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Strategy for Fabricating Wafer-Scale Platinum Disulfide
Xu, Hongjun,Huang, Hsin-Pan,Fei, HaiFeng,Feng, Jiafeng,Fuh, Huei-Ru,Cho, Jiung,Choi, Miri,Chen, Yanhui,Zhang, Lei,Chen, Dengyun,Zhang, Duan,Coileá,in, Cormac Ó,Han, Xiufeng,Chang, Ching-Ra American Chemical Society 2019 ACS APPLIED MATERIALS & INTERFACES Vol.11 No.8
<P>PtS<SUB>2</SUB> is a newly developed group 10 2D layered material with high carrier mobility, wide band gap tunability, strongly bound excitons, symmetrical metallic and magnetic edge states, and ambient stability, making it attractive in nanoelectronic, optoelectronic, and spintronic fields. To the aim of application, a large-scale synthesis is necessary. For transition-metal dichalcogenide (TMD) compounds, a thermally assisted conversion method has been widely used to fabricate wafer-scale thin films. However, PtS<SUB>2</SUB> cannot be easily synthesized using the method, as the tetragonal PtS phase is more stable. Here, we use a specified quartz part to locally increase the vapor pressure of sulfur in a chemical vapor deposition furnace and successfully extend this method for the synthesis of PtS<SUB>2</SUB> thin films in a scalable and controllable manner. Moreover, the PtS and PtS<SUB>2</SUB> phases can be interchangeably converted through a proposed strategy. Field-effect transistor characterization and photocurrent measurements suggest that PtS<SUB>2</SUB> is an ambipolar semiconductor with a narrow band gap. Moreover, PtS<SUB>2</SUB> also shows excellent gas-sensing performance with a detection limit of ∼0.4 ppb for NO<SUB>2</SUB>. Our work presents a relatively simple way of synthesizing PtS<SUB>2</SUB> thin films and demonstrates their promise for high-performance ultrasensitive gas sensing, broadband optoelectronics, and nanoelectronics in a scalable manner. Furthermore, the proposed strategy is applicable for making other PtX<SUB>2</SUB> compounds and TMDs which are compatible with modern silicon technologies.</P> [FIG OMISSION]</BR>
Threshold magnetoresistance in anistropic magnetic 2D transition metal dichalcogenides
Xu, Hongjun,Hsu, Ming-Chien,Fuh, Huei-Ru,Feng, Jiafeng,Han, Xiufeng,Zhao, Yanfeng,Zhang, Duan,Wang, Xinming,Liu, Fang,Liu, Huajun,Cho, Jiung,Choi, Miri,Chun, Byong Sun,Ó,Coileá,in, Cormac The Royal Society of Chemistry 2018 Journal of Materials Chemistry C Vol.6 No.12
<P>Recently many novel magnetoresistance (MR) phenomena have been reported from studies of two dimensional (2D) materials. Here, we report on the exotic transport behavior of VS2. A large negative and quadratic MR of −10% is observed for an in-plane magnetic field B up to 14 T. Remarkably, when the applied field deviates from the in-plane orientation there is a threshold field, Bc, and the MR shows a plateau of near zero MR. When B < Bc, only a single state exists and the transition between quantum spin states is forbidden. Our work sheds new light on the MR of magnetic 2D materials with localized states and may spur further investigations.</P>
Zhiying Liu,Yulin Li,Xiaohui Sun,Zhuyin Sui,Xiufeng Xu 한국공업화학회 2022 Journal of Industrial and Engineering Chemistry Vol.112 No.-
This study explored the feasibility of coupling N2O decomposition with ethylbenzene (EB) oxidativedehydrogenation, as an alternative approach for greenhouse gas elimination and styrene (ST) production,on the Co-Al mixed oxides and K-modified catalysts. It was found that N2O could decompose completelyover the K/Co2AlO4 catalyst, accompanied with 62.0% of EB conversion and 85.1% of styrene selectivity,which were much better than the existing catalyst systems for EB oxidative dehydrogenation. Characterization results showed that despite the decreased specific surface area of the catalysts withincreasing the Co/Al molar ratio, the improved reducibility, the reduced acid properties as well as thehigher ratio of Co3+/Co2+ were responsible for the enhanced performance. The K modification not onlychanged the electronic properties of active metal, resulting from the charge transfer from K cation tothe Co species, but also weakened the binding energy of Co3+-O, leading to the complete decompositionof N2O. Furthermore, the optimized strong acid properties inhibited the dealkylation or ring-openingreactions and significantly reduced the coke deposition on the catalyst surface, thus improving the STselectivity.