One-Dimensional Hollow Structures of 2O-PdS2 Decorated Carbon for Water Electrolysis
Source abstract
Abstract
Author: High surface area (∼90 ± 2 m2/g), one-dimensional (1D) graphitic structures (diameter ∼ 145 ± 5 nm, and length ∼ 3 ± 1 μm) decorated with pentagonal layered 2O-PdS2 nanoclusters (PdS2/C) were developed. The synthesis method consists of low temperature (280 °C) sulfurization of a palladium complex, namely, palladium bis(dimethylglyoxime) ([Pd(DMG)2]n). Electrocatalytic hydrogen evolution reaction (HER) efficiency of the PdS2/C studied in acidic condition indicates its potential in stable water electrolysis performance (>20 h) in contrast to the HER performance of benchmarked Pd(0) nanoparticle counterpart. The low overpotential (∼137 mV vs RHE) for HER initiation, low tafel slope (∼73 mV/dec), and high stability even after several cycles showcase PdS2/C as a viable electrocatalyst for water electrolysis process having a low mass loading of expensive palladium (0.016 mg cm–2) metal.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Electrocatalysts for Energy Conversion · Advanced Photocatalysis Techniques · Chalcogenide Semiconductor Thin Films
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Tata Institute of Fundamental Research−Hyderabad, Sy. No. 36/P, Gopanapally Village, Serilingampally Mandal, Hyderabad 500 046, India
Department of Mechanical Engineering and Materials Science, Rice University, Houston, Texas 77005, United States
School of Physics, University of Hyderabad, Hyderabad 500 046, India
Funding
Department of Atomic Energy, Government of India
References (29)
Show source-provided references
1. 10.1039/C3CS60468C10.1039/C3CS60468C ↗
2. 10.1038/nchem.111610.1038/nchem.1116 ↗
3. 10.1016/S1369-7021(08)70254-210.1016/S1369-7021(08)70254-2 ↗
4. 10.1039/C4EE00370E10.1039/C4EE00370E ↗
5. 10.1021/acscatal.8b0093810.1021/acscatal.8b00938 ↗
6. 10.1021/acsenergylett.1c0024610.1021/acsenergylett.1c00246 ↗
7. 10.1002/anie.20150437610.1002/anie.201504376 ↗
8. 10.1002/pssr.20190025710.1002/pssr.201900257 ↗
9. 10.1039/C6TA04082A10.1039/C6TA04082A ↗
10. 10.1039/C8TA06783J10.1039/C8TA06783J ↗
11. 10.3390/nano1012244110.3390/nano10122441 ↗
12. 10.1002/adma.20150427410.1002/adma.201504274 ↗
13. 10.1039/C9RA07445G10.1039/C9RA07445G ↗
14. 10.1016/j.nanoen.2018.04.01910.1016/j.nanoen.2018.04.019 ↗
15. 10.1002/adfm.20210232110.1002/adfm.202102321 ↗
16. 10.1038/srep1380110.1038/srep13801 ↗
17. 10.1103/PhysRevB.100.01450710.1103/PhysRevB.100.014507 ↗
18. 10.1002/anie.20191488610.1002/anie.201914886 ↗
19. 10.1107/S0365110X5700094810.1107/S0365110X57000948 ↗
20. 10.1039/C5TA04956C10.1039/C5TA04956C ↗
21. 10.1002/adfm.20190248310.1002/adfm.201902483 ↗
22. 10.1002/adfm.20070079710.1002/adfm.200700797 ↗
23. 10.1039/c3ee41182f10.1039/c3ee41182f ↗
24. 10.1021/acscatal.7b0003210.1021/acscatal.7b00032 ↗
25. 10.1039/C8QI00042E10.1039/C8QI00042E ↗
26. 10.1016/j.jcat.2015.03.01210.1016/j.jcat.2015.03.012 ↗
27. 10.1088/2515-7655/ab8e2510.1088/2515-7655/ab8e25 ↗
28. 10.1063/1.32353910.1063/1.323539 ↗
29. 10.1016/j.jcat.2017.07.00110.1016/j.jcat.2017.07.001 ↗