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The upregulation of programmed death-ligand 1 (PD-L1) and epidermal growth factor receptor 2 (HER2) may play a role in gastric adenocarcinoma (GAC).To study PD-L1 and HER-2 expression and prognosis in GAC.PD-L1 and HER2 expression was determined in tumor tissues of 75 patients with GAC. The correlations between PD-L1, HER2 expression, and clinicopathological factors were analyzed.The positive expression rate for PD-L1 was 57.3% (43/75) and the HER2 over-expression rate was 17.3% (13/75). PD-L1 expression negatively correlated with the grade of GAC differentiation (r =-0.26, P0.05). Approximately 85% of HER2-positive GACs were found to be PD-L1-positive and PD-L1 expression positively correlated with HER2 overexpression. The TNM stage and combined HER2 and PD-L1 expression were independent prognostic factors affecting the survival of patients with GAC. The median overall survival and recurrence-free survival of groups I (HER2 overexpression and PD-L1 positive), II (HER2 overexpression and PD-L1 negative), III (No HER2 overexpression and PD-L1 positive) and IV (No HER2 overexpression and PD-L1 negative) were (47 (17-77), 15 (0-44), 81 (62-101), and 78 (60-98) months, respectively.PD-L1 expression is upregulated in more than half of patients with GAC. Anti-PD-L1 treatment combined with anti-HER2 therapy may benefit patients with locally advanced GAC with HER2 overexpression.

Summary Aliovalent defects are extremely effective in manipulating charge transport and atomic vibrational properties for thermoelectric enhancements. Electronic performance of thermoelectrics is optimized at a reduced Fermi level of ∼0.3, which causes the optimal carrier concentration (nopt) to be strongly temperature dependent. This motivates a dynamic doping approach for electronic enhancements through an increase with temperature of solubility of aliovalent dopants. In addition, the defects could simultaneously act as scattering sources of phonons for reducing the lattice thermal conductivity. These effects are illustrated in this work by the temperature-dependent excess Cu solubility in n-PbTe0.75Se0.25 thermoelectrics, in which both carriers and dislocations are induced for regulating the electronic and phononic transport properties for a realization of an extraordinary thermoelectric figure of merit. The resultant defect structures and temperature gradient doping effects (for aliovalent solutes) could in principle open extra possibilities for optimizing charge and phonon transport properties in thermoelectrics.

Advanced functional materials 10(47), 2209980 (2022). doi:10.1002/adfm.202209980, Published by Wiley-VCH, Weinheim

Lithium-sulfur (Li-S) batteries have attracted widespread attention due to their high theoretical energy density. However, their practical application is still hindered by the shuttle effect and the sluggish conversion of lithium polysulfides (LiPSs). Herein, monodisperse molybdenum (Mo) nanoparticles embedded onto nitrogen-doped graphene (Mo@N-G) were developed and used as a highly efficient electrocatalyst to enhance LiPS conversion. The weight ratio of the electrocatalyst in the catalyst/sulfur cathode is only 9%. The unfilled d orbitals of oxidized Mo can attract the electrons of LiPS anions and form Mo–S bonds during the electrochemical process, thus facilitating fast conversion of LiPSs. Li-S batteries based on the Mo@N-G/S cathode can exhibit excellent rate performance, large capacity, and superior cycling stability. Moreover, Mo@N-G also plays an important role in room-temperature quasi-solid-state Li-S batteries. These interesting findings suggest the great potential of Mo nanoparticles in building high-performance Li-S batteries.

Summary Lattice vibrations in crystalline materials generate phonons as heat carriers for heat conduction, and the phonon dispersion (energy versus momentum) is fundamentally determined by the mass of lattice vibrators (atoms) and the interaction force between atoms. A significant manipulation of lattice thermal conductivity through a change in atomic mass usually requires a large variation in chemical composition, which is not always valid thermodynamically or may risk the resultant detriment of other functionalities (e.g., carrier mobility). Here we show a strategy of alternatively manipulating the interaction force between atoms through lattice strains without changing the composition, for remarkably reducing the lattice thermal conductivity without reducing carrier mobility, in Na0.03Eu0.03Sn0.02Pb0.92Te with stable lattice dislocations. This successfully leads to an extraordinarily high thermoelectric figure of merit, with the help of valence band convergence. This work offers both insights and solutions on lattice strain engineering for reducing lattice thermal conductivity, thus advancing thermoelectrics.

© 2020 Elsevier B.V. Molten salts are a unique type of electrolyte enabling high-temperature electrochemical energy storage (EES) with unmatched reversible electrode kinetics and high ion-conductivities, and hence impressive storage capacity and power capability. However, their high tendency to evaporate and flow at high temperatures challenges the design and fabrication of the respective EES devices in terms of manufacturing cost and cycling durability. On the other hand, most of these EES devices require lithium-containing molten salts as the electrolyte to enhance performances, which not only increases the cost but also demands a share of the already limited lithium resources. Here we report a novel quasi-solid-state (QSS) electrolyte, consisting of the molten eutectic mixture of Na2CO3-K2CO3 and nanoparticles of yttrium stabilized zirconia (YSZ) in a mass ratio of 1:1. The QSS electrolyte has relatively lower volatility in comparison with the pristine molten Na2CO3-K2CO3 eutectic, and therefore significantly suppresses the evaporation of molten salts, thanks to a strong interaction at the interface between molten salt and YSZ nanoparticles at high temperatures. The QSS electrolyte was used to construct an iron-air battery that performed excellently in charge-discharge cycling with high columbic and energy efficiencies. We also propose and confirm a redox mechanism at the three-phase interlines in the negative electrode. These findings can help establish a simpler and more efficient approach to designing low-cost and high-performance molten salt metal-air batteries with high stability and safety.

