Futureofdynamicrandom Accessmemoryasmainmemory
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Seong Keun Kim, Center for Electronic Materials, Korea Institute of Science and Technology, South Korea; s.k.kim@kist.re.kr
Mihaela Popovici, Semiconductor Technology and Systems Unit, IMEC, Belgium; mihaela.ioana.popovici@imec.be
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A
C = ε0 k , (1)
tphys
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with the thermal budget required in the DRAM fabrication relatively high work function (∼4.8 eV), and the ease with
process (<600°C). However, when grown on RuO2 conduc- which Ru can be dry etched is also advantageous for pat-
tive oxide, rutile TiO2 phase with similar lattice parameters terning the electrodes. The use of Ru as the electrode has
crystallizes at deposition temperatures (i.e., 250°C) owing to shown possibilities of lowering Jg.54–56 Forming a continu-
the template effect displayed by the substrate,12,13,37,38 thus ous and smooth Ru layer on oxides at a low Ru thickness
reducing both the EOT and Jg.12,15,34 Nevertheless, the scalabil- of <5 nm is difficult because of its high surface energy.
ity of tphys is limited to 10–12 nm. Doping TiO2 with Al11,39–42 Morphological issues such as blisters, which often occur
could further reduce Jg, leading to further reduction in tphys to on ALD Ru on oxides, must also be addressed for electrode
∼7 nm.39,41 application of Ru.57
A doping approach could also be considered for other Conducting oxides such as RuO2 and SrRuO3 have also
dielectrics (e.g., HfO2 and ZrO2). Dopants with lower elec- attracted attention as potential electrodes. The work func-
tronegativities and larger ionic radii than those correspond- tion of RuO2 and SrRuO3 is even higher than that of Ru,
ing to the host oxide led to higher-k and a reduction of Jg which is favorable for low Jg. In particular, the structural
for HfO243–45 and ZrO2.46,47 Higher symmetry phases are coherency with promising high-k materials (e.g., rutile
formed via doping (such as tetragonal or cubic) leading to TiO2/RuO213,58,59 and SrTiO3/SrRuO360,61) provides concur-
larger k, while the lower Jg was attributed to the shift of the rent decreases in EOT and Jg. However, these conducting
charge states of the oxygen vacancies into the conduction oxides have not yet been practically used in DRAM capaci-
bands.47 tors. Those Ru-containing oxides are easily reduced during
As previously described, continued downscaling of DRAM the back-end process, because of the weak bonding between
technology toward the sub-20-nm technology node will require ruthenium and oxygen. Ta-doped SnO2 has recently been sug-
a low tphys of ≤5 nm. At such a low thickness, other character- gested as a reduction-resistant oxide electrode for DRAM
istics of the capacitors become important, including electrode capacitors.62 Capacitors composed of rutile TiO2/Ta-doped
and dielectric surface roughness, lattice mismatch, and chemi- SnO2 stack showed both excellent dielectric properties and
cal compatibility of electrode/dielectric. A summary of the thermal stability in experiments.
lowest EOT – Jg – tphys at ±1 V for ALD dielectrics is given
in Figure 3c.17,20,41,48–51 This shows that the nanolaminates’ Summary and outlook
approach combining a high bandgap with a high-k dielectric DRAM is the representative memory used in modern com-
leads to the lowest Jg when thinning the dielectric. However, puters, but it appears to be facing serious challenges for
for tphys ≤ 5 nm, the nanolaminate approach is less likely to be further scaling toward the ∼10-nm technology node. Much
an option because of intermixing of the layers under the thermal effort has been dedicated to prolonging its scaling. Structural
budget applied to the capacitor. modification of cell transistors has been attempted to suppress
Comprehensive ab initio calculations of the bandgap and Jg and lower the bit-line capacitance. Transition of the cell
k52 (namely the generalized gradient approximation for band- architecture to 4 F2 has also been suggested for further DRAM
gap and local density approximation for k) showed that cubic scaling. To satisfy the stringent requirements of capacitors in
BeO can display the highest-k (∼300) and bandgap values ∼10-nm technology nodes, new higher-k dielectrics and elec-
(>9 eV). However, the cubic rock-salt structure of BeO is a trodes have been extensively investigated. Although high-k
high-pressure phase; therefore, stabilization under ambient oxides such as TiO2 and SrTiO3 show potential for further
conditions is required. Efforts are being devoted to depositing scaling of DRAM, their large Jg has to be resolved at a low
a high-bandgap BeO by ALD;53 however, no high-k material thickness of <5 nm. A new dielectric material with both large
has yet been achieved. bandgap (over ∼5 eV) and large k (>50) should be designed
for the ∼10-nm technology node. Otherwise, downscaling
Electrodes in DRAM capacitor of DRAM might end at approximately the 15-nm technol-
Further reduction in Jg can also be attained by electrode ogy node.
