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用于先进双碳钾离子电容器的纳米片网络分级多孔碳复合材料的可控构建

Controllable construction of hierarchically porous carbon composite of nanosheet network for advanced dual-carbon potassium-ion capacitors.

作者信息

Li Qian, Wang Tongde, Shu Tie, Miao Yidong, Pan Xiaoyi, Tao Yousheng, Qi Jiqiu, Sui Yanwei, He Yezeng, Meng Qingkun, Wei Fuxiang, Ren Yaojian, Zhao Yulong, Ju Zhicheng, Wei Lu

机构信息

College of Materials Science and Engineering, Sichuan University, Chengdu, 610065, People's Republic of China.

Jiangsu Province Engineering Laboratory of High Efficient Energy Storage Technology and Equipment, China University of Mining and Technology, Xuzhou 221116, People's Republic of China; School of Materials and Physics, China University of Mining and Technology, Xuzhou 221116, People's Republic of China.

出版信息

J Colloid Interface Sci. 2022 Sep;621:169-179. doi: 10.1016/j.jcis.2022.04.070. Epub 2022 Apr 15.

Abstract

Benefitting from the abundance and inexpensive nature of potassium resources, potassium-ion energy storage technology is considered a potential alternative to current lithium-ion systems. Potassium-ion capacitors (PICs) as a burgeoning K-ion electrochemical energy storage device, are capable of delivering high energy at high power without sacrificing lifespan. However, owing to the sluggish kinetics and significant volume change induced by the large K-diameter, matched electrode materials with good ion accessibility and fast K intercalation/deintercalation capability are urgently desired. In this work, pine needles and graphene oxide (GO) are utilized as precursors to fabricate oxygen-doped activated carbon/graphene (OAC/G) porous nanosheet composites. The introduction of GO not only induces the generation of interconnected nanosheet network, but also increases the oxygen-doping content of the composite, thus expanding the graphite interlayer spacing. Experimental analysis combined with first-principle calculations reveal the transport/storage mechanism of K in the OAC/G composite anode, demonstrating that the high surface area, sufficient reactive sites, enlarged interlayer distance and open channels in the porous nanosheet network contribute to rapid and effective K diffusion and storage. When incorporated with pine needle-activated carbon as cathode, the assembled dual-carbon PICs can function at a high voltage of 5 V, exhibiting a high energy density of 156.7 Wh kg at a power density of 500 W kg along with a satisfied cycle life, which highlights their potential application in economic and advanced PICs.

摘要

受益于钾资源的丰富性和廉价性,钾离子储能技术被认为是当前锂离子系统的一种潜在替代方案。钾离子电容器(PICs)作为一种新兴的钾离子电化学储能装置,能够在不牺牲寿命的情况下高功率地提供高能量。然而,由于大直径钾离子引起的动力学迟缓以及显著的体积变化,迫切需要具有良好离子可及性和快速钾离子嵌入/脱嵌能力的匹配电极材料。在这项工作中,松针和氧化石墨烯(GO)被用作前驱体来制备氧掺杂活性炭/石墨烯(OAC/G)多孔纳米片复合材料。GO的引入不仅诱导了相互连接的纳米片网络的生成,还增加了复合材料的氧掺杂含量,从而扩大了石墨层间距。实验分析与第一性原理计算相结合揭示了钾在OAC/G复合负极中的传输/存储机制,表明多孔纳米片网络中的高比表面积、充足的活性位点、扩大的层间距和开放通道有助于钾的快速有效扩散和存储。当与松针活性炭作为正极组装时,所制备的双碳PICs能够在5 V的高电压下工作,在500 W kg的功率密度下表现出156.7 Wh kg的高能量密度以及令人满意的循环寿命,这突出了它们在经济且先进的PICs中的潜在应用。

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