Ageing mechanisms of highly active and stable nickel-coated silicon photoanodes for water splitting. Issue 21 (23rd March 2016)
- Record Type:
- Journal Article
- Title:
- Ageing mechanisms of highly active and stable nickel-coated silicon photoanodes for water splitting. Issue 21 (23rd March 2016)
- Main Title:
- Ageing mechanisms of highly active and stable nickel-coated silicon photoanodes for water splitting
- Authors:
- Han, Tingting
Shi, Yuanyuan
Song, Xiaoxue
Mio, Antonio
Valenti, Luca
Hui, Fei
Privitera, Stefania
Lombardo, Salvatore
Lanza, Mario - Abstract:
- Abstract : The performance decay in 2 nm-thick metal-coated silicon photoanodes for water splitting is related to the formation of a thick SiO X film at the interface, while thicker coatings live longer and degrade due to the formation of holes. Abstract : The photoelectrochemical (PEC) water splitting cell, a device that uses sunlight to produce hydrogen, has garnered very much interest due to its simple structure, low fabrication cost and good performance. In these cells, a semiconductor photoelectrode is immersed in a liquid and, when illuminated, hydrogen and/or oxygen can be generated on its surface by electrolysis. Metal catalysts are often used to enhance the activity of the semiconductor, but the lifetime of the semiconductor photoelectrode is still the main bottleneck of this technology. In this manuscript we report the ageing mechanisms of silicon photoanodes coated with nickel films of different thicknesses (under the light-driven oxygen evolution reaction, OER). The n-Si photoanodes coated with 2 nm-thick, 5 nm-thick and 10 nm-thick nickel layers showed lifetimes of ∼18 h, ∼150 h and >260 h, respectively. While the 2 nm-thick sample degraded due to the formation of a thin SiO X layer at the metal–silicon interface, the performance of the thicker samples decreased due to the formation of holes. The 5 nm-thick and 10 nm-thick nickel films turned into homogeneous potassium-free NiO X films suitable for water splitting, and this conversion markedly enhanced theAbstract : The performance decay in 2 nm-thick metal-coated silicon photoanodes for water splitting is related to the formation of a thick SiO X film at the interface, while thicker coatings live longer and degrade due to the formation of holes. Abstract : The photoelectrochemical (PEC) water splitting cell, a device that uses sunlight to produce hydrogen, has garnered very much interest due to its simple structure, low fabrication cost and good performance. In these cells, a semiconductor photoelectrode is immersed in a liquid and, when illuminated, hydrogen and/or oxygen can be generated on its surface by electrolysis. Metal catalysts are often used to enhance the activity of the semiconductor, but the lifetime of the semiconductor photoelectrode is still the main bottleneck of this technology. In this manuscript we report the ageing mechanisms of silicon photoanodes coated with nickel films of different thicknesses (under the light-driven oxygen evolution reaction, OER). The n-Si photoanodes coated with 2 nm-thick, 5 nm-thick and 10 nm-thick nickel layers showed lifetimes of ∼18 h, ∼150 h and >260 h, respectively. While the 2 nm-thick sample degraded due to the formation of a thin SiO X layer at the metal–silicon interface, the performance of the thicker samples decreased due to the formation of holes. The 5 nm-thick and 10 nm-thick nickel films turned into homogeneous potassium-free NiO X films suitable for water splitting, and this conversion markedly enhanced the performance of the cells. The density/size of holes in the surface decreased/increased with the metal thickness. The potassium contamination in the 2 nm-thick Ni sample took place in the form of nanofilaments, and we demonstrated that the widely used X-ray photoelectron spectroscopy tests are blind to these features, which may have been ignored in all previous reports. These results could be useful for understanding the degradation and enhancing the yield of water-splitting solar cells. … (more)
- Is Part Of:
- Journal of materials chemistry. Volume 4:Issue 21(2016)
- Journal:
- Journal of materials chemistry
- Issue:
- Volume 4:Issue 21(2016)
- Issue Display:
- Volume 4, Issue 21 (2016)
- Year:
- 2016
- Volume:
- 4
- Issue:
- 21
- Issue Sort Value:
- 2016-0004-0021-0000
- Page Start:
- 8053
- Page End:
- 8060
- Publication Date:
- 2016-03-23
- Subjects:
- Materials -- Research -- Periodicals
Chemistry, Analytic -- Periodicals
Environmental sciences -- Research -- Periodicals
543.0284 - Journal URLs:
- http://pubs.rsc.org/en/journals/journalissues/ta ↗
http://www.rsc.org/ ↗ - DOI:
- 10.1039/c5ta09990k ↗
- Languages:
- English
- ISSNs:
- 2050-7488
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 5012.205100
British Library DSC - BLDSS-3PM
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