4.8 Review

Spin Selectivity in Photoinduced Charge-Transfer Mediated by Chiral Molecules

Journal

ACS NANO
Volume 13, Issue 5, Pages 4928-4946

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acsnano.9b01876

Keywords

chiral-induced spin selectivity; spin filter; photoluminescence; fluorescence quenching; optoelectronics; photospintronics; molecular spintronics

Funding

  1. National Science Foundation ECCS [1509794]
  2. DOE [ER46430]
  3. BSF-NSF program
  4. Department of Chemistry, IIT Kanpur
  5. Directorate For Engineering [1509794] Funding Source: National Science Foundation
  6. Div Of Electrical, Commun & Cyber Sys [1509794] Funding Source: National Science Foundation

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Optical control and readout of electron spin and spin currents in thin films and nanostructures have remained attractive yet challenging goals for emerging technologies designed for applications in information processing and storage. Recent advances in room-temperature spin polarization using nanometric chiral molecular assemblies suggest that chemically modified surfaces or interfaces can be used for optical spin conversion by exploiting photoinduced charge separation and injection from well-coupled organic chromophores or quantum dots. Using light to drive photoexcited charge-transfer processes mediated by molecules with central or helical chirality enables indirect measurements of spin polarization attributed to the chiral-induced spin selectivity effect and of the efficiency of spin-dependent electron transfer relative to competitive relaxation pathways. Herein, we highlight recent approaches used to detect and to analyze spin selectivity in photoinduced charge transfer including spin-transfer torque for local magnetization, nanoscale charge separation and polarization, and soft ferromagnetic substrate magnetization- and chirality-dependent photoluminescence. Building on these methods through systematic investigation of molecular and environmental parameters that influence spin filtering should elucidate means to manipulate electron spins and photoexcited states for room-temperature optoelectronic and photospintronic applications.

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