journal article·2014-07-09

Tungsten Sulfide Enhancing Solar-Driven Hydrogen Production from Silicon Nanowires

Zhipeng Huang, Chifang Wang, Zhibo Chen, Hua Meng, Cuncai Lv, Zhongzhong Chen, Ruqu Han, Chi Zhang

Publisher page

Abstract

Tungsten sulfides, including WS2 (crystalline) and WS3 (amorphous), were introduced to silicon nanowires, and both can promote the photoelectrochemical hydrogen production of silicon nanowires. In addition, more enhancement of energy conversion efficiency can be achieved by the loading of WS3, in comparison with loading of WS2. Polarization curves of WS3 and WS2 suggest that WS3 has higher catalytic activity in the hydrogen evolution reaction than WS2, affording higher energy conversion efficiency in silicon nanowires decorated with WS3. The higher electrocatalytic activity of WS3 correlates with the amorphous structure of WS3 and larger surface area of WS3, which result in more active sites in comparison with crystalline WS2.
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

China-Australia Joint Research Center for Functional Molecular Materials, Scientific Research Academy, Jiangsu University, Zhenjiang, Jiangsu 212013, People’s Republic of China

Research Institute of Refrigeration and Thermal Engineering, College of Mechanical Engineering, Tongji University, Shanghai 200092, People’s Republic of China

Department of Physics, Jiangsu University of Science and Technology, Zhenjiang, Jiangsu 212003, People’s Republic of China

References (31)

Show source-provided references
1. Walter M. G. · Chem. Rev. · 2010 · 110 · 644610.1021/cr1002326 ↗
2. Dominey R. N. · J. Am. Chem. Soc. · 1982 · 104 · 46710.1021/ja00366a016 ↗
3. Reece S. Y. · Science · 2011 · 334 · 64510.1126/science.1209816 ↗
4. Peng K. Q. · Small · 2005 · 1 · 106210.1002/smll.200500137 ↗
5. Garnett E. C. · J. Am. Chem. Soc. · 2008 · 130 · 922410.1021/ja8032907 ↗
6. Boettcher S. W. · J. Am. Chem. Soc. · 2011 · 133 · 121610.1021/ja108801m ↗
7. McKone J. R. · Energ Environ. Sci. · 2011 · 4 · 357310.1039/c1ee01488a ↗
8. Lin C. Y. · Chem. Sci. · 2012 · 3 · 348210.1039/c2sc20874a ↗
9. Hou Y. D. · Nat. Mater. · 2011 · 10 · 43410.1038/nmat3008 ↗
10. Seger B. · Angew. Chem., Int. Ed. · 2012 · 51 · 912810.1002/anie.201203585 ↗
11. Huang Z. P. · Nano Energy · 2013 · 2 · 133710.1016/j.nanoen.2013.06.016 ↗
12. Sobczynski A. · J. Phys. Chem. · 1988 · 92 · 231110.1021/j100319a042 ↗
13. Bonde J. · Faraday Discuss. · 2008 · 140 · 21910.1039/B803857K ↗
14. Jing D. W. · Catal. Commun. · 2007 · 8 · 79510.1016/j.catcom.2006.09.009 ↗
15. Zong X. · J. Phys. Chem. C · 2011 · 115 · 1220210.1021/jp2006777 ↗
16. Wu Z. Z. · Appl. Catal., B · 2012 · 125 · 5910.1016/j.apcatb.2012.05.013 ↗
17. Voiry D. · Nat. Mater. · 2013 · 12 · 85010.1038/nmat3700 ↗
18. Choi C. L. · Nano Research · 2013 · 6 · 92110.1007/s12274-013-0369-8 ↗
19. Huang Z. P. · Adv. Mater. · 2011 · 23 · 28510.1002/adma.201001784 ↗
20. Peng K. Q. · Adv. Mater. · 2002 · 14 · 116410.1002/1521-4095(20020816)14:16<1164::AID-ADMA1164>3.0.CO;2-E ↗
21. van der Vlies A. J. · J. Phys. Chem. B · 2002 · 106 · 344910.1021/jp0138734 ↗
22. Paola D. A. · J. Phys. Chem. B · 1999 · 103 · 823610.1021/jp9911797 ↗
23. Tran P. D. · Chem.—Eur. J. · 2012 · 18 · 1399410.1002/chem.201202214 ↗
24. Oh I. · Nano Lett. · 2013 · 12 · 29810.1021/nl203564s ↗
25. Lopes T. · Int. J. Hydogen Energy · 2010 · 35 · 1160110.1016/j.ijhydene.2010.04.001 ↗
26. Merki D. · Chem. Sci. · 2012 · 3 · 251510.1039/c2sc20539d ↗
27. Jaramillo T. F. · Science · 2007 · 317 · 10010.1126/science.1141483 ↗
28. Merki D. · Chem. Sci. · 2011 · 2 · 126210.1039/C1SC00117E ↗
29. Yan Y. · ACS Appl. Mater. Interfaces · 2013 · 5 · 1279410.1021/am404843b ↗
30. Xie J. F. · J. Am. Chem. Soc. · 2013 · 135 · 1788110.1021/ja408329q ↗
31. Chang Y. H. · Adv. Mater. · 2013 · 25 · 75610.1002/adma.201202920 ↗