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Yang, Q.*; Yang, X.*; Wang, Y.*; Fei, Y.*; Li, F.*; Zheng, H.*; Li, K.*; Han, Y.*; Hattori, Takanori; Zhu, P.*; et al.
Nature Communications (Internet), 15, p.7778_1 - 7778_9, 2024/09
Times Cited Count:9 Percentile:88.46(Multidisciplinary Sciences)Luminescent materials that simultaneously embody bright singlet and triplet excitons hold great potential in optoelectronics, signage, and information encryption. However, achieving high-performance white-light emission is severely hampered by their inherent unbalanced contribution of fluorescence and phosphorescence. Herein, we address this challenge by pressure treatment engineering via hydrogen bonding cooperativity effect to realize the mixture of n--
transitions, where the triplet state emission was boosted from 7% to 40% in isophthalic acid (IPA). A superior white-light emission based on hybrid fluorescence and phosphorescence was harvested in pressure-treated IPA, and the photoluminescence quantum yield was increased to 75% from the initial 19% (blue-light emission). In-situ high-pressure IR spectra, X ray diffraction, and neutron diffraction reveal continuous strengthening of the hydrogen bonds with the increase of pressure. Furthermore, this enhanced hydrogen bond is retained down to the ambient conditions after pressure treatment, awarding the targeted IPA efficient intersystem crossing for balanced singlet/triplet excitons population and resulting in efficient white-light emission. This work not only proposes a route for brightening triplet states in organic small molecule, but also regulates the ratio of singlet and triplet excitons to construct high-performance white-light emission.
Zhou, L.*; Zhang, H.*; Qin, T. Y.*; Hu, F. F.*; Xu, P. G.; Ao, N.*; Su, Y. H.; He, L. H.*; Li, X. H.*; Zhang, J. R.*; et al.
Metallurgical and Materials Transactions A, 55(7), p.2175 - 2185, 2024/07
Times Cited Count:3 Percentile:75.40(Materials Science, Multidisciplinary)Zhou, X.*; Fukutani, Katsuyuki; 9 of others*
Applied Physics Letters, 124(8), p.082103_1 - 082103_7, 2024/02
Times Cited Count:6 Percentile:89.50(Physics, Applied)Zhou, Y.*; Song, W.*; Zhang, F.*; Wu, Y.*; Lei, Z.*; Jiao, M.*; Zhang, X.*; Dong, J.*; Zhang, Y.*; Yang, M.*; et al.
Journal of Alloys and Compounds, 971, p.172635_1 - 172635_7, 2024/01
Times Cited Count:2 Percentile:12.80(Chemistry, Physical)Cao, Y.*; Zhou, H.*; Khmelevskyi, S.*; Lin, K.*; Avdeev, M.*; Wang, C.-W.*; Wang, B.*; Hu, F.*; Kato, Kenichi*; Hattori, Takanori; et al.
Chemistry of Materials, 35(8), p.3249 - 3255, 2023/04
Times Cited Count:2 Percentile:21.90(Chemistry, Physical)Hydrostatic and chemical pressure are efficient stimuli to alter the crystal structure and are commonly used for tuning electronic and magnetic properties in materials science. However, chemical pressure is difficult to quantify and a clear correspondence between these two types of pressure is still lacking. Here, we study intermetallic candidates for a permanent magnet with a negative thermal expansion (NTE). Based on in situ synchrotron X-ray diffraction, negative chemical pressure is revealed in HoFe
on Al doping and quantitatively evaluated by using temperature and pressure dependence of unit cell volume. A combination of magnetization and neutron diffraction measurements also allowed one to compare the effect of chemical pressure on magnetic ordering with that of hydrostatic pressure. Intriguingly, pressure can be used to control suppression and enhancement of NTE. Electronic structure calculations indicate that pressure affected the top of the majority band with respect to the Fermi level, which has implications for the magnetic stability, which in turn plays a critical role in modulating magnetism and NTE. This work presents a good example of understanding the effect of pressure and utilizing it to control properties of functional materials.
