Skip to main content

A perspective on auxetic nanomaterials

Abstract

Nanomaterials have recently been found to exhibit auxetic behavior, or a negative Poisson’s ratio, whereby the lateral dimensions of the material expand, rather than shrink, in response to applied tensile loading. In this brief review, we use the form of question–answer to highlight key points and outstanding issues related to the field of auxetic nanomaterials.

1 What are auxetic materials and why are they of interest?

Most materials, when subject to tensile mechanical forces, elongate in the direction of the applied force, and contract in the directions normal to the applied force. This phenomenon is described mathematically by the Poisson’s ratio \(\nu \). In two-dimensions, if a material is stretched in the x-direction, it would contract in the y-direction, and its Poisson’s ratio would be defined as \(\nu _{xy}=-\epsilon _{y}/\epsilon _{x}\), where \(\epsilon \) is the strain in either the x- or y-directions. The Poisson’s ratio is typically positive because the strain normal to the applied load \(\epsilon _{y}\), is usually negative. Classical elasticity theory does allow for a negative Poisson’s ratio (NPR), and the Poisson’s ratio for isotropic materials can lie in the range \(-1< \nu < 0.5\).

Materials that expand in the lateral directions in response to an applied tensile force were termed auxetic by Evans [1]. Beginning with seminal experiments of Lakes, who demonstrated NPR in a foam structure [2], various structures and materials have been shown to exhibit the NPR phenomenon [3,4,5,6,7,8,9,10,11,12,13,14,15].

Auxetic materials have been widely studied for a range of target applications due to this unique mechanical property. Auxetic materials also may have enhanced shear resistance, indentation resistance, fracture toughness, and enhanced damping of wave propagation and vibration transmission in periodic auxetic structures [16, 17].

2 What mechanisms for auxetic behavior in bulk materials have been observed to hold in nanomaterials?

One of the first mechanisms for enabling auxetic behavior in bulk materials was developed by Lakes, in which a structural foam was engineering to exhibit auxetic behavior via a microstructure containing a re-entrant unit cell with two orthogonal hinges. When this structure is under mechanical tension, one of the hinges opens along the tensile axis, whereas the other hinge expands in the lateral direction, resulting in a negative Poisson’s ratio in the out-of-plane direction [2].

Interestingly, certain two-dimensional (2D) nanomaterials have an intrinsic crystal structure that precisely mimics the re-entrant hinge mechanism first utilized by Lakes. One example is black phosphorus, which has, as shown in Fig. 1, a puckered lattice structure [18], with the two hinges formed by the angles \(\theta _{546}\) and \(\theta _{214}\), thus demonstrating a nanoscale version of the re-entrant hinge mechanism.

Fig. 1
figure 1

(Reproduced with permission from Jiang and Park [18]. Copyright 2014 Macmillan Publishers Ltd.)

The evolution of local structure in single-layer BP during uniaxial tension in the y-direction. a BP is stretched in the y-direction, i.e. atoms are moved in the direction of the attached arrows (blue online). b To accommodate the tension in the y-direction, BP contracts in the x-direction, i.e. atoms 1 and 4 move inward along the attached arrows (red online). The 1–4 bond thus becomes more closely aligned with the vertical (z)-direction. The green arrows display the movement of the four surrounding atoms following the movement of atoms 1 and 4

Black phosphorus is not the only puckered two-dimensional material. Other such materials include orthorhombic arsenic [19], borophane [20], and also the monochalcogenides, like GeSe and SnS [21].

Bulk materials have also been successfully patterned through cutting techniques to induce NPR [8, 22,23,24,25], and this approach also has produced similar success in creating NPR nanomaterials. Figure 2 illustrates this for patterned graphene, which exhibits NPR because the internal units rotate in response to the applied strain.

