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In Situ Growth of MoS2 Nanosheet Arraysand TS2 (T = Fe Co and Ni) Nanocubes onto Molybdate forEfficient Oxygen Evolution Reaction and Improved Hydrogen EvolutionReaction

机译:MoS2纳米片阵列的原位生长和TS2(T = FeCo和Ni)纳米晶在钼酸盐上用于高效的析氧反应和改进的析氢反应

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摘要

Rationally designing efficient and low-price bifunctional electrocatalysts for oxygen evolution reaction (OER) and hydrogen evolution reaction (HER) are vitally important to bring solar/electrical-to-hydrogen energy conversion processes into reality. Herein, we report on a synthetic method that leads to an in situ growth of ultrathin MoS2 nanosheets and transition metal disulfide nanocubes onto the surface of Fe1/3Co1/3Ni1/3MoO4 nanorods for the first time. Such hybrids are found to serve as a bifunctional electrocatalyst with high activities for OER and HER, as represented by an impressive anodic and cathodic current density of 10 mA cm–2 at 1.53 and −0.25 V, respectively. More importantly, the performance for OER is even better than that of IrO2, the conventional noble metal electrocatalyst. These striking observations were interpreted in terms of the combination of strongly synergistic effect of multimetal components, large amount of exposed active site, and superaerophobia. The present methodology has been confirmed universal for synthesizing other molybdate solid solutions, which would open up new possibilities for designing novelnon-noble bifunctional electrocatalysts for OER and HER.
机译:合理设计用于氧气析出反应(OER)和氢气析出反应(HER)的高效且价格低廉的双功能电催化剂,对于实现太阳能/电到氢的能量转化过程至关重要。在本文中,我们报道了一种合成方法,该方法首次导致超薄MoS2纳米片和过渡金属二硫化物纳米立方体原位生长到Fe1 / 3Co1 / 3Ni1 / 3MoO4纳米棒的表面。这些杂化物被发现对OER和HER具有高活性,可作为一种双功能电催化剂,其典型的阳极和阴极电流密度分别为1.53 V和-0.25 V时10 mA cm 。更重要的是,OER的性能甚至优于常规贵金属电催化剂IrO2。这些惊人的观察结果是根据多金属组分的强协同作用,大量暴露的活性位点和超级厌氧症的组合来解释的。已经证实本方法学可用于合成其他钼酸盐固溶体,这将为设计新颖的方法开辟新的可能性。用于OER和HER的非贵族双功能电催化剂。

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