Rui Lei, Guanan Guo, Lanlan Ye, Na Liu, Minglu Li, Shiyu Yu, Lei Liu, Qinyu Li, Weiningjing Zhou and Zaijiao Fei
{"title":"在不锈钢上可控合成垂直排列的 WO3 纳米板阵列,提高可见光光电催化活性†。","authors":"Rui Lei, Guanan Guo, Lanlan Ye, Na Liu, Minglu Li, Shiyu Yu, Lei Liu, Qinyu Li, Weiningjing Zhou and Zaijiao Fei","doi":"10.1039/D4NJ03397C","DOIUrl":null,"url":null,"abstract":"<p >Vertically aligned WO<small><sub>3</sub></small> nanoplate films were synthesized on stainless steel (SS) <em>via</em> a simple hydrothermal method. The prepared WO<small><sub>3</sub></small> films were characterized using scanning electron microscopy (SEM), X-ray diffraction (XRD) and high-resolution transmission electron microscopy (HRTEM). Results of these analyses reveal that the SS surface was well-covered with compact and vertical WO<small><sub>3</sub></small> nanoplates with a monoclinic single-crystalline structure. The film obtained through a 2.5 h hydrothermal reaction exhibited excellent photoelectrochemical performance under visible-light illumination and generated an anodic photocurrent of 0.754 mA cm<small><sup>−2</sup></small> at 0.8 V (<em>vs.</em> Ag/AgCl). WO<small><sub>3</sub></small> photoelectrodes could degrade 98.9% of methylene blue (MB) within 120 min through a photoelectrocatalytic (PEC) process. The stability of the as-prepared photoelectrode was also studied, and no significant reduction in PEC activity was observed after recycling for 5 times. The supreme PEC activity of the aligned WO<small><sub>3</sub></small> nanoplate films can be attributed to the direct charge transport pathway in the 2D structure and the bias potential applied to reduce the recombination of photogenerated electron–hole pairs.</p>","PeriodicalId":95,"journal":{"name":"New Journal of Chemistry","volume":" 46","pages":" 19472-19477"},"PeriodicalIF":2.7000,"publicationDate":"2024-10-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Controllable synthesis of vertically aligned WO3 nanoplate arrays on stainless steel for improved visible-light photoelectrocatalytic activity†\",\"authors\":\"Rui Lei, Guanan Guo, Lanlan Ye, Na Liu, Minglu Li, Shiyu Yu, Lei Liu, Qinyu Li, Weiningjing Zhou and Zaijiao Fei\",\"doi\":\"10.1039/D4NJ03397C\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p >Vertically aligned WO<small><sub>3</sub></small> nanoplate films were synthesized on stainless steel (SS) <em>via</em> a simple hydrothermal method. The prepared WO<small><sub>3</sub></small> films were characterized using scanning electron microscopy (SEM), X-ray diffraction (XRD) and high-resolution transmission electron microscopy (HRTEM). Results of these analyses reveal that the SS surface was well-covered with compact and vertical WO<small><sub>3</sub></small> nanoplates with a monoclinic single-crystalline structure. The film obtained through a 2.5 h hydrothermal reaction exhibited excellent photoelectrochemical performance under visible-light illumination and generated an anodic photocurrent of 0.754 mA cm<small><sup>−2</sup></small> at 0.8 V (<em>vs.</em> Ag/AgCl). WO<small><sub>3</sub></small> photoelectrodes could degrade 98.9% of methylene blue (MB) within 120 min through a photoelectrocatalytic (PEC) process. The stability of the as-prepared photoelectrode was also studied, and no significant reduction in PEC activity was observed after recycling for 5 times. The supreme PEC activity of the aligned WO<small><sub>3</sub></small> nanoplate films can be attributed to the direct charge transport pathway in the 2D structure and the bias potential applied to reduce the recombination of photogenerated electron–hole pairs.</p>\",\"PeriodicalId\":95,\"journal\":{\"name\":\"New Journal of Chemistry\",\"volume\":\" 46\",\"pages\":\" 19472-19477\"},\"PeriodicalIF\":2.7000,\"publicationDate\":\"2024-10-30\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"New Journal of Chemistry\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://pubs.rsc.org/en/content/articlelanding/2024/nj/d4nj03397c\",\"RegionNum\":3,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"CHEMISTRY, MULTIDISCIPLINARY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"New Journal of Chemistry","FirstCategoryId":"92","ListUrlMain":"https://pubs.rsc.org/en/content/articlelanding/2024/nj/d4nj03397c","RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
Controllable synthesis of vertically aligned WO3 nanoplate arrays on stainless steel for improved visible-light photoelectrocatalytic activity†
Vertically aligned WO3 nanoplate films were synthesized on stainless steel (SS) via a simple hydrothermal method. The prepared WO3 films were characterized using scanning electron microscopy (SEM), X-ray diffraction (XRD) and high-resolution transmission electron microscopy (HRTEM). Results of these analyses reveal that the SS surface was well-covered with compact and vertical WO3 nanoplates with a monoclinic single-crystalline structure. The film obtained through a 2.5 h hydrothermal reaction exhibited excellent photoelectrochemical performance under visible-light illumination and generated an anodic photocurrent of 0.754 mA cm−2 at 0.8 V (vs. Ag/AgCl). WO3 photoelectrodes could degrade 98.9% of methylene blue (MB) within 120 min through a photoelectrocatalytic (PEC) process. The stability of the as-prepared photoelectrode was also studied, and no significant reduction in PEC activity was observed after recycling for 5 times. The supreme PEC activity of the aligned WO3 nanoplate films can be attributed to the direct charge transport pathway in the 2D structure and the bias potential applied to reduce the recombination of photogenerated electron–hole pairs.