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石墨炔/石墨烯异质结构:一种用于选择性和持久CO电还原的锚定单分散过渡金属酞菁的通用二维支架

Graphdiyne/Graphene Heterostructure: A Universal 2D Scaffold Anchoring Monodispersed Transition-Metal Phthalocyanines for Selective and Durable CO Electroreduction.

作者信息

Gu Huoliang, Zhong Lixiang, Shi Guoshuai, Li Jiaqiang, Yu Ke, Li Jiong, Zhang Shuo, Zhu Chenyuan, Chen Shaohua, Yang Chunlei, Kong Ya, Chen Chen, Li Shuzhou, Zhang Jin, Zhang Liming

机构信息

Department of Chemistry and Shanghai Key Laboratory of Molecular Catalysis and Innovative Materials, Fudan University, Shanghai 200438, China.

School of Materials Science and Engineering, Nanyang Technological University, Singapore 639798, Singapore.

出版信息

J Am Chem Soc. 2021 Jun 16;143(23):8679-8688. doi: 10.1021/jacs.1c02326. Epub 2021 Jun 2.

Abstract

Electrochemical CO reduction (COR) is a sustainable way of producing carbon-neutral fuels, yet the efficiency is limited by its sluggish kinetics and complex reaction pathways. Developing active, selective, and stable COR electrocatalysts is challenging and entails intelligent material structure design and tailoring. Here we show a graphdiyne/graphene (GDY/G) heterostructure as a 2D conductive scaffold to anchor monodispersed cobalt phthalocyanine (CoPc) and reduce CO with an appreciable activity, selectivity, and durability. Advanced characterizations, e.g., synchrotron-based X-ray absorption spectroscopy (XAS), and density functional theory (DFT) calculation disclose that the strong electronic coupling between GDY and CoPc, together with the high surface area, abundant reactive centers, and electron conductivity provided by graphene, synergistically contribute to this distinguished electrocatalytic performance. Electrochemical measurements revealed a high FE of 96% at a partial current density of 12 mA cm in a H-cell and an FE of 97% at 100 mA cm in a liquid flow cell, along with a durability over 24 h. The per-site turnover frequency of CoPc reaches 37 s at -1.0 V vs RHE, outperforming most of the reported phthalocyanine- and porphyrin-based electrocatalysts. The usage of the GDY/G heterostructure as a scaffold can be further extended to other organometallic complexes beyond CoPc. Our findings lend credence to the prospect of the GDY/G hybrid contributing to the design of single-molecule dispersed COR catalysts for sustainable energy conversion.

摘要

电化学CO还原(COR)是一种生产碳中和燃料的可持续方法,但其效率受到缓慢动力学和复杂反应路径的限制。开发活性高、选择性好且稳定的COR电催化剂具有挑战性,需要智能的材料结构设计和剪裁。在这里,我们展示了一种石墨炔/石墨烯(GDY/G)异质结构作为二维导电支架,用于锚定单分散的钴酞菁(CoPc),并以可观的活性、选择性和耐久性还原CO。先进的表征,如基于同步加速器的X射线吸收光谱(XAS)和密度泛函理论(DFT)计算表明,GDY和CoPc之间的强电子耦合,以及石墨烯提供的高表面积、丰富的反应中心和电子导电性,协同促成了这种卓越的电催化性能。电化学测量显示,在H型电池中,在12 mA cm的部分电流密度下,FE高达96%;在液流电池中,在100 mA cm下,FE为97%,并且耐久性超过24小时。相对于可逆氢电极(RHE),CoPc在-1.0 V时的每活性位点周转频率达到37 s,优于大多数已报道的基于酞菁和卟啉的电催化剂。GDY/G异质结构作为支架的用途可以进一步扩展到CoPc以外的其他有机金属配合物。我们的研究结果为GDY/G杂化物有助于设计用于可持续能量转换的单分子分散COR催化剂的前景提供了可信度。

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