Miao, Z.-Q.*; Xia, C.-J.*; Lai, X.-Y.*; Maruyama, Toshiki; Xu, R.-X.*; Zhou, E.-P.*
International Journal of Modern Physics E, 31(4), p.2250037_1 - 2250037_20, 2022/04
Times Cited Count:11 Percentile:85.27(Physics, Nuclear)Naeem, M.*; Zhou, H.*; He, H.*; Harjo, S.; Kawasaki, Takuro; Lan, S.*; Wu, Z.*; Zhu, Y.*; Wang, X.-L.*
Applied Physics Letters, 119(13), p.131901_1 - 131901_7, 2021/09
Times Cited Count:20 Percentile:78.00(Physics, Applied)Qi, J.*; Hou, D.*; Chen, Y.*; Saito, Eiji; Jin, X.*
Journal of Magnetism and Magnetic Materials, 534, p.167980_1 - 167980_6, 2021/09
Times Cited Count:3 Percentile:16.61(Materials Science, Multidisciplinary)Yang, Z. H.*; Kubota, Yuki*; Corsi, A.*; Yoshida, Kazuki; Sun, X.-X.*; Li, J. G.*; Kimura, Masaaki*; Michel, N.*; Ogata, Kazuyuki*; Yuan, C. X.*; et al.
Physical Review Letters, 126(8), p.082501_1 - 082501_8, 2021/02
Times Cited Count:58 Percentile:95.97(Physics, Multidisciplinary)A quasifree (,
) experiment was performed to study the structure of the Borromean nucleus
B, which had long been considered to have a neutron halo. By analyzing the momentum distributions and exclusive cross sections, we obtained the spectroscopic factors for
and
orbitals, and a surprisingly small percentage of 9(2)% was determined for
. Our finding of such a small
component and the halo features reported in prior experiments can be explained by the deformed relativistic Hartree-Bogoliubov theory in continuum, revealing a definite but not dominant neutron halo in
B. The present work gives the smallest
- or
-orbital component among known nuclei exhibiting halo features and implies that the dominant occupation of
or
orbitals is not a prerequisite for the occurrence of a neutron halo.
Lai, W.-H.*; Wang, H.*; Zheng, L.*; Jiang, Q.*; Yan, Z.-C.*; Wang, L.*; Yoshikawa, Hirofumi*; Matsumura, Daiju; Sun, Q.*; Wang, Y.-X.*; et al.
Angewandte Chemie; International Edition, 59(49), p.22171 - 22178, 2020/12
Times Cited Count:103 Percentile:95.78(Chemistry, Multidisciplinary)Qin, J.*; Hou, D.*; Chen, Y.*; Saito, Eiji; Jin, X.*
Journal of Magnetism and Magnetic Materials, 501, p.166362_1 - 166362_4, 2020/05
Times Cited Count:4 Percentile:20.27(Materials Science, Multidisciplinary)Al-Shayeb, B.*; Sachdeva, R.*; Chen, L.-X.*; Ward, F.*; Munk, P.*; Devoto, A.*; Castelle, C. J.*; Olm, M. R.*; Bouma-Gregson, K.*; Amano, Yuki; et al.
Nature, 578(7795), p.425 - 431, 2020/02
Times Cited Count:291 Percentile:99.46(Multidisciplinary Sciences)Sun, M. D.*; Liu, Z.*; Huang, T. H.*; Zhang, W. Q.*; Andreyev, A. N.; Ding, B.*; Wang, J. G.*; Liu, X. Y.*; Lu, H. Y.*; Hou, D. S.*; et al.
Physics Letters B, 800, p.135096_1 - 135096_5, 2020/01
Times Cited Count:13 Percentile:74.01(Astronomy & Astrophysics)Wang, H.*; Hou, D.*; Qiu, Z.*; Kikkawa, Takashi*; Saito, Eiji; Jin, X.*
Journal of Applied Physics, 122(8), p.083907_1 - 083907_6, 2017/08
Times Cited Count:5 Percentile:22.22(Physics, Applied)Ding, F.*; Luo, G.-N.*; Pitts, R.*; Litnovsky, A.*; Gong, X.*; Ding, R.*; Mao, H.*; Zhou, H.*; Wampler, W. R.*; Stangeby, P. C.*; et al.
Journal of Nuclear Materials, 455(1-3), p.710 - 716, 2014/12
Times Cited Count:28 Percentile:88.43(Materials Science, Multidisciplinary)Wang, X.*; Hou, Z.*; Ikeda, Takashi; Terakura, Kiyoyuki*
Journal of Physical Chemistry C, 118(25), p.13929 - 13935, 2014/06
Times Cited Count:11 Percentile:33.66(Chemistry, Physical)The NMR chemical shifts of possible N-containing moieties at edges and defects of graphene are investigated by using the first-principles method. Our computations show that pyridine-like and graphite-like N are rather easily identifiable using N NMR technique, in agreement with experiment. On the other hand, pyridinium-like N is hardly distinguished from pyrrole-like one because these
N nuclei give nearly overlapping signals. However, our simulations suggest that
H NMR is useful to discriminate between them; The NMR chemical shift of
H directly bonded with pyridinium-like and pyrrole-like N is estimated as 0.8 and 10.8 ppm, respectively. The
N NMR signals for various moieties at edges we considered are found to be similar to the corresponding ones at defects except for pyridine-like nitrogens. Conversely, the
N NMR chemical shifts are altered sensitively by the degree of aggregation of pyridine-like
N atoms both along armchair edges and at defect sites.
