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方便地将 Pt-Sn 双金属催化剂固定在氮掺杂碳纳米管上,用于直接醇电化学催化氧化。

Convenient immobilization of Pt-Sn bimetallic catalysts on nitrogen-doped carbon nanotubes for direct alcohol electrocatalytic oxidation.

机构信息

Key Laboratory of Mesoscopic Chemistry of MOE, School of Chemistry and Chemical Engineering, Nanjing University, Nanjing, People's Republic of China.

出版信息

Nanotechnology. 2011 Sep 30;22(39):395401. doi: 10.1088/0957-4484/22/39/395401. Epub 2011 Sep 2.

DOI:10.1088/0957-4484/22/39/395401
PMID:21891845
Abstract

Pt-Sn alloy nanoparticles were conveniently immobilized on nitrogen-doped carbon nanotubes (NCNTs) through microwave-assisted ethylene glycol reduction. The nanoparticles have a narrow particle size distribution with the average particle size around 3 nm as measured by transmission electron microscopy and x-ray diffraction. The binding energy of metallic Sn passively shifts due to the charge transfer from Sn to Pt, as revealed by x-ray photoelectron spectroscopy. In comparison with the commercial Pt/C catalyst, Pt/NCNT presents a clear increase in activity for alcohol electro-oxidation due to the improved support, while the bimetallic Pt-Sn/NCNT has even higher activity owing to the alloying of Pt with Sn. Both Pt-Sn/NCNT and Pt/NCNT catalysts exhibit competitive long-term stability to Pt/C catalyst. The low cost, simple preparation and superior electrocatalytic performance indicate the great potential of Pt-Sn/NCNT in direct alcohol fuel cells.

摘要

通过微波辅助乙二醇还原,方便地将 Pt-Sn 合金纳米粒子固定在氮掺杂碳纳米管(NCNT)上。通过透射电子显微镜和 X 射线衍射测量,纳米粒子具有窄的粒径分布,平均粒径约为 3nm。X 射线光电子能谱表明,由于 Sn 向 Pt 的电荷转移,金属 Sn 的结合能被动移位。与商业 Pt/C 催化剂相比,由于载体的改善,Pt/NCNT 对醇电氧化的活性明显提高,而由于 Pt 与 Sn 的合金化,双金属 Pt-Sn/NCNT 具有更高的活性。Pt-Sn/NCNT 和 Pt/NCNT 催化剂都表现出比 Pt/C 催化剂更高的长期稳定性。低的成本,简单的制备和优越的电催化性能表明 Pt-Sn/NCNT 在直接醇燃料电池中有很大的应用潜力。

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