Highly Sensitive Chemical Detection with Tunable Sensitivity and Selectivity from Ultrathin Platinum Nanowires
Source abstract
Abstract
Ultrathin platinum nanowires obtained from wet-synthesis with no strong binding ligands exhibit very high sensitivity toward hydrogen gas (two orders of magnitude increase compared with state-of-the-art devices). Their chemical sensitivity, selectivity, and other sensing characteristics can be rationally tailored through further surface engineering. A significantly reduced cross-sensitivity toward humidity is achieved, while the hydrogen sensitivity is preserved or even enhanced. As a service to our authors and readers, this journal provides supporting information supplied by the authors. Such materials are peer reviewed and may be re-organized for online delivery, but are not copy-edited or typeset. Technical support issues arising from supporting information (other than missing files) should be addressed to the authors. Please note: The publisher is not responsible for the content or functionality of any supporting information supplied by the authors. Any queries (other than missing content) should be directed to the corresponding author for the article.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Semiconductor materials and devices · Analytical Chemistry and Sensors · Ferroelectric and Negative Capacitance Devices
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Department of Materials Science and Engineering University of California, Los Angeles Los Angeles CA 90095 USA
California NanoSystems Institute (CNSI) University of California, Los Angeles Los Angeles CA 90095 USA
Department of Chemistry and Biochemistry University of California, Los Angeles Los Angeles CA 90095 USA
References (39)
Show source-provided references
1. 10.1021/ja210278u10.1021/ja210278u ↗
2. 10.1021/nl200643810.1021/nl2006438 ↗
3. 10.1021/nl903888c10.1021/nl903888c ↗
4. 10.1002/anie.20070448810.1002/anie.200704488 ↗
5. 10.1002/ange.20070448810.1002/ange.200704488 ↗
6. 10.1021/ac901871d10.1021/ac901871d ↗
7. 10.1038/ncomms578110.1038/ncomms5781 ↗
8. 10.1021/nl401498t10.1021/nl401498t ↗
9. 10.1126/science.106318910.1126/science.1063189 ↗
10. 10.1021/nl900847410.1021/nl9008474 ↗
11. 10.1021/nl300602m10.1021/nl300602m ↗
12. 10.1063/1.490324510.1063/1.4903245 ↗
13. 10.1021/acsnano.5b0030210.1021/acsnano.5b00302 ↗
14. 10.1002/anie.20150530810.1002/anie.201505308 ↗
15. 10.1002/ange.20150530810.1002/ange.201505308 ↗
16. 10.1021/ja402955t10.1021/ja402955t ↗
17. 10.1002/adma.20120224110.1002/adma.201202241 ↗
18. 10.1038/ncomms886710.1038/ncomms8867 ↗
19. 10.1080/0001873011010218710.1080/00018730110102187 ↗
20. 10.1103/PhysRevB.22.606510.1103/PhysRevB.22.6065 ↗
21. 10.1002/sia.74017130410.1002/sia.740171304 ↗
22. 10.1002/adma.20100330410.1002/adma.201003304 ↗
23. 10.1073/pnas.100551210810.1073/pnas.1005512108 ↗
24. 10.1002/anie.20120104210.1002/anie.201201042 ↗
25. 10.1002/ange.20120104210.1002/ange.201201042 ↗
26. 10.1073/pnas.130725111010.1073/pnas.1307251110 ↗
27. 10.1038/nnano.2013.23610.1038/nnano.2013.236 ↗
28. 10.1002/anie.20150143410.1002/anie.201501434 ↗
29. 10.1002/ange.20150143410.1002/ange.201501434 ↗
30. 10.1021/ja201860g10.1021/ja201860g ↗
31. 10.1021/jz301711a10.1021/jz301711a ↗
32. 10.1021/ja402887v10.1021/ja402887v ↗
33. 10.1021/jz502631a10.1021/jz502631a ↗
34. 10.1021/nl302619p10.1021/nl302619p ↗
35. 10.1021/ja402423r10.1021/ja402423r ↗
36. 10.3390/s12030283110.3390/s120302831 ↗
37. 10.1016/j.snb.2012.02.01710.1016/j.snb.2012.02.017 ↗
38. 10.5194/jsss-3-29-201410.5194/jsss-3-29-2014 ↗
39. 10.1063/1.489323710.1063/1.4893237 ↗