Related Experiment Video
Updated: Aug 6, 2026

Single-Molecule Förster Resonance Energy Transfer Methods for Real-Time Investigation of the Holliday Junction Resolution by GEN1
Published on: September 18, 2019
Reversed Förster Resonance Energy Transfer in ReS2-Based Heterostructures
Shi Guo1, Cheng Sun2, Sung-Gyu Lee1,3
1School of Electrical and Electronic Engineering, Nanyang Technological University, Singapore, 639798, Singapore.
None:
Energy transfer (ET) is central to energy-harvesting and optoelectronic technologies. Conventional Förster resonance energy transfer (FRET) requires substantial spectral overlap between donor emission and acceptor absorption and downhill energy flow. Here, we demonstrate an unconventional FRET process that operates without spectral overlap and enables energy transfer from lower-energy donors to higher-energy acceptors. In ReS2/hBN/TMD (TMD = WSe2, WS2, and MoS2) heterostructures, efficient ET occurs from ReS2 to TMD monolayers despite the lower excitonic energies of ReS2. This reversed FRET originates from high energy excitonic states at the K and M valleys of ReS2 arising from the band-nesting effect, as supported by transient absorption spectroscopy. As a result, over 30-fold photoluminescence enhancement, more than 63% transfer efficiency, and sub-80 ps transfer time are achieved, outperforming most reported systems. Our findings open an unexplored route for engineering interlayer energy flow and enhancing quantum yield low-dimensional materials.
Related Concept Videos
Double Resonance Techniques: Overview
Spin decoupling is usually achieved by...
Photochemical Electrocyclic Reactions: Stereochemistry
Selection Rules: Photochemical Activation
Thermal Electrocyclic Reactions: Stereochemistry
Selection Rules: Thermal Activation
Conjugated systems containing an even number of π-electron pairs undergo a conrotatory ring closure. For example, thermal electrocyclization of (2E,4E)-2,4-hexadiene, a conjugated diene containing two π-electron pairs, gives trans-3,4-dimethylcyclobutene.
Woodward–Hoffmann Selection Rules and Microscopic Reversibility
Thermal and Photochemical Electrocyclic Reactions: Overview
[3,3] Sigmatropic Rearrangement of 1,5-Dienes: Cope Rearrangement

