Browsing by Author "Lee, Min-Han"

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A facile green antisolvent approach to Cu2+-doped ZnO nanocrystals with visible-light-responsive photoactivities
(2014-08-07)
Lu, Yi-Hsuan
;
Lin, Wei-Hao
;
Yang, Chao-Yao
;
Chiu, Yi-Hsuan
;
Pu, Ying-Chih
An environmentally benign antisolvent method has been developed to prepare Cu2+-doped ZnO nanocrystals with controllable dopant concentrations. A room temperature ionic liquid, known as a deep eutectic solvent (DES), was used as the solvent to dissolve ZnO powders. Upon the introduction of the ZnO-containing DES into a bad solvent which shows no solvation to ZnO, ZnO was precipitated and grown due to the dramatic decrease of solubility. By adding Cu2+ ions to the bad solvent, the growth of ZnO from the antisolvent process was accompanied by Cu2+ introduction, resulting in the formation of Cu2+-doped ZnO nanocrystals. The as-prepared Cu2+-doped ZnO showed an additional absorption band in the visible range (400-800 nm), which conduced to an improvement in the overall photon harvesting efficiency. Time-resolved photoluminescence spectra, together with the photovoltage information, suggested that the doped Cu2+ may otherwise trap photoexcited electrons during the charge transfer process, inevitably depressing the photoconversion efficiency. The photoactivity of Cu2+-doped ZnO nanocrystals for photoelectrochemical water oxidation was effectively enhanced in the visible region, which achieved the highest at 2.0 at% of Cu2+. A further increase in the Cu2+ concentration however led to a decrease in the photocatalytic performance, which was ascribed to the significant carrier trapping caused by the increased states given by excessive Cu2+. The photocurrent action spectra illustrated that the enhanced photoactivity of the Cu2+-doped ZnO nanocrystals was mainly due to the improved visible photon harvesting achieved by Cu2+ doping. These results may facilitate the use of transition metal ion-doped ZnO in other photoconversion applications, such as ZnO based dye-sensitized solar cells and magnetism-assisted photocatalytic systems.
A facile green antisolvent approach to Cu2+-doped ZnO nanocrystals with visible-light-responsive photoactivities
(2014-08-07)
Lu, Yi-Hsuan
;
Lin, Wei-Hao
;
Yang, Chao-Yao
;
Chiu, Yi-Hsuan
;
Pu, Ying-Chih
An environmentally benign antisolvent method has been developed to prepare Cu2+-doped ZnO nanocrystals with controllable dopant concentrations. A room temperature ionic liquid, known as a deep eutectic solvent (DES), was used as the solvent to dissolve ZnO powders. Upon the introduction of the ZnO-containing DES into a bad solvent which shows no solvation to ZnO, ZnO was precipitated and grown due to the dramatic decrease of solubility. By adding Cu2+ ions to the bad solvent, the growth of ZnO from the antisolvent process was accompanied by Cu2+ introduction, resulting in the formation of Cu2+-doped ZnO nanocrystals. The as-prepared Cu2+-doped ZnO showed an additional absorption band in the visible range (400-800 nm), which conduced to an improvement in the overall photon harvesting efficiency. Time-resolved photoluminescence spectra, together with the photovoltage information, suggested that the doped Cu2+ may otherwise trap photoexcited electrons during the charge transfer process, inevitably depressing the photoconversion efficiency. The photoactivity of Cu2+-doped ZnO nanocrystals for photoelectrochemical water oxidation was effectively enhanced in the visible region, which achieved the highest at 2.0 at% of Cu2+. A further increase in the Cu2+ concentration however led to a decrease in the photocatalytic performance, which was ascribed to the significant carrier trapping caused by the increased states given by excessive Cu2+. The photocurrent action spectra illustrated that the enhanced photoactivity of the Cu2+-doped ZnO nanocrystals was mainly due to the improved visible photon harvesting achieved by Cu2+ doping. These results may facilitate the use of transition metal ion-doped ZnO in other photoconversion applications, such as ZnO based dye-sensitized solar cells and magnetism-assisted photocatalytic systems.