engineering. The electrode in a DRAM capacitor should Although the scaling of DRAM will eventually end, DRAM
have a high work function and a sharp interface between might maintain its status as the main memory for a long
the electrode and dielectric for better dielectric perfor- time. The market for infrastructure such as servers, stor-
mance. TiN, grown by ALD using TiCl4 and NH3, currently age, and networking continues to grow rapidly. Bandwidth
functions as the electrode in DRAM capacitors. However, is the major challenge of DRAM for those applications.
the work function of TiN is insufficient to suppress Jg at the Although die stacking with conventional wire bonding has
thin dielectric thickness required in the ∼10-nm technol- limited data-transfer rates, the emergence of high-bandwidth
ogy node. Therefore, much effort has also been devoted to memory (HBM) through-silicon-via technology shows great
developing new electrodes, including noble metal and con- promise with much improved data rates and reduced power
ducting oxide electrodes. Among noble metals, ruthenium consumption. Die stacking of DRAM in the form of HBM
(Ru) is considered the most promising for DRAM capacitor could be the future of this long-standing main memory, fol-
electrodes. Ru is favorable for suppressing Jg because of its lowing the end of DRAM scaling.
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Acknowledgments 25. A. Kosola, M. Putkonen, L.-S. Johansson, L. Niinistö, Appl. Surf. Sci.
211, 102 (2003).
S.K.K. acknowledges support from the Future Semiconduc- 26. O.S. Kwon, S.K. Kim, M. Cho, C.S. Hwang, J. Jeong, J. Electrochem. Soc.
tor Device Technology Development Program (10047231) 152, C229 (2005).
27. O.S. Kwon, S.W. Lee, J.H. Han, C.S. Hwang, J. Electrochem. Soc. 154, G127
funded by the Ministry of Trade, Industry & Energy of South (2007).
Korea and the Korea Semiconductor Research Consortium, 28. W. Lee, J.H. Han, W. Jeon, Y.W. Yoo, S.W. Lee, S.K. Kim, C.H. Ko, C. Lansalot-
and from the National Research Foundation of Korea Grant Matras, C.S. Hwang, Chem. Mater. 25, 953 (2013).
29. V.V. Longo, N.N. Leick, F.F. Roozeboom, W.E. Kessels, ECS J. Solid State Sci.
funded by the Korean government (NRF-2018R1A2B2007525). Technol. 2, N15 (2013).
30. M. Popovici, B. Kaczer, V.V. Afanas’ev, G. Sereni, L. Larcher, A. Redolfi,
S.V. Elshocht, M. Jurczak, Phys. Status Solidi Rapid Res. Lett. 10, 420 (2016).
References 31. S.W. Lee, J.H. Han, S. Han, W. Lee, J.H. Jang, M. Seo, S.K. Kim, C. Dussarrat,
1. C.S. Hwang, Adv. Electron. Mater. 1, 1400056 (2015).
J. Gatineau, Y.-S. Min, C.S. Hwang, Chem. Mater. 23, 2227 (2011).
2. International Technology Roadmap for Semiconductors (2013), http://www.
32. W. Lee, J.H. Han, S.W. Lee, S. Han, W.J. Jeon, C.S. Hwang, J. Mater. Chem.
itrs2.net. 22, 15037 (2012).
3. J.Y. Kim, C.S. Lee, S.E. Kim, I.B. Chung, Y.M. Choi, B.J. Park, J.W. Lee, 33. W. Lee, W. Jeon, C.H. An, M.J. Chung, H.J. Kim, T. Eom, S.M. George, B.K. Park,
D.I. Kim, Y.S. Hwang, D.S. Hwang, H.K. Hwang, J.M. Park, D.H. Kim, N.J. Kang, J.H. Han, C.G. Kim, T.-M. Chung, S.W. Lee, C.S. Hwang, Chem. Mater. 27, 3881
M.H. Cho, M.Y. Jeong, H.J. Kim, J.N. Han, S.Y. Kim, B.Y. Nam, H.S. Park, (2015).
S.H. Chung, J.H. Lee, J.S. Park, H.S. Kim, Y.J. Park, K. Kim, Symp. VLSI Technol. 34. S.K. Kim, S.Y. Lee, M. Seo, G.J. Choi, C.S. Hwang, J. Appl. Phys. 102,
Dig. Tech. Pap. (2003), p. 11. 024109 (2007).
