journal article·2018-05-29

Phase Directing Ability of an Ionic Liquid Solvent for the Synthesis of HER-Active Ni2P Nanocrystals

Emily J. Roberts, Carlos G. Read, Nathan S. Lewis, Richard L. Brutchey

ACS Applied Energy Materials· Volume 1· Issue 5
Publisher page

Abstract

An ionic liquid (IL) solvent was used to synthesize small, phase-pure nickel phosphide (Ni2P) nanocrystals. In contrast, under analogous reaction conditions, substitution of the IL for the common high-boiling organic solvent 1-octadecene (ODE) results in phase-impure nanocrystals. The 5 nm Ni2P nanocrystals prepared in IL were electrocatalytically active toward the hydrogen evolution reaction. The synthesis in IL was also extended to alloyed Ni2–xCoxP nanocrystals, where 0.5 ≤ x ≤ 1.5.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: Electrocatalysts for Energy Conversion · Ionic liquids properties and applications · Catalysis and Hydrodesulfurization Studies

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

Affiliations

Department of Chemistry, University of Southern California, Los Angeles, California 90089, United States

Division of Chemistry and Chemical Engineering, California Institute of Technology, Pasadena, California 91125, United States

Funding

Resnick Sustainability Institute for Science, Energy and Sustainability, California Institute of Technology

References (34)

Show source-provided references
1. Wasserscheid P. · 2008
2. 10.1039/b602046a10.1039/b602046a ↗
3. 10.1021/am300441310.1021/am3004413 ↗
4. 10.1038/ncomms1078010.1038/ncomms10780 ↗
5. 10.1021/acs.chemmater.7b0069410.1021/acs.chemmater.7b00694 ↗
6. 10.1039/C3RA47801G10.1039/C3RA47801G ↗
7. 10.1039/c0gc00091d10.1039/c0gc00091d ↗
8. 10.1021/acs.cgd.6b0151110.1021/acs.cgd.6b01511 ↗
9. 10.1021/acs.chemmater.5b0214010.1021/acs.chemmater.5b02140 ↗
10. 10.1021/ja403440e10.1021/ja403440e ↗
11. 10.1021/acs.chemmater.5b0128410.1021/acs.chemmater.5b01284 ↗
12. 10.1021/acs.inorgchem.5b0112510.1021/acs.inorgchem.5b01125 ↗
13. 10.1021/nn103335710.1021/nn1033357 ↗
14. 10.1021/acs.chemmater.8b0029010.1021/acs.chemmater.8b00290 ↗
15. 10.1039/b802454e10.1039/b802454e ↗
16. 10.1021/cm034443o10.1021/cm034443o ↗
17. 10.1021/cm901073k10.1021/cm901073k ↗
18. 10.1021/jp910160g10.1021/jp910160g ↗
19. 10.1016/j.matlet.2009.07.03910.1016/j.matlet.2009.07.039 ↗
20. 10.1039/C5RA00117J10.1039/C5RA00117J ↗
21. 10.1021/ic061846s10.1021/ic061846s ↗
22. 10.1039/b822551f10.1039/b822551f ↗
23. 10.1002/cite.20150003610.1002/cite.201500036 ↗
24. 10.1039/b821659b10.1039/b821659b ↗
25. 10.1021/ic702071w10.1021/ic702071w ↗
26. 10.1021/cm303490y10.1021/cm303490y ↗
27. 10.1021/acs.chemmater.5b0350610.1021/acs.chemmater.5b03506 ↗
28. 10.1039/C4TA04867A10.1039/C4TA04867A ↗
29. 10.1002/sia.302610.1002/sia.3026 ↗
30. 10.1021/acs.chemmater.6b0118510.1021/acs.chemmater.6b01185 ↗
31. 10.1021/jp980375v10.1021/jp980375v ↗
32. 10.1016/0584-8539(87)80223-410.1016/0584-8539(87)80223-4 ↗
33. 10.1021/acs.chemmater.6b0214810.1021/acs.chemmater.6b02148 ↗
34. 10.1021/acs.chemmater.5b0095810.1021/acs.chemmater.5b00958 ↗