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Ir- and Ru-doped layered double hydroxides as affordable heterogeneous catalysts for electrochemical water oxidation

机译:IR-和Ru掺杂层状双氢氧化物作为用于电化学水氧化的实惠的异质催化剂

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摘要

Three M-doped LDHs (M = noble metal active site, LDH = layered double hydroxides; Ir-1, Ir-ZnAl; Ru, Ru-ZnAl; Ir-2, Ir-MgAl), containing small amounts of M (ca. 2 mol% and even <1 mol% for Ru and Ir, respectively), were prepared by following simple and established synthetic procedures. Their characterization indicates that M atoms are effectively incorporated into the brucite-like layers of LDH, without phase segregation. The resulting materials catalyse electrochemical water oxidation (WO), when immobilized in carbon paste electrodes, with performances that exceed those of the benchmark system IrO2, as probed by linear sweep voltammetry (LSV). Some of these catalysts undergo continuous activation upon chronoamperometric and chronopotentiometric treatments over several hours. The crystalline structure of all of them is preserved during electrocatalytic experiments, and no significant leaching of noble metal in solution is detected. The results herein reported highlight the remarkable potential of these doped M-LDHs and confirm that dispersing Ir and Ru centers in layered and cheap inorganic materials results in easily accessible metal centers, providing highly active catalysts, while minimizing the utilization of noble metals.
机译:三个M掺杂的LDH(M =贵金属活性位点,LDH =层叠双氢氧化物; IR-1,IR-ZNAL; Ru,Ru-Znal; IR-2,IR-MGAL),含有少量M(CA.通过以下简单和建立的合成方法制备2mol%甚至<1mol%的Ru和Ir%。它们的表征表明,M原子有效地掺入了LDH的布苏钛矿层中,没有相位偏析。当在碳浆电极中固定时,所得材料催化电化学水氧化(WO),其性能超过基准系统IRO2的性能,如线性扫描伏安法(LSV)探测。这些催化剂中的一些在几小时内时经历连续的活化和计时率测定的处理。在电催化实验期间保留所有它们的结晶结构,并且检测到溶液中贵金属的显着浸出。本文的结果报告突出了这些掺杂的M-LDH的显着潜力,并证实分散在分层和廉价的无机材料中的分散和Ru中心导致易于获得的金属中心,提供高活性催化剂,同时最小化贵金属的利用率。

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