4. J.V. Kim, H.J. Oh, D.S. Woo, Y.S. Lee, D.H. Kim, S.E. Kim, G.W. Ha, H.J. Kim, 35. W.D. Kim, G.W. Hwang, O.S. Kwon, S.K. Kim, M. Cho, D.S. Jeong, S.W. Lee,
N.J. Kang, J.M. Park, Y.S. Hwang, D.I. Kim, B.J. Park, M. Huh, B.H. Lee, M.H. Seo, C.S. Hwang, Y.S. Min, Y.J. Cho, J. Electrochem. Soc. 152, C552
S.B. Kim, M.H. Cho, M.Y. Jung, Y.I. Kim, C. Jin, D.W. Shin, M.S. Shim, C.S. Lee, (2005).
W.S. Lee, J.C. Park, G.Y. Jin, Y.J. Park, K. Kim, Symp. VLSI Technol. Dig. Tech. 36. M. Kadoshima, M. Hiratani, Y. Shimamoto, K. Torii, H. Miki, S. Kimura,
Pap. (2005), p. 34. T. Nabatame, Thin Solid Films 424, 224 (2003).
5. C. Lee, J.C. Park, S.H. Park, S.S. Lee, S.D. Hong, I.G. Kim, Y.J. Choi, T.W. Lee, 37. M. Popovici, J. Swerts, K. Tomida, D. Radisic, M.-S. Kim, B. Kaczer,
G.Y. Jin, K. Kim, International Conference on Solid State Devices and Materials O. Richard, H. Bender, A. Delabie, A. Moussa, C. Vrancken, K. Opsomer, A. Franquet,
(Tsukuba, Japan, 2007), p. 228. M.A. Pawlak, M. Schaekers, L. Altimime, S. Van Elshocht, J.A. Kittl, Phys. Status
6. K.-H. Park, K.-R. Han, J.-H. Lee, IEEE Electron Device Lett. 26, 690 (2005). Solidi Rapid Res. Lett. 5, 19 (2011).
7. C.M. Yang, C.K. Wei, Y.J. Chang, T.C. Wu, H.P. Chen, C.S. Lai, IEEE Trans. 38. S.K. Kim, G.W. Hwang, W.D. Kim, C.S. Hwang, Electrochem. Solid-State
Device Mater. Reliab. 16, 685 (2016). Lett. 9, F5 (2006).
8. C.S. Hwang, S.K. Kim, S.W. Lee, in Atomic Layer Deposition for Semiconduc- 39. S.K. Kim, G.J. Choi, S.Y. Lee, M. Seo, S.W. Lee, J.H. Han, H.S. Ahn, S. Han,
tors, C.S. Hwang, Ed. (Springer, Boston, 2014), chap. 4. C.S. Hwang, Adv. Mater. 20, 1429 (2008).
9. T. Schloesser, F. Jakubowski, J.V. Kluge, A. Graham, S. Slesazeck, M. Popp, 40. S.K. Kim, G.J. Choi, J.H. Kim, C.S. Hwang, Chem. Mater. 20, 3723
P. Baars, K. Muemmler, P. Moll, K. Wilson, A. Buerke, D. Koehler, J. Radecker, (2008).
E. Erben, U. Zimmermann, T. Vorrath, B. Fischer, G. Aichmayr, R. Agaiby, 41. W. Jeon, S. Yoo, H.K. Kim, W. Lee, C.H. An, M.J. Chung, C.J. Cho, S.K. Kim,
W. Pamler, T. Schster, W. Bergner, W. Mueller, Proc. IEEE Int. Electron Dev. Mtg. C.S. Hwang, ACS Appl. Mater. Interfaces 6, 21632 (2014).
(IEDM) (San Francisco, CA, 2008), p. 1. 42. G.J. Choi, S.K. Kim, S.J. Won, H.J. Kim, C.S. Hwang, J. Electrochem. Soc.
10. H. Chung, H. Kim, H. Kim, K. Kim, S. Kim, K.W. Song, J. Kim, Y.C. Oh, 156, G138 (2009).
Y. Hwang, H. Hong, G.Y. Jin, C. Chung, Proc. Eur. Solid-State Dev. Res. Conf. 43. S. Chen, Z. Liu, L. Feng, X. Che, X. Zhao, J. Rare Earths 32, 580 (2014).
(ESSDERC) (IEEE, Helsinki, Finland, 2011), p. 211. 44. W.-H. Kim, M.-K. Kim, I.-K. Oh, W.J. Maeng, T. Cheon, S.-H. Kim, A. Noori,
11. S.K. Kim, S.W. Lee, J.H. Han, B. Lee, S. Han, C.S. Hwang, Adv. Funct. Mater. D. Thompson, S. Chu, H. Kim, J. Am. Ceram. Soc. 97, 1164 (2014).
