Atomically thin metal oxide Titania as electrontransporting layer for Perovskite Solar Cells

碩士 === 國立臺灣大學 === 材料科學與工程學研究所 === 105 === A recently emerging class of solid-state hybrid organic–inorganic perovskite-based solar cells,using CH3NH3PbX3(X=Cl,Br,I) as light harvesting materials, had demonstrated remarkably high power conversion efficiencies of nearly 21%. Most state-of-the-art pero...

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Main Authors: CHUNG-WEI LIN, 林忠緯
Other Authors: CHUN-WEI CHEN
Format: Others
Language:zh-TW
Published: 2016
Online Access:http://ndltd.ncl.edu.tw/handle/31629514907756147120
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spelling ndltd-TW-105NTU051590022017-03-25T04:37:13Z http://ndltd.ncl.edu.tw/handle/31629514907756147120 Atomically thin metal oxide Titania as electrontransporting layer for Perovskite Solar Cells 利用原子級厚度二氧化鈦金屬氧化物作為鈣鈦礦電池之電子傳輸層 CHUNG-WEI LIN 林忠緯 碩士 國立臺灣大學 材料科學與工程學研究所 105 A recently emerging class of solid-state hybrid organic–inorganic perovskite-based solar cells,using CH3NH3PbX3(X=Cl,Br,I) as light harvesting materials, had demonstrated remarkably high power conversion efficiencies of nearly 21%. Most state-of-the-art perovskite solar cells typically have a device structure that is based on a hightemperature sintered metal oxide(compact TiO2) as electron transporting layer(ETL) which may cause the limitation of perovskite solar cells to be deposited on flexible substrates and affect their compatibility with fabrication processes in multi-junction solar cells. In this work, the utilization of atomically thin titania (atomic Ti0.87O2) deposited at room temperature as an ultra-thin electron transporting layer in perovskite solar cell was demonstrated.Through Langmuir-Blodgett deposition process at room temperature,atomic Ti0.87O2 was conformally deposited on FTO substrate with a high coverage and eliminated the requirement of high temperature process (over 500C) to deposit compact TiO2. The incorporation of multi-layer Ti0.87O2 (around 5 nm) effectively decreased the recombination of electron and hole and leaded to a reduced leakage current. This resulted in a promising device performance (14.05%) that is compatible to the device fabricated using high-temperature sintered metal oxide as electron selection layer. More importantly, we find devices using atomic Ti0.87O2 as electron transporting layer have a better stability in atomsphere. After 30 days, the atomic Ti0.87O2 devices remain about 70% of their original efficiency, unlike compact TiO2 devices, which remain 10% of original efficiency. With the atomic Ti0.87O2 electron transporting layer, we can successfully make a whole low temperature solution process, an atomically thin film ETL, and a stable deivces. CHUN-WEI CHEN 陳俊維 2016 學位論文 ; thesis 91 zh-TW
collection NDLTD
language zh-TW
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description 碩士 === 國立臺灣大學 === 材料科學與工程學研究所 === 105 === A recently emerging class of solid-state hybrid organic–inorganic perovskite-based solar cells,using CH3NH3PbX3(X=Cl,Br,I) as light harvesting materials, had demonstrated remarkably high power conversion efficiencies of nearly 21%. Most state-of-the-art perovskite solar cells typically have a device structure that is based on a hightemperature sintered metal oxide(compact TiO2) as electron transporting layer(ETL) which may cause the limitation of perovskite solar cells to be deposited on flexible substrates and affect their compatibility with fabrication processes in multi-junction solar cells. In this work, the utilization of atomically thin titania (atomic Ti0.87O2) deposited at room temperature as an ultra-thin electron transporting layer in perovskite solar cell was demonstrated.Through Langmuir-Blodgett deposition process at room temperature,atomic Ti0.87O2 was conformally deposited on FTO substrate with a high coverage and eliminated the requirement of high temperature process (over 500C) to deposit compact TiO2. The incorporation of multi-layer Ti0.87O2 (around 5 nm) effectively decreased the recombination of electron and hole and leaded to a reduced leakage current. This resulted in a promising device performance (14.05%) that is compatible to the device fabricated using high-temperature sintered metal oxide as electron selection layer. More importantly, we find devices using atomic Ti0.87O2 as electron transporting layer have a better stability in atomsphere. After 30 days, the atomic Ti0.87O2 devices remain about 70% of their original efficiency, unlike compact TiO2 devices, which remain 10% of original efficiency. With the atomic Ti0.87O2 electron transporting layer, we can successfully make a whole low temperature solution process, an atomically thin film ETL, and a stable deivces.
author2 CHUN-WEI CHEN
author_facet CHUN-WEI CHEN
CHUNG-WEI LIN
林忠緯
author CHUNG-WEI LIN
林忠緯
spellingShingle CHUNG-WEI LIN
林忠緯
Atomically thin metal oxide Titania as electrontransporting layer for Perovskite Solar Cells
author_sort CHUNG-WEI LIN
title Atomically thin metal oxide Titania as electrontransporting layer for Perovskite Solar Cells
title_short Atomically thin metal oxide Titania as electrontransporting layer for Perovskite Solar Cells
title_full Atomically thin metal oxide Titania as electrontransporting layer for Perovskite Solar Cells
title_fullStr Atomically thin metal oxide Titania as electrontransporting layer for Perovskite Solar Cells
title_full_unstemmed Atomically thin metal oxide Titania as electrontransporting layer for Perovskite Solar Cells
title_sort atomically thin metal oxide titania as electrontransporting layer for perovskite solar cells
publishDate 2016
url http://ndltd.ncl.edu.tw/handle/31629514907756147120
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