{"title":"Polarization-Driven Type-II and Z-Scheme Heterojunctions in GaN/ZrSO and GaN/ZrS2 for Enhanced Photocatalysis","authors":"Qiheng Ma, Xiaodong Hao, Cheng Wang, Jiahui Wang, Deqiang Yin, Shufang Ma, Bingshe Xu","doi":"10.1021/acs.jpcc.4c08602","DOIUrl":null,"url":null,"abstract":"In this work, the structural stability, electronic properties, and photocatalytic performance of three heterostructures─nonpolar/nonpolar GaN/ZrS<sub>2</sub> and nonpolar/polar GaN/ZrSO with different polarization directions (P↑ and P↓)─were systematically investigated using first-principles calculations. The GaN/ZrS<sub>2</sub> heterostructure was found to form a direct Z-scheme junction, with efficient charge separation driven by a built-in electric field. This internal field enhances the redox potential, making the GaN/ZrS<sub>2</sub> heterostructure highly suitable for overall photocatalytic water splitting. In contrast, the P↓ GaN/ZrSO heterostructure was shown to exhibit type II band alignment, where the presence of an intrinsic polarization field from the ZrSO monolayer further boosts its hydrogen evolution efficiency. Both GaN/ZrS<sub>2</sub> and P↓ GaN/ZrSO heterostructures demonstrated strong light absorption in the visible spectrum and favorable band-edge positions for redox reactions. Thermodynamic calculations of Gibbs free energy confirmed that spontaneous water splitting can occur under neutral conditions for both systems. Additionally, dielectric function analysis revealed enhanced visible light absorption, especially in the P↓ GaN/ZrSO system. These results indicate that GaN-based heterostructures offer significant potential as efficient and stable photocatalysts for water splitting, with the ability to harness visible light and optimize charge carrier dynamics through polarization effects. This study highlights the promise of these heterostructures for advancing sustainable energy applications.","PeriodicalId":61,"journal":{"name":"The Journal of Physical Chemistry C","volume":"6 1","pages":""},"PeriodicalIF":3.2000,"publicationDate":"2025-04-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"The Journal of Physical Chemistry C","FirstCategoryId":"1","ListUrlMain":"https://doi.org/10.1021/acs.jpcc.4c08602","RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, PHYSICAL","Score":null,"Total":0}
引用次数: 0
Abstract
In this work, the structural stability, electronic properties, and photocatalytic performance of three heterostructures─nonpolar/nonpolar GaN/ZrS2 and nonpolar/polar GaN/ZrSO with different polarization directions (P↑ and P↓)─were systematically investigated using first-principles calculations. The GaN/ZrS2 heterostructure was found to form a direct Z-scheme junction, with efficient charge separation driven by a built-in electric field. This internal field enhances the redox potential, making the GaN/ZrS2 heterostructure highly suitable for overall photocatalytic water splitting. In contrast, the P↓ GaN/ZrSO heterostructure was shown to exhibit type II band alignment, where the presence of an intrinsic polarization field from the ZrSO monolayer further boosts its hydrogen evolution efficiency. Both GaN/ZrS2 and P↓ GaN/ZrSO heterostructures demonstrated strong light absorption in the visible spectrum and favorable band-edge positions for redox reactions. Thermodynamic calculations of Gibbs free energy confirmed that spontaneous water splitting can occur under neutral conditions for both systems. Additionally, dielectric function analysis revealed enhanced visible light absorption, especially in the P↓ GaN/ZrSO system. These results indicate that GaN-based heterostructures offer significant potential as efficient and stable photocatalysts for water splitting, with the ability to harness visible light and optimize charge carrier dynamics through polarization effects. This study highlights the promise of these heterostructures for advancing sustainable energy applications.
期刊介绍:
The Journal of Physical Chemistry A/B/C is devoted to reporting new and original experimental and theoretical basic research of interest to physical chemists, biophysical chemists, and chemical physicists.