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박익재(Ik Jae Park),김동회(Dong Hoe Kim) 한국세라믹학회 2019 세라미스트 Vol.22 No.2
To overcome the theoretical efficiency of single-junction solar cells (> 30 %), tandem solar cells (or multi-junction solar cells) is considered as a strong nominee because of their excellent light utilization. Organic-inorganic halide perovskite has been regarded as a promising candidate material for next-generation tandem solar cell due to not only their excellent optoelectronic properties but also their bandgap-tune-ability and low-temperature processpossibility. As a result, they have been adopted either as a wide-bandgap top cell combined with narrow-bandgap silicon or CuIn x Ga (1-x) Se 2 bottom cells or for all-perovskite tandem solar cells using narrow- and wide-bandgap perovskites. To successfully transition perovskite materials from for single junction to tandem, substantial efforts need to focus on fabricating the high quality wide- and narrow-bandgap perovskite materials and semi-transparent electrode/recombination layer. In this paper, we present an overview of the current research and our outlook regarding perovskite-based tandem solar technology. Several key challenges discussed are: 1) a wide-bandgap perovskite for top-cell in multi-junction tandem solar cells; 2) a narrow-bandgap perovskite for bottom-cell in allperovskite tandem solar cells, and 3) suitable semi-transparent conducting layer for efficient electrode or recombination layer in tandem solar cells.
고효율 페로브스카이트-페로브스카이트 탠덤 태양전지의 연구 개발 동향
고재혁(Jaehyeok Koh),김채연(Chaeyoun Kim),박성주(Seongju Park),우다연(Dayeon Woo),신병하(Byungha Shin) 한국태양광발전학회 2024 Current Photovoltaic Research Vol.12 No.3
All-perovskite tandem solar cells have been developed as a next-generation solar cell technology to surpass the efficiency limits of single-junction solar cells. By using perovskite materials with different bandgaps in the top and bottom cells, these tandem solar cells can effectively utilize a wider range of the solar spectrum. All-perovskite tandem solar cells have been focused as a next-generation solar cell due to their ability to achieve high efficiency while being manufactured through low-cost solution processing. This paper focuses on key components for improving the performance of all-perovskite tandem solar cells and essential components: wide bandgap perovskite solar cells, narrow bandgap perovskite solar cells, and charge recombination layers. The characteristics, main challenges, and strategies for overcoming these issues are discussed. For wide bandgap perovskites, efficiency is reduced by high trap densities and halide ion phase segregation. Improvement methods through additives and surface passivation are proposed to overcome these issues. In narrow bandgap perovskites, composition control and surface treatment techniques are being developed to reduce the oxidation of Sn-based materials and charge recombination in the perovskite. Additionally, the charge recombination layer is an essential component for efficient electron-hole recombination and minimizing optical losses, with materials such as transparent conductive oxides and ultrathin metals being used. These studies make a significant contribution to enhancing the efficiency and stability of all-perovskite tandem solar cells and suggest future research directions for commercialization.
Kim, Yeonwoo,Yang, Sena,Jeon, Eun Hee,Baik, Jaeyoon,Kim, Namdong,Kim, Hyun Sung,Lee, Hangil Springer US 2016 NANOSCALE RESEARCH LETTERS Vol.11 No.1
<P>To design a high-performance photocatalytic system with TiO<SUB>2</SUB>, it is necessary to reduce the bandgap and enhance the absorption efficiency. The reduction of the bandgap to the visible range was investigated with reference to the surface distortion of anatase TiO<SUB>2</SUB> nanoparticles induced by varying Fe doping concentrations. Fe-doped TiO<SUB>2</SUB> nanoparticles (Fe@TiO<SUB>2</SUB>) were synthesized by a hydrothermal method and analyzed by various surface analysis techniques such as transmission electron microscopy, Raman spectroscopy, X-ray diffraction, scanning transmission X-ray microscopy, and high-resolution photoemission spectroscopy. We observed that Fe doping over 5 wt.% gave rise to a distorted structure, i.e., Fe<SUB>2</SUB>Ti<SUB>3</SUB>O<SUB>9</SUB>, indicating numerous Ti<SUP>3+</SUP> and oxygen-vacancy sites. The Ti<SUP>3+</SUP> sites act as electron trap sites to deliver the electron to O<SUB>2</SUB> as well as introduce the dopant level inside the bandgap, resulting in a significant increase in the photocatalytic oxidation reaction of thiol (–SH) of 2-aminothiophenol to sulfonic acid (–SO<SUB>3</SUB>H) under ultraviolet and visible light illumination.</P><P><B>Electronic supplementary material</B></P><P>The online version of this article (doi:10.1186/s11671-016-1263-6) contains supplementary material, which is available to authorized users.</P>
박영돈 대한화학회 2013 Bulletin of the Korean Chemical Society Vol.34 No.11
The fabrication of polymer field-effect transistors with good electrical properties requires the minimization of molecular defects caused by low molecular weight (MW) fractions of a conjugated polymer. Here we report that the electrical properties of a narrow bandgap conjugated polymer could be dramatically improved as a result of dipping a thin film into a poor solvent. The dipping time in hexanes was controlled to efficiently eliminate the low molecular weight fractions and concomitantly improve the molecular ordering of the conjugated polymer. The correlation between the structural order and the electrical properties was used to optimize the dipping time and investigate the effects of the low MW fraction on the electrical properties of the resulting thin film.
