...
首页> 外文期刊>Nanoscale >Structurally ordered PtSn intermetallic nanoparticles supported on ATO for efficient methanol oxidation reaction
【24h】

Structurally ordered PtSn intermetallic nanoparticles supported on ATO for efficient methanol oxidation reaction

机译:结构有序PtSn金属间化合物纳米粒子对ATO的有效支持甲醇氧化反应

获取原文
获取原文并翻译 | 示例
   

获取外文期刊封面封底 >>

       

摘要

The development of cost-effective methanol oxidation reaction (MOR) catalysts with a high activity and stability is highly desirable for direct methanol fuel cells. In this study, the structurally ordered PtSn intermetallic nanoparticles supported on Sb-doped SnO2 (ATO) have been successfully synthesized in ethylene glycol (EG) solution at 200 degrees C. Pt NPs were firstly formed on ATO, followed by the transformation from Pt into hexagonal PtSn on the surface of ATO. The obtained structurally ordered PtSn intermetallic NPs supported on ATO demonstrate significantly enhanced MOR activity and durability in comparison with commercial Pt/C. Our PtSn intermetallic NPs supported on ATO show a MOR activity 4.1 times higher than that of commercial Pt/C catalysts. Accelerated durability tests indicate that the commercial Pt/C catalysts lose about 50% of their initial current density after 500 cycles while the Pt/ATO-200-3 h catalyst loses only about 15% of its initial current density. Our PtSn intermetallic NPs supported on ATO are also found to have higher CO tolerance than commercial Pt/C. This work demonstrates an important strategy to rationally design high-performance structurally ordered Pt-based intermetallic NP catalysts for fuel cells and other applications.
机译:具有成本效益的发展甲醇氧化反应(铁道部)高的催化剂活性和稳定性是非常可取的直接甲醇燃料电池。结构有序PtSn金属间化合物纳米粒子支持Sb-doped SnO2 (ATO)已经成功地合成乙烯乙二醇(EG)的解决方案在200度c . Pt NPs首先形成了ATO,紧随其后的是吗从Pt转变成六角形PtSn上ATO的表面。在ATO PtSn金属间化合物NPs受支持证明显著增强铁道部活动和耐用性与商业相比Pt / C。显示一个铁道部活动的4.1倍商业Pt / C催化剂。测试表明,该商业Pt / C催化剂失去约50%的初始电流密度500年之后周期而Pt / ato - 200 - 3 h催化剂失去只有约15%的最初电流密度。支持ATO也发现高有限公司宽容比商业Pt / C。演示了理性的一个重要策略设计高性能的结构要求Pt-based金属间化合物NP催化剂对燃料细胞和其他应用程序。

著录项

相似文献

  • 外文文献
  • 中文文献
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号