Developments and Perspectives on Robust Nano- and Microstructured Binder-Free Electrodes for Bifunctional Water Electrolysis and Beyond
- Abstract
- The development of robust nano- and microstructured catalysts on highly conductive substrates is an effective approach to produce highly active binder-free electrodes for energy conversion and storage applications. As a result, nanostructured electrodes with binder-free designs have abundant advantages that provide superior electrocatalytic performance; these include more exposed active sites, large surface area, strong adhesion to substrates, facile charge transfer, high conductivity, high intrinsic catalytic activity, and fine-tuning of its electronic nature through nanostructure modification. Notably, the interface chemistry of an electrocatalyst plays a significant role in their optimized electrocatalytic activity and stability. This review provides an overview of recent progress in nano- and microstructured catalysts, such as one, two, and 3D catalysts as binder-free electrodes for electrocatalytic water splitting via the hydrogen evolution reaction and oxygen evolution reaction, and beyond. Furthermore, this review focuses on the current challenges and synthesis strategies of binder-free electrodes, with a focus on the impact of nanostructure on their functional property relationships and enhanced bifunctional electrocatalytic performance. Finally, an outlook for their future advances in energy conversion and storage is provided.
- Author(s)
- Sundaram Chandrasekaran; Mahima Khandelwal; Fan Dayong; Lijun Sui; Jin Suk Chung; R. D. K. Misra; Peng Yin; Eui Jung Kim; Woong Kim; Aravindan Vanchiappan; Yongping Liu; Seung Hyun Hur; Han Zhang; Chris Bowen
- Issued Date
- 2022
- Type
- Article
- Keyword
- binder-free electrodes; freestanding electrodes; HER; OER; watersplitting
- DOI
- 10.1002/aenm.202200409
- URI
- https://oak.ulsan.ac.kr/handle/2021.oak/14740
- Publisher
- Advanced Energy Materials
- Language
- 영어
- ISSN
- 1614-6832
- Citation Volume
- 12
- Citation Number
- 23
- Citation Start Page
- 1
- Citation End Page
- 73
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