Current Organizations / Institutes

The organizations/institutes from the scholar's latest article


Tsung-Ting Shih has a total of 37 co-authors. Here are the top co-authors by number of shared publications:


Latest Publications

  • Open Access

    Universal Analytical Framework Coupling Open-Source Platforms with Colorimetry for On-Site Water Quality Assessment

    by Cheng-Yu Wang, Ya-Cheng Tsai, Ji-Hao Chen, Yan-Ren Ke, Chun-Chung Cheng, Xuan-Yun Chen, Jia-Lin Tsai, Tsung-Ting Shih

    Various analytical methods for water quality monitoring have been standardized to date; however, implementation of these techniques necessitates considerable skill or expensive equipment, which impacts their use. In this study, a pragmatic strategy that employs an open-source Arduino platform coupled with visible-spectrum colorimetry for water quality assessment is proposed. Validation procedures demonstrate satisfactory application of the developed system to determine free residual chlorine (frCl) and ammonia–nitrogen (NH3–N) in collected water samples. The detection limits achieved, i.e., 0.04 and 0.03 mg L–1 for frCl and NH3–N, respectively, are considerably lower than the concentration levels recommended by regulations; thus, the proposed technique has sufficient detection capability for common use. Moreover, on-site water quality assessment can be achieved using a compact configuration, as the system weighs less than 100 g and is powered by a laptop. Remarkably, the system constructed in this study is more cost-effective than commercially available spectrophotometers, at approximately USD 35 per system.

  • Copper nitrite reduction by thiols: mechanistic insights into NO release en route to copper thiolate formation

    by Naorem Jemes Jemes Meitei, Yu-Ting Chu, Chien-Hung Li, Rahimeh Eshaghi Malekshah, Wei-Min Ching, Tsung-Ting Shih, Sodio C. N. Hsu

    β-Diketiminato Cu( ii )–nitrito complexes react with thiols ( t BuBzSH, BzSH, l -cysteine) to release NO and form a free ligand, disulfide, and an insoluble polymeric Cu( i )–thiolate (YP R ).


  • Open Access

    Fabrication of a Microfluidic-Based Device Coated with Polyelectrolyte-Capped Titanium Dioxide to Couple High-Performance Liquid Chromatography with Inductively Coupled Plasma Mass Spectrometry for Mercury Speciation

    by Ji-Hao Chen, Yu-Ting Luo, Yi-An Su, Yan-Ren Ke, Ming-Jay Deng, Wei-Yu Chen, Cheng-Yu Wang, Jia-Lin Tsai, Cheng-Hsing Lin, Tsung-Ting Shih

    Mercury (Hg) is a toxic element which impacts on biological systems and ecosystems. Because the toxicity of Hg species is highly dependent on their concentration levels and chemical forms, the sensitive identification of the chemical forms of Hg—i.e., Hg speciation—is of major significance in providing meaningful information about the sources of Hg exposure. In this study, a microfluidic-based device made of high-clarity poly(methyl methacrylate) (PMMA) was fabricated. Then, titanium dioxide nanoparticles (nano-TiO2s) were attached to the treated channel’s interior with the aid of poly(diallyldimethylammonium chloride) (PDADMAC). After coupling the nano-TiO2-coated microfluidic-based photocatalyst-assisted reduction device (the nano-TiO2-coated microfluidic-based PCARD) with high-performance liquid chromatography (HPLC) and inductively coupled plasma mass spectrometry (ICP-MS), a selective and sensitive, hyphenated system for Hg speciation was established. Validation procedures demonstrated that the method could be satisfactorily applied to the determination of mercury ions (Hg2+) and methylmercury ions (CH3Hg+) in both human urine and water samples. Remarkably, the zeta potential measured clearly indicated that the PDADMAC-capped nano-TiO2s with a predominance of positive charges indeed provided a steady force for firm attachment to the negatively charged device channel. The cause of the durability of the nano-TiO2-coated microfluidic-based PCARD was clarified thus.


