Self-Assembled MXene Supported on Carbonization-Free Wood for a Symmetrical All-Wood Eco-Supercapacitor.

ACS Appl Mater Interfaces

Key Laboratory of Bio-Based Material Science and Technology of Ministry of Education, Northeast Forestry University, Harbin 150040, P. R. China.

Published: July 2024

As an emerging two-dimensional (2D) material, MXene has garnered significant interest in advanced energy storage systems, yet the stackable structure, poor mechanical stability, and lack of moldability limit its large-scale applications. To address this challenge, herein, the self-assembly of MXene on carbonization-free wood was obtained to serve as high-performance electrodes for symmetrical all-wood eco-supercapacitors by a steam-driven self-assembly method. This method can be implemented in a low-temperature environment, significantly simplifying traditional high-temperature annealing processes and generating minimal impact on the environment, human health, and resource consumption. The environmentally friendly steam-driven self-assembly strategy can be further extended into various wood-based electrodes, regardless of the types and structures of wood. As a typical platform electrode, the optimized MXene@delignified balsa wood (MDBW) achieves high areal capacitance and specific capacitance values of 2.99 F cm and 580.55 F g at an extensive mass loading of 5.16 mg cm, respectively, with almost loss-free capacitance after 10,000 cycles at 50 mA cm. In addition, an all-solid-state symmetrical all-wood eco-supercapacitor was further assembled based on MDBW-20 as both positive and negative electrodes to achieve a high energy density of 19.22 μWh cm at a power density of 0.58 mW cm. This work provides an effective strategy to optimize wood-based electrodes for the practical application of biomass eco-supercapacitors.

Download full-text PDF

Source
http://dx.doi.org/10.1021/acsami.4c05129DOI Listing

Publication Analysis

Top Keywords

symmetrical all-wood
12
carbonization-free wood
8
all-wood eco-supercapacitor
8
steam-driven self-assembly
8
wood-based electrodes
8
self-assembled mxene
4
mxene supported
4
supported carbonization-free
4
wood
4
wood symmetrical
4

Similar Publications

High-mass loaded redox-active lignin functionalized carbonized wood collector to construct sustainable and high-performance supercapacitors.

Int J Biol Macromol

November 2024

Jiangsu Co-innovation Center of Efficient Processing and Utilization of Forestry Resources, College of Materials Science and Engineering, Nanjing Forestry University, Nanjing, Jiangsu 210037, China. Electronic address:

Traditional electrode materials for supercapacitors often face issues like high toxicity, cost, and non-renewability. To address these drawbacks, biomass-based alternatives are being explored, aligning with green development trends. Herein, carbonized wood (CW) with rich pore structure and redox-active lignin are combined to fabricate an all-wood-based sustainable supercapacitor electrode material.

View Article and Find Full Text PDF

Self-Assembled MXene Supported on Carbonization-Free Wood for a Symmetrical All-Wood Eco-Supercapacitor.

ACS Appl Mater Interfaces

July 2024

Key Laboratory of Bio-Based Material Science and Technology of Ministry of Education, Northeast Forestry University, Harbin 150040, P. R. China.

As an emerging two-dimensional (2D) material, MXene has garnered significant interest in advanced energy storage systems, yet the stackable structure, poor mechanical stability, and lack of moldability limit its large-scale applications. To address this challenge, herein, the self-assembly of MXene on carbonization-free wood was obtained to serve as high-performance electrodes for symmetrical all-wood eco-supercapacitors by a steam-driven self-assembly method. This method can be implemented in a low-temperature environment, significantly simplifying traditional high-temperature annealing processes and generating minimal impact on the environment, human health, and resource consumption.

View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!