# Collective behavior in the kinetics and equilibrium of solid-state photoreaction

Source: [Collective behavior in the kinetics and equilibrium of solid-state photoreaction](<https://www.sota2.com/research/paper/68fa3dd81e209131ce8e36d1>)

Collection index: [llms.txt](<https://www.sota2.com/research/llms.txt>)

Data updated: 2025-10-25T01:44:02.732Z

Authors: Ruobing Bai, Ying Shi Teh, Kaushik Bhattacharya

Published: 2020-11-02T16:03:56.000Z

## Abstract

There is current interest in developing photoactive materials that deform on illumination and can thus be used for photomechanical actuation. This is attractive since it can be affected at a distance, different frequencies can be used to actuate different modes and to sense, and corrosion-free lightweight fiber optic cables can deliver significant power over long distances. The strategy for developing new photomechanical materials is to first develop photoactive molecules in solution, and then to incorporate these in the solid-state either by crystallization or by inserting them into polymers. This letter shows that the kinetics and the nature of the photo-induced phase transitions are profoundly different in single molecules (solution) and in the solid state using a lattice spin model. In solution, where the molecules act independently, the photoreaction follows first-order kinetics. However, in the solid state where the photoactive molecules interact with each other and therefore behave collectively during reaction, photoreactions follow the sigmoidal kinetics of nucleation and growth as in a first-order phase transition. Further, we find that the exact nature of the photo-induced strain has a critical effect on the kinetics, equilibrium, and microstructure formation. These predictions agree qualitatively with experimental observations, and provide insights for the development of new photoactive materials.

## Recorded benchmark results

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## Original sources and implementation

[Original paper](<https://arxiv.org/abs/2011.01072>)

[PDF](<https://arxiv.org/pdf/2011.01072.pdf>)
