磷烯
阳极
材料科学
异质结
锂(药物)
黑磷
离子
半导体
带隙
化学工程
光电子学
化学
物理化学
电极
医学
有机化学
工程类
内分泌学
作者
Chandra Chowdhury,Sharmistha Karmakar,Ayan Datta
出处
期刊:ACS energy letters
[American Chemical Society]
日期:2016-06-13
卷期号:1 (1): 253-259
被引量:150
标识
DOI:10.1021/acsenergylett.6b00164
摘要
Black phosphorus (BP), despite possessing a favorable direct band gap, suffers from structural instability at ambient conditions that limits its utility for lithium ion batteries (LIB). In this Letter, we have proposed h-BN as an effective capping agent for black-phosphorene (Pn) for application as an anode material in both LIBs and sodium ion batteries (SIBs). The binding energy of Li/Na in the h-BN/black-Pn heterostructure is greatly enhanced (2.81 eV/2.55 eV) vis-a-vis pristine Pn (1.80 eV/1.59 eV) along with reduction in the barrier for movement of Li/Na within the layers. Significantly, lithiation/sodiation of these heterostructures does not alter the packing patterns due to insignificant volume changes (∼1.5–2.0%). The theoretical specific capacities for h-BN/black-Pn is 607 and 445 mA h g–1 for LIB and SIB, respectively, which are larger than those for existing commercial anode materials. Clearly, the high capacity, low open-circuit voltage, small volume change, and high mobility of Li/Na within the layers make h-BN-capped black-Pn an excellent anode material in LIBs/SIBs. The heterostructure exhibits an interesting semiconductor → metal electronic phase transition upon lithiation/sodiation.
科研通智能强力驱动
Strongly Powered by AbleSci AI