Wei E. I. Sha

Prof. Wei E. I. Sha

College of Information Science and Electronic Engineering, Zhejiang University, Hangzhou, China
orcid

Research Focus & Metrics

Academic Career Length

21Years (2006-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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8 May 2012 in Advanced Materials
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Journal Article
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XLXuanhua Li
Xuanhua Li
WCWallace Choy
Wallace Choy
LHLijun Huo
Lijun Huo
FXFengxian Xie
Fengxian Xie
WSWei E. I. Sha
Wei E. I. Sha
YYYang Yang
Yang Yang

1 June 2015 in Applied Physics Letters
Verified
Journal Article
Open access
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WSWei E. I. Sha
Wei E. I. Sha
Xingang RenXingang Ren
Xingang Ren
LCLuzhou Chen
Luzhou Chen
WCWallace Choy
Wallace Choy
With the consideration of photon recycling effect, the efficiency limit of methylammonium lead iodide (CH3NH3PbI3) perovskite solar cells is predicted by a detailed balance model. To obtain convincing predictions, both AM 1.5 spectrum of Sun and experimentally measured complex refractive index of perovskite material are employed in the detailed balance model. The roles of light trapping and angular restriction in improving the maximal output power of thin-film perovskite solar cells are also clarified. The efficiency limit of perovskite cells (without the angular restriction) is about 31%, which approaches to Shockley-Queisser limit (33%) achievable by gallium arsenide (GaAs) cells. Moreover, the Shockley-Queisser limit could be reached with a 200 nm-thick perovskite solar cell, through integrating a wavelength-dependent angular-restriction design with a textured light-trapping structure. Additionally, the influence of the trap-assisted nonradiative recombination on the device efficiency is investigated. The work is fundamentally important to high-performance perovskite photovoltaics.

9 July 2021 in Science Advances
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Journal Article
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QCQi Cao
Qi Cao
YLYongjiang Li
Yongjiang Li
Hong ZhangHong Zhang
Hong Zhang
JYJiabao Yang
Jiabao Yang
JHJian Han
Jian Han
MGMichael Grätzel
Michael Grätzel
A star-shaped polymer enables inverted perovskite solar cells with efficiency over 22% and a very high fill factor of 0.862.

6 January 2013 in Advanced Functional Materials
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Journal Article
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XLXuanhua Li
Xuanhua Li
WCWallace Choy
Wallace Choy
HLHaifei Lu
Haifei Lu
WSWei E. I. Sha
Wei E. I. Sha
AHAaron Ho Pui Ho
Aaron Ho Pui Ho

7 September 2011 in Journal of Materials Chemistry
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Journal Article
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DFDixon D. S. Fung
Dixon D. S. Fung
LQLinfang Qiao
Linfang Qiao
WCWallace Choy
Wallace Choy
CWChuandao Wang
Chuandao Wang
WSWei E. I. Sha
Wei E. I. Sha
Sailing HeSailing He
Sailing He
We unveil new device physics and provide details of device mechanisms by investigating polymer solar cells (PSCs) incorporating Au nanoparticles (NPs) into the hole collection poly(3,4-ethylenedioxythiophene) poly(styrenesulfonate) (PEDOT:PSS) layer. Theoretical and experimental results show that the very strong near field around Au NPs due to Localized Surface Plasmonic Resonance (LSPR) mainly distributes laterally along the PEDOT:PSS layer rather than vertically into the adjacent active layer, leading to minimal enhancement of light absorption in the active layer. This finding can be extended to a typical class of solar cells incorporating metallic NPs in spacing layers adjacent to the active layer. With optical effects proven to be minor contributors to device performance improvements, we investigate the electrical properties of the PSCs and obtain insights into the detailed device mechanisms. Improvements in power conversion efficiency (PCE) of solar cells are found to originate from the enlarged active layer/PEDOT:PSS interfacial area and improved PEDOT:PSS conductivity. At high NP concentrations, reduced exciton quenching at donor/acceptor junctions is found to cause PCE deterioration. Our findings indicate that it is highly important to investigate both optical and electrical effects for understanding and optimizing PSC performances.

27 June 2018 in Journal of Optics
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Journal Article
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NPNicolae Panoiu
Nicolae Panoiu
WSWei E. I. Sha
Wei E. I. Sha
DLDangyuan Lei
Dangyuan Lei
GLG-C Li
G-C Li