# Entropic force

In physics, an entropic force acting in a system is a force resulting from the entire system's thermodynamical tendency to increase its entropy, rather than from a particular underlying microscopic force.[1]

For instance, the internal energy of an ideal gas depends only on its temperature, and not on the volume of its containing box, so it is not an energy effect that tends to increase the volume of the box as gas pressure does. This implies that the pressure of an ideal gas has an entropic origin.[2]

What is the origin of such an entropic force? The most general answer is that the effect of thermal fluctuations tends to bring a thermodynamic system toward a macroscopic state that corresponds to a maximum in the number of microscopic states (or micro-states) that are compatible with this macroscopic state. In other words, thermal fluctuations tend to bring a system toward its macroscopic state of maximum entropy.[2]

## Mathematical formulation

In the canonical ensemble, the entropic force associated to a macrostate partition is given by:[3][4]

where is the temperature, is the entropy associated to the macrostate and is the present macrostate.

## Examples

### Brownian motion

The entropic approach to Brownian movement was initially proposed by R. M. Neumann,[3][5] Neumann derived the entropic force for a particle undergoing three-dimensional Brownian motion using the Boltzmann equation, denoting this force as a diffusional driving force or radial force. In the paper, three example systems are shown to exhibit such a force:

### Polymers

Main article: Ideal chain

A standard example of an entropic force is the elasticity of a freely-jointed polymer molecule.[5] For an ideal chain, maximizing its entropy means reducing the distance between its two free ends. Consequently, a force that tends to collapse the chain is exerted by the ideal chain between its two free ends. This entropic force is proportional to the distance between the two ends.[2][6]

### Hydrophobic force

Water drops on the surface of grass.

Another example of an entropic force is the hydrophobic force. At room temperature, it partly originates from the loss of entropy by the 3D network of water molecules when they interact with molecules of dissolved substance. Each water molecule is capable of

Therefore, water molecules can form an extended three-dimensional network. Introduction of a non-hydrogen-bonding surface disrupts this network. The water molecules rearrange themselves around the surface, so as to minimize the number of disrupted hydrogen bonds. This is in contrast to hydrogen fluoride (which can accept 3 but donate only 1) or ammonia (which can donate 3 but accept only 1), which mainly form linear chains.

If the introduced surface had an ionic or polar nature, there would be water molecules standing upright on 1 (along the axis of an orbital for ionic bond) or 2 (along a resultant polarity axis) of the four sp3 orbitals.[7] These orientations allow easy movement, i.e. degrees of freedom, and thus lowers entropy minimally. But a non-hydrogen-bonding surface with a moderate curvature forces the water molecule to sit tight on the surface, spreading 3 hydrogen bonds tangential to the surface, which then become locked in a clathrate-like basket shape. Water molecules involved in this clathrate-like basket around the non-hydrogen-bonding surface are constrained in their orientation. Thus, any event that would minimize such a surface is entropically favored. For example, when two such hydrophobic particles come very close, the clathrate-like baskets surrounding them merge. This releases some of the water molecules into the bulk of the water, leading to an increase in entropy.

Another related and counter-intuitive example of entropic force is protein folding, which is a spontaneous process and where hydrophobic effect also plays a role.[8] Structures of water-soluble proteins typically have a core in which hydrophobic side chains are buried from water, which stabilizes the folded state.[9] Charged and polar side chains are situated on the solvent-exposed surface where they interact with surrounding water molecules. Minimizing the number of hydrophobic side chains exposed to water is the principal driving force behind the folding process,[9][10] [11] although formation of hydrogen bonds within the protein also stabilizes protein structure.[12][13]

