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光介导的氧化锰电化学合成增强了其水氧化稳定性。

Light-Mediated Electrochemical Synthesis of Manganese Oxide Enhances Its Stability for Water Oxidation.

作者信息

Qin Chu, Luo Jiang, Zhang Dongyan, Brennan Logan, Tian Shijun, Berry Ashlynn, Campbell Brandon M, Sadtler Bryce

机构信息

Department of Chemistry, Washington University, St. Louis, Missouri 63130, United States.

Department of Physics, Zhejiang Sci-Tech University, Hangzhou, Zhejiang 310018, China.

出版信息

ACS Nanosci Au. 2023 Apr 24;3(4):310-322. doi: 10.1021/acsnanoscienceau.3c00002. eCollection 2023 Aug 16.

Abstract

New methods are needed to increase the activity and stability of earth-abundant catalysts for electrochemical water splitting to produce hydrogen fuel. Electrodeposition has been previously used to synthesize manganese oxide films with a high degree of disorder and a mixture of oxidation states for Mn, which has led to electrocatalysts with high activity but low stability for the oxygen evolution reaction (OER) at high current densities. In this study, we show that multipotential electrodeposition of manganese oxide under illumination produces nanostructured films with significantly higher stability for the OER compared to films grown under otherwise identical conditions in the dark. Manganese oxide films grown by multipotential deposition under illumination sustain a current density of 10 mA/cm at 2.2 V versus reversible hydrogen electrode for 18 h (pH 13). Illumination does not enhance the activity or stability of manganese oxide films grown using a constant potential, and films grown by multipotential deposition in the dark undergo a complete loss of activity within 1 h of electrolysis. Electrochemical and structural characterization indicate that photoexcitation of the films during growth reduces Mn ions and changes the content and structure of intercalated potassium ions and water molecules in between the disordered layers of birnessite-like sheets of MnO, which stabilizes the nanostructured film during electrocatalysis. These results demonstrate that combining multiple external stimuli (i.e., light and an external potential) can induce structural changes not attainable by either stimulus alone to make earth-abundant catalysts more active and stable for important chemical transformations such as water oxidation.

摘要

需要新方法来提高用于电化学水分解以生产氢燃料的储量丰富的地球催化剂的活性和稳定性。先前已使用电沉积来合成具有高度无序性和锰氧化态混合物的氧化锰薄膜,这导致了在高电流密度下对析氧反应(OER)具有高活性但稳定性低的电催化剂。在本研究中,我们表明,与在黑暗中其他相同条件下生长的薄膜相比,光照下氧化锰的多电位电沉积产生的纳米结构薄膜对OER具有明显更高的稳定性。在光照下通过多电位沉积生长的氧化锰薄膜在相对于可逆氢电极2.2 V的电压下,在pH 13时能维持10 mA/cm²的电流密度达18小时。光照不会提高使用恒电位生长的氧化锰薄膜的活性或稳定性,并且在黑暗中通过多电位沉积生长的薄膜在电解1小时内活性完全丧失。电化学和结构表征表明,生长过程中薄膜的光激发会还原锰离子,并改变MnO类水钠锰矿无序层间嵌入的钾离子和水分子的含量及结构,这在电催化过程中稳定了纳米结构薄膜。这些结果表明,结合多种外部刺激(即光和外部电位)可以诱导单独任何一种刺激都无法实现的结构变化,从而使储量丰富的地球催化剂对于诸如水氧化等重要化学转化更具活性和稳定性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ea23/10436374/77fd2e993592/ng3c00002_0002.jpg

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