Institute of High Energy Physics, Chinese Academy of Sciences

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Institute of High Energy Physics, Chinese Academy of Sciences
Short name
IHEP CAS
Country, city
China, Beijing
Publications
17 856
Citations
495 032
h-index
253
Top-3 journals
Journal of High Energy Physics
Journal of High Energy Physics (1187 publications)
Physical Review D
Physical Review D (1091 publications)
European Physical Journal C
European Physical Journal C (745 publications)
Top-3 organizations
Peking University
Peking University (1957 publications)
Top-3 foreign organizations
National Laboratory of Frascati
National Laboratory of Frascati (1763 publications)
Sapienza University of Rome
Sapienza University of Rome (1666 publications)

Most cited in 5 years

Zyla P.A., Barnett R.M., Beringer J., Dahl O., Dwyer D.A., Groom D.E., Lin C.-., Lugovsky K.S., Pianori E., Robinson D.J., Wohl C.G., Yao W.-., Agashe K., Aielli G., Allanach B.C., et. al.
2020-08-01 citations by CoLab: 3488 PDF Abstract  
The Review summarizes much of particle physics and cosmology. Using data from previous editions, plus 3,324 new measurements from 878 papers, we list, evaluate, and average measured properties of gauge bosons and the recently discovered Higgs boson, leptons, quarks, mesons, and baryons. We summarize searches for hypothetical particles such as supersymmetric particles, heavy bosons, axions, dark photons, etc. Particle properties and search limits are listed in Summary Tables. We give numerous tables, figures, formulae, and reviews of topics such as Higgs Boson Physics, Supersymmetry, Grand Unified Theories, Neutrino Mixing, Dark Energy, Dark Matter, Cosmology, Particle Detectors, Colliders, Probability and Statistics. Among the 120 reviews are many that are new or heavily revised, including a new review on High Energy Soft QCD and Diffraction and one on the Determination of CKM Angles from B Hadrons. The Review is divided into two volumes. Volume 1 includes the Summary Tables and 98 review articles. Volume 2 consists of the Particle Listings and contains also 22 reviews that address specific aspects of the data presented in the Listings. The complete Review (both volumes) is published online on the website of the Particle Data Group (pdg.lbl.gov) and in a journal. Volume 1 is available in print as the PDG Book. A Particle Physics Booklet with the Summary Tables and essential tables, figures, and equations from selected review articles is available in print and as a web version optimized for use on phones as well as an Android app.
Zhao S., Tan C., He C., An P., Xie F., Jiang S., Zhu Y., Wu K., Zhang B., Li H., Zhang J., Chen Y., Liu S., Dong J., Tang Z.
Nature Energy scimago Q1 wos Q1
2020-10-26 citations by CoLab: 821 Abstract  
Metal–organic frameworks (MOFs) are increasingly being investigated as electrocatalysts for the oxygen evolution reaction (OER). Despite their promising catalytic activity, many fundamental questions concerning their structure−performance relationships—especially those regarding the roles of active species—remain to be answered. Here we show the structural transformation of a Ni0.5Co0.5-MOF-74 during the OER by operando X-ray absorption spectroscopy analysis and high-resolution transmission electron microscopy imaging. We suggest that Ni0.5Co0.5OOH0.75, with abundant oxygen vacancies and high oxidation states, forms in situ and is responsible for the high OER activity observed. The ratio of Ni to Co in the bimetallic centres alters the geometric and electronic structure of as-formed active species and in turn the catalytic activity. Based on our understanding of this system, we fabricate a Ni0.9Fe0.1-MOF that delivers low overpotentials of 198 mV and 231 mV at 10 mA cm−2 and 20 mA cm−2, respectively. Metal–organic frameworks (MOFs) are increasingly being explored for electrocatalytic oxygen evolution, which is half of the water splitting reaction. Here the authors show that, under reaction conditions, mixed metal oxyhydroxides form at the nodes of bimetallic MOFs, which are highly catalytically active.
Ji S., Jiang B., Hao H., Chen Y., Dong J., Mao Y., Zhang Z., Gao R., Chen W., Zhang R., Liang Q., Li H., Liu S., Wang Y., Zhang Q., et. al.
