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用于选择性和持续海水氧化的MnO纳米片的电子和结构修饰

Electronic and Structural Modification of MnO Nanosheets for Selective and Sustained Seawater Oxidation.

作者信息

Ul Haq Tanveer, Mansour Said, Haik Yousef

机构信息

Sustainable Energy Engineering, Frank H. Dotterweich College of Engineering, Texas A&M University-Kingsville, Kingsville, Texas 78363-8202, United States.

Qatar Energy and Environment Research Institute, Hamad bin Khalifa University, Qatar Foundation, Doha 34110, Qatar.

出版信息

ACS Appl Mater Interfaces. 2022 May 11;14(18):20443-20454. doi: 10.1021/acsami.1c24304. Epub 2022 Feb 9.

Abstract

The accomplishment of seawater electrolysis to produce green hydrogen energy needs an efficient and durable electrocatalyst with high selectivity and corrosion resistance. Here we report a free-standing amorphous nanostructured oxygen evolution reaction (OER) electrocatalyst with microvoids developed by embedding Gd-doped MnO nanosheets in a CuO-Cu(OH) nanostructure array (Gd-MnO@ CuO-Cu(OH). The surface oxygen vacancies modulated the electronic structure of the catalyst and offered active sites with optimal chemisorption energy to OER intermediates. The hierarchical surface structure provides a large specific surface area, high electrical conductivity, ionic mobility, intrinsic activity for each active site, and efficient charge transfer, leading to an outstanding catalytic performance. The enhanced structural, chemical, and corrosion resistance ensures effectiveness as an anode in direct seawater electrolysis. Specifically, it needs an input voltage of 1.63 V to deliver a current density of 500 mA cm in alkaline seawater, with the stability of more than 75 h of continuous electrolysis without hypochlorite formation. The high Faradaic efficiency demonstrates its potential for hydrogen fuel production from seawater.

摘要

实现海水电解生产绿色氢能需要一种具有高选择性和耐腐蚀性的高效耐用的电催化剂。在此,我们报道了一种通过将钆掺杂的二氧化锰纳米片嵌入氧化铜 - 氢氧化铜纳米结构阵列(Gd - MnO@CuO - Cu(OH))中而开发的具有微孔的独立式非晶态纳米结构析氧反应(OER)电催化剂。表面氧空位调节了催化剂的电子结构,并为OER中间体提供了具有最佳化学吸附能的活性位点。分级表面结构提供了大的比表面积、高电导率、离子迁移率、每个活性位点的本征活性以及有效的电荷转移,从而导致出色的催化性能。增强的结构、化学和耐腐蚀性确保了其作为直接海水电解阳极的有效性。具体而言,在碱性海水中,要达到500 mA cm的电流密度需要输入1.63 V的电压,并且具有超过75小时的连续电解稳定性且不形成次氯酸盐。高法拉第效率证明了其从海水中生产氢燃料的潜力。

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