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Now showing 1 - 10 of 12
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    Ultrahigh Power Factor in Thermoelectric System Nb0.95M0.05FeSb (M = Hf, Zr, and Ti)
    (Chichester : John Wiley and Sons Ltd, 2018) Ren, W.; Zhu, H.; Zhu, Q.; Saparamadu, U.; He, R.; Liu, Z.; Mao, J.; Wang, C.; Nielsch, K.; Wang, Z.; Ren, Z.
    Conversion efficiency and output power are crucial parameters for thermoelectric power generation that highly rely on figure of merit ZT and power factor (PF), respectively. Therefore, the synergistic optimization of electrical and thermal properties is imperative instead of optimizing just ZT by thermal conductivity reduction or just PF by electron transport enhancement. Here, it is demonstrated that Nb0.95Hf0.05FeSb has not only ultrahigh PF over ≈100 µW cm−1 K−2 at room temperature but also the highest ZT in a material system Nb0.95M0.05FeSb (M = Hf, Zr, Ti). It is found that Hf dopant is capable to simultaneously supply carriers for mobility optimization and introduce atomic disorder for reducing lattice thermal conductivity. As a result, Nb0.95Hf0.05FeSb distinguishes itself from other outstanding NbFeSb-based materials in both the PF and ZT. Additionally, a large output power density of ≈21.6 W cm−2 is achieved based on a single-leg device under a temperature difference of ≈560 K, showing the realistic prospect of the ultrahigh PF for power generation.
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    Measurements of gaseous H2SO4 by AP-ID-CIMS during CAREBeijing 2008 Campaign
    (München : European Geopyhsical Union, 2011) Zheng, J.; Hu, M.; Zhang, R.; Yue, D.; Wang, Z.; Guo, S.; Li, X.; Bohn, B.; Shao, M.; He, L.; Huang, X.; Wiedensohler, A.; Zhu, T.
    As part of the 2008 Campaign of Air Quality Research in Beijing and Surrounding Regions (CAREBeijing 2008), measurements of gaseous sulfuric acid (H2SO4) have been conducted at an urban site in Beijing, China from 7 July to 25 September 2008 using atmospheric pressure ion drift – chemical ionization mass spectrometry (AP-ID-CIMS). This represents the first gaseous H2SO4 measurements in China. Diurnal profile of sulfuric acid is strongly dependent on the actinic flux, reaching a daily maximum around noontime and with an hourly average concentration of 5 × 106 molecules cm−3. Simulation of sulfuric acid on the basis of the measured sulfur dioxide concentration, photolysis rates of ozone and nitrogen dioxide, and aerosol surface areas captures the trend of the measured H2SO4 diurnal variation within the uncertainties, indicating that photochemical production and condensation onto preexisting particle surface dominate the observed diurnal H2SO4 profile. The frequency of the peak H2SO4 concentration exceeding 5 × 106 molecules cm−3 increases by 16 % during the period of the summer Olympic Games (8–24 August 2008), because of the implementation of air quality control regulations. Using a multivariate statistical method, the critical nucleus during nucleation events is inferred, containing two H2SO4 molecules (R2 = 0.85). The calculated condensation rate of H2SO4 can only account for 10–25 % of PM1 sulfate formation, indicating that either much stronger sulfate production exists at the SO2 source region or other sulfate production mechanisms are responsible for the sulfate production.
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    Scanning supersaturation condensation particle counter applied as a nano-CCN counter for size-resolved analysis of the hygroscopicity and chemical composition of nanoparticles
    (München : European Geopyhsical Union, 2015) Wang, Z.; Su, H.; Wang, X.; Ma, N.; Wiedensohler, A.; Pöschl, U.; Cheng, Y.
    Knowledge about the chemical composition of aerosol particles is essential to understand their formation and evolution in the atmosphere. Due to analytical limitations, however, relatively little information is available for sub-10 nm particles. We present the design of a nano-cloud condensation nuclei counter (nano-CCNC) for measuring size-resolved hygroscopicity and inferring chemical composition of sub-10 nm aerosol particles. We extend the use of counting efficiency spectra from a water-based condensation particle counter (CPC) and link it to the analysis of CCN activation spectra, which provides a theoretical basis for the application of a scanning supersaturation CPC (SS-CPC) as a nano-CCNC. Measurement procedures and data analysis methods are demonstrated through laboratory experiments with monodisperse particles of diameter down to 2.5 nm, where sodium chloride, ammonium sulfate, sucrose and tungsten oxide can be easily discriminated by different characteristic supersaturations of water droplet formation. A near-linear relationship between hygroscopicity parameter κ and organic mass fraction is also found for sucrose-ammonium sulfate mixtures. The design is not limited to the water CPC, but also applies to CPCs with other working fluids (e.g. butanol, perfluorotributylamine). We suggest that a combination of SS-CPCs with multiple working fluids may provide further insight into the chemical composition of nanoparticles and the role of organic and inorganic compounds in the initial steps of atmospheric new particle formation and growth.