### Colloids

Entropic forces are important and widespread in the physics of colloids,[14] where they are responsible for the depletion force, and the ordering of hard particles, such as the crystallization of hard spheres, the isotropic-nematic transition in liquid crystal phases of hard rods, and the ordering of hard polyhedra.[14][15] Entropic forces arise in colloidal systems due to the osmotic pressure that comes from particle crowding. This was first discovered in, and is most intuitive for, colloid-polymer mixtures described by the Asakura-Oosawa model. In this model, polymers are approximated as finite-sized spheres that can penetrate one another, but cannot penetrate the colloidal particles. The inability of the polymers to penetrate the colloids leads to a region around the colloids in which the polymer density is reduced. If the regions of reduced polymer density around two colloids overlap with one another, by means of the colloids approaching one another, the polymers in the system gain an additional free volume that is equal to the volume of the intersection of the reduced density regions. The additional free volume causes an increase in the entropy of the polymers, and drives them to form locally dense-packed aggregates. A similar effect occurs in sufficiently dense colloidal systems without polymers, where osmotic pressure also drives the local dense packing[14] of colloids into a diverse array of structures [15] that can be rationally designed by modifying the shape of the particles.[16]

## Controversial examples

Some forces that are generally regarded as conventional forces have been argued to be actually entropic in nature. These theories remain controversial and are the subject of ongoing work. Matt Visser, professor of mathematics at Victoria University of Wellington, NZ in "Conservative Entropic Forces" [17] criticizes selected approaches but generally concludes:

There is no reasonable doubt concerning the physical reality of entropic forces, and no reasonable doubt that classical (and semi-classical) general relativity is closely related to thermodynamics. Based on the work of Jacobson, Thanu Padmanabhan, and others, there are also good reasons to suspect a thermodynamic interpretation of the fully relativistic Einstein equations might be possible.

### Gravity

Main article: Entropic gravity

In 2009, Erik Verlinde argued that gravity can be explained as an entropic force.[18] It claimed (similar to Jacobson's result) that gravity is a consequence of the "information associated with the positions of material bodies". This model combines the thermodynamic approach to gravity with Gerard 't Hooft's holographic principle. It implies that gravity is not a fundamental interaction, but an emergent phenomenon.[18]

### Other forces

In the wake of the discussion started by Verlinde, entropic explanations for other fundamental forces have been suggested,[17] including Coulomb's law,[19][20][21] the electroweak and strong forces.[22] The same approach was argued to explain dark matter, dark energy and Pioneer effect.[23]

It was argued that causal entropic forces lead to spontaneous emergence of tool use and social cooperation.[24][25][26] Causal entropic forces by definition maximize entropy production between the present and future time horizon, rather than just greedily maximizing instantaneous entropy production like typical entropic forces.

A formal simultaneous connection between the mathematical structure of the discovered laws of nature, intelligence and the entropy-like measures of complexity was previously noted in 2000 by Andrei Soklakov[27] in the context of Occam's razor principle.

