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Highly active anode electrocatalysts derived from electrochemical leaching of Ru from metallic Ir 0.7 Ru 0.3 for proton exchange membrane electrolyzers

机译:对于质子交换膜电解器的金属IR 0.7 ru 0.3,高活性阳极电催化剂来自Ru的电化学浸出。

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摘要

Hydrogen produced by water splitting is a promising solution for a sustained economy from renewable energy sources. Proton exchange membrane (PEM) electrolysis is the utmost suitable technology for this purpose, although the quest for low cost, highly active and durable catalysts is persistent. Here we develop a nanostructured iridium catalyst after electrochemically leaching ruthenium from metallic iridium-ruthenium, Ir0.7Ru0.3Ox (EC), and compare its physical and electrochemical properties to the thermally treated counterpart: Ir0.7Ru0.3O2 (TT). Ir0.7Ru0.3Ox (EC) shows an unparalleled 13-fold higher oxygen evolution reaction (OER) activity compared to the Ir0.7Ru0.3O2 (TT). PEM electrolyzer tests at 1 A cm-2 show no increase of cell voltage for almost 400 h, proving that Ir0.7Ru0.3Ox (EC) is one of the most efficient anodes so far developed.
机译:水分裂产生的氢是一种从可再生能源持续经济的有希望的解决方案。质子交换膜(PEM)电解是最适合的技术为此目的,尽管追求低成本,高活性和耐用的催化剂是持久的。在这里,我们在从金属铱 - 钌,IR0.7RU0.3X(EC)中电化学浸出钌后开发纳米结构铱催化剂,并将其物理和电化学性能与热处理的对应物进行比较:IR0.7Ru0.3O2(TT)。 IR0.7RU0.3X(EC)显示与IR0.7RU0.3O2(TT)相比的无与伦比的13倍高氧进化反应(OER)活性。 PEM电解槽在1个CM-2的测试显示近400小时的电池电压的增加显示,IR0.7RU0.3X(EC)是到目前为止发达的最有效的阳极之一。

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