首页> 外文期刊>Bulletin of the Korean Chemical Society >Effect of a Surface Area and a d-Band Oxidation State on the Activity and Stability of RuOx Electrocatalysts for Oxygen Evolution Reaction
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Effect of a Surface Area and a d-Band Oxidation State on the Activity and Stability of RuOx Electrocatalysts for Oxygen Evolution Reaction

机译:表面积和d波段氧化态对析氧反应RuOx电催化剂活性和稳定性的影响

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摘要

It is widely recognized that RuO2 is the best electrocatalysts for oxygen evolution reaction (OER) in water splitting in acidic media. In this study, we investigated the effect of a surface area and a d-band oxidation state on the activity and the stability of RuOx electrocatalysts for OER. We synthesized RuOx thin film on glassy carbon electrode by the radio frequency magnetic sputtering and controlled the deposition temperature to vary the surface morphology and the electronic structure. In particular, we obtained a precise d-band valence structure by using the synchrotron beam. A higher surface area and a more stable Ru4+ state were obtained at a lower deposition temperature owing to a smaller grain size and a lower oxidation state, respectively. As a result, the order of activity and stability is clearly consistent with that of surface area and stable Ru4+ state (RuOx > RuO(x)200 > RuO(x)400 > RuO(x)600). Hence, we suggest that the surface area and the Ru d-band oxidation state should be carefully controlled in the synthesis process in order to enhance the activity and the stability of RuOx electrocatalysts for OER.
机译:众所周知,RuO2是在酸性介质中进行水分解时氧气释放反应(OER)的最佳电催化剂。在这项研究中,我们研究了表面积和d波段氧化态对RuOx电催化剂对OER的活性和稳定性的影响。我们通过射频磁溅射在玻璃碳电极上合成RuOx薄膜,并控制沉积温度以改变表面形态和电子结构。特别是,我们通过使用同步加速器束获得了精确的d波段价结构。由于较低的晶粒尺寸和较低的氧化态,分别在较低的沉积温度下获得了较高的表面积和更稳定的Ru4 +状态。结果,活性和稳定性的顺序与表面积和稳定的Ru4 +状态的顺序明显一致(RuOx> RuO(x)200> RuO(x)400> RuO(x)600)。因此,我们建议在合成过程中应小心控制表面积和Ru d带的氧化态,以增强RuOx电催化剂对OER的活性和稳定性。

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