Improvement of the short-term stability of atomic fountain clock with state preparation by two-laser optical pumping

To improve the signal to noise ratio(SNR) and the short-term stability of cesium atomic fountain clocks, the work of two-laser optical pumping is presented theoretically and experimentally. The short-term stability of the NIM6 fountain clock has been improved by preparing more cold atoms in the |F = 4, mF= 0〉 clock state with a shortened cycle time.Two π-polarized laser beams overlapped in the horizontal plane have been applied after launching, one is resonant with|F = 4〉→ |F = 4〉 transition and the other is resonant with |F = 3〉→ |F = 4〉 transition. With optical pumping, the population accumulated in the |mF= 0〉 clock state is improved from 11% to 63%, and the detection signal is increased by a factor of 4.2, the SNR of the clock transition probability and the short-term stability are also improved accordingly.     

激光冷却SH~–阴离子的理论研究

本文采用多组态相互作用及Davidson修正方法和全电子基组计算了SH~-阴离子的X~1∑~+,a~3∏和A~1∏态的势能曲线、电偶极矩和跃迁偶极矩.计算的光谱常数与实验值及已有的理论值符合得很好.在计算中考虑了自旋-轨道耦合效应.计算得到a~3∏_1(v'=0)?X~1∑_(0+)~+(v"=0)和A~1∏_1(v'=0)?X~1Σ_(0+)~+(v"=0)跃迁具有高对角分布的弗兰克-康登因子,分别为0.9990和0.9999;计算得到a~3∏_1和A~1∏_1态的自发辐射寿命分别为1.472和0.188 ms.A~1∏_1?X~1∑_(0+)~+跃迁存在中间态a~3∏_(0+)和a~3∏_1,但中间态对激光冷却SH~-阴离子的影响可以忽略.分别利用a~3∏_1(v'=0)? X~1∑_(0+)~+(v"=0)和A~1∏_1(v'=0)? X~1∑_(0+)~+(v"=0)跃迁构建了准闭合的能级系统,冷却所需的激光波长分别为492.27和478.57 nm.最后预测了激光冷却SH~-阴离子能达到的多普勒温度和反冲温度.这些结果为进一步实验提供了理论参数.     

Characteristics of temperature fluctuation in two-dimensional turbulent Rayleigh-Bénard convection

We study the characteristics of temperature fluctuation in two-dimensional turbulent Rayleigh–Benard convection in′a square cavity by direct numerical simulations.The Rayleigh number range is 1×10⁸≤Ra≤1×10¹³,and the Prandtl number is selected as Pr=0.7 and Pr=4.3.It is found that the temperature fluctuation profiles with respect to Ra exhibit two different distribution patterns.In the thermal boundary layer,the normalized fluctuationθrms/θrms,max is independent of Ra and a power law relation is identified,i.e.,θrms/θrms,max～(z/δ)0.99±0.01,where z/δis a dimensionless distance to the boundary(δis the thickness of thermal boundary layer).Out of the boundary layer,when Ra≤5×10⁹,the profiles ofθrms/θrms,max descend,then ascend,and finally drop dramatically as z/δincreases.While for Ra≥1×10¹⁰,the profiles continuously decrease and finally overlap with each other.The two different characteristics of temperature fluctuations are closely related to the formation of stable large-scale circulations and corner rolls.Besides,there is a critical value of Ra indicating the transition,beyond which the fluctuation hθrmsiV has a power law dependence on Ra,given by hθrmsiV～Ra?0.14±0.01.     

On Realization of an Extremely Small Shift of MR Frequency in a Wide Range of Operating Temperatures in Rubidium Atomic Clock on 87 Rb Cell with Two Anti-Relaxation Components (Coating + Inert Gas, 40 Ar)

