TY - JOUR
T1 - Two-dimensional mesoporous heterostructure delivering superior pseudocapacitive sodium storage via bottom-up monomicelle assembly
AU - Lan, Kun
AU - Wei, Qiulong
AU - Wang, Ruicong
AU - Xia, Yuan
AU - Tan, Shuangshuang
AU - Wang, Yanxiang
AU - Elzatahry, Ahmed
AU - Feng, Pingyun
AU - Mai, Liqiang
AU - Zhao, Dongyuan
N1 - Publisher Copyright:
© 2019 American Chemical Society.
PY - 2019/10/23
Y1 - 2019/10/23
N2 - Two-dimensional (2D) heterostructures endowed with mesoporosities offer exciting opportunities in electrocatalysis, photocatalysis, energy storage, and conversion technologies due to their integrated functionalities, abundant active sites and shortened diffusion distance. However, layered mesostructures have not been combined due to the immense difficulties by conventional chemical, mechanical exfoliation or self-assembly approaches. Herein, we explore a bottom-up strategy, carried out under mild conditions, for the facile synthesis of monolayered mesoporous-titania-mesoporous-carbon vertical heterostructure with uniform mesopore size, which enables ultrahigh rate capability and cycling longevity for pseudocapacitive sodium-ion storage in nonaqueous electrolyte. Such a brand-new type of heterostructure consists of well-ordered monolayered mesoporous titania nanosheets and surrounding two mesoporous carbon monolayers assembled at both sides. Remarkably, the combination of interconnected large mesoporosity and heterointerface leads to highly promoted reversible pseudocapacitance (96.4% of total charge storage at a sweep rate of 1 mV s-1), and it enables the material to retain strong mechanical stability during the rapid sodiation and desodiation processes. This study reveals the importance of incorporating mesopores into heterointerface as a strategy for enhancing charge storage kinetics of electroactive materials.
AB - Two-dimensional (2D) heterostructures endowed with mesoporosities offer exciting opportunities in electrocatalysis, photocatalysis, energy storage, and conversion technologies due to their integrated functionalities, abundant active sites and shortened diffusion distance. However, layered mesostructures have not been combined due to the immense difficulties by conventional chemical, mechanical exfoliation or self-assembly approaches. Herein, we explore a bottom-up strategy, carried out under mild conditions, for the facile synthesis of monolayered mesoporous-titania-mesoporous-carbon vertical heterostructure with uniform mesopore size, which enables ultrahigh rate capability and cycling longevity for pseudocapacitive sodium-ion storage in nonaqueous electrolyte. Such a brand-new type of heterostructure consists of well-ordered monolayered mesoporous titania nanosheets and surrounding two mesoporous carbon monolayers assembled at both sides. Remarkably, the combination of interconnected large mesoporosity and heterointerface leads to highly promoted reversible pseudocapacitance (96.4% of total charge storage at a sweep rate of 1 mV s-1), and it enables the material to retain strong mechanical stability during the rapid sodiation and desodiation processes. This study reveals the importance of incorporating mesopores into heterointerface as a strategy for enhancing charge storage kinetics of electroactive materials.
UR - https://www.scopus.com/pages/publications/85073248634
U2 - 10.1021/jacs.9b06962
DO - 10.1021/jacs.9b06962
M3 - Article
C2 - 31564098
AN - SCOPUS:85073248634
SN - 0002-7863
VL - 141
SP - 16755
EP - 16762
JO - Journal of the American Chemical Society
JF - Journal of the American Chemical Society
IS - 42
ER -