TY - JOUR
T1 - Layer-by-Layer Assembly of Polyaniline Nanofibers and MXene Thin-Film Electrodes for Electrochemical Energy Storage
AU - Yun, Junyeong
AU - Echols, Ian
AU - Flouda, Paraskevi
AU - Wang, Shaoyang
AU - Easley, Alexandra
AU - Zhao, Xiaofei
AU - Tan, Zeyi
AU - Prehn, Evan
AU - Zi, Goangseup
AU - Radovic, Miladin
AU - Green, Micah J.
AU - Lutkenhaus, Jodie L.
N1 - Publisher Copyright:
Copyright © 2019 American Chemical Society.
PY - 2019/12/26
Y1 - 2019/12/26
N2 - The growing demand for compact energy storage devices may be met through the use of thin-film microbatteries, which generally rely on charge storage in thin or conformal layers. A promising technique for creating thin-film electrodes is layer-by-layer (LbL) assembly, based on the alternating adsorption of oppositely charged species to a surface to form a nanostructured electrode. Thin-film energy storage devices must have a high energy density within a limited space, so new electrode structures, materials, and assembly methods are important. To this end, both two-dimensional MXenes and polyaniline nanofibers (PNFs) have shown promising energy storage properties. Here, we report on the LbL assembly of positively charged PNFs and negatively charged Ti3C2Tx MXenes into hybrid electrodes for thin-film energy storage devices. The successful assembly is demonstrated in which MXenes and PNFs are deposited in films of 49 nm/layer pair thickness. The resulting composition was 77 wt % PNFs and 23 wt % MXenes. The charge storage process was deconvoluted into faradaic/non-faradaic contributions and separated into contributions from PNFs and MXenes. A sandwich cell showed a maximum areal capacity, energy, and power of 17.6 μA h cm-2, 22.1 μW h cm-2, and 1.5 mW cm-2, respectively, for PNF/MXene multilayers of about 2 μm thickness. This work suggests the possibility of using LbL PNF/MXene thin films as electrode materials for thin-film energy storage devices used in next-generation small electronics.
AB - The growing demand for compact energy storage devices may be met through the use of thin-film microbatteries, which generally rely on charge storage in thin or conformal layers. A promising technique for creating thin-film electrodes is layer-by-layer (LbL) assembly, based on the alternating adsorption of oppositely charged species to a surface to form a nanostructured electrode. Thin-film energy storage devices must have a high energy density within a limited space, so new electrode structures, materials, and assembly methods are important. To this end, both two-dimensional MXenes and polyaniline nanofibers (PNFs) have shown promising energy storage properties. Here, we report on the LbL assembly of positively charged PNFs and negatively charged Ti3C2Tx MXenes into hybrid electrodes for thin-film energy storage devices. The successful assembly is demonstrated in which MXenes and PNFs are deposited in films of 49 nm/layer pair thickness. The resulting composition was 77 wt % PNFs and 23 wt % MXenes. The charge storage process was deconvoluted into faradaic/non-faradaic contributions and separated into contributions from PNFs and MXenes. A sandwich cell showed a maximum areal capacity, energy, and power of 17.6 μA h cm-2, 22.1 μW h cm-2, and 1.5 mW cm-2, respectively, for PNF/MXene multilayers of about 2 μm thickness. This work suggests the possibility of using LbL PNF/MXene thin films as electrode materials for thin-film energy storage devices used in next-generation small electronics.
KW - MXene
KW - layer-by-layer assembly
KW - polyaniline nanofiber
KW - thin-film energy storage
UR - http://www.scopus.com/inward/record.url?scp=85077296597&partnerID=8YFLogxK
U2 - 10.1021/acsami.9b16692
DO - 10.1021/acsami.9b16692
M3 - Article
C2 - 31774650
AN - SCOPUS:85077296597
SN - 1944-8244
VL - 11
SP - 47929
EP - 47938
JO - ACS Applied Materials and Interfaces
JF - ACS Applied Materials and Interfaces
IS - 51
ER -