# Elucidating the Role of the Mixing Entropy in Equilibrated Nanoconfined Reactions

**Authors:** Leonid Rubinovich, Micha Polak

PMC · DOI: 10.3390/e27060564 · Entropy · 2025-05-27

## TL;DR

This paper explores how mixing entropy affects chemical reactions in nanoscale environments, revealing new insights into equilibrium behavior.

## Contribution

The paper introduces a novel concept of fluctuating mixing entropy for nanoreactions and models its interplay with reaction extent.

## Key findings

- A distinct inverse correlation exists between mixing entropy and reaction extent in nanosystems.
- Smallest nanosystems show step-like entropy behavior due to discrete probability distributions.
- The approach is extendable to other confined systems like molecular adsorption and spin polarization.

## Abstract

By introducing the concept of nanoreaction-based fluctuating mixing entropy, the challenge posed by the smallness of a closed molecular system is addressed through equilibrium statistical–mechanical averaging over fluctuating reaction extent. Based on the canonical partition function, the interplay between the mixing entropy and fluctuations in the reaction extent in nanoscale environments is unraveled while maintaining consistency with macroscopic behavior. The nanosystem size dependence of the mixing entropy, the reaction extent, and a concept termed the “reaction extent entropy” are modeled for the combination reactions A+B↔2C and the specific case of H2+I2↔2HI. A distinct inverse correlation is found between the first two properties, revealing consistency with the nanoconfinement entropic effect on chemical equilibrium (NCECE). To obtain the time dependence of the instantaneous mixing entropy following equilibration, the Stochastic Simulation (Gillespie) Algorithm is employed. In particular, the smallest nanosystems exhibit a step-like behavior that deviates significantly from the smooth mean values and is associated with the discrete probability distribution of the reaction extent. As illustrated further for molecular adsorption and spin polarization, the current approach can be extended beyond nanoreactions to other confined systems with a limited number of species.

## Linked entities

- **Chemicals:** H2 (PubChem CID 783), I2 (PubChem CID 807), HI (PubChem CID 24841)

## Full-text entities

- **Chemicals:** I2 (MESH:D007455), 2HI (-)

## Full text

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## Figures

11 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12192152/full.md

## References

37 references — full list in the complete paper: https://tomesphere.com/paper/PMC12192152/full.md

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Source: https://tomesphere.com/paper/PMC12192152