Fig. 2
figure 2

(Reproduced with permission from Ho et al. [43]. Copyright 2016, Wiley-VCH)

Patterned porous graphene under uniaxial loading. Size = 24.6 × 24.7 nm2. Configurations of the patterned porous graphene at strain a \(\epsilon =0\) and b \(\epsilon =0.1\) under uniaxial loading in the zigzag direction

3 What new mechanisms for auxetic behavior emerge at the nanoscale?

One of the distinct nanoscale effects that strongly impacts the mechanical properties of nanomaterials is the surface stress (or edge stress for 2D materials) [26, 27], which result from the fact that surface atoms have fewer bonding neighbors than atoms that lie within the material bulk. Edge buckling due to edge stresses has been found to induce NPR in narrow graphene ribbons [28], as illustrated in Fig. 3. Similarly, surface stresses have previously been shown to induce phase transformations [29], as well as shape memory and pseudoelasticity in metal nanostructures [30, 31], and were recently shown to, by inducing phase transformations in metal nanoplates, induce auxetic behavior in the metal nanostructures, including nanoplates [32, 33] and nanowires [34].

Fig. 3
figure 3

(Reprinted (adapted) with permission from Jiang and Park [28]. Copyright (2016) American Chemical Society)

Poisson’s ratio for graphene from Set I. a Strain dependence for Poisson’s ratio. Inset displays the strain–strain relation for graphene with width 29.51 Å, in which graphene expands in the y-direction when it is stretched in the x-direction by strain smaller than \(\epsilon _c=0.005\), indicating the NPR effect. b The strain dependence for the z positions of two atoms in the peak (valley) of the warped edge in graphene. Data are fitted to functions \(z=\pm b_0\sin [\theta _0(1-\epsilon /\epsilon _c)]\) with constraint \(b_0=z_0/\sin \theta _0\). Inset displays these two atoms; i.e. the atom on the peak (red arrow) and valley (blue arrow) of the warped edge. Both atoms fall into the graphene plane for strain larger than \(\epsilon _c\). c Width dependence for the Poisson’s ratio. Inset shows the critical strain in graphene ribbons of different width

2D nanomaterials, due to being only a single, or few atoms thick, are mechanically resistant to in-plane stretching, but can easily be induced to deform out of the 2D plane due to their small bending modulus [35, 36]. Thus, one mechanism that has been widely exploited to generate NPR in 2D materials, is that of rippling. Rippling induces NPR in 2D materials because in-plane stretching causes the ripples to flatten, and an expansion of the in-plane dimensions, resulting in a NPR.

Rippling-induced NPR has been generated in 2D materials in various ways, including thermally-induced ripples [37], introduction of 5-8-5 double vacancies in graphene [38] and hydrogenation of graphene [39]. The mechanism by which rippling induced by vacancies in graphene leads to NPR is illustrated in Fig. 4.

Fig. 4
figure 4

(Reproduced with permission from Grima et al. [38]. Copyright 2016 Wiley-VCH)

a Typical images of a crumpled sheet of paper at different levels of applied strain and b typical images of a graphene sheet having 3.0% defects at different levels of applied strain. Note that both systems undergo a de-wrinkling process so as to assume a more planar conformation resulting in an in-plane negative Poisson’s ratio

4 What are the key challenges and open issues?

There are many possibilities and challenges in the field of auxetic nanomaterials, particularly since the first report of NPR in a single-crystal nanomaterial occurred only in 2014 for both black phosphorus and metal nanoplates. One key challenge is in determining how an in-plane NPR can be induced in nanomaterials. This is because currently, essentially all examples of NPR reported so far for nanomaterials are out-of-plane, i.e. via the rippling mechanism, and also the hinge mechanism for black phosphorus. However, very few reports of in-plane NPR have emerged. For example, transition metal dichalcogenides MX2 (MoSe2, MoTe2, WSe2, WTe2, TcTe2, ReSe2, and ReTe2) shows in-plane auxeticity in the elastic range [40], and pristine graphene [41] and semi-fluorinated graphene [42] exhibit in-plane auxeticity for large tensile strains exceeding about 6 and 9%, respectively.

