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Article: Nickel-coated silicon photocathode for water splitting in alkaline electrolytes
Title | Nickel-coated silicon photocathode for water splitting in alkaline electrolytes |
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Authors | |
Keywords | nickel photoelectrochemical water splitting silicon photocathode |
Issue Date | 2015 |
Citation | Nano Research, 2015, v. 8, n. 5, p. 1577-1583 How to Cite? |
Abstract | Photoelectrochemical (PEC) water splitting is a promising approach to harvest and store solar energy [1]. Silicon has been widely investigated for PEC photoelectrodes due to its suitable band gap (1.12 eV) matching the solar spectrum [2]. Here we investigate employing nickel both as a catalyst and protecting layer of a p-type silicon photocathode for photoelectrochemical hydrogen evolution in basic electrolytes for the first time. The silicon photocathode was made by depositing 15 nm Ti on a p-type silicon wafer followed by 5 nm Ni. The photocathode afforded an onset potential of ∼0.3 V vs. the reversible hydrogen electrode (RHE) in alkaline solution (1 M KOH). The stability of the Ni/Ti/p-Si photocathode showed a 100 mV decay over 12 h in KOH, but the stability was significantly improved when the photocathode was operated in potassium borate buffer solution (pH ≈ 9.5). The electrode surface was found to remain intact after 12 h of continuous operation at a constant current density of 10 mA/cm2 in potassium borate buffer, suggesting that Ni affords good protection of Si based photocathodes in borate buffers. |
Persistent Identifier | http://hdl.handle.net/10722/334395 |
ISSN | 2023 Impact Factor: 9.5 2023 SCImago Journal Rankings: 2.539 |
ISI Accession Number ID |
DC Field | Value | Language |
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dc.contributor.author | Feng, Ju | - |
dc.contributor.author | Gong, Ming | - |
dc.contributor.author | Kenney, Michael J. | - |
dc.contributor.author | Wu, Justin Z. | - |
dc.contributor.author | Zhang, Bo | - |
dc.contributor.author | Li, Yanguang | - |
dc.contributor.author | Dai, Hongjie | - |
dc.date.accessioned | 2023-10-20T06:47:50Z | - |
dc.date.available | 2023-10-20T06:47:50Z | - |
dc.date.issued | 2015 | - |
dc.identifier.citation | Nano Research, 2015, v. 8, n. 5, p. 1577-1583 | - |
dc.identifier.issn | 1998-0124 | - |
dc.identifier.uri | http://hdl.handle.net/10722/334395 | - |
dc.description.abstract | Photoelectrochemical (PEC) water splitting is a promising approach to harvest and store solar energy [1]. Silicon has been widely investigated for PEC photoelectrodes due to its suitable band gap (1.12 eV) matching the solar spectrum [2]. Here we investigate employing nickel both as a catalyst and protecting layer of a p-type silicon photocathode for photoelectrochemical hydrogen evolution in basic electrolytes for the first time. The silicon photocathode was made by depositing 15 nm Ti on a p-type silicon wafer followed by 5 nm Ni. The photocathode afforded an onset potential of ∼0.3 V vs. the reversible hydrogen electrode (RHE) in alkaline solution (1 M KOH). The stability of the Ni/Ti/p-Si photocathode showed a 100 mV decay over 12 h in KOH, but the stability was significantly improved when the photocathode was operated in potassium borate buffer solution (pH ≈ 9.5). The electrode surface was found to remain intact after 12 h of continuous operation at a constant current density of 10 mA/cm2 in potassium borate buffer, suggesting that Ni affords good protection of Si based photocathodes in borate buffers. | - |
dc.language | eng | - |
dc.relation.ispartof | Nano Research | - |
dc.subject | nickel | - |
dc.subject | photoelectrochemical water splitting | - |
dc.subject | silicon photocathode | - |
dc.title | Nickel-coated silicon photocathode for water splitting in alkaline electrolytes | - |
dc.type | Article | - |
dc.description.nature | link_to_subscribed_fulltext | - |
dc.identifier.doi | 10.1007/s12274-014-0643-4 | - |
dc.identifier.scopus | eid_2-s2.0-84935889204 | - |
dc.identifier.volume | 8 | - |
dc.identifier.issue | 5 | - |
dc.identifier.spage | 1577 | - |
dc.identifier.epage | 1583 | - |
dc.identifier.eissn | 1998-0000 | - |
dc.identifier.isi | WOS:000354625600013 | - |