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吹糖诱导的多孔磷化钴/氮掺杂碳纳米结构对水和其他小分子具有增强的电化学氧化性能

Sugar Blowing-Induced Porous Cobalt Phosphide/Nitrogen-Doped Carbon Nanostructures with Enhanced Electrochemical Oxidation Performance toward Water and Other Small Molecules.

作者信息

Zhu Chengzhou, Fu Shaofang, Xu Bo Z, Song Junhua, Shi Qiurong, Engelhard Mark H, Li Xiaolin, Beckman Scott P, Sun Junming, Du Dan, Lin Yuehe

机构信息

School of Mechanical and Materials Engineering, Washington State University, Pullman, WA, 99164, USA.

Environmental Molecular Science Laboratory, Pacific Northwest National Laboratory, Richland, WA, 99352, USA.

出版信息

Small. 2017 Sep;13(33). doi: 10.1002/smll.201700796. Epub 2017 Jun 28.

Abstract

Rational design of high active and robust nonprecious metal catalysts with excellent catalytic efficiency in oxygen evolution reaction (OER) is extremely vital for making the water splitting process more energy efficient and economical. Among these noble metal-free catalysts, transition-metal-based nanomaterials are considered as one of the most promising OER catalysts due to their relatively low-cost intrinsic activities, high abundance, and diversity in terms of structure and morphology. Herein, a facile sugar-blowing technique and low-temperature phosphorization are reported to generate 3D self-supported metal involved carbon nanostructures, which are termed as Co P@Co/nitrogen-doped carbon (Co P@Co/N-C). By capitalizing on the 3D porous nanostructures with high surface area, homogeneously dispersed active sites, the intimate interaction between active sites, and 3D N-doped carbon, the resultant Co P@Co/N-C exhibits satisfying OER performance superior to CoO@Co/N-C, delivering 10 mA cm at overpotential of 0.32 V. It is worth noting that in contrast to the substantial current density loss of RuO , Co P@Co/N-C shows much enhanced catalytic activity during the stability test and a 1.8-fold increase in current density is observed after stability test. Furthermore, the obtained Co P@Co/N-C can also be served as an excellent nonprecious metal catalyst for methanol and glucose electrooxidation in alkaline media, further extending their potential applications.

摘要

合理设计在析氧反应(OER)中具有优异催化效率的高活性和稳健的非贵金属催化剂对于提高水分解过程的能源效率和经济性至关重要。在这些无贵金属催化剂中,过渡金属基纳米材料因其相对低成本的本征活性、高丰度以及结构和形态的多样性,被认为是最有前途的OER催化剂之一。在此,报道了一种简便的吹糖技术和低温磷化方法来制备3D自支撑金属掺杂碳纳米结构,即CoP@Co/氮掺杂碳(CoP@Co/N-C)。利用具有高表面积、均匀分散的活性位点、活性位点之间的紧密相互作用以及3D氮掺杂碳的3D多孔纳米结构,所得的CoP@Co/N-C表现出令人满意的OER性能,优于CoO@Co/N-C,在0.32V的过电位下实现10mA cm的电流密度。值得注意的是,与RuO的大量电流密度损失相比,CoP@Co/N-C在稳定性测试期间表现出大大增强的催化活性,并且在稳定性测试后观察到电流密度增加了1.8倍。此外,所获得的CoP@Co/N-C还可以用作碱性介质中甲醇和葡萄糖电氧化的优异非贵金属催化剂,进一步扩展了它们的潜在应用。

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