Another question that emerges is to move past the discovery phase of NPR in nanomaterials, and to develop a mechanistic understanding of how to controllably tune the NPR in nanomaterials, either by controllably altering the structure of nanomaterials, most likely via cutting and patterning.

Finally, most reports of NPR have so-far been in 2D materials. However, the mechanisms for NPR in 2D materials, which to-date have primarily exploited the low bending modulus to achieve an out-of-plane NPR, may not be operant for other nanomaterials, like 1D nanowires. Thus, it remains to be determined what new mechanisms can be found for other important nanomaterials.

References

  1. K.E. Evans, Endeavour 15(4), 170 (1991)

    Article  Google Scholar 

  2. R.S. Lakes, Science 235, 1038 (1987)

    Article  Google Scholar 

  3. L. Rothenburg, A.A. Berlint, R.J. Bathurst, Nature 354, 470 (1991)

    Article  Google Scholar 

  4. R. Lakes, Adv. Mater. 5, 293 (1993)

    Article  Google Scholar 

  5. R.H. Baughman, D.S. Galvao, Nature 365, 735 (1993)

    Article  Google Scholar 

  6. K.E. Evans, A. Alderson, Adv. Mater. 12(9), 617 (2000)

    Article  Google Scholar 

  7. W. Yang, Z.M. Li, W. Shi, B.H. Xie, M.B. Yang, J. Mater. Sci. 39, 3269 (2004)

    Article  Google Scholar 

  8. N. Ravirala, A. Alderson, K.L. Alderson, J . Mater. Sci. 42, 7433 (2007)

    Article  Google Scholar 

  9. Z.A. Lethbridge, R.I. Walton, A.S. Marmier, C.W. Smith, K.E. Evans, Acta Mater. 58, 6444 (2010)

    Article  Google Scholar 

  10. K. Bertoldi, P.M. Reis, S. Willshaw, T. Mullin, Adv. Mater. 22, 361 (2010)

    Article  Google Scholar 

  11. K. Alderson, A. Alderson, S. Anand, V. Simkins, S. Nazare, N. Ravirala, Phys. Status Solidi B 249(7), 1322 (2012)

    Article  Google Scholar 

  12. A. Clausen, F. Wang, J.S. Jensen, O. Sigmund, J.A. Lewis, Adv. Mater. 27, 5523 (2015)

    Article  Google Scholar 

  13. F. Milstein, K. Huang, Phys. Rev. B 19(4), 2030 (1979)

    Article  Google Scholar 

  14. R.H. Baughman, J.M. Shacklette, A.A. Zakhidov, S. Stafstrom, Nature 392, 362 (1998)

    Article  Google Scholar 

  15. J.W. Jiang, S.Y. Kim, H.S. Park, Appl. Phys. Rev. 3, 041101 (2016)

    Article  Google Scholar 

  16. K.K. Saxena, R. Das, E.P. Calius, Adv. Eng. Mater. 18(11), 1847 (2016)

    Article  Google Scholar 

  17. C. Huang, L. Chen, Adv. Mater. 28, 8079 (2016)

    Article  Google Scholar 

  18. J.W. Jiang, H.S. Park, Nat. Commun. 5, 4727 (2014)

    Google Scholar 

  19. J. Han, J. Xie, Z. Zhang, D. Yang, M. Si, D. Xue, Appl. Phys. Expr. 8(4), 041801 (2015)

    Article  Google Scholar 

  20. L. Kou, Y. Ma, C. Tang, Z. Sun, A. Du, C. Chen, Nano Lett. 16(12), 7910 (2016)

    Article  Google Scholar 

  21. P.Z. Hanakata, A. Carvalho, D.K. Campbell, H.S. Park, Phys. Rev. B 94, 035304 (2016)

    Article  Google Scholar 

  22. J.N. Grima, K.E. Evans, J. Mater. Sci. Lett. 19, 1563 (2000)

    Article  Google Scholar 

  23. C.W. Smith, J.N. Grima, K.E. Evans, Acta Mater. 48, 4349 (2000)

