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将有序亲氧铟位点固定在铂上以实现碱性电解质中的高效氢氧化反应

Immobilizing Ordered Oxophilic Indium Sites on Platinum Enabling Efficient Hydrogen Oxidation in Alkaline Electrolyte.

作者信息

Wu Jie, Gao Xin, Liu Guimei, Qiu Xiaoyi, Xia Qing, Wang Xinzhong, Zhu Wenxiang, He Tiwei, Zhou Yunjie, Feng Kun, Wang Jiaxuan, Huang Hui, Liu Yang, Shao Minhua, Kang Zhenhui, Zhang Xiao

机构信息

Department of Mechanical Engineering, The Hong Kong Polytechnic University, Hung Hom, Kowloon, Hong Kong SAR 999077, China.

Institute of Functional Nano & Soft Materials (FUNSOM), Jiangsu Key Laboratory for Carbon-Based Functional Materials & Devices, Soochow University, Suzhou 215123, Jiangsu, China.

出版信息

J Am Chem Soc. 2024 Jul 24;146(29):20323-20332. doi: 10.1021/jacs.4c05844. Epub 2024 Jul 12.

Abstract

Addressing the sluggish kinetics in the alkaline hydrogen oxidation reaction (HOR) is a pivotal yet challenging step toward the commercialization of anion-exchange membrane fuel cells (AEMFCs). Here, we have successfully immobilized indium (In) atoms in an orderly fashion into platinum (Pt) nanoparticles supported by reduced graphene oxide (denoted as O-PtIn/rGO), significantly enhancing alkaline HOR kinetics. We have revealed that the ordered atomic matrix enables uniform and optimized hydrogen binding energy (HBE), hydroxyl binding energy (OHBE), and carbon monoxide binding energy (COBE) across the catalyst. With a mass activity of 2.3066 A mg at an overpotential of 50 mV, over 10 times greater than that of Pt/C, the catalyst also demonstrates admirable CO resistance and stability. Importantly, the AEMFC implementing this catalyst as the anode catalyst has achieved an impressive power output compared to Pt/C. This work not only highlights the significance of constructing ordered oxophilic sites for alkaline HOR but also sheds light on the design of well-structured catalysts for energy conversion.

摘要

解决碱性氢氧化反应(HOR)中缓慢的动力学问题是阴离子交换膜燃料电池(AEMFC)商业化进程中的关键且具有挑战性的一步。在此,我们成功地将铟(In)原子有序地固定在还原氧化石墨烯负载的铂(Pt)纳米颗粒中(记为O-PtIn/rGO),显著提高了碱性HOR动力学。我们发现,有序的原子基质能够使整个催化剂的氢结合能(HBE)、羟基结合能(OHBE)和一氧化碳结合能(COBE)均匀且优化。在50 mV过电位下,该催化剂的质量活性为2.3066 A mg,比Pt/C高出10倍以上,同时还表现出令人钦佩的抗CO性能和稳定性。重要的是,以这种催化剂作为阳极催化剂的AEMFC与Pt/C相比,实现了令人印象深刻的功率输出。这项工作不仅突出了构建用于碱性HOR的有序亲氧位点的重要性,还为能量转换中结构良好的催化剂设计提供了思路。

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