One of the most important problems in achieving daily frequency instability $$\sigma _{y} < 5 \cdot 10^{{ - 14}}$$ of on-board rubidium atomic clocks on absorption cell with working 87Rb atoms and mixture of buffer gases is realization of the TFS parameter — of temperature frequency shift $$\delta \nu \left( T \right)$$ at the level of $$\ \le 3 \cdot 10^{{ - 12}} /\, {^\circ } {\text{C}}.$$ The temperature dependence of the microwave “0–0” transition frequency $$\nu \left( T \right)$$ has an extremum with a small flat top ∆T ~ 0.5 °C to which the 87Rb-cell operating temperature is tuned. Significant difficulties arise in maintaining the high stability of this small ∆T zone under conditions of increased 87Rb cell operating temperature, $$T>70\, ^\circ{\rm C}$$, with an accuracy of < 0.005 °C for a day or more. To solve this problem, authors proposed a new type of 87Rb absorption cell with two dissimilar anti-relaxation (AR) components (wall coating + buffer gas, 40Ar) and created a special physical setup for optical spin pumping of 87Rb atoms at the microwave magnetic resonance frequency, $$\nu \sim \;6.834\,\;{\text{GHz}}$$, with a resolution $$0.01 \,\mathrm{H}\mathrm{z}$$. Investigations have shown TFS $$\sim 1.4 \cdot 10^{{ - 12}} /\;{{^\circ }} {\text{C}}$$ in significantly expanded (by an order of magnitude) zone, $$\Delta T$$ ≃ $$5 \left(\pm 1\right)\,\, ^\circ{\rm C} ,$$ in the operating temperature range of $$\left( {35 \div 41} \right)\;^{ \circ } {\text{C}},$$ which is ensured inside a satellite, for example. The simultaneous effect of AR-components causes the maximum mutual compensation of temperature frequency shifts in the extended ∆T zone. The experimental data show the possibility realizing daily frequency instability $$\sigma _{y} \sim 1 \cdot 10^{{ - 14}}$$ of the on-board atomic clock on 87Rb cell with two dissimilar AR-components (wall coating + inert gas, 40Ar).     

Laboratory demonstration of geopotential measurement using transportable optical clocks

We report an experimental demonstration of geopotential difference measurement using a pair of transportable $^{40}$Ca$^{+}$ optical clocks (TOC-729-1 and TOC-729-3) in the laboratory, each of them has an uncertainty of $1.3 \times 10^{-17}$ and an instability of $4.8 \times 10^{-15}/\sqrt{ \tau } $. Referenced to a stationary clock of TOC-729-1, the geopotential difference measurements are realized by moving TOC-729-3 to three different locations and the relevant altitude differences are measured with uncertainties at the level of 20 cm. After correcting the systematic shifts (including gravitational red shift), the two-clock frequency difference is measured to be $-0.7(2.2) \times 10^{-17}$, considering both the statistic $(1.0 \times 10^{-17})$ and the systematic $(1.9 \times 10^{-17})$ uncertainties. The frequency difference between these two clocks is within their respective uncertainties, verifying the reliability of transportable $^{40}$Ca$^{+}$ optical clocks at the low level of 10$^{-17}$.     

Searching for isotropic stochastic gravitational-wave background in the international pulsar timing array second data release

We search for isotropic stochastic gravitational-wave background (SGWB) in the International Pulsar Timing Array second data release. By modeling the SGWB as a power-law, we find very strong Bayesian evidence for a common-spectrum process, and further this process has scalar transverse (ST) correlations allowed in general metric theory of gravity as the Bayes factor in favor of the ST-correlated process versus the spatially uncorrelated common-spectrum process is 30 ± 2. The median and the 90% equal-tail amplitudes of ST mode are ${{ \mathcal A }}_{\mathrm{ST}}={1.29}_{-0.44}^{+0.51}\times {10}^{-15}$, or equivalently the energy density parameter per logarithm frequency is ${{\rm{\Omega }}}_{\mathrm{GW}}^{\mathrm{ST}}={2.31}_{-1.30}^{+2.19}\times {10}^{-9}$, at frequency of 1 year⁻¹. However, we do not find any statistically significant evidence for the tensor transverse (TT) mode and then place the 95% upper limits as ${{ \mathcal A }}_{\mathrm{TT}}\lt 3.95\times {10}^{-15}$, or equivalently ${{\rm{\Omega }}}_{\mathrm{GW}}^{\mathrm{TT}}\lt 2.16\times {10}^{-9}$, at frequency of 1 year⁻¹.     

Constructing the three-qudit unextendible product bases with strong nonlocality

Unextendible product bases (UPBs) are interesting members of a family of orthogonal product bases. Here, we investigate the construction of 3-qudit UPBs with strong nonlocality. First, a UPB set in ${{C}^{3}}\otimes {{C}^{3}}\otimes {{C}^{3}}$ of size 19 is presented based on the shift UPBs. By mapping the system to a Rubik's cube, we provide a general method of constructing UPBs in ${{C}^{d}}\otimes {{C}^{d}}\otimes {{C}^{d}}$ of size ${{\left(d-1 \right)}^{3}}+2d+5$, whose corresponding Rubik's cube is composed of four parts. Second, for the more general case where the dimensions of parties are different, we extend the classical tile structure to the 3-qudit system and propose the tri-tile structure. By means of this structure, a ${{C}^{4}}\otimes {{C}^{4}}\otimes {{C}^{5}}$ system of size 38 is obtained based on a ${{C}^{3}}\otimes {{C}^{3}}\otimes {{C}^{4}}$ system of size 19. Then, we generalize this approach to the ${{C}^{{{d}_{1}}}}\otimes {{C}^{{{d}_{2}}}}\otimes {{C}^{{{d}_{3}}}}$ system which also consists of four parts. Our research provides a positive answer to the open question raised in by Halder et al. [$Phys. Rev. Lett$. 122 040403 (2019)], indicating that there do exist UPBs that can exhibit strong quantum nonlocality without entanglement.     

