TY - JOUR
T1 - Generic synthesis of high-entropy phosphides for fast and stable Li-ion storage
AU - Li, Wenwu
AU - Li, Yanhong
AU - Wang, Jeng Han
AU - Huang, Shengchi
AU - Chen, Anjie
AU - Yang, Lufeng
AU - Chen, Jie
AU - He, Lunhua
AU - Pang, Wei Kong
AU - Thomsen, Lar
AU - Cowie, Bruce
AU - Xiong, Peixun
AU - Zhou, Yucun
AU - Jang, Gun
AU - Min, Dong Hyun
AU - Byun, Jin Suk
AU - Xu, Lei
AU - Huang, Jia Qi
AU - Roh, Kwang Chul
AU - Kang, Seo Hui
AU - Liu, Meilin
AU - Duan, Xiangfeng
AU - Park, Ho Seok
N1 - Publisher Copyright:
© 2024 The Royal Society of Chemistry.
PY - 2024/4/16
Y1 - 2024/4/16
N2 - Monophosphides and bi-metallic phosphides have attracted considerable interest for their high-capacity Li-storage capacity, but are currently plagued by the sluggish charge transfer kinetics and large volume changes that hinder their practical applications. Herein, we design a triple-disordered-cation phosphide of GaGeSiP3 that combines the benefits of the high capacity of Si, high reactivity of P, fast Li ion conduction of Ge, and the self-healing capability of liquid metallic Ga. The GaGeSiP3 multinary compound features high configurational entropy, with excellent electronic conductivity, rapid Li-ion diffusion, and better resistance to volume change compared to the parent phases of GaGe2P3, GaSi2P3, Ge, and Si. Crystallographic and spectrographic analyses, electrochemical characterization and theoretical simulations confirm that GaGeSiP3 undergoes a reversible lithium storage mechanism based on a combination of intercalation and conversion reactions. The GaGeSiP3 anode delivers a high specific capacity of 1667 mA h g−1 with an initial coulombic efficiency of 90.3% and a low average operating potential of 0.47 V. Moreover, we further create graphite-modified GaGeSiP3 that combines intercalation and conversion storage to deliver a high rate capacity of 949 mA h g−1 at 20.0 mA cm−2, and an exceptional cycling stability to retain a capacity of 1121 mA h g−1 after 2000 cycles at 6.0 mA cm−2. Inspired by this unique feature of high structural entropy, we further synthesized quaternary mixed-cation ZnGaGeSiP4, CuGaGeSiP4, and AlGaGeSiP4; quinary mixed-cation ZnCuGaGeSiP5, ZnAlGaGeSiP5, and CuAlGaGeSiP5; and hexanary mixed-cation ZnCuAlGaGeSiP6, where the crystalline size was reduced due to the enhanced structural entropy. This work opens up a new synthesis paradigm, which overcomes the thermodynamic immiscibility among different metals and non-metals, for creating an attractive family of high-entropy multinary mixed-cation phosphides as advanced energy storage materials.
AB - Monophosphides and bi-metallic phosphides have attracted considerable interest for their high-capacity Li-storage capacity, but are currently plagued by the sluggish charge transfer kinetics and large volume changes that hinder their practical applications. Herein, we design a triple-disordered-cation phosphide of GaGeSiP3 that combines the benefits of the high capacity of Si, high reactivity of P, fast Li ion conduction of Ge, and the self-healing capability of liquid metallic Ga. The GaGeSiP3 multinary compound features high configurational entropy, with excellent electronic conductivity, rapid Li-ion diffusion, and better resistance to volume change compared to the parent phases of GaGe2P3, GaSi2P3, Ge, and Si. Crystallographic and spectrographic analyses, electrochemical characterization and theoretical simulations confirm that GaGeSiP3 undergoes a reversible lithium storage mechanism based on a combination of intercalation and conversion reactions. The GaGeSiP3 anode delivers a high specific capacity of 1667 mA h g−1 with an initial coulombic efficiency of 90.3% and a low average operating potential of 0.47 V. Moreover, we further create graphite-modified GaGeSiP3 that combines intercalation and conversion storage to deliver a high rate capacity of 949 mA h g−1 at 20.0 mA cm−2, and an exceptional cycling stability to retain a capacity of 1121 mA h g−1 after 2000 cycles at 6.0 mA cm−2. Inspired by this unique feature of high structural entropy, we further synthesized quaternary mixed-cation ZnGaGeSiP4, CuGaGeSiP4, and AlGaGeSiP4; quinary mixed-cation ZnCuGaGeSiP5, ZnAlGaGeSiP5, and CuAlGaGeSiP5; and hexanary mixed-cation ZnCuAlGaGeSiP6, where the crystalline size was reduced due to the enhanced structural entropy. This work opens up a new synthesis paradigm, which overcomes the thermodynamic immiscibility among different metals and non-metals, for creating an attractive family of high-entropy multinary mixed-cation phosphides as advanced energy storage materials.
UR - http://www.scopus.com/inward/record.url?scp=85192483479&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85192483479&partnerID=8YFLogxK
U2 - 10.1039/d3ee02392c
DO - 10.1039/d3ee02392c
M3 - Article
AN - SCOPUS:85192483479
SN - 1754-5692
VL - 17
SP - 5387
EP - 5398
JO - Energy and Environmental Science
JF - Energy and Environmental Science
IS - 15
ER -