Journal
JOURNAL OF POWER SOURCES
Volume 532, Issue -, Pages -Publisher
ELSEVIER
DOI: 10.1016/j.jpowsour.2022.231353
Keywords
Spontaneous redox synthesis; Self-supported bifunctional electrocatalysts; Overall water/seawater splitting
Funding
- ShanghaiTech University
- Shanghai Key Research Program [20ZR1436700]
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This study presents a novel and simple synthesis strategy to prepare a self-supported high-performance water/seawater splitting bifunctional electro-catalyst. The catalyst exhibits excellent catalytic activity and enhanced chemical stability, which is highly relevant for commercial applications.
The development of high-performance, low-cost and large-scale water/seawater splitting bifunctional electro-catalysts still faces huge challenges. Here, we deliver a novel and simple spontaneous redox synthesis strategy to fabricate a self-supported Pt-CoFe(II) layered double hydroxide (LDH) electrocatalyst. The three-dimensional porous structure of the catalyst and the synergistic effect of Pt clusters and CoFe hydroxides jointly contribute to its excellent catalytic activity and enhanced chemical stability. Specifically, in 1 M KOH, the overpotentials for oxygen evolution reaction (OER) and hydrogen evolution reaction (HER) of Pt-CoFe(II) LDH at 10 mA cm(-2) are 214 mV and 15 mV, respectively. The catalysts are stable for at least 40 h at high current densities of 100 and 500 mA cm-2. Compared with previously reported electrocatalysts, Pt-CoFe(II) LDHs || Pt-CoFe(II) LDHs overall water (seawater) electrolyzers only require 1.634 (1.651) and 1.798 (1.858) V to reach 100 and 500 mA cm-2 in 1 M KOH water (seawater) electrolyte, confirming the superior catalytic activity of the self-supported Pt-CoFe(II) layered double hydroxide electrocatalysts. This study provides a novel and simple synthesis strategy to prepare advanced water/seawater splitting electrocatalysts, which is highly relevant for commercial applications.
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