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    Discovery of TaFeSb-based half-Heuslers with high thermoelectric performance
    (London : Nature Publishing Group, 2019) Zhu, H.; Mao, J.; Li, Y.; Sun, J.; Wang, Y.; Zhu, Q.; Li, G.; Song, Q.; Zhou, J.; Fu, Y.; He, R.; Tong, T.; Liu, Z.; Ren, W.; You, L.; Wang, Z.; Luo, J.; Sotnikov, A.; Bao, J.; Nielsch, K.; Chen, G.; Singh, D.J.; Ren, Z.
    Discovery of thermoelectric materials has long been realized by the Edisonian trial and error approach. However, recent progress in theoretical calculations, including the ability to predict structures of unknown phases along with their thermodynamic stability and functional properties, has enabled the so-called inverse design approach. Compared to the traditional materials discovery, the inverse design approach has the potential to substantially reduce the experimental efforts needed to identify promising compounds with target functionalities. By adopting this approach, here we have discovered several unreported half-Heusler compounds. Among them, the p-type TaFeSb-based half-Heusler demonstrates a record high ZT of ~1.52 at 973 K. Additionally, an ultrahigh average ZT of ~0.93 between 300 and 973 K is achieved. Such an extraordinary thermoelectric performance is further verified by the heat-to-electricity conversion efficiency measurement and a high efficiency of ~11.4% is obtained. Our work demonstrates that the TaFeSb-based half-Heuslers are highly promising for thermoelectric power generation.
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    Engineering new limits to magnetostriction through metastability in iron-gallium alloys
    ([London] : Nature Publishing Group UK, 2021) Meisenheimer, P.B.; Steinhardt, R.A.; Sung, S.H.; Williams, L.D.; Zhuang, S.; Nowakowski, M.E.; Novakov, S.; Torunbalci, M.M.; Prasad, B.; Zollner, C. J.; Wang, Z.; Dawley, N.M.; Schubert, J.; Hunter, A.H.; Manipatruni, S.; Nikonov, D.E.; Young, I.A.; Chen, L.Q.; Bokor, J.; Bhave, S.A.; Ramesh, R.; Hu, J.-M.; Kioupakis, E.; Hovden, R.; Schlom, D.G.; Heron, J.T.
    Magnetostrictive materials transduce magnetic and mechanical energies and when combined with piezoelectric elements, evoke magnetoelectric transduction for high-sensitivity magnetic field sensors and energy-efficient beyond-CMOS technologies. The dearth of ductile, rare-earth-free materials with high magnetostrictive coefficients motivates the discovery of superior materials. Fe1−xGax alloys are amongst the highest performing rare-earth-free magnetostrictive materials; however, magnetostriction becomes sharply suppressed beyond x = 19% due to the formation of a parasitic ordered intermetallic phase. Here, we harness epitaxy to extend the stability of the BCC Fe1−xGax alloy to gallium compositions as high as x = 30% and in so doing dramatically boost the magnetostriction by as much as 10x relative to the bulk and 2x larger than canonical rare-earth based magnetostrictors. A Fe1−xGax − [Pb(Mg1/3Nb2/3)O3]0.7−[PbTiO3]0.3 (PMN-PT) composite magnetoelectric shows robust 90° electrical switching of magnetic anisotropy and a converse magnetoelectric coefficient of 2.0 × 10−5 s m−1. When optimally scaled, this high coefficient implies stable switching at ~80 aJ per bit.
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    Tomonaga–Luttinger liquid behavior and spinon confinement in YbAlO 3
    ([London] : Nature Publishing Group UK, 2019) Wu, L.S.; Nikitin, S.E.; Wang, Z.; Zhu, W.; Batista, C.D.; Tsvelik, A.M.; Samarakoon, A.M.; Tennant, D.A.; Brando, M.; Vasylechko, L.; Frontzek, M.; Savici, A.T.; Sala, G.; Ehlers, G.; Christianson, A.D.; Lumsden, M.D.; Podlesnyak, A.
    Low dimensional quantum magnets are interesting because of the emerging collective behavior arising from strong quantum fluctuations. The one-dimensional (1D) S = 1/2 Heisenberg antiferromagnet is a paradigmatic example, whose low-energy excitations, known as spinons, carry fractional spin S = 1/2. These fractional modes can be reconfined by the application of a staggered magnetic field. Even though considerable progress has been made in the theoretical understanding of such magnets, experimental realizations of this low-dimensional physics are relatively rare. This is particularly true for rare-earth-based magnets because of the large effective spin anisotropy induced by the combination of strong spin–orbit coupling and crystal field splitting. Here, we demonstrate that the rare-earth perovskite YbAlO3 provides a realization of a quantum spin S = 1/2 chain material exhibiting both quantum critical Tomonaga–Luttinger liquid behavior and spinon confinement–deconfinement transitions in different regions of magnetic field–temperature phase diagram.
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    Discovery of ZrCoBi based half Heuslers with high thermoelectric conversion efficiency
    (London : Nature Publishing Group, 2018) Zhu, H.; He, R.; Mao, J.; Zhu, Q.; Li, C.; Sun, J.; Ren, W.; Wang, Y.; Liu, Z.; Tang, Z.; Sotnikov, A.; Wang, Z.; Broido, D.; Singh, D.J.; Chen, G.; Nielsch, K.; Ren, Z.