20, 2989 (2010). 45. S. Govindarajan, T.S. Böscke, P. Sivasubramani, P.D. Kirsch, B.H. Lee,
12. S.K. Kim, W.D. Kim, K.M. Kim, C.S. Hwang, J. Jeong, Appl. Phys. Lett. 85, H.-H. Tseng, R. Jammy, U. Schröder, S. Ramanathan, B.E. Gnade, Appl. Phys.
4112 (2004). Lett. 91, 062906 (2007).
13. K. Fröhlich, J. Aarik, M. Ťapajna, A. Rosová, A. Aidla, E. Dobročka, K. Hušková, 46. L. Lamagna, C. Wiemer, S. Baldovino, A. Molle, M. Perego, S. Schamm-
J. Vac. Sci. Technol. B 27, 266 (2009). Chardon, P.E. Coulon, M. Fanciulli, Appl. Phys. Lett. 95, 122902 (2009).
14. N. Menou, M. Popovici, S. Clima, K. Opsomer, W. Polspoel, B. Kaczer, 47. B.-E. Park, I.-K. Oh, C. Mahata, C.W. Lee, D. Thompson, H.-B.-R. Lee,
G. Rampelberg, K. Tomida, M.A. Pawlak, C. Detavernier, D. Pierreux, J. Swerts, W.J. Maeng, H. Kim, J. Alloys Compd. 722, 307 (2017).
J.W. Maes, D. Manger, M. Badylevich, V. Afanasiev, T. Conard, P. Favia, H. Bender, 48. M. Popovici, J. Swerts, A. Redolfi, B. Kaczer, M. Aoulaiche, I. Radu,
B. Brijs, W. Vandervorst, S.V. Elshocht, G. Pourtois, D.J. Wouters, S. Biesemans, S. Clima, J.-L. Everaert, S.V. Elshocht, M. Jurczak, Appl. Phys. Lett. 104,
J.A. Kittl, J. Appl. Phys. 106, 094101 (2009). 082908 (2014).
15. M. Popovici, M.-S. Kim, K. Tomida, J. Swerts, H. Tielens, A. Moussa, 49. R. Padmanabhan, S. Mohan, Y. Morozumi, S. Kaushal, N. Bhat, IEEE Trans.
O. Richard, H. Bender, A. Franquet, T. Conard, L. Altimime, S.V. Elshocht, J.A. Kittl, Electron Devices 63, 3928 (2016).
Microelectron. Eng. 88, 1517 (2011). 50. Y. Shin, K.K. Min, S.-H. Lee, S.K. Lim, J.S. Oh, K.-J. Lee, K. Hong, B.J. Cho,
16. M.A. Pawlak, J. Swerts, M. Popovici, B. Kaczer, M.-S. Kim, W.-C. Wang, Appl. Phys. Lett. 98, 173505 (2011).
K. Tomida, B. Govoreanu, J. Delmotte, V.V. Afanas’ev, M. Schaekers, W. Vandervorst, 51. J.-H. Ahn, S.-H. Kwon, ACS Appl. Mater. Interfaces 7, 15587 (2015).
J.A. Kittl, Appl. Phys. Lett. 101, 042901 (2012). 52. K. Yim, Y. Yong, J. Lee, K. Lee, H.-H. Nahm, J. Yoo, C. Lee, C.S. Hwang,
17. J. Swerts, M. Popovici, B. Kaczer, M. Aoulaiche, A. Redolfi, S. Clima, C. Caillat, S. Han, NPG Asia Mater. 7, e190 (2015).
W.C. Wang, V.V. Afanas’ev, N. Jourdan, C. Olk, H. Hody, S.V. Elshocht, M. Jurczak, 53. W.C. Lee, C.J. Cho, S. Kim, E.S. Larsen, J.H. Yum, C.W. Bielawski, C.S. Hwang,
IEEE Electron Device Lett. 35, 753 (2014). S.K. Kim, J. Phys. Chem. C 121, 17498 (2017).
18. S.K. Kim, K.M. Kim, D.S. Jeong, W. Jeon, K.J. Yoon, C.S. Hwang, J. Mater. 54. J. Swerts, A. Delabie, M.M. Salimullah, M. Popovici, M.-S. Kim, M. Schaekers,
Res. 28, 313 (2013). S. Van Elshocht, ECS Solid State Lett. 1, P19 (2012).
