{"title":"电子束蒸发氧化镍在高性能钙钛矿太阳能电池中的协同界面改性。","authors":"Qiyu Shi,Le Wei,Yudong Shao,Jiale Su,Bitao Chen,Disheng Yao,Jilin Wang,Shuyi Mo,Bing Zhou,Guoyuan Zheng,Fei Long","doi":"10.1021/acsami.5c15868","DOIUrl":null,"url":null,"abstract":"Nickel oxide (NiOx) is considered an ideal hole transport layer (HTL) in inverted perovskite solar cells (PSCs) due to its excellent carrier mobility and low cost. Electron-beam-evaporated NiOx (E-beam-NiOx) exhibits exceptional commercial potential due to its process compatibility. However, there are surface defects in E-beam-NiOx, which are incompatible with perovskite (PVK) and limit its development. In this work, we used [4-(3,6-dimethyl-9H-carbazol-9-yl)butyl]phosphonic acid (Me-4PACz) as a self-assembled monolayer (SAM) and l-α-glycerylphosphorylcholine (GPC) to double modify the buried interface of E-beam-NiOx films. SAM is used to modify interface defects of NiOx, while GPC improves the wetting property and uniformity of the interface. Under the joint modification of SAM and GPC, the interface defects of NiOx films were passivated, and the hole extraction ability of HTL was improved. At the same time, the growth quality of PVK films was improved, and the energy level matching between NiOx and PVK was optimized. After optimization, the small-area (0.0575 cm2) PSCs achieved a champion power conversion efficiency (PCE) of 23.31%, providing an effective strategy and direction for the preparation of high-efficiency PSCs by E-beam-NiOx.","PeriodicalId":5,"journal":{"name":"ACS Applied Materials & Interfaces","volume":"33 1","pages":""},"PeriodicalIF":8.2000,"publicationDate":"2025-10-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Synergistic Interface Modification of Electron-Beam-Evaporated NiOx for High-Performance Perovskite Solar Cells.\",\"authors\":\"Qiyu Shi,Le Wei,Yudong Shao,Jiale Su,Bitao Chen,Disheng Yao,Jilin Wang,Shuyi Mo,Bing Zhou,Guoyuan Zheng,Fei Long\",\"doi\":\"10.1021/acsami.5c15868\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Nickel oxide (NiOx) is considered an ideal hole transport layer (HTL) in inverted perovskite solar cells (PSCs) due to its excellent carrier mobility and low cost. Electron-beam-evaporated NiOx (E-beam-NiOx) exhibits exceptional commercial potential due to its process compatibility. However, there are surface defects in E-beam-NiOx, which are incompatible with perovskite (PVK) and limit its development. In this work, we used [4-(3,6-dimethyl-9H-carbazol-9-yl)butyl]phosphonic acid (Me-4PACz) as a self-assembled monolayer (SAM) and l-α-glycerylphosphorylcholine (GPC) to double modify the buried interface of E-beam-NiOx films. SAM is used to modify interface defects of NiOx, while GPC improves the wetting property and uniformity of the interface. Under the joint modification of SAM and GPC, the interface defects of NiOx films were passivated, and the hole extraction ability of HTL was improved. At the same time, the growth quality of PVK films was improved, and the energy level matching between NiOx and PVK was optimized. After optimization, the small-area (0.0575 cm2) PSCs achieved a champion power conversion efficiency (PCE) of 23.31%, providing an effective strategy and direction for the preparation of high-efficiency PSCs by E-beam-NiOx.\",\"PeriodicalId\":5,\"journal\":{\"name\":\"ACS Applied Materials & Interfaces\",\"volume\":\"33 1\",\"pages\":\"\"},\"PeriodicalIF\":8.2000,\"publicationDate\":\"2025-10-23\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"ACS Applied Materials & Interfaces\",\"FirstCategoryId\":\"88\",\"ListUrlMain\":\"https://doi.org/10.1021/acsami.5c15868\",\"RegionNum\":2,\"RegionCategory\":\"材料科学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"MATERIALS SCIENCE, MULTIDISCIPLINARY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"ACS Applied Materials & Interfaces","FirstCategoryId":"88","ListUrlMain":"https://doi.org/10.1021/acsami.5c15868","RegionNum":2,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"MATERIALS SCIENCE, MULTIDISCIPLINARY","Score":null,"Total":0}
Synergistic Interface Modification of Electron-Beam-Evaporated NiOx for High-Performance Perovskite Solar Cells.
Nickel oxide (NiOx) is considered an ideal hole transport layer (HTL) in inverted perovskite solar cells (PSCs) due to its excellent carrier mobility and low cost. Electron-beam-evaporated NiOx (E-beam-NiOx) exhibits exceptional commercial potential due to its process compatibility. However, there are surface defects in E-beam-NiOx, which are incompatible with perovskite (PVK) and limit its development. In this work, we used [4-(3,6-dimethyl-9H-carbazol-9-yl)butyl]phosphonic acid (Me-4PACz) as a self-assembled monolayer (SAM) and l-α-glycerylphosphorylcholine (GPC) to double modify the buried interface of E-beam-NiOx films. SAM is used to modify interface defects of NiOx, while GPC improves the wetting property and uniformity of the interface. Under the joint modification of SAM and GPC, the interface defects of NiOx films were passivated, and the hole extraction ability of HTL was improved. At the same time, the growth quality of PVK films was improved, and the energy level matching between NiOx and PVK was optimized. After optimization, the small-area (0.0575 cm2) PSCs achieved a champion power conversion efficiency (PCE) of 23.31%, providing an effective strategy and direction for the preparation of high-efficiency PSCs by E-beam-NiOx.
期刊介绍:
ACS Applied Materials & Interfaces is a leading interdisciplinary journal that brings together chemists, engineers, physicists, and biologists to explore the development and utilization of newly-discovered materials and interfacial processes for specific applications. Our journal has experienced remarkable growth since its establishment in 2009, both in terms of the number of articles published and the impact of the research showcased. We are proud to foster a truly global community, with the majority of published articles originating from outside the United States, reflecting the rapid growth of applied research worldwide.