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Bin Ren

Researcher at Xiamen University

Publications -  528
Citations -  30728

Bin Ren is an academic researcher from Xiamen University. The author has contributed to research in topics: Raman spectroscopy & Surface-enhanced Raman spectroscopy. The author has an hindex of 73, co-authored 470 publications receiving 23452 citations. Previous affiliations of Bin Ren include Pacific Northwest National Laboratory & Max Planck Society.

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Correlating the Shape, Surface Plasmon Resonance, and Surface-Enhanced Raman Scattering of Gold Nanorods

TL;DR: In this article, the shape, surface plasmon resonance (SPR), and surface-enhanced Raman scattering (SERS) of gold nanorods (NRs) in dilute colloids were correlated.
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Quantifying Surface Temperature of Thermoplasmonic Nanostructures.

TL;DR: A method capable of measuring the surface temperature of plasmonic nanostructures with surface-enhanced Raman spectroscopy with high spatial resolution is presented, which allows us to successfully monitor the extracellular temperature distribution of a single living cell experiencing cold resistance and the intracellular temperature change during the calcium ion transport process.
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Distinctive Enhanced and Tunable Plasmon Resonant Absorption from Controllable Au@Cu2O Nanoparticles: Experimental and Theoretical Modeling

TL;DR: In this paper, the authors proposed a method to improve the performance of the NFFTBS NFF-TBS project in terms of energy efficiency and energy efficiency in China.
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Transient Electrochemical Surface-Enhanced Raman Spectroscopy: A Millisecond Time-Resolved Study of an Electrochemical Redox Process.

TL;DR: A transient Electrochemical surface-enhanced Raman spectroscopy (TEC-SERS) to monitor the structural evolution of surface species at a time resolution that equals the transient electrochemical methods, so that the Raman signal with the molecular signature information and the electrochemical current signal can be precisely correlated.
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Carbonic Anhydrase Inhibitors with Dual-Tail Moieties To Match the Hydrophobic and Hydrophilic Halves of the Carbonic Anhydrase Active Site

TL;DR: This novel dual-tail approach to carbonic anhydrase II (CA II) inhibitor design has provided an enhanced opportunity to more fully exploit interactions with the CA active site by enabling these molecules to interact with the distinct halves of the active site.