journal article·2020-04-15

Mo-Doped FeP Nanospheres for Artificial Nitrogen Fixation

Yu-Xi Luo, Wei-Bin Qiu, Ru-Ping Liang, Xing-Hua Xia, Jian-Ding Qiu

ACS Applied Materials & Interfaces· Volume 12· Issue 15
Publisher page

Abstract

Electrochemical conversion of N2 to NH3 under ambient conditions is a promising and environmentally friendly route compared with the CO2-emitting and energy-intensive Haber–Bosch process. Nevertheless, due to ultrahigh stability of N2, it is urgent to explore efficient catalysts to weaken and activate the N≡N bond. Here, we report the Mo-doped iron phosphide (Mo-FeP) nanosphere as a valid transition-metal-based catalyst for electrochemical N2-to-NH3 fixation under ambient conditions. This catalyst exhibits excellent catalytic performance with a NH4+ yield rate (13.1 μg h–1 mg–1) and Faradaic efficiency (7.49%) at −0.3 and −0.2 V vs reversible hydrogen electrode (RHE), respectively. However, the FeP catalyst without doped Mo species displays weak catalytic performance. We found that the better catalytic performance of Mo-FeP might be due to the doping of Mo species, which is favorable for the polarization of adsorbed N2 molecules, making the N≡N bond more viable to dissociate.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: Ammonia Synthesis and Nitrogen Reduction · Nanomaterials for catalytic reactions · Advanced Photocatalysis Techniques

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

Affiliations

College of Chemistry, Nanchang University, Nanchang 330031, China

State Key Laboratory of Analytical Chemistry for Life Science, School of Chemistry and Chemical Engineering, Nanjing University, Nanjing 210023, China

College of Materials and Chemical Engineering, Pingxiang University, Pingxiang 337055, China

Funding

National Natural Science Foundation of China

References (58)

Show source-provided references
1. 10.1038/ngeo32510.1038/ngeo325 ↗
2. Smil V. · Nature · 1999 · 400 · 41510.1038/22672 ↗
3. 10.1126/science.aar661110.1126/science.aar6611 ↗
4. 10.1002/adfm.20180330910.1002/adfm.201803309 ↗
5. 10.1039/c4cs00085d10.1039/c4cs00085d ↗
6. 10.1039/C7EE02220D10.1039/C7EE02220D ↗
7. 10.1021/acsaem.9b0010210.1021/acsaem.9b00102 ↗
8. 10.1016/j.cattod.2016.06.01410.1016/j.cattod.2016.06.014 ↗
9. 10.1021/ja00464a01510.1021/ja00464a015 ↗
10. 10.1126/science.108532610.1126/science.1085326 ↗
11. 10.1002/adma.20180019110.1002/adma.201800191 ↗
12. 10.1126/science.aad499810.1126/science.aad4998 ↗
13. 10.1002/adma.20160479910.1002/adma.201604799 ↗
14. 10.1039/C7TA06139K10.1039/C7TA06139K ↗
15. 10.1016/j.nanoen.2018.04.03910.1016/j.nanoen.2018.04.039 ↗
16. 10.1038/s41467-018-04213-910.1038/s41467-018-04213-9 ↗
17. 10.1016/j.chempr.2018.10.00710.1016/j.chempr.2018.10.007 ↗
18. 10.1039/C7TA10866D10.1039/C7TA10866D ↗
19. 10.1002/smtd.20180020410.1002/smtd.201800204 ↗
20. 10.1002/adma.20190270910.1002/adma.201902709 ↗
21. 10.1002/aenm.20180393510.1002/aenm.201803935 ↗
22. 10.1021/acscatal.8b0258510.1021/acscatal.8b02585 ↗
23. 10.1039/C8NR04524K10.1039/C8NR04524K ↗
24. 10.1016/j.carbon.2018.12.10610.1016/j.carbon.2018.12.106 ↗
25. 10.1021/acssuschemeng.8b0171410.1021/acssuschemeng.8b01714 ↗
26. 10.1039/C8CC03870H10.1039/C8CC03870H ↗
27. 10.1002/adfm.20170600810.1002/adfm.201706008 ↗
28. 10.1016/j.apcatb.2019.11852510.1016/j.apcatb.2019.118525 ↗
29. 10.1021/acs.inorgchem.9b0182310.1021/acs.inorgchem.9b01823 ↗
30. 10.1002/cctc.20190107510.1002/cctc.201901075 ↗
31. 10.1002/aenm.20190317210.1002/aenm.201903172 ↗
32. 10.1146/annurev.biochem.78.070907.10381210.1146/annurev.biochem.78.070907.103812 ↗
33. 10.1126/science.aaf209110.1126/science.aaf2091 ↗
34. 10.1002/aenm.20180135710.1002/aenm.201801357 ↗
35. 10.1016/j.matchemphys.2018.05.05410.1016/j.matchemphys.2018.05.054 ↗
36. 10.1039/C4NR06321J10.1039/C4NR06321J ↗
37. 10.1021/acsami.7b0942810.1021/acsami.7b09428 ↗
38. 10.1016/j.nanoen.2018.03.03410.1016/j.nanoen.2018.03.034 ↗
39. 10.1002/adfm.20170232410.1002/adfm.201702324 ↗
40. 10.1002/aenm.20150175810.1002/aenm.201501758 ↗
41. 10.1016/j.nanoen.2018.08.02810.1016/j.nanoen.2018.08.028 ↗
42. 10.1039/C5TA08715E10.1039/C5TA08715E ↗
43. 10.1016/j.jnoncrysol.2014.10.01110.1016/j.jnoncrysol.2014.10.011 ↗
44. 10.1016/j.watres.2016.05.01810.1016/j.watres.2016.05.018 ↗
45. 10.1002/chem.20150377710.1002/chem.201503777 ↗
46. 10.1039/C5TA03438H10.1039/C5TA03438H ↗
47. 10.1016/j.matchemphys.2016.06.06310.1016/j.matchemphys.2016.06.063 ↗
48. 10.1016/j.ijhydene.2015.02.09910.1016/j.ijhydene.2015.02.099 ↗
49. 10.1016/j.micromeso.2012.01.02810.1016/j.micromeso.2012.01.028 ↗
50. 10.1016/j.jallcom.2006.08.23110.1016/j.jallcom.2006.08.231 ↗
51. 10.1038/nmat369610.1038/nmat3696 ↗
52. 10.1021/ac60072a04410.1021/ac60072a044 ↗
53. 10.1039/C9CC03413G10.1039/C9CC03413G ↗
54. 10.1021/acscatal.9b0040710.1021/acscatal.9b00407 ↗
55. 10.1021/acsnano.7b0650110.1021/acsnano.7b06501 ↗
56. 10.1038/s41467-019-12312-410.1038/s41467-019-12312-4 ↗
57. 10.1016/j.joule.2018.06.00710.1016/j.joule.2018.06.007 ↗
58. 10.1126/science.aaq168410.1126/science.aaq1684 ↗