Catalytic Decomposition Mechanism of PH3 on 3DCuO/C and High Value Utilization of Deactivated Catalysts
Source abstract
Abstract
Abstract With the widespread application of lithium iron phosphate batteries, the production capacity of the yellow phosphorus industry has increased sharply, and the treatment of the highly toxic by‐product PH3 is facing severe challenges. In this study, a 3D copper‐based catalyst (3DCuO/C) that can efficiently decompose PH3 at low temperatures and low oxygen concentrations is synthesized. The PH3 capacity is up to 181.41 mg g−1, which is superior to that previously reported in the literature. Further studies indicated that the special 3D structure of 3DCuO/C induces oxygen vacancies on the surface of CuO, which is beneficial to the activation of O2, and then promotes the adsorption and dissociation of PH3. The doping of P after dissociation determines the formation of Cu‐P, and the eventual conversion to Cu3P leads to the deactivation of CuO active sites. More strikingly, due to the appearance of Cu3P, the deactivated De‐3DCuO/C (Cu3P/C) exhibited significant activity in the photocatalytic degradation of rhodamine B and photocatalytic oxidation of Hg0 (gas) and can also be a candidate as an anode material for Li batteries after modification, which will provide a more thorough and economical treatment scheme for deactivated catalysts.
Source: crossref · Quality: baseline
Research context
OpenAlex topics: Extraction and Separation Processes · Advancements in Battery Materials · Nanomaterials for catalytic reactions
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Faculty of Environmental Science and Engineering Kunming University of Science and Technology Yunnan 650500 P. R. China
School of Chemistry and Environment Yunnan Minzu University Yunnan 650500 P. R. China
State Key Laboratory of Clean and Efficient Coal Utilization Taiyuan University of Technology Shanxi 030024 P. R. China
Faculty of Chemical Engineering Kunming University of Science and Technology Kunming 650500 P. R. China
Funding
National Natural Science Foundation of China · China Scholarship Council
References (55)
Show source-provided references
1. 10.1002/aenm.20190016110.1002/aenm.201900161 ↗
2. 10.1016/j.energy.2019.06.07710.1016/j.energy.2019.06.077 ↗
3. 10.1038/s41586-019-1682-510.1038/s41586-019-1682-5 ↗
4. 10.1016/j.rser.2015.04.13010.1016/j.rser.2015.04.130 ↗
5. 10.1016/j.cej.2023.14127710.1016/j.cej.2023.141277 ↗
6. 10.1016/j.apsusc.2020.14726410.1016/j.apsusc.2020.147264 ↗
7. 10.1021/jp108565x10.1021/jp108565x ↗
8. 10.1016/j.talanta.2004.10.00410.1016/j.talanta.2004.10.004 ↗
9. 10.1016/j.jclepro.2011.05.00110.1016/j.jclepro.2011.05.001 ↗
10. 10.1016/j.cej.2016.05.03710.1016/j.cej.2016.05.037 ↗
11. 10.1016/j.cej.2017.01.10310.1016/j.cej.2017.01.103 ↗
12. 10.1080/09593330.2020.176035910.1080/09593330.2020.1760359 ↗
13. 10.1021/ie101622x10.1021/ie101622x ↗
14. 10.1039/C5RA05443E10.1039/C5RA05443E ↗
15. 10.1021/es405006710.1021/es4050067 ↗
16. 10.1039/C5RA00578G10.1039/C5RA00578G ↗
17. 10.1021/ie071074n10.1021/ie071074n ↗
18. 10.1016/j.jtice.2018.03.00710.1016/j.jtice.2018.03.007 ↗
19. 10.1016/j.seppur.2021.11942010.1016/j.seppur.2021.119420 ↗
20. 10.1016/j.cej.2020.12490610.1016/j.cej.2020.124906 ↗
21. 10.1080/10408347.2017.135669910.1080/10408347.2017.1356699 ↗
22. 10.1016/j.cej.2019.12333710.1016/j.cej.2019.123337 ↗
23. 10.1016/j.jcis.2021.01.02310.1016/j.jcis.2021.01.023 ↗
24. 10.1021/acs.est.0c0825610.1021/acs.est.0c08256 ↗
25. 10.1016/j.seppur.2020.11820510.1016/j.seppur.2020.118205 ↗
26. 10.1021/acsami.1c0258410.1021/acsami.1c02584 ↗
27. 10.1021/acs.est.0c0050310.1021/acs.est.0c00503 ↗
28. 10.1038/s41467-019-13993-710.1038/s41467-019-13993-7 ↗
29. 10.1002/jctb.648710.1002/jctb.6487 ↗
30. 10.1016/j.jallcom.2017.02.17910.1016/j.jallcom.2017.02.179 ↗
31. 10.1016/j.apsusc.2014.04.11210.1016/j.apsusc.2014.04.112 ↗
32. 10.1016/j.jcis.2018.07.05010.1016/j.jcis.2018.07.050 ↗
33. 10.1021/acs.est.8b0344810.1021/acs.est.8b03448 ↗
34. 10.1006/jcat.1996.013610.1006/jcat.1996.0136 ↗
35. 10.1021/ja310999c10.1021/ja310999c ↗
36. 10.1021/acs.est.1c0049010.1021/acs.est.1c00490 ↗
37. 10.1002/advs.20170065910.1002/advs.201700659 ↗
38. 10.1016/j.apcatb.2013.04.04310.1016/j.apcatb.2013.04.043 ↗
39. 10.1021/acscatal.7b0379910.1021/acscatal.7b03799 ↗
40. 10.1039/D0RA02403A10.1039/D0RA02403A ↗
41. 10.1016/j.mcat.2019.11075510.1016/j.mcat.2019.110755 ↗
42. 10.1016/j.carbon.2019.09.03710.1016/j.carbon.2019.09.037 ↗
43. 10.1038/ncomms216310.1038/ncomms2163 ↗
44. 10.1016/j.cej.2020.12511310.1016/j.cej.2020.125113 ↗
45. 10.3155/1047-3289.60.5.62910.3155/1047-3289.60.5.629 ↗
46. 10.1016/j.apsusc.2015.02.01810.1016/j.apsusc.2015.02.018 ↗
47. 10.1021/j100122a02710.1021/j100122a027 ↗
48. 10.1016/j.seppur.2021.11922310.1016/j.seppur.2021.119223 ↗
49. 10.1016/j.ijhydene.2020.03.13910.1016/j.ijhydene.2020.03.139 ↗
50. 10.1016/j.powera.2020.10003110.1016/j.powera.2020.100031 ↗
51. 10.1002/cssc.20170145010.1002/cssc.201701450 ↗
52. 10.1002/adma.20130468310.1002/adma.201304683 ↗
53. 10.1016/j.apsusc.2021.14987410.1016/j.apsusc.2021.149874 ↗
54. 10.1016/j.apcatb.2018.09.01010.1016/j.apcatb.2018.09.010 ↗
55. 10.1021/acssuschemeng.7b0440310.1021/acssuschemeng.7b04403 ↗