{"title":"MXene quantum dots-engineered NiOₓ nanoparticles for high-efficiency wide-bandgap perovskite solar cells","authors":"Zihao Wang, Weidong Zhu, Laijun Liang, Dandan Chen, Xiaomeng Wu, Wenming Chai, He Xi, Peng Zhong, Zhiming Li, Chunfu Zhang, Jincheng Zhang, Yue Hao","doi":"10.1016/j.cej.2025.166305","DOIUrl":null,"url":null,"abstract":"NiOₓ is a promising hole-transporting layer (HTL) for inverted perovskite solar cells (PSCs), but its practical application is hindered by high defect density, low conductivity, and poor compatibility with self-assembled monolayers (SAMs). Here, we report a strategy to enhance commercial NiOₓ nanoparticles (NPs) by incorporating Ti₃C₂Tₓ MXene quantum dots (MQDs), which offer abundant surface functional groups (–OH, <img alt=\"single bond\" src=\"https://sdfestaticassets-us-east-1.sciencedirectassets.com/shared-assets/55/entities/sbnd.gif\" style=\"vertical-align:middle\"/>O, <img alt=\"single bond\" src=\"https://sdfestaticassets-us-east-1.sciencedirectassets.com/shared-assets/55/entities/sbnd.gif\" style=\"vertical-align:middle\"/>F) and high conductivity. Moreover, MQDs promote surface hydroxylation and the formation of NiOOH species in NiOₓ NPs, while co-addition of H₂O₂ narrows their particle size distribution and suppresses aggregation, yielding NiOₓ films with improved morphology, conductivity, energy alignment, and SAM anchoring. When combined with 1.68 eV-bandgap perovskites, the modified NiOₓ enables better crystallinity, enlarged grains, and fewer interfacial defects, boosting the efficiency of opaque PSCs to 22.96 %. This strategy also enables efficient two-terminal TOPCon/perovskite and four-terminal HBC/perovskite tandem cells, achieving champion efficiencies of 31.06 % and 32.20 %, respectively. All devices show excellent ambient humidity stability, underscoring the potential of MQDs-engineered NiOₓ HTLs for scalable, high-performance photovoltaics.","PeriodicalId":270,"journal":{"name":"Chemical Engineering Journal","volume":"14 1","pages":""},"PeriodicalIF":13.2000,"publicationDate":"2025-07-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Chemical Engineering Journal","FirstCategoryId":"5","ListUrlMain":"https://doi.org/10.1016/j.cej.2025.166305","RegionNum":1,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"ENGINEERING, CHEMICAL","Score":null,"Total":0}
引用次数: 0
Abstract
NiOₓ is a promising hole-transporting layer (HTL) for inverted perovskite solar cells (PSCs), but its practical application is hindered by high defect density, low conductivity, and poor compatibility with self-assembled monolayers (SAMs). Here, we report a strategy to enhance commercial NiOₓ nanoparticles (NPs) by incorporating Ti₃C₂Tₓ MXene quantum dots (MQDs), which offer abundant surface functional groups (–OH, O, F) and high conductivity. Moreover, MQDs promote surface hydroxylation and the formation of NiOOH species in NiOₓ NPs, while co-addition of H₂O₂ narrows their particle size distribution and suppresses aggregation, yielding NiOₓ films with improved morphology, conductivity, energy alignment, and SAM anchoring. When combined with 1.68 eV-bandgap perovskites, the modified NiOₓ enables better crystallinity, enlarged grains, and fewer interfacial defects, boosting the efficiency of opaque PSCs to 22.96 %. This strategy also enables efficient two-terminal TOPCon/perovskite and four-terminal HBC/perovskite tandem cells, achieving champion efficiencies of 31.06 % and 32.20 %, respectively. All devices show excellent ambient humidity stability, underscoring the potential of MQDs-engineered NiOₓ HTLs for scalable, high-performance photovoltaics.
期刊介绍:
The Chemical Engineering Journal is an international research journal that invites contributions of original and novel fundamental research. It aims to provide an international platform for presenting original fundamental research, interpretative reviews, and discussions on new developments in chemical engineering. The journal welcomes papers that describe novel theory and its practical application, as well as those that demonstrate the transfer of techniques from other disciplines. It also welcomes reports on carefully conducted experimental work that is soundly interpreted. The main focus of the journal is on original and rigorous research results that have broad significance. The Catalysis section within the Chemical Engineering Journal focuses specifically on Experimental and Theoretical studies in the fields of heterogeneous catalysis, molecular catalysis, and biocatalysis. These studies have industrial impact on various sectors such as chemicals, energy, materials, foods, healthcare, and environmental protection.