    Thermoelectric materials are capable of converting waste heat into electricity. The dimensionless figure-of-merit (ZT), as the critical measure for the material's thermoelectric performance, plays a decisive role in the energy conversion efficiency. Half-Heusler materials, as one of the most promising candidates for thermoelectric power generation, have relatively low ZTs compared to other material systems. Here we report the discovery of p-type ZrCoBi-based half-Heuslers with a record-high ZT of ∼1.42 at 973 K and a high thermoelectric conversion efficiency of ∼9% at the temperature difference of ∼500 K. Such an outstanding thermoelectric performance originates from its unique band structure offering a high band degeneracy (N v) of 10 in conjunction with a low thermal conductivity benefiting from the low mean sound velocity (v m ∼2800 m s-1). Our work demonstrates that ZrCoBi-based half-Heuslers are promising candidates for high-temperature thermoelectric power generation.
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    Two types of magnetic shape-memory effects from twinned microstructure and magneto-structural coupling in Fe1 +yTe
    (Washington : National Academy of Sciences, 2019) Rößler, S.; Koz, C.; Wang, Z.; Skourski, Y.; Doerr, M.; Kasinathan, D.; Rosner, H.; Schmidt, M.; Schwarz, U.; Rößler, U.K.; Wirth, S.
    A detailed experimental investigation of Fe1+yTe (y = 0.11, 0.12) using pulsed magnetic fields up to 60 T confirms remarkable magnetic shape-memory (MSM) effects. These effects result from magnetoelastic transformation processes in the low-temperature antiferromagnetic state of these materials. The observation of modulated and finely twinned microstructure at the nanoscale through scanning tunneling microscopy establishes a behavior similar to that of thermoelastic martensite. We identified the observed, elegant hierarchical twinning pattern of monoclinic crystallographic domains as an ideal realization of crossing twin bands. The antiferromagnetism of the monoclinic ground state allows for a magnetic-field–induced reorientation of these twin variants by the motion of one type of twin boundaries. At sufficiently high magnetic fields, we observed a second isothermal transformation process with large hysteresis for different directions of applied field. This gives rise to a second MSM effect caused by a phase transition back to the field-polarized tetragonal lattice state.
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    Exploring the intrinsic limit of the charge-carrier-induced increase of the Curie temperature of Lu- and La-doped EuO thin films
    (College Park, MD : APS, 2020) Held, R.; Mairoser, T.; Melville, A.; Mundy, J.A.; Holtz, M.E.; Hodash, D.; Wang, Z.; Heron, J.T.; Dacek, S.T.; Holländer, B.; Muller, D.A.; Schlom, D.G.
    Raising the Curie temperature TC of the highly spin-polarized semiconductor EuO by doping it with rare-earth elements is a strategy to make EuO more technologically relevant to spintronics. The increase of TC with free carrier density n and the surprisingly low dopant activation p, found in Gd-doped EuO thin films [Mairoser et al., Phys. Rev. Lett. 105, 257206 (2010)], raised the important question of whether TC could be considerably enhanced by increasing p. Using a low-temperature growth method for depositing high-quality Lu-doped EuO films we attain high dopant activation (p) values of up to 67%, effectively more than doubling p as compared to adsorption-controlled growth of Lu- and Gd-doped EuO. Relating n, p, and lattice compression of La- and Lu-doped EuO films grown at different temperatures to the TC of these samples allows us to identify several different mechanisms influencing TC and causing an experimental maximum in TC. In addition, scanning transmission electron microscopy in combination with electron energy loss spectroscopy measurements on La-doped EuO indicate that extensive dopant clustering is one, but not the sole reason for dopant deactivation in rare-earth doped EuO films.
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    Onymity promotes cooperation in social dilemma experiments
    (Washington : American Association for the Advancement of Science (A A A S), 2017) Wang, Z.; Jusup, M.; Wang, R.-W.; Shi, L.; Iwasa, Y.; Moreno, Y.; Kurths, J.
    One of the most elusive scientific challenges for over 150 years has been to explain why cooperation survives despite being a seemingly inferior strategy from an evolutionary point of view. Over the years, various theoretical scenarios aimed at solving the evolutionary puzzle of cooperation have been proposed, eventually identifying several cooperation-promoting mechanisms: kin selection, direct reciprocity, indirect reciprocity, network reciprocity, and group selection. We report the results of repeated Prisoner’s Dilemma experiments with anonymous and onymous pairwise interactions among individuals. We find that onymity significantly increases the frequency of cooperation and the median payoff per round relative to anonymity. Furthermore, we also show that the correlation between players’ ranks and the usage of strategies (cooperation, defection, or punishment) underwent a fundamental shift, whereby more prosocial actions are rewarded with a better ranking under onymity. Our findings prove that reducing anonymity is a valid promoter of cooperation, leading to higher payoffs for cooperators and thus suppressing an incentive—anonymity—that would ultimately favor defection.