Chin-Hung Lai

Dr. Chin-Hung Lai

Department of Medical Applied Chemistry, Chung Shan Medical University, Taichung, Taiwan
orcid

Research Focus & Metrics

Academic Career Length

26Years (2001-Present)

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

Representative Publications

View All Publications
5 February 2008 in Chemistry of Materials
Verified
Journal Article
Closed access
K. R. Justin ThomasK. R. Justin Thomas
K. R. Justin Thomas
YHYing-Chan Hsu
Ying-Chan Hsu
JLJiann T. Lin
Jiann T. Lin
Kun-Mu LeeKun-Mu Lee
Kun-Mu Lee
KHKuo-Chuan Ho
Kuo-Chuan Ho
PCPi-Tai Chou
Pi-Tai Chou

19 February 2009 in Advanced Functional Materials
Verified
Journal Article
Closed access
PDF file
CCChen‐Han Chien
Chen‐Han Chien
CCChing‐Kun Chen
Ching‐Kun Chen
FHFang‐Ming Hsu
Fang‐Ming Hsu
CSChing‐Fong Shu
Ching‐Fong Shu
PCPi-Tai Chou
Pi-Tai Chou
Chin-Hung LaiChin-Hung Lai
Chin-Hung Lai

24 September 2008 in Chemical Communications
Verified
Journal Article
Closed access
PDF file
WLWei-Hsin Liu
Wei-Hsin Liu
IWI-Che Wu
I-Che Wu
Chin-Hung LaiChin-Hung Lai
Chin-Hung Lai
CLCheng-Hsuan Lai
Cheng-Hsuan Lai
PCPi-Tai Chou
Pi-Tai Chou
Yun CHIYun CHI
Yun CHI
3,4-Ethylenedioxythiophene and bis[2-(2-methoxyethoxy)ethoxy]thiophene bridged donor–acceptor molecules for dye-sensitized solar cells have been synthesized, one of which achieved a solar-to-energy conversion efficiency of 7.3%, compared to 7.7% optimized for N719 dye.

1 September 2009 in Advanced Functional Materials
Verified
Journal Article
Closed access
PDF file
FHFang‐Ming Hsu
Fang‐Ming Hsu
CCChen‐Han Chien
Chen‐Han Chien
CSChing‐Fong Shu
Ching‐Fong Shu
Chin-Hung LaiChin-Hung Lai
Chin-Hung Lai
CHCheng‐Chih Hsieh
Cheng‐Chih Hsieh
PCPi-Tai Chou
Pi-Tai Chou

15 September 2006 in Chemical Communications
Verified
Journal Article
Closed access
PDF file
KCKew-Yu Chen
Kew-Yu Chen
CHCheng-Chih Hsieh
Cheng-Chih Hsieh
YCYi-Ming Cheng
Yi-Ming Cheng
Chin-Hung LaiChin-Hung Lai
Chin-Hung Lai
PCPi-Tai Chou
Pi-Tai Chou
Via a systematic derivatization of the excited-state intramolecular proton-transfer system, 10-hydroxybenzo[h] quinoline, the proton-transfer emission can be extensively tuned from 550 nm (1) to 675 nm (6), in which amplified spontaneous emission was readily observed for 1–3, generating a new family of proton transfer laser dyes.

3 August 2009 in Advanced Functional Materials
Verified
Journal Article
Closed access
PDF file
MVMarappan Velusamy
Marappan Velusamy
JSJiun‐Yi Shen
Jiun‐Yi Shen
JLJiann T. Lin
Jiann T. Lin
YLYi‐Chih Lin
Yi‐Chih Lin
CHCheng‐Chih Hsieh
Cheng‐Chih Hsieh
JHJong‐Kai Hsiao
Jong‐Kai Hsiao