Noble-Metal-Free CdS Nanoparticle-Coated Graphene Oxide Nanosheets Favoring Electron Transfer for Efficient Photoreduction of CO2
Source abstract
Abstract
Graphene oxide (GO) nanosheets are promising noble-metal-free catalysts. However, the catalytic activity and selectivity of GO are still very low. Herein, GO is first functionalized via noncovalent interactions by an aspartic acid modified anhydride having COOH groups to form A-GO. A-GO is more conductive and hydrophilic than GO and P-GO synthesized via functionalizing GO by a COOH-free anhydride. Then, we load CdS nanoparticles, which are responsible for absorbing light to produce charge carriers, on A-GO to fabricate a CdS/A-GO photocatalyst without noble metals for the photoreduction of CO2 by H2O. CdS/A-GO exhibits a higher photoreduction efficiency than that of CdS/GO and CdS/P-GO. The main carbon-based photoreduction product of CdS/A-GO is CH3OH, whereas that of CdS/GO and CdS/P-GO is CO. The more conductive and hydrophilic A-GO triggers a more efficient electron transfer, CO2 adsorption, and production of hydrogen atoms from H2O dissociation, thus leading to the higher photoreduction efficiency and product change on CdS/A-GO. Besides, the COOH groups of the aspartic acid modified anhydride supply their hydrogen atoms to promote the conversion from CO2 to CH3OH on CdS/A-GO. Therefore, noncovalently functionalizing GO with different active species can efficiently improve the catalytic performance of GO. This opens a new way to design and construct noble-metal-free catalysts with enhanced activity and selectivity.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Advanced Photocatalysis Techniques · Covalent Organic Framework Applications · CO2 Reduction Techniques and Catalysts
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Key Laboratory of Organo-Pharmaceutical Chemistry, Gannan Normal University, Ganzhou 341000, P. R. China
Department of Instrument Science and Engineering, School of Electronic Information and Electrical Engineering, Shanghai Jiao Tong University, Shanghai 200240, P. R. China
Funding
Gannan Normal University · National Natural Science Foundation of China · Institute of Chemistry, Chinese Academy of Sciences
References (50)
Show source-provided references
1. 10.1038/s41467-018-07397-210.1038/s41467-018-07397-2 ↗
2. 10.1021/acs.chemrev.8b0040010.1021/acs.chemrev.8b00400 ↗
3. 10.1016/j.gee.2017.06.00310.1016/j.gee.2017.06.003 ↗
4. 10.1039/C6GC02856J10.1039/C6GC02856J ↗
5. 10.1002/anie.20190805810.1002/anie.201908058 ↗
6. 10.1021/jacs.9b0299710.1021/jacs.9b02997 ↗
7. 10.1016/j.apcatb.2018.01.00510.1016/j.apcatb.2018.01.005 ↗
8. 10.1016/j.cej.2018.04.18010.1016/j.cej.2018.04.180 ↗
9. 10.1007/s12274-018-2269-410.1007/s12274-018-2269-4 ↗
10. 10.1016/j.apcatb.2014.11.03510.1016/j.apcatb.2014.11.035 ↗
11. 10.1021/acsami.8b2074410.1021/acsami.8b20744 ↗
12. 10.1021/cr300115g10.1021/cr300115g ↗
13. 10.1039/C8TA03404D10.1039/C8TA03404D ↗
14. 10.1016/j.nanoen.2011.11.00110.1016/j.nanoen.2011.11.001 ↗
15. 10.1016/j.ccr.2019.02.01710.1016/j.ccr.2019.02.017 ↗
16. 10.1021/acsami.9b0297110.1021/acsami.9b02971 ↗
17. 10.1021/ar300122m10.1021/ar300122m ↗
18. 10.1002/anie.20140278010.1002/anie.201402780 ↗
19. 10.1021/acs.chemrev.5b0062010.1021/acs.chemrev.5b00620 ↗
20. 10.1016/j.apcatb.2012.05.02310.1016/j.apcatb.2012.05.023 ↗
21. 10.1002/adma.20150537110.1002/adma.201505371 ↗
22. 10.1002/smll.20120219610.1002/smll.201202196 ↗
23. 10.1007/s12274-014-0622-910.1007/s12274-014-0622-9 ↗
24. 10.1016/j.polymer.2013.06.02710.1016/j.polymer.2013.06.027 ↗
25. 10.1021/jz300802k10.1021/jz300802k ↗
26. 10.1016/j.aca.2012.03.00710.1016/j.aca.2012.03.007 ↗
27. 10.1016/j.snb.2012.03.04410.1016/j.snb.2012.03.044 ↗
28. 10.1039/C6TA02880B10.1039/C6TA02880B ↗
29. 10.1016/j.carbon.2017.04.07110.1016/j.carbon.2017.04.071 ↗
30. 10.1002/sia.600910.1002/sia.6009 ↗
31. 10.1016/j.apcatb.2017.12.04610.1016/j.apcatb.2017.12.046 ↗
32. 10.1002/cssc.20140233410.1002/cssc.201402334 ↗
33. 10.1021/jacs.7b0026610.1021/jacs.7b00266 ↗
34. 10.1021/jacs.8b0855210.1021/jacs.8b08552 ↗
35. 10.1016/j.ijhydene.2016.07.22710.1016/j.ijhydene.2016.07.227 ↗
36. 10.1016/j.apcatb.2018.08.06010.1016/j.apcatb.2018.08.060 ↗
37. 10.1103/PhysRevB.54.1116910.1103/PhysRevB.54.11169 ↗
38. 10.1103/PhysRevB.48.1311510.1103/PhysRevB.48.13115 ↗
39. 10.1103/PhysRevB.50.1795310.1103/PhysRevB.50.17953 ↗
40. 10.1103/PhysRevB.59.175810.1103/PhysRevB.59.1758 ↗
41. 10.1002/adfm.20150555410.1002/adfm.201505554 ↗
42. 10.1021/acsnano.5b0043810.1021/acsnano.5b00438 ↗
43. 10.1016/j.apcatb.2019.01.06810.1016/j.apcatb.2019.01.068 ↗
44. 10.1039/c3nr03043a10.1039/c3nr03043a ↗
45. 10.1021/acsami.9b1783310.1021/acsami.9b17833 ↗
46. 10.1016/j.apcatb.2019.11808810.1016/j.apcatb.2019.118088 ↗
47. 10.1016/j.cej.2017.12.11310.1016/j.cej.2017.12.113 ↗
48. 10.1021/acscatal.9b0029110.1021/acscatal.9b00291 ↗
49. 10.1016/j.jcat.2010.04.00310.1016/j.jcat.2010.04.003 ↗
50. 10.1021/jacs.8b0160110.1021/jacs.8b01601 ↗