A high-resolution Ramsey-Bordé spectrometer for optical clocks based on cold Mg atoms

We report on recent progress in our Ramsey-Bordé interferometer with cold magnesium atoms at 457.2 nm. A resolution as high as was achieved, which corresponds to a quality factor of Q = 2.3×10¹². An upper limit of 170 Hz for the laser oscillator line width is inferred from the interferometric analysis of the contrast decay induced by the residual atomic motion and spontaneous emission. The performance of the spectrometer allows to realize an optical frequency standard at 457.2 nm with a short-term stability of up to with 10⁵ atoms similar to state-of-the art, non-cryogenic microwave clocks or oscillators.     

Parity-violating neutron spin rotation in hydrogen and deuterium

We calculate the (parity-violating) spin-rotation angle of a polarized neutron beam through hydrogen and deuterium targets, using pionless effective field theory up to next-to-leading order. Our result is part of a program to obtain the five leading independent low-energy parameters that characterize hadronic parity violation from few-body observables in one systematic and consistent framework. The two spin-rotation angles provide independent constraints on these parameters. Our result for np spin rotation is $\frac{1} {\rho }\frac{{d\varphi _{PV}^{np} }} {{dl}} = \left[ {4.5 \pm 0.5} \right] rad MeV^{ - \frac{1} {2}} \left( {2g^{\left( {^3 S_1 - ^3 P_1 } \right)} + g^{\left( {^3 S_1 - ^3 P_1 } \right)} } \right) - \left[ {18.5 \pm 1.9} \right] rad MeV^{ - \frac{1} {2}} \left( {g_{\left( {\Delta {\rm I} = 0} \right)}^{\left( {^1 S_0 - ^3 P_0 } \right)} - 2g_{\left( {\Delta {\rm I} = 2} \right)}^{\left( {^1 S_0 - ^3 P_0 } \right)} } \right)$\frac{1} {\rho }\frac{{d\varphi _{PV}^{np} }} {{dl}} = \left[ {4.5 \pm 0.5} \right] rad MeV^{ - \frac{1} {2}} \left( {2g^{\left( {^3 S_1 - ^3 P_1 } \right)} + g^{\left( {^3 S_1 - ^3 P_1 } \right)} } \right) - \left[ {18.5 \pm 1.9} \right] rad MeV^{ - \frac{1} {2}} \left( {g_{\left( {\Delta {\rm I} = 0} \right)}^{\left( {^1 S_0 - ^3 P_0 } \right)} - 2g_{\left( {\Delta {\rm I} = 2} \right)}^{\left( {^1 S_0 - ^3 P_0 } \right)} } \right), while for nd spin rotation we obtain $\frac{1} {\rho }\frac{{d\varphi _{PV}^{nd} }} {{dl}} = \left[ {8.0 \pm 0.8} \right] rad MeV^{ - \frac{1} {2}} g^{\left( {^3 S_1 - ^1 P_1 } \right)} + \left[ {17.0 \pm 1.7} \right] rad MeV^{ - \frac{1} {2}} g^{\left( {^3 S_1 - ^3 P_1 } \right)} + \left[ {2.3 \pm 0.5} \right] rad MeV^{ - \frac{1} {2}} \left( {3g_{\left( {\Delta {\rm I} = 0} \right)}^{\left( {^1 S_0 - ^3 P_0 } \right)} - 2g_{\left( {\Delta {\rm I} = 1} \right)}^{\left( {^1 S_0 - ^3 P_0 } \right)} } \right)$\frac{1} {\rho }\frac{{d\varphi _{PV}^{nd} }} {{dl}} = \left[ {8.0 \pm 0.8} \right] rad MeV^{ - \frac{1} {2}} g^{\left( {^3 S_1 - ^1 P_1 } \right)} + \left[ {17.0 \pm 1.7} \right] rad MeV^{ - \frac{1} {2}} g^{\left( {^3 S_1 - ^3 P_1 } \right)} + \left[ {2.3 \pm 0.5} \right] rad MeV^{ - \frac{1} {2}} \left( {3g_{\left( {\Delta {\rm I} = 0} \right)}^{\left( {^1 S_0 - ^3 P_0 } \right)} - 2g_{\left( {\Delta {\rm I} = 1} \right)}^{\left( {^1 S_0 - ^3 P_0 } \right)} } \right), where the g ^(X-Y), in units of $MeV^{ - \frac{3} {2}}$MeV^{ - \frac{3} {2}}, are the presently unknown parameters in the leading-order parity-violating Lagrangian. Using naıve dimensional analysis to estimate the typical size of the couplings, we expect the signal for standard target densities to be $\left| {\frac{{d\varphi _{PV} }} {{dl}}} \right| \approx \left[ {10^{ - 7} \ldots 10^{ - 6} } \right]\frac{{rad}} {m}$\left| {\frac{{d\varphi _{PV} }} {{dl}}} \right| \approx \left[ {10^{ - 7} \ldots 10^{ - 6} } \right]\frac{{rad}} {m} for both hydrogen and deuterium targets. We find no indication that the nd observable is enhanced compared to the np one. All results are properly renormalized. An estimate of the numerical and systematic uncertainties of our calculations indicates excellent convergence. An appendix contains the relevant partial-wave projectors of the three-nucleon system.     