Park, Yeong Don Korean Chemical Society 2013 Bulletin of the Korean Chemical Society Vol.34 No.11
The fabrication of polymer field-effect transistors with good electrical properties requires the minimization of molecular defects caused by low molecular weight (MW) fractions of a conjugated polymer. Here we report that the electrical properties of a narrow bandgap conjugated polymer could be dramatically improved as a result of dipping a thin film into a poor solvent. The dipping time in hexanes was controlled to efficiently eliminate the low molecular weight fractions and concomitantly improve the molecular ordering of the conjugated polymer. The correlation between the structural order and the electrical properties was used to optimize the dipping time and investigate the effects of the low MW fraction on the electrical properties of the resulting thin film.
End‐Capping Effect of a Narrow Bandgap Conjugated Polymer on Bulk Heterojunction Solar Cells
Park, Jin Kuen,Jo, Jang,Seo, Jung Hwa,Moon, Ji Sun,Park, Yeong Don,Lee, Kwanghee,Heeger, Alan J.,Bazan, Guillermo C. WILEY‐VCH Verlag 2011 Advanced Materials Vol.23 No.21
<P><B>Device performances of BHJ solar cells</B> based on poly[(4,4‐didodecyldithieno[3,2‐b:2’,3’‐d]silole)‐2,6‐diyl‐<I>alt</I>‐(2,1,3‐benzoxadiazole)‐4,7‐diyl]and PC<SUB>71</SUB>BM improve by capping the chain ends with thiophene fragments. This structural modification yields materials that are more thermally robust and that can be used in devices with thicker films – important considerations for enabling the mass production of plastic solar cells. </P>
Parveen Akhter,Iqrash Shafiq,Faisal Ali,Faiza Hassan,Roeya Rehman,Nasir Shezad,Ashfaq Ahmed,Farrukh Jamil,Murid Hussain,Young-Kwon Park 한국공업화학회 2023 Journal of Industrial and Engineering Chemistry Vol.123 No.-
Textile effluents may harm the human body as well as cause environmental pollution. For several decadesresearchers have been attempting to overcome this issue by introducing environmentally friendly technologiesthat degrade bulk dyes to mitigate hazards. Synthetic dyes are carcinogenic for humans as wellas for other living organisms. Various techniques have been developed for the removal of these toxiccompounds, advanced oxidation processes (AOPs) being the most used processes. In this study,Montmorillonite (MMT) supported BiVO4 nanocomposite was prepared by the sol–gel method to degradeBrilliant Red 80 dye using photocatalysis. The BiVO4/MMT composite was comprehensively characterizedby several characterization techniques including X-ray diffraction (XRD), Fourier-transform infraredspectroscopy (FTIR), Scanning electron microscopy (SEM), Raman, Photoluminescence spectroscopy(PL), and UV–Vis diffuse reflectance spectroscopy (UV–Vis-DRS). Interestingly, the composite materialshowed a narrow bandgap of 2.26 eV with strong light absorption in the visible range. A 1000-wattXenon Lamp was used for activity performance measurement. The photocatalytic Brilliant Red 80 degradationactivity was observed to be 99% degraded within 120 min of illumination compared to conventionalBiVO4 which showed around 80% degradation. Moreover, in this work, an acidic media wasfound to favor the degradation of Brilliant Red 80 dye.
Lim, Hyung-Seok,Lee, JaeSoul,Lee, Seunghyun,Kang, Yong Soo,Sun, Yang-Kook,Suh, Kyung-Do Elsevier 2017 Acta materialia Vol.122 No.-
<P><B>Abstract</B></P> <P>In this study, we propose a fine fabrication method of walnut-like ZnO@Zn<SUB>2</SUB>TiO<SUB>4</SUB> multicore-shell submicron spheres for the solar light-responsive photocatalysis. Poly(methacrylic acid/ethylene glycol dimethacrylate) [poly(MAA/EGDMA)] microspheres were used as sacrificial template to create the hierarchically-structured hybrid metal oxide spheres with a thin carbon layer. Heterogeneous multicore-shell structure like a walnut depends on the monomer ratio of poly(MAA/EGDMA) microspheres. The thin carbon layer formed on the surface of ZnO nano-grains can cause visible light response and effectively impede the recombination of photo-generated electron-hole. When the walnut-like ZnO@Zn<SUB>2</SUB>TiO<SUB>4</SUB> multicore-shell submicron spheres with a thin carbon layer are tested as photocatalysts under solar light, the photodegradation of organic dye of above 93% is exhibited for 1 h due to the multiple light scattering originated from the unique structure and a coexistence of ZnO and Zn<SUB>2</SUB>TIO<SUB>4</SUB>.</P> <P><B>Graphical abstract</B></P> <P>[DISPLAY OMISSION]</P>