Journal
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
Volume 144, Issue 21, Pages 9354-9362Publisher
AMER CHEMICAL SOC
DOI: 10.1021/jacs.2c01412
Keywords
-
Categories
Funding
- National Key Research and Development Program of China [2021YFB2500300]
- National Natural Science Fund for Excellent Young Scholars [21722508]
Ask authors/readers for more resources
This study investigates the interfacial evolution at the electrode/electrolyte interface of all-carbon graphdiyne-based materials using in situ optical microscopy and atomic force microscopy monitoring. The results reveal the growth and continuous accumulation of the solid electrolyte interphase (SEI) at the surface of the graphdiyne electrode, as well as the homogeneous propagation of nanoparticle-shaped SEI when nitrogen configurations are involved.
All-carbon graphdiyne (GDY)-based materials have attracted extensive attention owing to their extraordinary structures and outstanding performance in electrochemical energy storage. Straightforward insights into the interfacial evolution at GDY electrode/electrolyte interface could crucially enrich the fundamental comprehensions and inspire targeted regulations. Herein, in situ optical microscopy and atomic force microscopy monitoring of the GDY and N-doped GDY electrodes reveal the interplay between the solid electrolyte interphase (SEI) and Li deposition. The growth and continuous accumulation of the flocculent-like SEI is directly tracked at the surface of GDY electrode. Moreover, the nanoparticle-shaped SEI homogeneously propagates at the interface when N configurations are involved, providing a critical clue for the N-doping effects of stabilizing interfaces and homogenizing Li deposition. This work probes into the dynamic evolution and structure-reactivity correlation in detail, creating effective strategies for GDY-based materials optimization in lithium-ion batteries.
Authors
I am an author on this paper
Click your name to claim this paper and add it to your profile.
Reviews
Recommended
No Data Available