A carbonization/interfacial assembly-driven electroplating approach for water-splitting textile electrodes with remarkably low overpotentials and high operational stability. Issue 9 (15th July 2022)

• Record Type: Journal Article
• Authors: Mo, Jeongmin; Ko, Younji; Yun, Young Soo; Huh, June; Cho, Jinhan
• Is Part Of: Energy & environmental science. Volume 15:Issue 9(2022)
• Page Start: 3815
• Page End: 3829
• Publication Date: 2022-07-15
• Subjects: Energy conversion -- Periodicals; Fuel switching -- Periodicals; Environmental sciences -- Periodicals; Environmental chemistry -- Periodicals; 333.79
• DOI: 10.1039/d2ee01510b
• Languages: English
• ISSNs: 1754-5692

Abstract

Abstract : We introduce silk textile-based water-splitting electrodes that can significantly increase the electrocatalytic performance for both HER and OER by a carbonization/interfacial assembly-driven electroplating approach. Abstract : A key requirement for realizing highly efficient commercial water-splitting devices is to develop non-noble metal-based electrodes that can generate a large amount of hydrogen fuels with low overpotentials and high operational stability. Herein, we introduce high-performance water-splitting electrodes (WSEs) with extremely low overpotentials and unprecedently high operation stability via a carbonization/interfacial assembly-induced electroplating approach. To this end, silk textiles were first converted to carboxylic acid-functionalized conductive textiles using carbonization and subsequent acid treatment. Then, amine linkers were assembled onto the conductive textiles to achieve favorable interfacial interactions with electrocatalysts. For a hydrogen evolution reaction (HER) electrode, Ni was electroplated onto the interface-modified textile, while to prepare an oxygen evolution reaction (OER) electrode, NiFeCo was additionally electroplated onto the Ni-electroplated textile. These HER and OER electrodes exhibited extremely low overpotentials in alkaline media (12 mV at 10 mA cm −2 for the HER and 186 mV at 50 mA cm −2 for the OER), outperforming the conventional non-noble metal-based electrodes. Additionally, the overall-water-splitting reaction of full-cell electrodes was stably maintained at a remarkably high current density of 2000 mA cm −2 and a low cell voltage of 1.70 V. We believe that our approach can provide a basis for developing commercially available high-performance WSEs.