Caixia Li
Shandong University
79 Papers
40 Citations
Caixia Li is an academic researcher from Shandong University. The author has contributed to research in topics: Medicine & Chemistry. The author has an hindex of 21, co-authored 29 publications.
Chat about Author
Papers
Reduced graphene oxide wrapped MOFs-derived cobalt-doped porous carbon polyhedrons as sulfur immobilizers as cathodes for high performance lithium sulfur batteries
TL;DR: In this paper, reduced graphene oxide (RGO) wrapped metal-organic frameworks (MOFs) derived cobalt doped porous carbon polyhedrons synthesized via a carbonization process, are for the first time used for sulfur immobilizers as cathodes for high performance lithium-sulfur (Li-S) batteries.
435
ZnS-Sb2S3@C Core-Double Shell Polyhedron Structure Derived from Metal–Organic Framework as Anodes for High Performance Sodium Ion Batteries
TL;DR: The polyhedron composite with a ZnS inner-core and Sb2S3/C double-shell as anode for sodium ion batteries (SIBs) shows a significantly improved electrochemical performance with stable cycle stability, high Coulombic efficiency and specific capacity.
348
Core-shell structured CoP/FeP porous microcubes interconnected by reduced graphene oxide as high performance anodes for sodium ion batteries
TL;DR: In this article, a unique core-shell porous FeP@CoP phosphide micocubes interconnected via reduced graphene oxide (RGO) nanosheets are for the first time synthesized via a low-temperature phosphorization process using prussion blue as reactant template.
328
Atomically dispersed cobalt catalyst anchored on nitrogen-doped carbon nanosheets for lithium-oxygen batteries
Peng Wang,Yingying Ren,Rutao Wang,Peng Zhang,Mingjie Ding,Caixia Li,Danyang Zhao,Zhao Qian,Zhiwei Zhang,Luyuan Zhang,Longwei Yin +10 more
TL;DR: The achieved electrode with maximized exposed atomic active sites is beneficial for tailoring formation/decomposition mechanisms of uniformly distributed nano-sized lithium peroxide during oxygen reduction/evolution reactions due to abundant cobalt-nitrogen coordinate catalytic sites, thus demonstrating greatly enhanced redox kinetics and efficiently ameliorated over-potentials.
322