Wang Jiamei, Zhu Gang, Zhang Zelei, Wang Yi, Wang Hui, Bai Jintao, Wang Gang
State Key Laboratory of Photoelectric Technology and Functional Materials, International Collaborative Center on Photoelectric Technology and Nano Functional Materials, Institute of Photonics & Photon-Technology, Northwest University, Xi'an, 710127, China.
Shaanxi Joint Lab of Graphene, Northwest University, Xi'an, 710127, China.
Chemistry. 2021 Jan 21;27(5):1713-1723. doi: 10.1002/chem.202003261. Epub 2020 Dec 16.
Urchin-type cobalt phosphide microparticles assembled by nanorod were encapsulated in a graphene framework membrane (CoP@GF), and used as a binder-free electrode for alkali metal ion batteries. Electrochemical measurements indicate that this membrane exhibits enhanced reversible lithium, sodium, and potassium storage capabilities. Moreover, the energy storage properties of CoP@GF electrodes in alkali metal ion batteries display an order of Li>Na>K. DFT calculations on adsorption energy of CoP surfaces for Li, Na, and K indicated that CoP surfaces were more favorable to transfer electrons to Li atoms than Na and K, and the surface reactivity can be ordered as Li-CoP>Na-CoP>K-CoP; thus, CoP@GF exhibits better storage capacity for lithium. This work provides experimental and theoretical basis for understanding the electrochemical performance of cobalt phosphide-based membranes for alkali metal ion batteries.
由纳米棒组装而成的海胆型磷化钴微粒被封装在石墨烯框架膜(CoP@GF)中,并用作碱金属离子电池的无粘结剂电极。电化学测量表明,这种膜展现出增强的可逆锂、钠和钾存储能力。此外,CoP@GF电极在碱金属离子电池中的储能性能呈现出Li>Na>K的顺序。对CoP表面对Li、Na和K的吸附能进行的密度泛函理论计算表明,CoP表面比Na和K更有利于将电子转移给Li原子,且表面反应活性顺序为Li-CoP>Na-CoP>K-CoP;因此,CoP@GF对锂表现出更好的存储容量。这项工作为理解基于磷化钴的膜在碱金属离子电池中的电化学性能提供了实验和理论依据。