journal article·2020-07-08

Can Half-a-Monolayer of Pt Simulate Activity Like That of Bulk Pt? Solar Hydrogen Activity Demonstration with Quasi-artificial Leaf Device

Himanshu Bajpai, Kshirodra Kumar Patra, Ravi Ranjan, Naresh Nalajala, Kasala Prabhakar Reddy, Chinnakonda S. Gopinath

ACS Applied Materials & Interfaces· Volume 12· Issue 27
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Abstract

Pt is the best cocatalyst for hydrogen production. It is also well-known that the surface atomic layer is critical for catalysis. To minimize the Pt content as cocatalyst, herein we report on half-a-monolayer of Pt (0.5θPt) decorated on earth-abundant Ni–Cu cocatalyst, which is integrated with a quasi-artificial leaf (QuAL) device (TiO2/ZnS/CdS) and demonstrated for efficient solar hydrogen production. For the QuAL, TiO2 is sensitized with ZnS and CdS quantum dots by the SILAR method. The 0.5θPt-decorated Ni–Cu shows an onset potential of 0.05 V vs reversible hydrogen electrode for the hydrogen evolution reaction, which is almost similar to that of commercial Pt/C. Photoactivity of the present QuAL device with either bulk Pt or 0.5θPt-coated Ni–Cu cocatalyst is, surprisingly, equal. Our findings underscore that a fraction of a monolayer of Pt can enhance the activity of the cocatalyst, and it is worth exploring further for the high activity associated with atomic Pt and other noble metals.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: Advanced Photocatalysis Techniques · Electrocatalysts for Energy Conversion · Quantum Dots Synthesis And Properties

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

Affiliations

Catalysis and Inorganic Chemistry Division, CSIR-National Chemical Laboratory, Dr. Homi Bhabha Road, Pune 411 008, India

Academy of Scientific and Innovative Research (AcSIR), CSIR-National Chemical Laboratory, Pune 411 008, India

Funding

Council of Scientific and Industrial Research · University Grants Commission · Department of Science and Technology, Ministry of Science and Technology

References (40)

Show source-provided references
1. 10.1002/anie.20060237310.1002/anie.200602373 ↗
2. 10.1021/acssuschemeng.8b0425010.1021/acssuschemeng.8b04250 ↗
3. 10.1073/pnas.060339510310.1073/pnas.0603395103 ↗
4. 10.1039/C8CS00542G10.1039/C8CS00542G ↗
5. 10.1126/science.110319710.1126/science.1103197 ↗
6. 10.1021/ar200301310.1021/ar2003013 ↗
7. 10.1039/C5NR02613J10.1039/C5NR02613J ↗
8. 10.1021/acsami.9b0707010.1021/acsami.9b07070 ↗
9. 10.1021/jz301890m10.1021/jz301890m ↗
10. 10.1246/bcsj.2018025810.1246/bcsj.20180258 ↗
11. 10.1246/bcsj.2018025010.1246/bcsj.20180250 ↗
12. 10.1007/s12039-014-0747-010.1007/s12039-014-0747-0 ↗
13. 10.1038/414625a10.1038/414625a ↗
14. 10.1021/jp210677d10.1021/jp210677d ↗
15. 10.1002/cctc.20160093710.1002/cctc.201600937 ↗
16. 10.1039/C5NR03735B10.1039/C5NR03735B ↗
17. 10.1021/acs.jpcc.9b0598310.1021/acs.jpcc.9b05983 ↗
18. 10.1039/C4DT01268B10.1039/C4DT01268B ↗
19. 10.1021/ar300227e10.1021/ar300227e ↗
20. 10.1016/j.cej.2020.12510110.1016/j.cej.2020.125101 ↗
21. 10.1126/science.271.5251.93310.1126/science.271.5251.933 ↗
22. 10.1007/BF0033153510.1007/BF00331535 ↗
23. 10.1016/j.apcatb.2017.06.03310.1016/j.apcatb.2017.06.033 ↗
24. 10.1039/C8RA09982K10.1039/C8RA09982K ↗
25. 10.1038/s41598-017-06849-x10.1038/s41598-017-06849-x ↗
26. 10.1039/c2ee03250c10.1039/c2ee03250c ↗
27. 10.1039/C8TA11307F10.1039/C8TA11307F ↗
28. 10.1039/C3CS60425J10.1039/C3CS60425J ↗
29. 10.1039/C4CC02747G10.1039/C4CC02747G ↗
30. 10.1039/C6DT02531E10.1039/C6DT02531E ↗
31. 10.1021/cm903368r10.1021/cm903368r ↗
32. 10.1021/cm900682q10.1021/cm900682q ↗
33. 10.1039/c0gc00236d10.1039/c0gc00236d ↗
34. 10.1016/j.pnsc.2014.07.00210.1016/j.pnsc.2014.07.002 ↗
35. 10.1016/j.apcatb.2004.09.00710.1016/j.apcatb.2004.09.007 ↗
36. 10.1002/cctc.20140258110.1002/cctc.201402581 ↗
37. 10.1021/ac404102610.1021/ac4041026 ↗
38. 10.1016/j.electacta.2016.08.14510.1016/j.electacta.2016.08.145 ↗
39. 10.1039/C5TA09322H10.1039/C5TA09322H ↗
40. 10.1021/ja407115p10.1021/ja407115p ↗