Related Experiment Video
Updated: Aug 30, 2025

Morphology Control for Fully Printable Organic–Inorganic Bulk-heterojunction Solar Cells Based on a Ti-alkoxide and Semiconducting Polymer
Published on: January 10, 2017
Simultaneously Enhancing Exciton/Charge Transport in Organic Solar Cells by an Organoboron Additive.
Heng Lu1, Kai Chen2,3, Raja Sekhar Bobba4
1School of Materials Science and Engineering, Peking University, Beijing, 100871, China.
Adding trans-bis(dimesitylboron)stilbene (BBS) to organic solar cells (OSCs) enhances exciton diffusion and charge transport. This boosts the power conversion efficiency (PCE) of PM6:Y6-based devices to 17.6%.
Area of Science:
- Materials Science
- Organic Electronics
- Photovoltaics
Background:
- Efficient exciton diffusion and charge transport are crucial for high power conversion efficiency (PCE) in organic solar cells (OSCs).
- The PM6:Y6 system is a widely studied benchmark for OSCs, but further optimization of charge dynamics is needed.
- Understanding and controlling molecular aggregation and energy transfer pathways are key to improving device performance.
Purpose of the Study:
- To investigate the effect of a highly emissive solid additive, trans-bis(dimesitylboron)stilbene (BBS), on exciton/charge transport in PM6:Y6-based OSCs.
- To elucidate the mechanisms by which BBS enhances exciton diffusion, dissociation, and charge transport.
- To achieve improved power conversion efficiency (PCE) in PM6:Y6:BBS devices.
Main Methods:
- Employing trans-bis(dimesitylboron)stilbene (BBS) as a solid additive in PM6:Y6 blend films.
- Utilizing transient gated photoluminescence spectroscopy to study exciton diffusion and dissociation.
- Employing transient absorption spectroscopy to analyze charge generation dynamics.
- Characterizing film morphology and charge-carrier diffusion length using current-sensing atomic force microscopy.
Main Results:
- BBS transforms emissive sites from H-type to J-type aggregates, facilitating resonance energy transfer and exciton diffusion.
- Addition of BBS improves exciton diffusion coefficient and dissociation of PM6 excitons.
- Faster charge generation and improved charge-carrier diffusion length were observed in PM6:Y6:BBS films.
- BBS addition enhances Y6 crystallization.
Conclusions:
- The addition of BBS effectively enhances exciton diffusion, exciton dissociation, charge generation, and charge transport in PM6:Y6 OSCs.
- BBS leads to reduced charge recombination and energy loss, contributing to higher device performance.
- PM6:Y6:BBS devices achieved a significantly improved PCE of 17.6% compared to 16.2% for devices without BBS, with simultaneous improvements in open-circuit voltage, short-circuit current density, and fill factor.
More Related Videos
06:49In situ Grazing Incidence Small Angle X-ray Scattering on Roll-To-Roll Coating of Organic Solar Cells with Laboratory X-ray Instrumentation
Published on: March 2, 2021
11:44Using Cyclic Voltammetry, UV-Vis-NIR, and EPR Spectroelectrochemistry to Analyze Organic Compounds
Published on: October 18, 2018
Related Concept Videos
P-N junction
Hydroboration-Oxidation of Alkenes
Preparation of Alcohols via Addition Reactions
The acid-catalyzed addition of water to the double bond of alkenes is a large-scale industrial method used to synthesize low-molecular-weight alcohols. An acidic atmosphere is required to allow the hydrogen in the water molecule to act as an electrophile and attack the double bond in an alkene. The addition of a proton to the double bond creates a carbocation intermediate. The proton preferentially bonds to the less substituted end of the double bond to create a more stable carbocation...
Photochemical Electrocyclic Reactions: Stereochemistry
Selection Rules: Photochemical Activation
Regioselectivity and Stereochemistry of Hydroboration
Hydroboration proceeds in a concerted fashion with the attack of borane on the π bond, giving a cyclic four-centered transition state. The –BH2 group is bonded to the less substituted carbon and –H to the more substituted carbon. The concerted nature requires the simultaneous addition of –H and –BH2 across the same face of the alkene giving syn...
Electrophilic 1,2- and 1,4-Addition of X2 to 1,3-Butadiene