19. K.H. Kuesters, M.F. Beug, U. Schroeder, N. Nagel, U. Bewersdorff, G. Dallmann, 55. J.H. Han, S.W. Lee, G.-J. Choi, S.Y. Lee, C.S. Hwang, C. Dussarrat, J. Gatineau,
S. Jakschik, R. Knoefler, S. Kudelka, C. Ludwig, D. Manger, W. Mueller, A. Tilke, Adv. Chem. Mater. 21, 207 (2009).
Eng. Mater. 11, 241 (2009). 56. G.J. Choi, S.K. Kim, S.Y. Lee, W.Y. Park, M. Seo, B.J. Choi, C.S. Hwang,
20. S. Knebel, M. Pešić, K. Cho, J. Chang, H. Lim, N. Kolomiiets, V.V. Afanas’ev, J. Electrochem. Soc. 156, G71 (2009).
U. Muehle, U. Schroeder, T. Mikolajick, J. Appl. Phys. 117, 224102 (2015). 57. J.-Y. Kim, D.-S. Kil, J.-H. Kim, S.-H. Kwon, J.-H. Ahn, J.-S. Roh, S.-K. Park,
21. D.S. Kil, H.S. Song, K.J. Lee, K. Hong, J.H. Kim, K.S. Park, S.J. Yeom, J.S. Roh, J. Electrochem. Soc. 159, H560 (2012).
N.J. Kwak, H.C. Sohn, J.W. Kim, S.W. Park, Symp. VLSI Technol. Dig. Tech. Pap. 58. J.H. Han, S. Han, W. Lee, S.W. Lee, S.K. Kim, J. Gatineau, C. Dussarrat,
(2006), p. 38. C.S. Hwang, Appl. Phys. Lett. 99, 022901 (2011).
22. J. Robertson, Eur. Phys. J. Appl. Phys. 28, 265 (2004). 59. J.-H. Kim, D.-S. Kil, S.-J. Yeom, J.-S. Roh, N.-J. Kwak, J.-W. Kim, Appl.
23. M. Popovici, S. Van Elshocht, N. Menou, J. Swerts, D. Pierreux, A. Delabie, Phys. Lett. 91, 052908 (2007).
B. Brijs, T. Conard, K. Opsomer, J.W. Maes, D.J. Wouters, J.A. Kittl, J. Electrochem. 60. S. Schmelzer, D. Bräuhaus, S. Hoffmann-Eifert, P. Meuffels, U. Böttger,
Soc. 157, G1 (2010). L. Oberbeck, P. Reinig, U. Schröder, R. Waser, Appl. Phys. Lett. 97, 132907
24. D.S. Kil, J.M. Lee, J.S. Roh, Chem. Vap. Depos. 8, 195 (2002). (2010).
338
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Future of dynamic random-access memory as main memory
61. D. Popescu, B. Popescu, G. Jegert, S. Schmelzer, U. Boettger, P. Lugli, IEEE Mihaela Popovici has been a senior researcher
Trans. Electron Devices 61, 2130 (2014). in the Semiconductor Technology and Sys-
62. C.J. Cho, M.-S. Noh, W.C. Lee, C.H. An, C.-Y. Kang, C.S. Hwang, S.K. Kim, tems Unit at IMEC, Belgium, since 2007. She
J. Mater. Chem. C 5, 9405 (2017). received her BSc and MSc degrees in chemi-
cal engineering and her PhD degree in materials
science and engineering in 2004 at Politehnica
University of Timisoara, Romania. She com-
pleted postdoctoral research at Philips Research,
Seong Keun Kim has been a principal researcher The Netherlands, in the Photonic Materials
in the Center for Electronic Materials at the and Devices Department. Her research focuses
Korea Institute of Science and Technology, on dielectric oxides and metal thin-film devel-
South Korea, since 2012. He received his BSc opment, physical and electrical characteriza-
degree in 2001 and PhD degree in 2007, both in tion, and design of complex materials stacks
materials science and engineering from Seoul with applications in microelectronic electronic
National University, South Korea. From 2007 to devices. She has an h-index of 15. Popovici can be reached by email at
2009, he worked as an Alexander von Humboldt mihaela.ioana.popovici@imec.be.
Research Fellow at Forschungszentrum Jülich,
Germany. In 2010, he joined Argonne National
Laboratory as a postdoctoral researcher. His
current research interests include high-k dielec-
trics and novel electrodes, atomic layer deposi-
tion of those materials, and thin-film transistors
utilizing oxides and two-dimensional metal chalcogenides. He has published
more than 120 papers. Kim can be reached by email at s.k.kim@kist.re.kr.
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