表面改性
阳极
石墨烯
锂(药物)
纳米颗粒
化学
电极
化学工程
材料科学
纳米技术
物理化学
医学
内分泌学
工程类
作者
Bo Lan,Xueqian Zhang,Lianyu Zhao,Peng Wang,Chuncheng Wei,Yishan Wang,Guangwu Wen
标识
DOI:10.1016/j.electacta.2023.141910
摘要
Compounding CoP nanoparticles with graphene can serve as promising anode materials for high-performance lithium-ion batteries. However, the weak binding and dispersion between CoP and graphene usually lead to poor structural stability limiting the lithium storage performance. Herein, an amino-functionalization-assisted one pot self-assembly method is employed to synthesize CoP/nitrogen, phosphorus co-doped graphene composites (CoP/NPG) with a highly stable 3D porous structure. The negatively charged phytic acid can act as a bridging connection between the positively charged amino-functionalized graphene and Co2+ by strong electrostatic attraction, ensuring the synthesized CoP nanoparticles are uniformly distributed on NPG sheets with high conductivity and plenty of active centers. Meanwhile, establishing strong C–P and Co–O–C surface chemical bonds between CoP and NPG improves the structural strength and promotes fast electron/ion transport, which effectively alleviates the volume expansion of CoP. Benefiting from these advantages, the CoP/NPG electrode displays high lithium storage capacity (917.9 mAh g − 1 at 0.5 A g − 1 after 600 cycles), ultra-long cyclic stability (434.8 and 350.5 mAh g − 1 at 3.0 and 5.0 A g − 1 after 3000 cycles) and fast pseudocapacitive charge storage (contribution even up to 97% at 2.0 mV s − 1). This strategy offers promising prospects for the preparation of highly stable anode materials.
科研通智能强力驱动
Strongly Powered by AbleSci AI