Li, G. S.*; Liu, M. L.*; Zhou, X. H.*; Zhang, Y. H.*; Liu, Y. X.*; Zhang, N. T.*; Hua, W.*; Zheng, Y. D.*; Fang, Y. D.*; Guo, S.*; et al.
Physical Review C, 89(5), p.054303_1 - 054303_9, 2014/05
Times Cited Count:5 Percentile:36.43(Physics, Nuclear)High-spin states of Pt have been reinvestigated using the
Yb(
O, 4
) reaction at a beam energy of 88 MeV. The previously known positive parity band associated with the
(
being
or
) configuration has been revised and extended significantly. A new negative parity band has been established and proposed to be based on the
configuration. Possible structure evolution of the yrast line from predominantly vibrational to rotational with increasing spin is discussed with the help of E
over spin curves. Additionally, calculations of Total Routhian surfaces have been performed to investigate the band properties.
Kikkawa, Takashi*; Uchida, Kenichi*; Daimon, Shunsuke*; Shiomi, Yuki*; Adachi, Hiroto; Qiu, Z.*; Hou, D.*; Jin, X.-F.*; Maekawa, Sadamichi; Saito, Eiji
Physical Review B, 88(21), p.214403_1 - 214403_11, 2013/12
Times Cited Count:137 Percentile:96.38(Materials Science, Multidisciplinary)Povinec, P. P.*; Aoyama, Michio*; Biddulph, D.*; Breier, R.*; Buesseler, K. O.*; Chang, C. C.*; Golser, R.*; Hou, X. L.*; Jekovsk
, M.*; Jull, A. J. T.*; et al.
Biogeosciences, 10(8), p.5481 - 5496, 2013/08
Times Cited Count:107 Percentile:94.03(Ecology)Radionuclide impact of the Fukushima Dai-ichi Nuclear Power Plant accident on the distribution of radionuclides in seawater of the NW Pacific Ocean is compared with global fallout from atmospheric tests of nuclear weapons. Surface and water column seawater samples collected during the international expedition in June 2011 were analyzed for Cs,
Cs,
I and
H. The
Cs,
I and
H levels in surface seawater offshore Fukushima varied between 0.002-3.5 Bq/L, 0.01-0.8
Bq/L, and 0.05-0.15 Bq/L, respectively. At the sampling site about 40 km from the coast, where all three radionuclides were analyzed, the Fukushima impact on the levels of these three radionuclides represent an increase above the global fallout background by factors of about 1000, 30 and 3, respectively. The water column data indicate that the transport of Fukushima-derived radionuclides downward to the depth of 300 m has already occurred. The observed
Cs levels in surface waters and in the water column are in reasonable agreement with predictions obtained from the Ocean General Circulation Model, which indicates that the radionuclides have been transported from the Fukushima coast eastward. Due to a suitable residence time in the ocean, Fukushima-derived radionuclides will provide useful tracers for isotope oceanography studies on the transport of water masses in the NW Pacific Ocean.
Hou, Z.*; Wang, X.*; Ikeda, Takashi; Terakura, Kiyoyuki*; Oshima, Masaharu*; Kakimoto, Masaaki*
Physical Review B, 87(16), p.165401_1 - 165401_16, 2013/04
Times Cited Count:115 Percentile:95.34(Materials Science, Multidisciplinary)We have performed the DFT calculations to study the electronic structures of N-doped graphene with vacancies and Stone-Wales defect. Our results show that monovacancies in graphene act as hole dopants and that two substitutional N dopants are needed to compensate for the hole introduced by a monovacancy. On the other hand, divacancy does not produce any free carriers. Interestingly, a single N dopant at divacancy acts as an acceptor rather than a donor. Compared with the case of an isolated N dopant in perfect graphene, the electrons donated by substitutional N dopants would be localized significantly when a N-N pair is formed. The N-N interaction and the interference between native point defect and N dopant strongly modify the role of N doping regarding the free carrier production in the bulk bands. Our results are qualitatively consistent with the experimental observation that the concentration of free electrons introduced by N dopants would be lower than that of doped N.