The interaction of red phosphorus with supporting carbon additives in lithium-ion battery anodes

被引:7
|
作者
Smajic, Jasmin [1 ]
Alazmi, Amira [1 ,2 ]
Alzahrani, Areej [1 ,3 ]
Emwas, Abdul-Hamid [4 ]
Costa, Pedro M. F. J. [1 ]
机构
[1] King Abdullah Univ Sci & Technol KAUST, Phys Sci & Engn Div, Thuwal 239556900, Saudi Arabia
[2] Univ Hafr Al Batin, Univ Coll Nairiyah, Dept Chem, Hafar al Batin 39524, Saudi Arabia
[3] Al Baha Univ, Fac Sci & Arts, Dept Phys, Al Makhwah 65931, Saudi Arabia
[4] King Abdullah Univ Sci & Technol KAUST, Core Labs, Thuwal 239556900, Saudi Arabia
关键词
Phosphorus; Carbon; Lithium; Battery; Anode; BLACK PHOSPHORUS; GRAPHENE OXIDE; MESOPOROUS CARBON; HIGH-CAPACITY; PERFORMANCE; COMPOSITE; ELECTRODE; NANOTUBE;
D O I
10.1016/j.jelechem.2022.116852
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
In theory, red P is a promising alloying-type anode material for Li-ion batteries (LIBs). However, we are chal-lenged by reports of poor electrochemical performance due to P pulverization. So far, our best approach is to use composites of P and C as these dramatically improve the anode's stability in regards to the lithiation/ delithiation process. Admittedly, success is dependent on the C additives providing electronic conductivity and structural integrity to the composite whilst also ensuring an adequate P dispersion. Here, three of the most commonly used C additives (carbon nanotubes, reduced graphene oxide and graphite flakes) are compared in their ability to stabilize the capacity of red P and its adherence to the current collector in a LIB. Our experi-ments show that nanotubes are the most promising stabilization agents due to their mechanical elasticity, high surface area/pore volume, and superior P uptake of their elastic web-like aggregates. As a result, the adherence of the C/P composite to the current collector is ensured. Notwithstanding the additive's performance, we also observe that the interconversion between different P phases is not fully reversible at room temperature, con-stituting an added reason for the capacity fade of C/P anodes.
引用
收藏
页数:9
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