Nature Catalysis scimago Q1 wos Q1
2021-05-06 citations by CoLab: 777 Abstract  
Developing artificial enzymes with the excellent catalytic performance of natural enzymes has been a long-standing goal for chemists. Single-atom catalysts with well-defined atomic structure and electronic coordination environments can effectively mimic natural enzymes. Here, we report an engineered FeN3P-centred single-atom nanozyme (FeN3P-SAzyme) that exhibits comparable peroxidase-like catalytic activity and kinetics to natural enzymes, by controlling the electronic structure of the single-atom iron active centre through the precise coordination of phosphorus and nitrogen. In particular, the engineered FeN3P-SAzyme, with well-defined geometric and electronic structures, displays catalytic performance that is consistent with Michaelis–Menten kinetics. We rationalize the origin of the high enzyme-like activity using density functional theory calculations. Finally, we demonstrate that the developed FeN3P-SAzyme with superior peroxidase-like activity can be used as an effective therapeutic strategy for inhibiting tumour cell growth in vitro and in vivo. Therefore, SAzymes show promising potential for developing artificial enzymes that have the catalytic kinetics of natural enzymes. Nanozymes can provide cost and stability advantages over natural enzymes, but they usually display low catalytic activity and inferior kinetics. Now, a highly active nanozyme is developed that shows comparable kinetics to horseradish peroxidase in the oxidation of a commonly used artificial substrate.
Shang H., Zhou X., Dong J., Li A., Zhao X., Liu Q., Lin Y., Pei J., Li Z., Jiang Z., Zhou D., Zheng L., Wang Y., Zhou J., Yang Z., et. al.
Nature Communications scimago Q1 wos Q1 Open Access
2020-06-16 citations by CoLab: 728 PDF Abstract  
Atomic interface regulation is thought to be an efficient method to adjust the performance of single atom catalysts. Herein, a practical strategy was reported to rationally design single copper atoms coordinated with both sulfur and nitrogen atoms in metal-organic framework derived hierarchically porous carbon (S-Cu-ISA/SNC). The atomic interface configuration of the copper site in S-Cu-ISA/SNC is detected to be an unsymmetrically arranged Cu-S1N3 moiety. The catalyst exhibits excellent oxygen reduction reaction activity with a half-wave potential of 0.918 V vs. RHE. Additionally, through in situ X-ray absorption fine structure tests, we discover that the low-valent Cuprous-S1N3 moiety acts as an active center during the oxygen reduction process. Our discovery provides a universal scheme for the controllable synthesis and performance regulation of single metal atom catalysts toward energy applications. Engineering the coordination environment of single atom catalysts offers to opportunity to optimize electrocatalytic activity. In this work, the authors prepare an unsymmetrical Cu-S1N3 single atom site on porous carbon with high performance in the oxygen reduction reaction.
Hui W., Chao L., Lu H., Xia F., Wei Q., Su Z., Niu T., Tao L., Du B., Li D., Wang Y., Dong H., Zuo S., Li B., Shi W., et. al.
Science scimago Q1 wos Q1 Open Access
2021-03-26 citations by CoLab: 636 PDF Abstract  
Perovskite synthesis out in the open Although methods have been developed that create the photoactive black perovskite phase of formamidinium lead iodide (α-FAPbI 3 ), these routes are temperature and humidity sensitive and less compatible with large-scale solar cell production. Hui et al. report an alternative route in which vertically aligned lead iodide thin films are grown from the ionic liquid methylamine formate. Nanoscale channels in the films lower the barrier to permeation of formamidinium iodide and enable transformation to α-FAPbI 3 , even at high humidity and room temperature. Solar cells made with these films have power conversion efficiencies as high as 24.1% that display high stability. Science , this issue p. 1359
Li Z., Chen Y., Ji S., Tang Y., Chen W., Li A., Zhao J., Xiong Y., Wu Y., Gong Y., Yao T., Liu W., Zheng L., Dong J., Wang Y., et. al.
