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Non-noble metal Fe 2 O 3 @NiO as efficient bifunctional catalysts for water splitting

机译:非贵金属Fe 2 O 3 @NiO作为高效的水分解双功能催化剂

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The development of non-noble metal catalysts is crucial for hydrogen production. In this study, electrochemically reconfigurable Fe2O3@NiO-x composite catalysts were synthesized within tens of seconds using a simple microwave deposition method. Interestingly, Fe2O3@NiO-5 exhibited a high-speed and deep surface reconstruction capability, greatly enhancing the hydrogen evolution reaction (HER) activity. DFT calculations also confirmed that the reconstruction process optimized the adsorption energy of H2O and H intermediate to promote HER kinetics. The optimized Fe2O3@NiO-5 electrode only afforded an overpotential of 295 mV at 10 mA cm(-2) and it steadily functioned for 25 h for HER in 1 M KOH. In addition, benefiting from the combination of Fe2O3 and NiO layer during the synthesis process, Fe2O3 and NiO converted into FeOOH and NiOOH, respectively, resulted in the excellent oxygen evolution reaction (OER) activity of Fe2O3@NiO-5. The as-prepared Fe2O3@NiO-5 only required an overpotential of 186 mV at 10 mA cm(-2) and exhibited excellent stability for up to 144 h. As a bifunctional catalyst, the Fe2O3@NiO-5 electrode can deliver a current density of 20 mA cm(-2) at a low voltage of 1.78 V with high durability for water splitting. This work can provide a new perspective for constructing advanced non-noble metal electrode.
机译:非贵金属催化剂的开发对于制氢至关重要。本研究采用简单的微波沉积法,在数十秒内合成了电化学重构的Fe2O3@NiO-x复合催化剂。有趣的是,Fe2O3@NiO-5表现出高速和深层的表面重建能力,大大增强了析氢反应(HER)的活性。DFT计算也证实了重构过程优化了H2O和H中间体的吸附能,促进了HER动力学。优化后的Fe2O3@NiO-5电极在10 mA cm(-2)时仅提供295 mV的过电位,并且在1 M KOH下HER稳定工作25 h。此外,得益于合成过程中Fe2O3和NiO层的结合,Fe2O3和NiO分别转化为FeOOH和NiOOH,使Fe2O3@NiO-5具有优异的析氧反应(OER)活性。制备的Fe2O3@NiO-5在10 mA cm(-2)时仅需186 mV的过电位,在长达144 h的时间内表现出优异的稳定性。作为双功能催化剂,Fe2O3@NiO-5电极可在1.78 V的低电压下提供20 mA cm(-2)的电流密度,具有很高的水分解耐久性。本工作可为构建先进的非贵金属电极提供新的视角。

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