Harnessing nano-particles on thin film CIGS solar cells studied by ultrabroadband pump-probe spectroscopy

碩士 === 國立交通大學 === 電子物理系所 === 104 === In this study, we have employed the ultrabroadband pump-probe spectroscopy to investigate the enhancement of efficiency in CIGS thin film solar cells via nanoparticles. Using the plasmonic effect of gold nano-partilce is an approach to improve the efficiency of C...

Full description

Bibliographic Details
Main Authors: Li, Jia-Xing, 李嘉興
Other Authors: 吳光雄
Format: Others
Language:zh-TW
Published: 2015
Online Access:http://ndltd.ncl.edu.tw/handle/6gu8vh
id ndltd-TW-104NCTU5429003
record_format oai_dc
spelling ndltd-TW-104NCTU54290032019-05-15T22:34:03Z http://ndltd.ncl.edu.tw/handle/6gu8vh Harnessing nano-particles on thin film CIGS solar cells studied by ultrabroadband pump-probe spectroscopy 利用超寬頻激發探測光譜研究奈米粒子提昇銅銦鎵硒薄膜太陽能電池之研究 Li, Jia-Xing 李嘉興 碩士 國立交通大學 電子物理系所 104 In this study, we have employed the ultrabroadband pump-probe spectroscopy to investigate the enhancement of efficiency in CIGS thin film solar cells via nanoparticles. Using the plasmonic effect of gold nano-partilce is an approach to improve the efficiency of CIGS solar cells. Another way is utilizing the down-shifting effect of CdSe quantum dots to enhance the photocurrent. We have performed the ultrabroadband femtosecond pump-probe spectroscopy of CuIn1-xGaxSe2 (CIGS) thin films with and without Au nanoparticles (NPs) incorporation, and elaborately analyzed the lifetimes and zero momentum for the hot carrier relaxation. The signals of enhanced photobleach (PB) and waned photoinduced absorption (PIA) attributed to surface plasmon resonance (SPR) of Au NPs were observed in the transient differential absorption spectrum. This result has suggested the carriers can be considerably excited from ground state to lower energy level. The improvements of electrical transport by suppressing the surface recombination of photoinduced carriers via enhanced local electromagnetic field (LEMF) was also confirmed by extracted hot carrier lifetime and calculated electromagnetic field distribution. Finally, the theoretical calculation for resonant energy transfer (RET)-induced enhancement in probability of exciting electron-hole pairs was conducted and the result is well corresponding to the enhanced PB peak of transient differential absorption in plasmonic CIGS. In CdSe quantum dots CIGS solar cells was observed by an external quantum efficiency, we confirmed the success of the photon down conversion mechanism to enhance optical conversion efficiency. These result has suggested that Surface Plasma Resonance and photon down-conversion mechanism are viable approachs to boosting high-efficiency CIGS solar cells. 吳光雄 2015 學位論文 ; thesis 42 zh-TW
collection NDLTD
language zh-TW
format Others
sources NDLTD
description 碩士 === 國立交通大學 === 電子物理系所 === 104 === In this study, we have employed the ultrabroadband pump-probe spectroscopy to investigate the enhancement of efficiency in CIGS thin film solar cells via nanoparticles. Using the plasmonic effect of gold nano-partilce is an approach to improve the efficiency of CIGS solar cells. Another way is utilizing the down-shifting effect of CdSe quantum dots to enhance the photocurrent. We have performed the ultrabroadband femtosecond pump-probe spectroscopy of CuIn1-xGaxSe2 (CIGS) thin films with and without Au nanoparticles (NPs) incorporation, and elaborately analyzed the lifetimes and zero momentum for the hot carrier relaxation. The signals of enhanced photobleach (PB) and waned photoinduced absorption (PIA) attributed to surface plasmon resonance (SPR) of Au NPs were observed in the transient differential absorption spectrum. This result has suggested the carriers can be considerably excited from ground state to lower energy level. The improvements of electrical transport by suppressing the surface recombination of photoinduced carriers via enhanced local electromagnetic field (LEMF) was also confirmed by extracted hot carrier lifetime and calculated electromagnetic field distribution. Finally, the theoretical calculation for resonant energy transfer (RET)-induced enhancement in probability of exciting electron-hole pairs was conducted and the result is well corresponding to the enhanced PB peak of transient differential absorption in plasmonic CIGS. In CdSe quantum dots CIGS solar cells was observed by an external quantum efficiency, we confirmed the success of the photon down conversion mechanism to enhance optical conversion efficiency. These result has suggested that Surface Plasma Resonance and photon down-conversion mechanism are viable approachs to boosting high-efficiency CIGS solar cells.
author2 吳光雄
author_facet 吳光雄
Li, Jia-Xing
李嘉興
author Li, Jia-Xing
李嘉興
spellingShingle Li, Jia-Xing
李嘉興
Harnessing nano-particles on thin film CIGS solar cells studied by ultrabroadband pump-probe spectroscopy
author_sort Li, Jia-Xing
title Harnessing nano-particles on thin film CIGS solar cells studied by ultrabroadband pump-probe spectroscopy
title_short Harnessing nano-particles on thin film CIGS solar cells studied by ultrabroadband pump-probe spectroscopy
title_full Harnessing nano-particles on thin film CIGS solar cells studied by ultrabroadband pump-probe spectroscopy
title_fullStr Harnessing nano-particles on thin film CIGS solar cells studied by ultrabroadband pump-probe spectroscopy
title_full_unstemmed Harnessing nano-particles on thin film CIGS solar cells studied by ultrabroadband pump-probe spectroscopy
title_sort harnessing nano-particles on thin film cigs solar cells studied by ultrabroadband pump-probe spectroscopy
publishDate 2015
url http://ndltd.ncl.edu.tw/handle/6gu8vh
work_keys_str_mv AT lijiaxing harnessingnanoparticlesonthinfilmcigssolarcellsstudiedbyultrabroadbandpumpprobespectroscopy
AT lǐjiāxìng harnessingnanoparticlesonthinfilmcigssolarcellsstudiedbyultrabroadbandpumpprobespectroscopy
AT lijiaxing lìyòngchāokuānpínjīfātàncèguāngpǔyánjiūnàimǐlìzitíshēngtóngyīnjiāxībáomótàiyángnéngdiànchízhīyánjiū
AT lǐjiāxìng lìyòngchāokuānpínjīfātàncèguāngpǔyánjiūnàimǐlìzitíshēngtóngyīnjiāxībáomótàiyángnéngdiànchízhīyánjiū
_version_ 1719131837560782848