the mechanisms for tuning microscopic reactivity of HO molecules in aqueous electrolytes remain elusive. This study employs six ether molecules with distinct structures and solvation powers to regulate the microstructure of aqueous solutions.
View Article and Find Full Text PDFSci Adv
September 2025
Department of Electrical and Computer Engineering, National University of Singapore, Singapore 117583, Singapore.
Embodied intelligence in soft robotics offers unprecedented capabilities for operating in uncertain, confined, and fragile environments that challenge conventional technologies. However, achieving true embodied intelligence-which requires continuous environmental sensing, real-time control, and autonomous decision-making-faces challenges in energy management and system integration. We developed deformation-resilient flexible batteries with enhanced performance under magnetic fields inherently present in magnetically actuated soft robots, with capacity retention after 200 cycles improved from 31.
View Article and Find Full Text PDFSmall
September 2025
School of Mechanical Engineering, Yonsei University, 50, Yonsei-ro, Seodaemun-gu, Seoul, 03722, Republic of Korea.
Core-shell electrodes provide a potential and innovative approach for significantly enhancing the performance and capacity of supercapacitors (SCs) by combining two distinct materials. The capabilities of these advanced electrodes surpass those of conventional single electrodes. Specifically, these exhibit better energy storage, higher power density, and improved overall performance.
View Article and Find Full Text PDFChem Commun (Camb)
September 2025
Department of Applied Chemistry, School of Chemistry and Chemical Engineering, Chongqing University, Chongqing 401331, China.
Herein, 1,3,5-benzenetricarboxylate (BTC) intercalation and oxygen vacancy engineering are proposed to enhance the electrochemical performance of layered double hydroxide (LDH) nanosheets. The optimized LDH exhibits a remarkable capacity of 426 mAh g at 3 A g and 70% capacity retention after 15 000 cycles, attributed to improved ion transport, abundant active sites, and structural stability.
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