Jindi Yang, Hanqing Yin, Aijun Du, Mike Tebyetekerwa, Chuanbiao Bie, Zhuyuan Wang, Zhimeng Sun, Zhongguo Zhang, Xiangkang Zeng, Xiwang Zhang
{"title":"Unveiling O2 adsorption on non-metallic active site for selective photocatalytic H2O2 production","authors":"Jindi Yang, Hanqing Yin, Aijun Du, Mike Tebyetekerwa, Chuanbiao Bie, Zhuyuan Wang, Zhimeng Sun, Zhongguo Zhang, Xiangkang Zeng, Xiwang Zhang","doi":"10.1016/j.apcatb.2024.124586","DOIUrl":null,"url":null,"abstract":"Photocatalytic oxygen reduction reaction (ORR) offers a promising pathway for sustainable hydrogen peroxide (HO) production but faces challenges in developing catalysts with good ORR selectivity. Herein, we report that tailoring O adsorption on non-metallic active sites can optimize ORR selectivity. This concept is demonstrated on three carbon nitrides with different atomic configurations: polymeric carbon nitride (PCN), lithium-poly triazine imide (Li-PTI), and sodium-poly heptazine imide (Na-PHI). Na-PHI emerges as a strong candidate for HO production due to the end-on adsorption mode and suitable adsorption strength with O. Synthesized Na-PHI, PCN, and Li-PTI are characterized, with Na-PHI showing superior light absorption, charge carrier separation, and remarkable selectivity (92 %) for two-electron ORR. Consequently, Na-PHI achieves a high HO generation rate of 3.48 mmol g h, surpassing Li-PTI and PCN by 9.2 and 33 times, respectively. This study underscores the importance of O adsorption on non-metallic active sites for selective photocatalytic HO generation.","PeriodicalId":516528,"journal":{"name":"Applied Catalysis B: Environment and Energy","volume":"112 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2024-09-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Applied Catalysis B: Environment and Energy","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1016/j.apcatb.2024.124586","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
Photocatalytic oxygen reduction reaction (ORR) offers a promising pathway for sustainable hydrogen peroxide (HO) production but faces challenges in developing catalysts with good ORR selectivity. Herein, we report that tailoring O adsorption on non-metallic active sites can optimize ORR selectivity. This concept is demonstrated on three carbon nitrides with different atomic configurations: polymeric carbon nitride (PCN), lithium-poly triazine imide (Li-PTI), and sodium-poly heptazine imide (Na-PHI). Na-PHI emerges as a strong candidate for HO production due to the end-on adsorption mode and suitable adsorption strength with O. Synthesized Na-PHI, PCN, and Li-PTI are characterized, with Na-PHI showing superior light absorption, charge carrier separation, and remarkable selectivity (92 %) for two-electron ORR. Consequently, Na-PHI achieves a high HO generation rate of 3.48 mmol g h, surpassing Li-PTI and PCN by 9.2 and 33 times, respectively. This study underscores the importance of O adsorption on non-metallic active sites for selective photocatalytic HO generation.