## References

1. A history of thermodynamics: the doctrine of energy and entropy by Ingo Müller, p115
2. Taylor; Tabachnik (2013). "Entropic forces—making the connection between mechanics and thermodynamics in an exactly soluble model". European Journal of Physics. 34 (3).
3. Neumann RM (1980). "Entropic approach to Brownian movement". American Journal of Physics. 48 (5): 354. Bibcode:1980AmJPh..48..354N. doi:10.1119/1.12095.
4. Neumann RM (1977). "The entropy of a single Gaussian macromolecule in a noninteracting solvent". The Journal of Chemical Physics. 66 (2): 870. Bibcode:1977JChPh..66..870N. doi:10.1063/1.433923.
5. Smith, SB; Finzi, L; Bustamante, C (1992). "Direct mechanical measurements of the elasticity of single DNA molecules by using magnetic beads". Science. 258 (5085): 1122–6. Bibcode:1992Sci...258.1122S. doi:10.1126/science.1439819. PMID 1439819.
6. Encyclopedia of Life Science Article on Hydrophobic Effect; See Figure 4: http://xibalba.lcg.unam.mx/~rgalindo/bioquimica/BQPosgrado2011/I%20FQ%20repaso/HydrophobicEffect.pdf
7. http://www.wiley.com/college/pratt/0471393878/student/review/thermodynamics/7_relationship.html
8. Pace CN, Shirley BA, McNutt M, Gajiwala K (1 January 1996). "Forces contributing to the conformational stability of proteins". FASEB J. 10 (1): 75–83. PMID 8566551.
9. Compiani M, Capriotti E (Dec 2013). "Computational and theoretical methods for protein folding" (PDF). Biochemistry. 52 (48): 8601–24. doi:10.1021/bi4001529. PMID 24187909.
10. Callaway, David J. E. (1994). "Solvent-induced organization: a physical model of folding myoglobin". Proteins: Structure, Function, and Bioinformatics. 20 (1): 124–138. arXiv:. doi:10.1002/prot.340200203. PMID 7846023.
11. Rose GD, Fleming PJ, Banavar JR, Maritan A (2006). "A backbone-based theory of protein folding". Proc. Natl. Acad. Sci. U.S.A. 103 (45): 16623–33. doi:10.1073/pnas.0606843103. PMC . PMID 17075053.
12. Gerald Karp (2009). Cell and Molecular Biology: Concepts and Experiments. John Wiley and Sons. pp. 128–. ISBN 978-0-470-48337-4.
13. van Anders, Greg; Klotsa, Daphne; Ahmed, N. Khalid; Engel, Michael; Glotzer, Sharon C. (2014). "Understanding shape entropy through local dense packing". Proc Natl Acad Sci USA. 111: E4812–E4821. arXiv:. doi:10.1073/pnas.1418159111.
14. Damasceno, Pablo F.; Engel, Michael; Glotzer, Sharon C. (2012). "Predictive Self-Assembly of Polyhedra into Complex Structures". Science. 337: 453–457. arXiv:. doi:10.1126/science.1220869.
15. van Anders, Greg; Ahmed, N. Khalid; Smith, Ross; Engel, Michael; Glotzer, Sharon C. (2014). "Entropically Patchy Particles: Engineering Valence through Shape Entropy". ACS Nano. 8: 931–940. arXiv:. doi:10.1021/nn4057353.
16. Visser, Matt. "Conservative entropic forces". arXiv:.
17. E.P. Verlinde. "On the Origin of Gravity and the Laws of Newton". JHEP. 2011 (04): 29. arXiv:. Bibcode:2011JHEP...04..029V. doi:10.1007/JHEP04(2011)029.
18. http://arxiv.org//abs/1001.4965, Coulomb Force as an Entropic Force, T. Wang
19. http://arxiv.org//abs/0809.4631, Simple field theoretical approach of Coulomb systems. Entropic effects, D. di Caprio, J.P. Badiali, M. Holovko
20. http://arxiv.org//abs/1009.5561, Entropic Corrections to Coulomb's Law, A. Sheykhi, S. H. Hendi
21. http://arxiv.org//abs/1008.4147, Emergent Gauge Fields, Peter G.O. Freund
22. http://arxiv.org//abs/1009.1506 Unification of Dark Matter and Dark Energy in a Modified Entropic Force Model, Zhe Chang, Ming-Hua Li, Xin Li
23. Wissner-Gross, A.D.; Freer, C.E. (2013). "Causal Entropic Forces" (PDF). Physical Review Letters. 110 (16). Bibcode:2013PhRvL.110p8702W. doi:10.1103/PhysRevLett.110.168702.
24. http://arxiv.org/abs/1308.4375, Comment on Phys. Rev. Lett. 110, 168702 (2013): Causal Entropic Forces, E. Canessa
25. http://arxiv.org/abs/1312.4185, Comment: Causal entropic forces, H.J. Kappen
26. Andrei N. Soklakov, "Occam's razor as a formal basis for a physical theory" (arXiv:math-ph/0009007, September 2000; Foundations of Physics Letters, 2002), "Complexity analysis for algorithmically simple strings" (arXiv:cs/0009001, September 2000).