Competing Anisotropy-Tunneling Correlation of the CoFeB/MgO Perpendicular Magnetic Tunnel Junction: An Electronic Approach
(2015-11-24)
Yang, Chao-Yao
;
Chang, Shu-Jui
;
Lee, Min-Han
;
Shen, Kuei-Hung
;
Yang, Shan-Yi
We intensively investigate the physical principles regulating the tunneling magneto-resistance (TMR) and perpendicular magnetic anisotropy (PMA) of the CoFeB/MgO magnetic tunnel junction (MTJ) by means of angle-resolved x-ray magnetic spectroscopy. The angle-resolved capability was easily achieved, and it provided greater sensitivity to symmetry-related d-band occupation compared to traditional x-ray spectroscopy. This added degree of freedom successfully solved the unclear mechanism of this MTJ system renowned for controllable PMA and excellent TMR. As a surprising discovery, these two physical characteristics interact in a competing manner because of opposite band-filling preference in space-correlated symmetry of the 3d-orbital. An overlooked but harmful superparamagnetic phase resulting from magnetic inhomogeneity was also observed. This important finding reveals that simultaneously achieving fast switching and a high tunneling efficiency at an ultimate level is improbable for this MTJ system owing to its fundamental limit in physics. We suggest that the development of independent TMR and PMA mechanisms is critical towards a complementary relationship between the two physical characteristics, as well as the realization of superior performance, of this perpendicular MTJ. Furthermore, this study provides an easy approach to evaluate the futurity of any emerging spintronic candidates by electronically examining the relationship between their magnetic anisotropy and transport.
Soft and hard natures of Nd2Fe14B permanent magnet explored by first-order-reversal-curves
(2014-12-01)
Chen, Po-An
;
Yang, Chao-Yao
;
Chang, Shu-Jui
;
Lee, Min-Han
;
Tang, Nai-Kuang
Two commercial Nd2Fe14B samples, MQP-B and sintered-NdFeB were investigated using synchrotron based x-ray diffraction and first-order-reversal-curves (FORCs). Despite differing in magnetic and structural properties, the two samples were found to comprise two major ferromagnetic components in FORCs. For the sintered-NdFeB case, the soft component may originate from the intrinsically soft Nd-f site which was coupled with its local Fe atomic environment that differs in magnetic anisotropy from the Nd-g site (intrinsically hard). It may directly originate from the Nd-rich phase or microstructural imperfection, while the former possibility (Nd-f sire) appears greater than the latter While for the MQP-B, the minor second phase resulting from high structural disorder was likely in charge of the presence of the soft component. Sophisticated FORCs analyses revealed the natures of the soft and hard components, soft hard coupling and switching reversibility of the two cases, irrespective of the origins of their two components. This provides insights to the origin of magnetic stability and reversal dynamics of Nd2Fe14B that have not been fully understood by conventional magnetic analyses. The coexistence of the two components led to an incoherent reversal undermining the magnetic stability of Nd2Fe14B. This is a fundamental problem as to why the performance extremity can only be improved finitely through extrinsic tuning. From FORCs simulation we understand that the soft-hard coupling was moderate in a real Nd2Fe14B compound. A stronger soft-hard coupling is necessary to conquer the anisotropic competition to enable a coherent reversal that will promote the magnetic hardness. (C) 2014 Elsevier B.V. All rights reserved,
Structural imperfections and attendant localized/itinerant ferromagnetism in ZnO nanoparticles
(2014-08-30)
Yang, Chao-Yao
;
Lu, Yi-Hsuan
;
Lin, Wei-Hao
;
Lee, Min-Han
;
Hsu, Yung-Jung
Using synchrotron-based x-ray magnetic spectroscopy, we report a study focusing on the local symmetry of Cu-dopant and resultant structural imperfections in mediating Cu-doped ZnO nanoparticles\' ferromagnetism (FM). Prepared by an antisolvent method, Cu appeared to preferably populate on the basal plane of ZnO with a local symmetry of [CuO4]. This unique symmetry was antiferromagnetic in nature, while electronically and structurally coupled to surrounded oxygen vacancies (V-o) that yielded a localized FM, because of a strong dependency on the number/location of the [CuO4] symmetry. Surprisingly, the FM of undoped but oxygen-deficient ZnO appeared to be more itinerant and long-range, where V-o percolated the FM effectively and isotropically through oxygen\'s delocalized orbital. By adopting the approach of structural imperfection, this study clearly identifies V-o\'s (defect\'s) true characters in mediating the FM of magnetic semiconductors which has been thought of as a long-standing debate, and thus provides a different thinking about the traditional extrinsic ferromagnetic-tuning in the semiconductors. It even illuminates recent research concerning the intrinsic FM of low-dimensional systems that contain defects but non-magnetic elements.