Lead single atoms anchored on reduced graphene oxide as multifunctional additive for lead–carbon battery

石墨烯 氧化物 碳纤维 电池(电) 材料科学 纳米技术 扫描透射电子显微镜 吸附 电化学 透射电子显微镜 化学工程 化学 电极 冶金 有机化学 复合材料 复合数 物理化学 物理 工程类 量子力学 功率(物理)
作者
Daiwen Tao,Xiong Liu,Zeming Li,Hui Yang,Jinyu Wang,Qilong Zhang
出处
期刊:Chemical Engineering Journal [Elsevier BV]
卷期号:461: 141992-141992 被引量:18
标识
DOI:10.1016/j.cej.2023.141992
摘要

The application of lead–carbon batteries (LCBs) in hybrid electric vehicles and large-scale energy storage was limited by gradual sulfation and parasitic hydrogen evolution reaction (HER) of negative plates. Here, Pb single atoms anchored on reduced graphene oxide ([email protected]) were prepared through electrostatic adsorption and thermal reduction method, and confirmed by two aberration-corrected transmission electron microscopy (TEM and STEM) and synchrotron-based X-ray absorption fine structure spectroscopy (XAFS). By anchoring PbSAs on rGO surfaces where HER is prone to occur, the HER rate was greatly reduced. Moreover, PbSAs could serve as seeds to induce three-dimensional growth of Pb branches, which endows the NAM containing [email protected] additives with a specific surface areas (SSA) about 2.3 times than that of control one. The increased SSA can help to delay the sulfation of negative plate. Meanwhile, PbSAs can help enhance the affinity of rGO towards negative active material (NAM), which enable electrochemical reduction reaction proceeds at a higher rate. Thanks to the coordination of various functions from multifunctional additives, service life of LCBs under high-rate partial-state-of-charge (HRPSoC) have been extend from 3529 to 16,097 cycles, and from 4692 to 22,606 cycles, in 50% state of charge (SoC) and 75% SoC, respectively.
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