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空间受限客体合成法制备用于无阳极钠电池的锡单分散氮掺杂介孔主体材料

Space-Confined Guest Synthesis to Fabricate Sn-Monodispersed N-Doped Mesoporous Host toward Anode-Free Na Batteries.

作者信息

Li Siwu, Zhu Haolin, Liu Yuan, Wu Qiang, Cheng Shijie, Xie Jia

机构信息

State Key Laboratory of Advanced Electromagnetic Engineering and Technology, School of Electrical and Electronic Engineering, Huazhong University of Science and Technology, Wuhan, 430074, P. R. China.

Key Laboratory for Renewable Energy, Beijing Key Laboratory for New Energy Materials and Devices, Beijing National Laboratory for Condensed Matter Physics, Institute of Physics, Chinese Academy of Sciences, Beijing, 100190, P. R. China.

出版信息

Adv Mater. 2023 Aug;35(32):e2301967. doi: 10.1002/adma.202301967. Epub 2023 Jun 28.

Abstract

Severe issues including volume change and dendrite growth on sodium metal anodes hinder the pursuit of applicable high-energy-density sodium metal batteries. Herein, an in situ reaction approach is developed that takes metal-organic frameworks as nano-reactor and pore-former to produce a mesoporous host comprised of nitrogen-doped carbon fibers embedded with monodispersed Sn clusters (SnNCNFs). The hybrid host shows outstanding sodiophilicity that enables rapid Na infusion and ultralow Na nucleation overpotential of 2 mV. Its porous structure holds a high Na content and guides uniform Na deposition. Such host provides favorable Na plating/stripping with an average Coulombic efficiency of 99.96% over 2000 cycles (at 3 mA cm and 3 mA h cm ). The Na-infused SnNCNF anode delivers extreme Na utilization of 86% in symmetric cells (at 10 mA cm and 10 mA h cm ), outstanding rate capability and cycle life in Na-SnNCNF||Na V (PO ) full cells (at 1 A g for over 1000 cycles with capacity retention of 92.1%). Furthermore, high-energy/power-density anode-less and anode-free Na cells are achieved. This work presents an effective heteroatom-doping approach for fabricating multifunctional porous carbon materials and developing high-performance metal batteries.

摘要

包括钠金属阳极上的体积变化和枝晶生长在内的严重问题阻碍了实用型高能量密度钠金属电池的发展。在此,开发了一种原位反应方法,该方法以金属有机框架作为纳米反应器和造孔剂,以制备由嵌入单分散Sn团簇的氮掺杂碳纤维组成的介孔主体(SnNCNFs)。这种混合主体表现出出色的亲钠性,能够实现快速的钠注入和2 mV的超低钠成核过电位。其多孔结构容纳了高钠含量并引导钠均匀沉积。这种主体提供了良好的钠电镀/剥离性能,在2000次循环中(在3 mA cm²和3 mA h cm²下)平均库仑效率为99.96%。注入钠的SnNCNF阳极在对称电池中(在10 mA cm²和10 mA h cm²下)实现了86%的极高钠利用率,在Na-SnNCNF||Na₃V₂(PO₄)₃全电池中具有出色的倍率性能和循环寿命(在1 A g下循环超过1000次,容量保持率为92.1%)。此外,还实现了高能量/功率密度的无阳极和无负极钠电池。这项工作提出了一种有效的杂原子掺杂方法,用于制备多功能多孔碳材料和开发高性能金属电池。

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