Nature Chemistry scimago Q1 wos Q1
2020-06-15 citations by CoLab: 564 Abstract  
Single-atom catalysts not only maximize metal atom efficiency, they also display properties that are considerably different to their more conventional nanoparticle equivalents, making them a promising family of materials to investigate. Herein we developed a general host–guest strategy to fabricate various metal single-atom catalysts on nitrogen-doped carbon (M1/CN, M = Pt, Ir, Pd, Ru, Mo, Ga, Cu, Ni, Mn). The iridium variant Ir1/CN electrocatalyses the formic acid oxidation reaction with a mass activity of 12.9 $${{{\rm{A}}\,{\rm{mg}}^{-1}_{{\rm{Ir}}}}}$$ whereas an Ir/C nanoparticle catalyst is almost inert (~4.8 × 10−3 $${{{\rm{A}}\,{\rm{mg}}^{-1}_{{\rm{Ir}}}}}$$). The activity of Ir1/CN is also 16 and 19 times greater than those of Pd/C and Pt/C, respectively. Furthermore, Ir1/CN displays high tolerance to CO poisoning. First-principle density functional theory reveals that the properties of Ir1/CN stem from the spatial isolation of iridium sites and from the modified electronic structure of iridium with respect to a conventional nanoparticle catalyst. Single-atom catalysts maximize metal atom efficiency and exhibit properties that can be considerably different to their nanoparticle equivalent. Now a general host–guest strategy to make various single-atom catalysts on nitrogen-doped carbon has been developed; the iridium variant electrocatalyses the formic acid oxidation reaction with high mass activity and displays high tolerance to CO poisoning.
Yang C., Wang L., Yin P., Liu J., Chen M., Yan Q., Wang Z., Xu S., Chu S., Cui C., Ju H., Zhu J., Lin Y., Shui J., Liang H.
Science scimago Q1 wos Q1 Open Access
2021-10-22 citations by CoLab: 561 PDF Abstract  
Sulfur-stabilized intermetallic nanoparticles Nanoparticles of intermetallic alloys of platinum could have enhanced electronic properties that improve their catalytic activity, but the high temperatures needed to ensure complete atomic diffusion often lead to the growth of larger nanoparticles—sintering—with low surface area and hence low overall activity. Yang et al . show that sulfur-doped carbon supports create strong platinum-sulfur bonds that stabilize small platinum alloy nanoparticles (<5 nanometers in diameter) to temperatures up to 1000ºC. They screened libraries of platinum alloys and identified ones with high mass activity for the oxygen reduction reaction in hydrogen fuel cells. —PDS
Chen Y., Gao R., Ji S., Li H., Tang K., Jiang P., Hu H., Zhang Z., Hao H., Qu Q., Liang X., Chen W., Dong J., Wang D., Li Y.
2020-12-10 citations by CoLab: 548 Abstract  
Demonstrated here is the correlation between atomic configuration induced electronic density of single-atom Co active sites and oxygen reduction reaction (ORR) performance by combining density-functional theory (DFT) calculations and electrochemical analysis. Guided by DFT calculations, a MOF-derived Co single-atom catalyst with the optimal Co1 -N3 PS active moiety incorporated in a hollow carbon polyhedron (Co1 -N3 PS/HC) was designed and synthesized. Co1 -N3 PS/HC exhibits outstanding alkaline ORR activity with a half-wave potential of 0.920 V and superior ORR kinetics with record-level kinetic current density and an ultralow Tafel slope of 31 mV dec-1 , exceeding that of Pt/C and almost all non-precious ORR electrocatalysts. In acidic media the ORR kinetics of Co1 -N3 PS/HC still surpasses that of Pt/C. This work offers atomic-level insight into the relationship between electronic density of the active site and catalytic properties, promoting rational design of efficient catalysts.
Zhang B., Wang L., Cao Z., Kozlov S.M., García de Arquer F.P., Dinh C.T., Li J., Wang Z., Zheng X., Zhang L., Wen Y., Voznyy O., Comin R., De Luna P., Regier T., et. al.
Nature Catalysis scimago Q1 wos Q1
2020-10-19 citations by CoLab: 539 Abstract  
Multimetal oxyhydroxides have recently been reported that outperform noble metal catalysts for oxygen evolution reaction (OER). In such 3d-metal-based catalysts, the oxidation cycle of 3d metals has been posited to act as the OER thermodynamic-limiting process; however, further tuning of its energetics is challenging due to similarities among the electronic structures of neighbouring 3d metal modulators. Here we report a strategy to reprogram the Fe, Co and Ni oxidation cycles by incorporating high-valence transition-metal modulators X (X = W, Mo, Nb, Ta, Re and MoW). We use in situ and ex situ soft and hard X-ray absorption spectroscopies to characterize the oxidation transition in modulated NiFeX and FeCoX oxyhydroxide catalysts, and conclude that the lower OER overpotential is facilitated by the readier oxidation transition of 3d metals enabled by high-valence modulators. We report an ~17-fold mass activity enhancement compared with that for the OER catalysts widely employed in industrial water-splitting electrolysers. Multimetal oxyhydroxides are among the most active catalysts for alkaline water oxidation, but tuning their properties remains a challenge. Now, the performance of NiFe- and FeCo-based catalysts is optimized with the incorporation of high-valence modulator metals, which shifts the active metals towards lower valence states and enables lower overpotentials.
