{"title":"Surface Engineering of GaN Photoelectrode by NH3 Treatment for Solar Water Oxidation","authors":"Soon Hyung Kang, Jun-Seok Ha","doi":"10.33961/jecst.2023.00339","DOIUrl":null,"url":null,"abstract":"Photoelectrochemical (PEC) water splitting is a vital source of clean and sustainable hydrogen energy. Moreover, the large-scale H 2 production is currently necessary, while long-term stability and high PEC activity still remain important issues. In this study, a GaN-based photoelectrode was modified by an additional NH 3 treatment (900°C for 10 min) and its PEC behavior was monitored. The bare GaN exhibited a highly crystalline wurtzite structure with the (002) plane and the optical bandgap was approximately 3.2 eV. In comparison, the NH 3 -treated GaN film exhibited slightly reduced crystallinity and a small improvement in light absorption, resulting from the lattice stress or cracks induced by the excessive N supply. The minor surface nanotexturing created more surface area, providing electroactive reacting sites. From the surface XPS analysis, the formation of an N-Ga-O phase on the surface region of the GaN film was confirmed, which suppressed the charge recombination process and the positive shift of E FB . Therefore, these effects boosted the PEC activity of the NH 3 -treated GaN film, with J values of approximately 0.35 and 0.78 mA·cm –2 at 0.0 and 1.23 V RHE , respectively, and an onset potential (V on ) of −0.24 V RHE . In addition, there was an approximate 50% improvement in the J value within the highly applied potential region with a positive shift of V on . This result could be explained by the increased nanotexturing on the surface structure, the newly formed defect/trap states correlated to the positive V on shift, and the formation of a GaO x N 1-x phase, which partially blocked the charge recombination reaction.","PeriodicalId":15542,"journal":{"name":"Journal of electrochemical science and technology","volume":"12 1","pages":"0"},"PeriodicalIF":2.2000,"publicationDate":"2023-09-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of electrochemical science and technology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.33961/jecst.2023.00339","RegionNum":4,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"ELECTROCHEMISTRY","Score":null,"Total":0}
引用次数: 0
Abstract
Photoelectrochemical (PEC) water splitting is a vital source of clean and sustainable hydrogen energy. Moreover, the large-scale H 2 production is currently necessary, while long-term stability and high PEC activity still remain important issues. In this study, a GaN-based photoelectrode was modified by an additional NH 3 treatment (900°C for 10 min) and its PEC behavior was monitored. The bare GaN exhibited a highly crystalline wurtzite structure with the (002) plane and the optical bandgap was approximately 3.2 eV. In comparison, the NH 3 -treated GaN film exhibited slightly reduced crystallinity and a small improvement in light absorption, resulting from the lattice stress or cracks induced by the excessive N supply. The minor surface nanotexturing created more surface area, providing electroactive reacting sites. From the surface XPS analysis, the formation of an N-Ga-O phase on the surface region of the GaN film was confirmed, which suppressed the charge recombination process and the positive shift of E FB . Therefore, these effects boosted the PEC activity of the NH 3 -treated GaN film, with J values of approximately 0.35 and 0.78 mA·cm –2 at 0.0 and 1.23 V RHE , respectively, and an onset potential (V on ) of −0.24 V RHE . In addition, there was an approximate 50% improvement in the J value within the highly applied potential region with a positive shift of V on . This result could be explained by the increased nanotexturing on the surface structure, the newly formed defect/trap states correlated to the positive V on shift, and the formation of a GaO x N 1-x phase, which partially blocked the charge recombination reaction.