Cheng-Kang Mai
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Previous Organizations / Institutes
The organizations / institutes from the scholar's other articles in the past ten years
Cheng-Kang Mai has a total of 65 co-authors. Here are the top co-authors by number of shared publications:
- Guillermo Carlos Bazan
Department of Chemistry National University of Singapore Singapore Singapore
10 shared publications Guillermo C. Bazan
Center for Polymers and Organic Solids, Department of Chemistry and Biochemistry, University of California, Santa Barbara, CA 93106, USA
8 shared publicationsStephanie L. Fronk
Department of Chemistry and Biochemistry , University of California , Santa Barbara , CA 93106 , USA
6 shared publicationsHuiqiong Zhou
Center for Polymers and Organic Solids, University of California Santa Barbara, Santa Barbara, CA, 93106, USA
5 shared publicationsYuan Zhang
Center for Polymers and Organic Solids University of California Santa Barbara Santa Barbara CA 93106 USA
5 shared publicationsAlan J. Heeger
Center for Polymers and Organic Solids, University of California, Santa Barbara, Santa Barbara, California 93106, United States
4 shared publications
Latest Publications
- 8 January 2019
- Published by Fundacio Scito
Ultrafast Properties of a Self-Doped Conjugated Polyelectrolyte
- 8 January 2019
- Published by Fundacio Scito
Ultrafast Properties of a Self-Doped Conjugated Polyelectrolyte
- Open Access
- 9 December 2015
- Published by Royal Society of Chemistry (RSC) in Chemical Science
- Vol. 7 (3) , 1914-1919
Tethered tertiary amines as solid-state n-type dopants for solution-processable organic semiconductors
Tertiary amines covalently tethered to electron-deficient aromatic molecules by alkyl spacers enable solid-state n-doping.
- 9 December 2015
- Published by Royal Society of Chemistry (RSC) in Chemical Science
- Vol. 7 (3) , 1914-1919
Open AccessTethered tertiary amines as solid-state n-type dopants for solution-processable organic semiconductors
Tertiary amines covalently tethered to electron-deficient aromatic molecules by alkyl spacers enable solid-state n-doping.
- 30 November 2015
- Published by Royal Society of Chemistry (RSC) in Chemical Communications
- Vol. 52 (11) , 2237-2240
One-pot synthesis of semicrystalline/amorphous multiblock copolymers via divinyl-terminated telechelic polyolefins
A one-pot synthesis of random semicrystalline/amorphous multiblock copolymers is demonstrated via acyclic diene metathesis (ADMET) polymerization of α,ω-divinyl-terminated telechelic polyolefins.
- 30 November 2015
- Published by Royal Society of Chemistry (RSC) in Chemical Communications
- Vol. 52 (11) , 2237-2240
One-pot synthesis of semicrystalline/amorphous multiblock copolymers via divinyl-terminated telechelic polyolefins
A one-pot synthesis of random semicrystalline/amorphous multiblock copolymers is demonstrated via acyclic diene metathesis (ADMET) polymerization of α,ω-divinyl-terminated telechelic polyolefins.
- 28 September 2015
- Published by Royal Society of Chemistry (RSC) in Chemical Communications
- Vol. 51 (99) , 17607-17610
Electrical properties of doped conjugated polyelectrolytes with modulated density of the ionic functionalities
We report the synthesis of a series of water soluble anionic narrow band-gap conjugated polyelectrolytes with a varied density of the ionic functional groups.
- 28 September 2015
- Published by Royal Society of Chemistry (RSC) in Chemical Communications
- Vol. 51 (99) , 17607-17610
Electrical properties of doped conjugated polyelectrolytes with modulated density of the ionic functionalities
We report the synthesis of a series of water soluble anionic narrow band-gap conjugated polyelectrolytes with a varied density of the ionic functional groups.
- 21 September 2015
- Published by American Chemical Society (ACS) in Macromolecules
- Vol. 48 (19) , 7383-7384
Correction to End-Group-Mediated Aggregation of Poly(3-hexylthiophene)
- 21 September 2015
- Published by American Chemical Society (ACS) in Macromolecules
- Vol. 48 (19) , 7383-7384
Correction to End-Group-Mediated Aggregation of Poly(3-hexylthiophene)
- 19 August 2015
- Published by American Chemical Society (ACS) in Macromolecules
- Vol. 48 (17) , 6224-6232
End-Group-Mediated Aggregation of Poly(3-hexylthiophene)
- 19 August 2015
- Published by American Chemical Society (ACS) in Macromolecules
- Vol. 48 (17) , 6224-6232
End-Group-Mediated Aggregation of Poly(3-hexylthiophene)
- 6 August 2015
- Published by Royal Society of Chemistry (RSC) in Journal of Materials Chemistry B
- Vol. 3 (37) , 7340-7346
Narrow band gap conjugated polyelectrolytes for photothermal killing of bacteria
We report the demonstration of antimicrobial conjugated polyelectrolytes (CPEs) with high NIR absorbance for selective and efficient photothermal killing of bacteria over mammalian cells. The antimicrobial CPE possessing quaternary ammonium (QA) terminated side chains (P1) shows higher binding preference and increased dark toxicity towards Gram-positive and Gram-negative bacteria over mammalian cells. Bestowed by π-conjugated backbones, P1 exhibits a high molar absorptivity of 39.8 L g−1 cm−1 at 808 nm with an efficient photothermal conversion efficiency of 33 ± 1%. Upon 808 nm laser irradiation, P1 shows enhanced bactericidal effects, but not to mammalian cells. Although the anionic CPE counterpart with the same polymer backbone but sulfonate terminated side chains (P2) possesses a similar photothermal conversion ability, it exhibits much lower antibacterial effects due to its low binding affinity. This study thus reveals that bacteria–CPE electrostatic interactions play a major role in bacterial recognition, although hydrophobic interactions also contribute.
