journal article·2021-02-17Open access

One-Pot Hydrothermal Synthesis of Solution-Processable MoS2/PEDOT:PSS Composites for High-Performance Supercapacitors

Yunfeng Chao, Yu Ge, Zhiqi Chen, Xiaoling Cui, Chen Zhao, Caiyun Wang, Gordon G. Wallace

Abstract

It is challenging to hydrothermally synthesize solution-processable MoS2, as the strong van der Waals force between MoS2 nanosheets induces self-assembly of agglomerates. Here, we introduce poly(3,4-ethylenedioxythiophene):poly(styrenesulfonate) (PEDOT:PSS) into the precursor to impede aggregate formation in the hydrothermal process. A hybrid MoS2/PEDOT:PSS (MP) hydrogel is formed due to the electrostatic interactions between the negatively charged MoS2 and positively charged PEDOT chains. This hydrogel can be easily dispersed in water for subsequent solution processing such as vacuum filtration to form free-standing flexible films or extrusion 3D printing to create novel patterns. The MP film with a fracture strength of 18.59 MPa displays excellent electrochemical performance in both aqueous Na2SO4 electrolyte (474 mF cm–2) and solid-state PVA–H3PO4 electrolyte (360 mF cm–2). Flexibility and robustness can be evidenced by high capacitance retention rates of 94 and 89% after being repeatedly bent to 180° for 5000 cycles in aqueous and solid-state electrolytes, respectively.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: Supercapacitor Materials and Fabrication · MXene and MAX Phase Materials · Advanced Sensor and Energy Harvesting Materials

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

Intelligent Polymer Research Institute, ARC Centre of Excellence for Electromaterials Science, AIIM Facility, Innovation Campus, University of Wollongong, Wollongong, New South Wales 2522, Australia

College of petrochemical technology, Lanzhou University of Technology, Lanzhou 730050, PR China

School of Materials and Energy, Guangdong University of Technology, Guangzhou 510006, China

Funding

Australian Research Council Centre of Excellence Scheme

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