Spray drying induced engineering a hierarchical reduced graphene oxide supported heterogeneous Tin dioxide and Zinc oxide for Lithium-ion storage

被引:9
|
作者
Zhang, Rui [1 ]
Tan, Qingke [1 ]
Bao, Shouchun [1 ]
Deng, Jianbin [1 ]
Xie, Yan [1 ]
Zheng, Fei [1 ]
Wu, Guanglei [1 ]
Xu, Binghui [1 ]
机构
[1] Qingdao Univ, Coll Mat Sci & Engn, Inst Mat Energy & Environm, State Key Lab Biofibersfv & Ecotext, Qingdao 266071, Peoples R China
基金
中国博士后科学基金;
关键词
Zinc oxide; Tin dioxide; Hierarchical; Reduced graphene oxide; Spray drying; Lithium-ion batteries; N-DOPED CARBON; ANODE MATERIALS; ZNO NANOPARTICLES; POROUS MATERIALS; PERFORMANCE; FRAMEWORK; COMPOSITE; NANORODS; NANOMATERIALS; ELECTRODES;
D O I
10.1016/j.jcis.2021.10.026
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
In this work, a hierarchical reduced graphene oxide (RGO) supportive matrix consisting of both larger two-dimensional RGO sheets and smaller three-dimensional RGO spheres was engineered with ZnO and SnO2 nanoparticles immobilized. The ZnO and SnO2 nanocrystals with controlled size were in sequence engineered on the surface of the RGO sheets during the deoxygenation of graphene oxide sample (GO), where the zinc-containing ZIF-8 sample and metal tin foil were used as precursors for ZnO and SnO2, respectively. After a spray drying treatment and calcination, the final ZnO@SnO2/RGO-H sample was obtained, which delivered an outstanding specific capacity of 982 mAh.g(-1) under a high current density of 1000 mA.g(-1) after 450 cycles. Benefitting from the unique hierarchical structure, the mechanical strength, ionic and electric conductivities of the ZnO@SnO2/RGO-H sample have been simultaneously promoted. The joint contributions from pseudocapacitive and battery behaviors in lithium-ion storage processes bring in both large specific capacity and good rate capability. The industrially mature spray drying method for synthesizing RGO based hierarchical products can be further developed for wider applications. (C) 2021 Elsevier Inc. All rights reserved.
引用
收藏
页码:1758 / 1768
页数:11
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