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用于高效甲醇氧化的聚电解质诱导的富含晶界的铂纳米蠕虫在TiCT MXene纳米片上的立体组装

Polyelectrolyte-Induced Stereoassembly of Grain Boundary-Enriched Platinum Nanoworms on TiCT MXene Nanosheets for Efficient Methanol Oxidation.

作者信息

Yang Cuizhen, Jiang Quanguo, Huang Huajie, He Haiyan, Yang Lu, Li Weihua

机构信息

College of Mechanics and Materials, Hohai University, Nanjing 210098, China.

College of Chemical Engineering and Technology, Sun Yat-sen University, Tangjiawan, Zhuhai 519082, China.

出版信息

ACS Appl Mater Interfaces. 2020 May 27;12(21):23822-23830. doi: 10.1021/acsami.0c02806. Epub 2020 May 12.

Abstract

Direct methanol fuel cells with high energy conversion efficiency and low hazard emissions have aroused great attention from both academic and industrial communities, but their large-scale commercial application has been blocked by high costs as well as short lifespan of the anode Pt catalysts. Here, we demonstrate a simple and scalable noncovalent strategy for the synthesis of quasi-one-dimensional (1D) Pt nanoworms grown on poly(diallyldimethyl-ammonium chloride) (PDDA)-functionalized TiCT nanosheets as anode catalysts for methanol electrooxidation. Interestingly, the introduction of PDDA on TiCT nanosheets can not only effectively adjust their surface charge property to strengthen the electrostatic interaction between metal and support but also induce the stereoassembly of worm-shaped Pt nanocrystals with abundant catalytically active grain boundaries, which enable the resulting hybrid to express high electrocatalytic activity, remarkable durability, and strong antipoisoning ability for methanol electrooxidation, which are better than those of the traditional Pt nanoparticle electrocatalysts loaded on carbon black, carbon nanotubes, reduced graphene oxide, and MXene matrixes. Theoretical simulations disclose that the more stable worm-shaped Pt configuration with an optimized electronic structure on the TiCT surface possesses a weaker CO adsorption ability than that of the Pt nanoclusters, thereby providing a dramatically enhanced and sustainable electrocatalytic performance.

摘要

具有高能量转换效率和低有害排放的直接甲醇燃料电池引起了学术界和工业界的极大关注,但其大规模商业应用却因成本高昂以及阳极铂催化剂寿命短而受阻。在此,我们展示了一种简单且可扩展的非共价策略,用于合成在聚(二烯丙基二甲基氯化铵)(PDDA)功能化的TiCT纳米片上生长的准一维(1D)铂纳米蠕虫,作为甲醇电氧化的阳极催化剂。有趣的是,在TiCT纳米片上引入PDDA不仅可以有效调节其表面电荷性质,以增强金属与载体之间的静电相互作用,还能诱导具有丰富催化活性晶界的蠕虫状铂纳米晶体的立体组装,这使得所得的杂化物对甲醇电氧化表现出高电催化活性、卓越的耐久性和强大的抗中毒能力,优于负载在炭黑、碳纳米管、还原氧化石墨烯和MXene基体上的传统铂纳米颗粒电催化剂。理论模拟表明,在TiCT表面具有优化电子结构的更稳定的蠕虫状铂构型比铂纳米团簇具有更弱的CO吸附能力,从而提供了显著增强且可持续的电催化性能。

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