    Article  Google Scholar 

  24. N. Gaspar, X. Ren, C. Smith, J. Grima, K. Evans, Acta Mater. 53, 2439 (2005)

    Article  Google Scholar 

  25. J.N. Grima, K. Evans, J. Mater. Sci. 41, 3193 (2006)

    Article  Google Scholar 

  26. R.C. Cammarata, Prog. Surf. Sci. 46(1), 1 (1994)

    Article  Google Scholar 

  27. W. Haiss, Rep. Prog. Phys. 64, 591 (2001)

    Article  Google Scholar 

  28. J.W. Jiang, H.S. Park, Nano Lett. 16, 2657 (2016)

    Article  Google Scholar 

  29. J. Diao, K. Gall, M.L. Dunn, Nat. Mater. 2, 656 (2003)

    Article  Google Scholar 

  30. H.S. Park, K. Gall, J.A. Zimmerman, Phys. Rev. Lett. 95(25), 255504 (2005)

    Article  Google Scholar 

  31. W. Liang, M. Zhou, F. Ke, Nano Lett. 5(10), 2039 (2005)

    Article  Google Scholar 

  32. D.T. Ho, S.D. Park, S.Y. Kwon, K. Park, S.Y. Kim, Nat. Commun. 5, 3255 (2014)

    Google Scholar 

  33. D.T. Ho, H. Kim, S.Y. Kwon, S.Y. Kim, Phys. Status Solidi B 252(7), 1492 (2015)

    Article  Google Scholar 

  34. D.T. Ho, S.Y. Kwon, S.Y. Kim, Sci. Rep. 6, 27560 (2016)

    Article  Google Scholar 

  35. Q. Lu, M. Arroyo, R. Huang, J. Phys. D 42, 102002 (2009)

    Article  Google Scholar 

  36. J.W. Jiang, Z. Qi, H.S. Park, T. Rabczuk, Nanotechnology 24, 435705 (2013)

    Article  Google Scholar 

  37. K.V. Zakharchenko, M.I. Katsnelson, A. Fasolino, Phys. Rev. Lett. 102(4), 046808 (2009)

    Article  Google Scholar 

  38. J.N. Grima, S. Winczewski, L. Mizzi, M.C. Grech, R. Cauchi, R. Gatt, D. Attard, K.W. Wojciechowski, J. Rybicki, Adv. Mater. 27, 1455 (2015)

    Article  Google Scholar 

  39. J.W. Jiang, T. Chang, X. Guo, Nanoscale 8, 15948 (2016)

    Article  Google Scholar 

  40. L. Yu, Q. Yan, A. Ruzsinszky, https://arxiv.org/abs/1701.06529 (2017)

  41. J.W. Jiang, T. Chang, X. Guo, H.S. Park, Nano Lett. 16, 5286 (2016)

    Article  Google Scholar 

  42. R. Qin, J. Zheng, W. Zhu, Nanoscale 9, 128 (2017)

    Article  Google Scholar 

  43. V.H. Ho, D.T. Ho, S.Y. Kwon, S.Y. Kim, Phys. Status Solidi B 253(7), 1303 (2016)

    Article  Google Scholar 

Download references

Authors’ contributions

HSP and SYK wrote the manuscript. Both authors read and approved the final manuscript.

Acknowledgements

HSP acknowledges helpful discussions with Prof. Jin-Wu Jiang.

Competing interests

The authors declare that they have no competing interests.

Funding

S.Y.K. acknowledges the support from the Mid-Career Researcher Support Program (Grant No. 2014R1A2A2A09052374) of the National Research Foundation (NRF) of Korea.

Publisher’s Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Harold S. Park.

Rights and permissions

Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Park, H.S., Kim, S.Y. A perspective on auxetic nanomaterials. Nano Convergence 4, 10 (2017). https://doi.org/10.1186/s40580-017-0104-3

Download citation

  • Received:

  • Accepted:

  • Published:

  • DOI: https://doi.org/10.1186/s40580-017-0104-3

Keywords