Ren H., Yu S., Chao L., Xia Y., Sun Y., Zuo S., Li F., Niu T., Yang Y., Ju H., Li B., Du H., Gao X., Zhang J., Wang J., et. al.
Nature Photonics scimago Q1 wos Q1
2020-01-13 citations by CoLab: 502 Abstract  
Two-dimensional Ruddlesden–Popper phase (2DRP) perovskites are known to exhibit improved photostability and environmental stability compared with their three-dimensional (3D) counterparts. However, fundamental questions remain over the interaction between the bulky alkylammoniums and the 2DRP perovskite framework. Here, we unambiguously demonstrate that a sulfur–sulfur interaction is present for a new bulky alkylammonium, 2-(methylthio)ethylamine hydrochloride (MTEACl). In addition to a weaker van der Waals interaction, the interaction between sulfur atoms in two MTEA molecules enables a (MTEA)2(MA)4Pb5I16 (n = 5) perovskite framework with enhanced charge transport and stabilization. The result is 2DRP perovskite solar cells with significantly improved efficiency and stability. Cells with a power conversion efficiency as high as 18.06% (17.8% certified) are achieved, along with moisture tolerance for up to 1,512 h (under 70% humidity conditions), thermal stability for 375 h (at 85 °C) and stability under continuous light stress (85% of the initial efficiency retained over 1,000 h of operation at the maximum power point). Two-dimensional perovskite solar cells have been engineered to be robust against moisture, high temperatures and light stress.
Cao J., Wang M., Pei Y., Li Q., Zhao L., Xu Q., Zhang M., Yang H., Ning F.
2025-05-01 citations by CoLab: 0
Chen Y., Guo L., Jia Q., Xie X., Zhu W., Wang P.
Energies scimago Q1 wos Q3 Open Access
2025-03-10 citations by CoLab: 0 PDF Abstract  
The research on the thermal insulation performance of experimental systems in the liquid helium temperature range is relatively scarce. This paper presents the theoretical design and establishment of a liquid helium storage system for insulation research, consisting of a liquid helium Dewar, a daily boil-off rate test subsystem, and a helium recovery subsystem. The passive thermal insulation structure consisted of a multilayer insulation (MLI) system with hollow glass microspheres serving as spacers. Based on self-built data acquisition, experiments were conducted to investigate the liquid helium insulation characteristics of an experimental system. A theoretical thermal analysis of the Dewar was conducted, resulting in the derivation of an expression for the heat leak of the Dewar. The analysis indicates that the evaporation capacity from the liquid helium Dewar was significantly affected by the structure of the neck tube. The overall relative error between the simulated and experimental temperature distribution of the insulation layer is 14.3%, with a maximum error of 22.3%. The system had an average daily boil-off rate of 14.4%, a heat leakage of 7.5 W, and a heat flux of 2.254 W/m2, while the effective thermal conductivity of the MLI with hollow glass microspheres was determined to be 2.887 × 10−4 W/(m·K). Furthermore, the apparent thermal conductivity between different layers of MLI significantly fluctuated with increasing temperature, ranging from a maximum of 5.342 × 10−4 W/(m·K) to a minimum of 1.721 × 10−4 W/(m·K).
Wang J., Zeng M., Li D., Gao J.
2025-03-07 citations by CoLab: 0 PDF Abstract  
In recent years, the field of positron acceleration in plasma wakefield accelerators has witnessed rapid theoretical advancements, and several effective schemes have been proposed. In these studies, longitudinally uniform plasma is taken into account, with the positron beam located at the start of the second wakefield bubble. The electron filament near the positron beam provides Coulomb attraction force for the guiding of the positron beam. However, the influence of vacuum-plasma transition on positron beams has not been considered yet, where wakefield bubble is larger than that in the density plateau region, and the positron beam is in the defocusing region. In this paper, we study the evolution of positron beam size in the vacuum-plasma transition region and find out that the transition is detrimental to low-energy positron beams. Wide drive beams with relatively large transverse sizes are proposed as a possible solution to this difficulty. Published by the American Physical Society 2025
Mojahed M.A., Schmitz K., Xu X.