  • Open Access

    Fabrication of a Microfluidic-Based Device Coated with Polyelec-Trolyte-Capped-Titanium Dioxide to Couple High-Performance Liquid Chromatography with Inductively Coupled Plasma-Mass Spectrometry for Mercury Speciation

    by Ji-Hao Chen, Yu-Ting Luo, Yi-An Su, Yan-Ren Ke, Ming-Jay Deng, Wei-Yu Chen, Cheng-Yu Wang, Jia-Lin Tsai, Cheng-Hsing Lin, Tsung-Ting Shih

    Mercury (Hg) is a toxic element impacting on biological systems and ecosystems. Because the toxicity of Hg species is highly dependent on concentration levels and chemical forms, sensitive identification of chemical forms for Hg, i.e., Hg speciation, is of major significance in providing meaningful information about the source of Hg exposure. In this study, a microfluidic-based device made of high clarity poly(methyl methacrylate) (PMMA) was fabricated. Then titanium dioxide nanoparticles (nano-TiO2) were attached to the treated channel interior with the aid of poly(diallyldimethylammonium chloride) (PDADMAC). After coupling the nano-TiO2-coated microfluidic-based photocatalyst-assisted reduction device (the nano-TiO2-coated microfluid-ic-based PCARD) with high-performance liquid chromatography (HPLC) and inductively coupled plasma-mass spectrometry (ICP-MS), a selective and sensitive hyphenated system for Hg specia-tion was established. Validation procedures demonstrated that the method could be satisfactorily applied to the determination of mercuric ion (Hg2+) and methylmercury ion (CH3Hg+) in both human urine and water samples. Remarkably, the zeta potential measured clearly indicated the PDADMAC-capped nano-TiO2 with predominance of positive charges indeed provided steady force for firm attachment to the negatively charged device channel. The cause for the durability of the nano-TiO2-coated microfluidic-based PCARD was clarified thus.


  • Rapid determination of metallic additives in century eggs by microwave plasma‐atomic emission spectrometer and microwave‐assisted digestion

    by Ji‐Hao Chen, Chi‐Feng Weng, Wei‐Chung Wang, Yi‐Peng Kao, Jia‐Lin Tsai, Yi‐Ju Chen, Hui‐Ling Lee, Tsung‐Ting Shih


  • Open Access

    Evaluation of Polymer Gel Electrolytes for Use in MnO2 Symmetric Flexible Electrochemical Supercapacitors

    by Yu-Hao Lin, Wan-Tien Huang, Yi-Ting Huang, Yi-Ni Jhang, Tsung-Ting Shih, Murat Yılmaz, Ming-Jay Deng

    Flexible electrochemical supercapacitors (FESCs) are emerging as innovative energy storage systems, characterized by their stable performance, long cycle life, and portability/foldability. Crucial components of FESCs, such as electrodes and efficient electrolytes, have become the focus of extensive research. Herein, we examine deep eutectic solvent (DES)–based polymer gel systems for their cost-effective accessibility, simple synthesis, excellent biocompatibility, and exceptional thermal and electrochemical stability. We used a mixture a DES, LiClO4–2-Oxazolidinone as the electroactive species, and a polymer, either polyvinyl alcohol (PVA) or polyacrylamide (PAAM) as a redox additive/plasticizer. This combination facilitates a unique ion-transport process, enhancing the overall electrochemical performance of the polymer gel electrolyte. We manufactured and used LiClO4–2-Oxazolidinone (LO), polyvinyl alcohol–LiClO4–2-Oxazolidinone (PVA–LO), and polyacrylamide–LiClO4–2-Oxazolidinone (PAAM–LO) electrolytes to synthesize an MnO2 symmetric FESC. To evaluate their performance, we analyzed the MnO2 symmetric FESC using various electrolytes with cyclic voltammetry (CV), galvanostatic charge–discharge (GCD), and electrochemical impedance spectroscopy (EIS). The FESC featuring the PVA–LO electrolyte demonstrated superior electrochemical and mechanical performances. This solid-state MnO2 symmetric FESC exhibited a specific capacitance of 121.6 F/g within a potential window of 2.4 V. Due to the excellent ionic conductivity and the wide electrochemical operating voltage range of the PVA–LO electrolyte, a high energy density of 97.3 Wh/kg at 1200 W/kg, and a long-lasting energy storage system (89.7% capacitance retention after 5000 cycles of GCD at 2 A/g) are feasibly achieved. For practical applications, we employed the MnO2 symmetric FESCs with the PVA–LO electrolyte to power a digital watch and a light-emitting diode, further demonstrating their real-world utility.