journal article·2017-08-09

Dentritic CuPtPd Catalyst for Enhanced Electrochemical Oxidation of Methanol

Xiaoqin Shi, Ying Wen, Xiaoyu Guo, Yuxia Pan, Yuanyuan Ji, Ye Ying, Haifeng Yang

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Abstract

The CuPtPd catalyst is designed and synthesized successfully via directly reducing metal ions. The composition, morphology, and structure of the as-prepared CuPtPd nanohybrids are characterized by scanning electron microscopy and transmission electron microscopy, energy-dispersive spectrometry, selected-area electron diffraction, X-ray diffraction, and inductively coupled plasma atomic emission spectrometry. By comparison of the electrocatalytic properties of the ternary CuPtPd catalyst with bimetallic catalysts, we find that ternary nanocomposites perform better electrocatalytic and antipoisoning activity toward oxidation of methanol. The catalytic mass activity of the CuPtPd nanoparticles is 5.51-fold of commercial Pd black and 12.1-fold of Pt black.
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Research context

OpenAlex topics: Electrocatalysts for Energy Conversion · Catalytic Processes in Materials Science · Electrochemical Analysis and Applications

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

The Education Ministry Key Lab of Resource Chemistry, Department of Chemistry, Shanghai Normal University, Shanghai 200234, People’s Republic of China

Funding

Shanghai Municipal Education Commission · National Natural Science Foundation of China · International Joint Laboratory on Resource Chemistry, Shanghai Normal University · Shanghai Key Laboratory of Rare Earth Functional Materials, Shanghai Normal University

References (38)

Show source-provided references
1. 10.1016/S0378-7753(99)00407-310.1016/S0378-7753(99)00407-3 ↗
2. 10.1016/j.jpowsour.2008.03.07510.1016/j.jpowsour.2008.03.075 ↗
3. 10.1016/j.nantod.2011.04.00710.1016/j.nantod.2011.04.007 ↗
4. 10.1039/c2cs35173k10.1039/c2cs35173k ↗
5. 10.1002/anie.20110520410.1002/anie.201105204 ↗
6. 10.1021/ja111160r10.1021/ja111160r ↗
7. 10.1002/anie.20100586810.1002/anie.201005868 ↗
8. 10.1002/adma.20100437710.1002/adma.201004377 ↗
9. 10.1021/ja100571h10.1021/ja100571h ↗
10. 10.1023/A:101753122517110.1023/A:1017531225171 ↗
11. 10.1039/c2cs35173k10.1039/c2cs35173k ↗
12. 10.1016/j.jpowsour.2010.10.09310.1016/j.jpowsour.2010.10.093 ↗
13. 10.1021/ja200329p10.1021/ja200329p ↗
14. 10.1002/chem.20120290910.1002/chem.201202909 ↗
15. 10.1021/jp101243k10.1021/jp101243k ↗
16. 10.1016/j.jpowsour.2008.12.03110.1016/j.jpowsour.2008.12.031 ↗
17. 10.1038/nchem.55310.1038/nchem.553 ↗
18. 10.1021/ja101966a10.1021/ja101966a ↗
19. 10.1021/ja204046410.1021/ja2040464 ↗
20. 10.1021/ja212206m10.1021/ja212206m ↗
21. 10.1039/C2CS35261C10.1039/C2CS35261C ↗
22. 10.1021/acs.chemrev.5b0048210.1021/acs.chemrev.5b00482 ↗
23. 10.1038/nmat280610.1038/nmat2806 ↗
24. 10.1039/ft991870012510.1039/ft9918700125 ↗
25. 10.1021/cr800250510.1021/cr8002505 ↗
26. 10.1038/srep0829410.1038/srep08294 ↗
27. 10.1021/ja508256g10.1021/ja508256g ↗
28. 10.1021/ja207308b10.1021/ja207308b ↗
29. 10.1002/anie.20130209010.1002/anie.201302090 ↗
30. 10.1039/C4SC04037F10.1039/C4SC04037F ↗
31. 10.1039/C3NR06186H10.1039/C3NR06186H ↗
32. 10.1021/acsami.5b0382610.1021/acsami.5b03826 ↗
33. 10.1021/nn901448310.1021/nn9014483 ↗
34. 10.1016/j.carbon.2014.07.07610.1016/j.carbon.2014.07.076 ↗
35. 10.1016/j.apcatb.2016.01.01910.1016/j.apcatb.2016.01.019 ↗
36. 10.1016/j.jpowsour.2010.03.02210.1016/j.jpowsour.2010.03.022 ↗
37. 10.1016/j.electacta.2014.02.05510.1016/j.electacta.2014.02.055 ↗
38. 10.1021/ja072367a10.1021/ja072367a ↗