Physical Review D scimago Q1 wos Q1
2025-03-06 citations by CoLab: 0 Abstract  
Wash-in leptogenesis is an attractive mechanism to produce the baryon asymmetry of the Universe. It treats right-handed-neutrino interactions as spectator processes, on the same footing as electroweak sphalerons, that reprocess primordial charge asymmetries in the thermal plasma into a baryon-minus-lepton asymmetry. The origin of these primordial charges must be accounted for by new CP-violating dynamics at very high energies. In this paper, we propose such a scenario of chargegenesis that, unlike earlier proposals, primarily relies on new interactions in the gravitational sector. We point out that a coupling of a conserved current to the divergence of the Ricci scalar during reheating can lead to nonzero effective chemical potentials in the plasma that, together with a suitable charge-violating interaction, can result in the production of a primordial charge asymmetry. Gravitational chargegenesis represents a substantial generalization of the idea of gravitational baryogenesis. We provide a detailed analysis of a generic and minimal realization that is consistent with inflation and show that it can successfully explain the baryon asymmetry of the Universe. Published by the American Physical Society 2025
Song X.
Physical Review D scimago Q1 wos Q1
2025-03-06 citations by CoLab: 1 Abstract  
The possibility of compact stars as hideouts for color-spin-locked (CSL) quark matter (QM) is investigated in both the MIT bag model and the Nambu-Jona-Lasinio (NJL) model. Within the framework of the NJL model, the idea of absolutely stable quark matter and the existence of the conventional pure quark star (QS) are not supported; in addition, there appears to be no stable hybrid configuration above 2M⊙ as the hideout for CSL QM. The stable configurations of massive strange quark stars could be reproduced in the MIT bag model with QCD corrections being taken into account; moreover, they could act as the hiding place for the CSL QM. An interesting scenario is proposed that the phase transition to the CSL phase could occur in the cooling process. The CSL quark matter is an electromagnetic (EM) superconductor of type I, and a complete Meissner effect is expected. However, the analysis for this sizable superconductor indicates that most of the magnetic field is frozen inside the quark core with a critical strength, while in some special cases a small fraction could be expelled from a thin layer near the surface in a short time. The analysis on energetics and timescale suggests that this process could act as an inducement mechanism to power typical fast radio bursts, but as a single source of energy, it is unlikely to generate other EM emissions such as gamma-ray bursts and giant flares. Published by the American Physical Society 2025
Yang Y., Bi X., Yin P.
Physical Review D scimago Q1 wos Q1
2025-03-04 citations by CoLab: 0
Yang C., Yao J., Meng S., Wang P., He M., Li P., Xiao P., Xiao J., Liu Y., Li Z.
2025-03-04 citations by CoLab: 1
Xu R., Xia X., Han Z., Wang D., Ji G., Wang H., Cui X., Liu Y., Shi X., Jiang W., Fan R., Liang H.
IEEE Electron Device Letters scimago Q1 wos Q2
2025-03-01 citations by CoLab: 0
Ma X., Ma Y., Li Z., Zhang Y., Zhang J., Wei W., Li H., Ji X., Liu P., Chen Y.
2025-03-01 citations by CoLab: 0
Yang X., Ji X., Zhu K., Zhang S., Li H., Yu Z., Xiao P., Shi Y., Ma X.
2025-03-01 citations by CoLab: 0
Xu C., Zhang H., Zhou J., Chen Y., Yan Z., Liang Z., Wu T., Hu J., Wei W., Zhang Y.
2025-03-01 citations by CoLab: 0
Li H., Ye M., Xie X., Liu S., Huang S., Jiang X., Hu J.
2025-03-01 citations by CoLab: 0
Xu C., Zhou J., Zhang H., Zheng W., Zhou Y., Dong S., Dong J., Lu Y., Ouyang Q.
2025-03-01 citations by CoLab: 0
Wu Y., Yu Z., Zhang S., Chen C., Zhang H., Li F., Gu M., Zhu K.
2025-03-01 citations by CoLab: 0
Zhao X., Ke Y., Xie S., Sun M., Jiang H., Li B., Wang X.
