MANA International Symposium 2025


Semiconductor Materials - 08

Title

Realization of a Highly Reactive Sulfur Source Using a Plasma Cracking Cell and Growth of Group-IV Chalcogenide Thin Films

Author's photo

Authors

Ryo Matsumura, Naoki Fukata

Affiliations

Nanostructured Semiconducting Materials Group, MANA, NIMS

URL

https://www.nims.go.jp/nanosemicon/english/index.html

Abstract

Group-IV chalcogenide materials such as tin sulfide (SnSx) and germanium sulfide (GeSx) have attracted significant attention due to their wide range of potential applications, including next-generation transistors, solar cells, and anode materials for lithium-ion batteries. Various growth techniques have been reported, such as vapor-phase deposition [1] and reactive sputtering [2]. In this study, we investigated molecular beam deposition (MBD), which enables deposition under high vacuum conditions with high cleanliness and excellent controllability of film thickness.

In the experiments, Si(100) substrates with a 100-nm thermal oxide layer were cleaned and then introduced into an MBD chamber (base pressure: ~10-6 Pa). During deposition, substrates were heated at temperatures ranging from room temperature (RT) to 500 °C, while Sn and S were co-supplied to form SnSx films [Fig. 1]. Here, while a solid K-cell was used as the Sn source, since elemental sulfur typically exists in a stable 8-membered ring structure with low reactivity, we employed a cracking cell equipped with an Ar plasma source to enhance the reactivity of sulfur [3], thereby promoting the formation of SnSx.

The XRD results of the deposited films are shown in Fig. 2. A diffraction peak corresponding to SnS(400) was observed in samples deposited at 200–300 °C, indicating crystallization of SnS. In contrast, the peak disappeared in samples deposited above 350 °C. Thickness measurements confirmed that the SnS layer vanished at these higher substrate temperatures [Fig. 3], suggesting that the disappearance was due to re-evaporation of SnS. Furthermore, compositional analysis revealed that the deposited films maintained the stoichiometric ratio of SnS [Fig. 3].

Fig. 1 Schematic of experiment
Fig.2 XRD results of samples
Fig. 3 S concentration and film thickness after deposition with various Tsub. Photos of samples are shown as insets.

Reference

  1. Q. Zhang et al., ACS Appl. Nano Mater. 6, 6920 (2023). DOI: 10.1021/acsanm.3c00669
  2. D. Modai et al., 71st JSAP Spring Meeting , 23p-12L-10 (2024).
  3. R. Matsumura et al., Jpn. J. Appl. Phys. , 64 08SP05 (2025). DOI: 10.35848/1347-4065/adf3be