- 6 August 2015
- Published by Royal Society of Chemistry (RSC) in Journal of Materials Chemistry B
- Vol. 3 (37) , 7340-7346
Narrow band gap conjugated polyelectrolytes for photothermal killing of bacteria
We report the demonstration of antimicrobial conjugated polyelectrolytes (CPEs) with high NIR absorbance for selective and efficient photothermal killing of bacteria over mammalian cells. The antimicrobial CPE possessing quaternary ammonium (QA) terminated side chains (P1) shows higher binding preference and increased dark toxicity towards Gram-positive and Gram-negative bacteria over mammalian cells. Bestowed by π-conjugated backbones, P1 exhibits a high molar absorptivity of 39.8 L g−1 cm−1 at 808 nm with an efficient photothermal conversion efficiency of 33 ± 1%. Upon 808 nm laser irradiation, P1 shows enhanced bactericidal effects, but not to mammalian cells. Although the anionic CPE counterpart with the same polymer backbone but sulfonate terminated side chains (P2) possesses a similar photothermal conversion ability, it exhibits much lower antibacterial effects due to its low binding affinity. This study thus reveals that bacteria–CPE electrostatic interactions play a major role in bacterial recognition, although hydrophobic interactions also contribute.
- Open Access
- 17 June 2015
- Published by Springer Nature in Nature Communications
- Vol. 6 (1) , 7348
Conjugated polyelectrolyte hole transport layer for inverted-type perovskite solar cells
Organic–inorganic hybrid perovskite materials offer the potential for realization of low-cost and flexible next-generation solar cells fabricated by low-temperature solution processing. Although efficiencies of perovskite solar cells have dramatically improved up to 19% within the past 5 years, there is still considerable room for further improvement in device efficiency and stability through development of novel materials and device architectures. Here we demonstrate that inverted-type perovskite solar cells with pH-neutral and low-temperature solution-processable conjugated polyelectrolyte as the hole transport layer (instead of acidic PEDOT:PSS) exhibit a device efficiency of over 12% and improved device stability in air. As an alternative to PEDOT:PSS, this work is the first report on the use of an organic hole transport material that enables the formation of uniform perovskite films with complete surface coverage and the demonstration of efficient, stable perovskite/fullerene planar heterojunction solar cells.
- 17 June 2015
- Published by Springer Nature in Nature Communications
- Vol. 6 (1) , 7348
Open AccessConjugated polyelectrolyte hole transport layer for inverted-type perovskite solar cells
Organic–inorganic hybrid perovskite materials offer the potential for realization of low-cost and flexible next-generation solar cells fabricated by low-temperature solution processing. Although efficiencies of perovskite solar cells have dramatically improved up to 19% within the past 5 years, there is still considerable room for further improvement in device efficiency and stability through development of novel materials and device architectures. Here we demonstrate that inverted-type perovskite solar cells with pH-neutral and low-temperature solution-processable conjugated polyelectrolyte as the hole transport layer (instead of acidic PEDOT:PSS) exhibit a device efficiency of over 12% and improved device stability in air. As an alternative to PEDOT:PSS, this work is the first report on the use of an organic hole transport material that enables the formation of uniform perovskite films with complete surface coverage and the demonstration of efficient, stable perovskite/fullerene planar heterojunction solar cells.
- 30 April 2015
- Published by Royal Society of Chemistry (RSC) in Energy & Environmental Science
- Vol. 8 (8) , 2341-2346
Varying the ionic functionalities of conjugated polyelectrolytes leads to both p- and n-type carbon nanotube composites for flexible thermoelectrics
Selective doping of single-walled carbon nanotubes can be achieved by varying pendant ionic functionalities of conjugated polyelectrolytes.
- 30 April 2015
- Published by Royal Society of Chemistry (RSC) in Energy & Environmental Science
- Vol. 8 (8) , 2341-2346
Varying the ionic functionalities of conjugated polyelectrolytes leads to both p- and n-type carbon nanotube composites for flexible thermoelectrics
Selective doping of single-walled carbon nanotubes can be achieved by varying pendant ionic functionalities of conjugated polyelectrolytes.
- Top Cited Papers
- 21 January 2015
- Published by Wiley in Advanced Materials
- Vol. 27 (10) , 1767-1773
Polymer Homo‐Tandem Solar Cells with Best Efficiency of 11.3%
Rational materials design and interface engineering are both essential to realize a high performance for tandem cells. Two identical bulk heterojunctions are connected in series using novel interconnection layers combining pH-neutral conjugated polyelectrolytes and a thin film of ZnO nanoparticles by a solution process. The best performing tandem cells achieve a power conversion efficiency of 11.3%, with 25% enhancement in efficiency compared with single cells, which arises primarily from the increased light absorption.
- 21 January 2015
- Published by Wiley in Advanced Materials
- Vol. 27 (10) , 1767-1773
Top Cited PapersPolymer Homo‐Tandem Solar Cells with Best Efficiency of 11.3%
Rational materials design and interface engineering are both essential to realize a high performance for tandem cells. Two identical bulk heterojunctions are connected in series using novel interconnection layers combining pH-neutral conjugated polyelectrolytes and a thin film of ZnO nanoparticles by a solution process. The best performing tandem cells achieve a power conversion efficiency of 11.3%, with 25% enhancement in efficiency compared with single cells, which arises primarily from the increased light absorption.