2025-03-01 citations by CoLab: 1 Abstract  
Solid-state precipitation is an effective strategy for tuning the mechanical and functional properties of advanced alloys. Structure design and modification necessitate good knowledge of the kinetic evolution of precipitates during fabrication, which is strongly correlated with defect concentration. For Fe-Ga alloys, giant magnetostriction can be induced by the precipitation of the nanoscale tetragonal L60 phase. By introducing quenched-in vacancies, we significantly enhance the magnetostriction of the aged Fe81Ga19 polycrystalline alloys to ∼305 ppm, which is close to the level of single crystals. Although vacancies were found to facilitate the generation of the L60 phase, their impact on the precipitation mechanism and kinetics has yet to be revealed. This study combined transmission electron microscopy (TEM) and time-resolved small-angle neutron scattering (SANS) to investigate the precipitation of the L60 phase during the isothermal aging at 350 and 400 °C, respectively. The evolution of L60 nanophase in morphology and number density in as-cast (AC) and liquid nitrogen quenched (LN) Fe81Ga19 alloys with aging time were quantitatively compared. Interestingly, the nucleation of the L60 phase proceeds progressively in AC while suddenly in LN specimens, indicating the homogenous to heterogeneous mechanism switching induced by concentrated vacancies. Moreover, excess vacancies can change the shape of nanoprecipitates and significantly accelerate the growth and coarsening kinetics. The magnetostrictive coefficient is optimized when the size (long-axis) of L60 precipitates lies between 100 and 110 Å with a number density between 3.2–4.3 × 10–7 Å–3. Insight from this study validates the feasibility of achieving high magnetoelastic properties through precise manipulation of the nanostructure.

Since 1966

Total publications
17856
Total citations
495032
Citations per publication
27.72
Average publications per year
302.64
Average authors per publication
216.42
h-index
253
Metrics description

Top-30

Fields of science

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Nuclear and High Energy Physics, 5056, 28.32%
Astronomy and Astrophysics, 1950, 10.92%
Instrumentation, 1938, 10.85%
General Chemistry, 1841, 10.31%
General Materials Science, 1809, 10.13%
General Physics and Astronomy, 1695, 9.49%
Condensed Matter Physics, 1409, 7.89%
Physics and Astronomy (miscellaneous), 1308, 7.33%
Electronic, Optical and Magnetic Materials, 874, 4.89%
Space and Planetary Science, 847, 4.74%
Physical and Theoretical Chemistry, 804, 4.5%
Nuclear Energy and Engineering, 762, 4.27%
Engineering (miscellaneous), 750, 4.2%
Atomic and Molecular Physics, and Optics, 740, 4.14%
Materials Chemistry, 702, 3.93%
General Medicine, 654, 3.66%
Catalysis, 625, 3.5%
Electrical and Electronic Engineering, 596, 3.34%
Mechanical Engineering, 513, 2.87%
Mechanics of Materials, 504, 2.82%
Surfaces, Coatings and Films, 488, 2.73%
Biochemistry, 460, 2.58%
General Chemical Engineering, 454, 2.54%
Inorganic Chemistry, 408, 2.28%
Environmental Chemistry, 379, 2.12%
Mathematical Physics, 378, 2.12%
Renewable Energy, Sustainability and the Environment, 366, 2.05%
Analytical Chemistry, 340, 1.9%
Pollution, 335, 1.88%
Metals and Alloys, 332, 1.86%
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USA, 3377, 18.91%
Germany, 2358, 13.21%
Italy, 2309, 12.93%
United Kingdom, 2007, 11.24%
France, 1853, 10.38%
Switzerland, 1779, 9.96%
Spain, 1745, 9.77%
Poland, 1695, 9.49%
Russia, 1694, 9.49%
Brazil, 1559, 8.73%
Turkey, 1480, 8.29%
Colombia, 1471, 8.24%
Australia, 1439, 8.06%
Czech Republic, 1430, 8.01%
Austria, 1420, 7.95%
Greece, 1389, 7.78%
Georgia, 1365, 7.64%
Portugal, 1340, 7.5%
Serbia, 1336, 7.48%
Japan, 1272, 7.12%
Belarus, 1143, 6.4%
Netherlands, 1108, 6.21%
Armenia, 1089, 6.1%
Hungary, 1081, 6.05%
Sweden, 1024, 5.73%
Romania, 983, 5.51%
Canada, 967, 5.42%
Republic of Korea, 944, 5.29%
Bulgaria, 934, 5.23%
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  • We do not take into account publications without a DOI.
  • Statistics recalculated daily.
  • Publications published earlier than 1966 are ignored in the statistics.
  • The horizontal charts show the 30 top positions.
  • Journals quartiles values are relevant at the moment.