Please use this identifier to cite or link to this item: https://hdl.handle.net/10356/166406
Title: Pd-PdO nanodomains on amorphous Ru metallene oxide for high-performance multifunctional electrocatalysis
Authors: Do, Viet-Hung
Prabhu, P.
Jose, Vishal
Yoshida, Takefumi
Zhou, Yingtang
Miwa, Hiroko
Kaneko, Takuma
Uruga, Tomoya
Iwasawa, Yasuhiro
Lee, Jong-Min
Keywords: Engineering::Chemical technology
Issue Date: 2023
Source: Do, V., Prabhu, P., Jose, V., Yoshida, T., Zhou, Y., Miwa, H., Kaneko, T., Uruga, T., Iwasawa, Y. & Lee, J. (2023). Pd-PdO nanodomains on amorphous Ru metallene oxide for high-performance multifunctional electrocatalysis. Advanced Materials, 35(12), 2208860-. https://dx.doi.org/10.1002/adma.202208860
Project: RG105/19 
Journal: Advanced Materials 
Abstract: Developing highly efficient multifunctional electrocatalysts is crucial for future sustainable energy  pursuits, but remains a great challenge. Herein, a facile synthetic strategy is used to confine atomically thin Pd-PdO nanodomains to amorphous Ru metallene oxide (RuO2 ). The as-synthesized electrocatalyst (Pd2 RuOx-0.5 h) exhibits excellent catalytic activity toward the pH-universal hydrogen evolution reaction (η10  = 14 mV in 1 m KOH, η10  = 12 mV in 0.5 m H2 SO4 , and η10  = 22 mV in 1 m PBS), alkaline oxygen evolution reaction (η10  = 225 mV), and overall water splitting (E10  = 1.49 V) with high mass activity and operational stability. Further reduction endows the material (Pd2 RuOx-2 h) with a promising alkaline oxygen reduction activity, evidenced by high halfway potential, four-electron selectivity, and excellent poison tolerance. The enhanced catalytic activity is attributed to the rational integration of favorable nanostructures, including 1) the atomically thin nanosheet morphology, 2) the coexisting amorphous and defective crystalline phases, and 3) the multi-component heterostructural features. These structural factors effectively regulate the material's electronic configuration and the adsorption of intermediates at the active sites for favorable reaction energetics.
URI: https://hdl.handle.net/10356/166406
ISSN: 0935-9648
DOI: 10.1002/adma.202208860
Schools: Interdisciplinary Graduate School (IGS) 
School of Chemistry, Chemical Engineering and Biotechnology 
Research Centres: Energy Research Institute @ NTU (ERI@N) 
Rights: © 2023 Wiley-VCH GmbH. All rights reserved.
Fulltext Permission: none
Fulltext Availability: No Fulltext
Appears in Collections:CCEB Journal Articles
ERI@N Journal Articles
IGS Journal Articles

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