PdCuPt Nanocrystals with Multibranches for Enzyme-Free Glucose Detection
Source abstract
Abstract
By carefully controlling the synthesis condition, branched PtCu bimetallic templates were synthesized in aqueous solution. After the galvanic replacement reaction between PtCu templates and the Pt precursors, PdCuPt trimetallic nanocrystals with branched structures were obtained. Owing to the open structure and the optimized composition, the electrochemical experimental results reveal that the PdCuPt trimetallic nanocrystals possess high electrocatalytic activity, selectivity and stability for the oxidation of glucose in alkaline solution. In detail, a detection limit of 1.29 μM and a sensitivity of 378 μA/mM/cm(2) are achieved. The good electrocatalytic performance should be attributed to the unique branched nanostructure as well as the synergistic effect among metals. The superior catalytic properties suggest that these nanocrystals are promising for enzyme-free detection of glucose.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Electrochemical sensors and biosensors · Electrochemical Analysis and Applications · Advanced Nanomaterials in Catalysis
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
The School of Mechanical and Materials Engineering, Washington State University, Pullman, Washington 99164, United States
Environmental Molecular Sciences Laboratory, Pacific Northwest National Laboratory, Richland, Washington 99352, United States
State Key Laboratory of Crystal Materials, Shandong University, Jinan 250100, People’s Republic of China
Funding
Washington State University
References (32)
Show source-provided references
1. 10.1021/ac400292n10.1021/ac400292n ↗
2. 10.1038/srep1611510.1038/srep16115 ↗
3. 10.1039/C5AY03181H10.1039/C5AY03181H ↗
4. 10.1016/j.snb.2013.12.04510.1016/j.snb.2013.12.045 ↗
5. 10.1016/j.biortech.2012.12.02010.1016/j.biortech.2012.12.020 ↗
6. 10.1039/C3TA14173J10.1039/C3TA14173J ↗
7. 10.1039/c2cs35475f10.1039/c2cs35475f ↗
8. 10.1039/C2CC16601A10.1039/C2CC16601A ↗
9. 10.1021/ac403250w10.1021/ac403250w ↗
10. 10.1002/chem.20120337810.1002/chem.201203378 ↗
11. 10.1021/ja209044g10.1021/ja209044g ↗
12. 10.1021/ac503986310.1021/ac5039863 ↗
13. 10.1021/acs.chemrev.5b0025510.1021/acs.chemrev.5b00255 ↗
14. 10.1016/j.electacta.2014.02.12310.1016/j.electacta.2014.02.123 ↗
15. 10.1002/adma.20110495110.1002/adma.201104951 ↗
16. 10.1016/j.apcatb.2013.08.03710.1016/j.apcatb.2013.08.037 ↗
17. 10.1021/jp312652210.1021/jp3126522 ↗
18. 10.1021/ac701790z10.1021/ac701790z ↗
19. 10.1021/nn400482d10.1021/nn400482d ↗
20. 10.1002/smll.20150274110.1002/smll.201502741 ↗
21. 10.1021/am200563f10.1021/am200563f ↗
22. 10.1016/j.jelechem.2014.05.01210.1016/j.jelechem.2014.05.012 ↗
23. 10.1038/srep1061710.1038/srep10617 ↗
24. Lin K. C. · Int. J. Electrochem. Sci. · 2015 · 10 · 372610.1016/S1452-3981(23)06574-4 ↗
25. 10.1016/j.aca.2007.05.04710.1016/j.aca.2007.05.047 ↗
26. 10.1002/adfm.20040032110.1002/adfm.200400321 ↗
27. 10.1038/srep0332310.1038/srep03323 ↗
28. 10.1016/j.jcis.2011.12.07410.1016/j.jcis.2011.12.074 ↗
29. 10.1021/la201521w10.1021/la201521w ↗
30. 10.1016/j.bios.2011.10.03310.1016/j.bios.2011.10.033 ↗
31. 10.1002/smll.20120100810.1002/smll.201201008 ↗
32. 10.1002/elan.20140001810.1002/elan.201400018 ↗