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Layer-by-Layer Doping of Few-Layer Graphene Film
Gü,neş,, Fethullah,Shin, Hyeon-Jin,Biswas, Chandan,Han, Gang Hee,Kim, Eun Sung,Chae, Seung Jin,Choi, Jae-Young,Lee, Young Hee American Chemical Society 2010 ACS NANO Vol.4 No.8
<P>We propose a new method of layer-by-layer (LbL) doping of thin graphene films. Large area monolayer graphene was synthesized on Cu foil by using the chemical vapor deposition method. Each layer was transferred on a polyethylene terephthalate substrate followed by a salt-solution casting, where the whole process was repeated several times to get LbL-doped thin layers. With this method, sheet resistance was significantly decreased up to ∼80% with little sacrifice in transmittance. Unlike samples fabricated by topmost layer doping, our sample shows better environmental stability due to the presence of dominant neutral Au atoms on the surface which was confirmed by angle-resolved X-ray photoelectron spectroscopy. The sheet resistance of the LbL-doped four-layer graphene (11 × 11 cm<SUP>2</SUP>) was 54 Ω/sq at 85% transmittance, which meets the technical target for industrial applications.</P><P><B>Graphic Abstract</B> <IMG SRC='http://pubs.acs.org/appl/literatum/publisher/achs/journals/content/ancac3/2010/ancac3.2010.4.issue-8/nn1008808/production/images/medium/nn-2010-008808_0006.gif'></P><P><A href='http://pubs.acs.org/doi/suppl/10.1021/nn1008808'>ACS Electronic Supporting Info</A></P>
Jin Young Kim,Hee-Wang Yoo,Pyung-Gang Lee,SUN-GU LEE,Joo-Hyun Seo,Byung-Gee Kim 한국생물공학회 2019 Biotechnology and Bioprocess Engineering Vol.24 No.1
In vivo protein evolution is a protein engineering approach that is performed by both generating mutagenesis libraries and selecting desired mutants in a cell. Despite its clear advantages in some aspects, the approach has not much been popularized compared to in vitro protein evolution methods which employ in vitro mutagenesis. The reason behind this unpopularity is the limitations in the low library diversity and specificity of in vivo mutagenic methods compared to those of in vitro mutagenic methods. While various non-specific and specific in vitro mutagenic methods, which allowed us to use computational design principles as well as random approach in the design of mutant library, had been developed, in vivo mutagenic methods were stalled at the step of random mutagenesis since the in vivo generation of target-specific library with high specificity and broad mutational spectra is quite challenging. Recently, various in vivo protein mutagenesis methods have been developed to generate rather focused libraries in a target-specific manner, thanks to the significant decrease in the price of oligomer synthesis and better understanding of DNA targeting systems. In this review, we examined the trends of in vivo protein evolution and inspect some of the state-of-the-art techniques that were recently introduced for in vivo protein mutagenesis in a target-specific manner. In vivo protein mutagenesis is a subject undergoing intense study and will become more specific and thorough simultaneously.