In‐grain dislocation‐induced lattice strain fluctuations are recently revealed as an effective avenue for minimizing the lattice thermal conductivity. This effect could be integratable with electronic enhancements such as by band convergence, for a great advancement in thermoelectric performance. This motivates the current work to focus on the thermoelectric enhancements of p‐type PbTe alloys, where monotelluride‐alloying and Na‐doping are used for a simultaneous manipulation on both dislocation and band structures. As confirmed by synchrotron X‐ray diffractions and Raman measurements, the resultant dense in‐grain dislocations induce lattice strain fluctuations for broadening the phonon dispersion, leading to an exceptionally low lattice thermal conductivity of ≈0. 4 W m‐K−1. Band structure calculations reveal the convergence of valence bands due to monotelluride‐alloying. Eventually, the integration of both electronic and thermal improvements lead to a realization of an extraordinary figure of merit zT of ≈2.5 in Na0.03Eu0.03Cd0.03Pb0.91Te alloy at 850 K., Simultaneous manipulation of in‐grain dislocations for lattice thermal conductivity reduction and band convergence for electronic enhancement leads to a realization of an extraordinary thermoelectric figure of merit in p‐PbTe alloys.

Maximizing band degeneracy and minimizing phonon relaxation time are proven to be successful for advancing thermoelectrics. Alloying with monotellurides has been known to be an effective approach for converging the valence bands of PbTe for electronic improvements, while the lattice thermal conductivity of the materials remains available room for being further reduced. It is recently revealed that the broadening of phonon dispersion measures the strength of phonon scattering, and lattice dislocations are particularly effective sources for such broadening through lattice strain fluctuations. In this work, a fine control of MnTe and EuTe alloying enables a significant increase in density of electron states near the valence band edge of PbTe due to involvement of multiple transporting bands, while the creation of dense in-grain dislocations leads to an effective broadening in phonon dispersion for reduced phonon lifetime due to the large strain fluctuations of dislocations as confirmed by synchrotron X-ray diffraction. The synergy of both electronic and thermal improvements successfully leads the average thermoelectric figure of merit to be higher than that ever reported for p-type PbTe at working temperatures.

GeSe is a IV-VI semiconductor, like the excellent thermoelectric materials PbTe and SnSe. Orthorhombic GeSe has been predicted theoretically to have good thermoelectric performance but is difficult to dope experimentally. Like PbTe, rhombohedral GeTe has a multivalley band structure, which is ideal for thermoelectrics and also promotes the formation of Ge vacancies to provide enough carriers for electrical transport. Herein, we investigate the thermoelectric properties of GeSe alloyed with AgSbSe2, which stabilizes a new rhombohedral structure with higher symmetry that leads to a multivalley Fermi surface and a dramatic increase in carrier concentration. The zT of GeAg0.2Sb0.2Se1.4 reaches 0.86 at 710 K, which is 18 times higher than that of pristine GeSe and over four times higher than doped orthorhombic GeSe. Our results open a new avenue towards developing novel thermoelectric materials via crystal phase engineering using a strategy of entropy stabilization of high symmetry alloys.

Perovskite manganite Ca0.9R0.1MnO3−δ (R = Dy, Yb) ceramics have been synthesized by a traditional solid-state reaction with multicalcination processes. A heterogeneous microstructure including large and small micrometer-sized grains, coherent interfaces, and oxygen defects has been formed with optimized calcination time. The carrier concentration of the third-calcined samples is enhanced approximately 3 times compared with those synthesized through conventional methods. Thus, the electrical resistivity of the third-calcined Ca0.9R0.1MnO3−δ (R = Dy, Yb) ceramic samples obviously decreases, leading to a higher power factor. Additionally, the thermal conductivity is also reduced by multiscale scattering of the heterogeneous structure. The lowest lattice thermal conductivities of Dy- or Yb-doped samples are 1.24 and 1.22 W m–1 K–1, respectively. Thus, the high thermoelectric performance for Ca0.9R0.1MnO3−δ (R = Dy, Yb) has been achieved by the multicalcination process. The highest figure of merit is almost 30% higher than that of the first-calcined samples. Therefore, a heterogeneous microstructure formed by optimized multicalcination can effectively optimize the thermoelectric performance of oxides., The work is financially supported by the National Basic Research Program of China (2013CB632506), the Natural Science Fund of China under Grants 51501105, 51672159, and 51611540342, the Young Scholars Program of Shandong University under Grant 2015WLJH21, the China Postdoctoral Science Foundation under Grants 2015M580588 and 2016T90631, the Postdoctoral Innovation Foundation of Shandong Province under Grant 201603027, the Fundamental Research Funds of Shandong University under Grant 2015TB019, and the Foundation of the State Key Laboratory of Metastable Materials Science and Technology under Grant 201703.