A 532 nm molecular iodine optical frequency standard based on modulation transfer spectroscopy

We report construction of an iodine-stabilized laser frequency standard at 532 nm based on modulation transfer spectroscopy(MTS) technology with good reproducibility. A frequency stability of 2.5 × 10~(-14) at 1 s averaging time is achieved,and the frequency reproducibility has a relative uncertainty of 3.5×10~(-13), demonstrating the great stability of our setup.The systematic uncertainty of the iodine-stabilized laser frequency standard is evaluated, especially the contribution of the residual amplitude modulation(RAM). The contribution of the RAM in MTS cannot be evaluated directly. To solve this problem, we theoretically deduce the MTS signal with RAM under large modulation depth, and prove that the nonsymmetric shape of the MTS signal is directly related to the MTS effect. The non-symmetric shape factor r can be calibrated with a frequency comb, and in real experiments, this r value can be obtained by least-squares fitting of the MTS signal,from which we can infer the RAMinduced frequency shift. The full frequency uncertainty is evaluated to be 5.3 k Hz(corresponding to a relative frequency uncertainty of 9.4×10~(-12)). The corrected transition frequency has a difference from the BIPM-recommended value of 2 k Hz, which is within 1σ uncertainty, proving the validity of our evaluation.     

Frequency stabilization of CO laser using RF optogalvanic Lamb-dip

The Lamb dip of CO rovibrational transition is detected by a room temperature extracavity RF optogalvanic cell and employed to stabilize the frequency of a CO laser. The S/N ratio of optogalvanic signal is about 2000  at optical power < 1 W. The relative depth of Lamb dip is 2.3%. The S/N ratios of first and third harmonic demodulated saturation signals are about 40  and 10  , respectively. The CO laser is stabilized using the first harmonic demodulated signal, and the frequency stability is better than 300 kHz. Concurrently, the influences of operational parameters, which include the coil current, partial pressures of gas mixture, are investigated. A simple model for the influence of coil current is presented, and further improvements are addressed as well.     

AC Stark-shift in CPT-based Cs miniature atomic clocks

We report on studies on the light-shift in caesium miniature atomic clocks based on coherent population trapping (CPT) using a micro-fabricated buffer-gas cell (MEMS cell). The CPT signal is observed on the Cs D1-line by coupling the two hyperfine ground-state Zeeman sublevels involved in the clock transition to a common excited state, using two coherent electromagnetic fields. These light fields are created with a distributed feedback laser and an electro-optical modulator. We study the light-shift phenomena at different cell temperatures and laser wavelengths around 894.6?nm. By adjusting the cell temperature, conditions are identified where a miniature CPT atomic clock can be operated with simultaneously low temperature coefficient and suppressed light-shift. The impact of the light-shift on the clock frequency stability is evaluated. These results are relevant for improving the long-term frequency stability of CPT-based Cs vapour-cell clocks.     

Coherent interaction and action-counteraction theory in small polaron systems,and ground state properties

Based on the coherent interaction and action-counteraction principles, we investigate the ground state properties for small polaron systems, the coherent-squeezed fluctuation correction, and the anomalous lattice quantum fluctuation, with the new variational generator containing correlated squeezed-coherent coupling and quantum entanglement. Noting that $-2t $ is the T.B.A. energy, for the coherent interaction effect, we find the ground-state energy $E_0$ to be $-2.428t$, in which the coherent squeezed fluctuation correction $-A_0 t$ is $-0.463t $ (where $ t $ is the hopping integral, $\omega $ is the phonon frequency), with the electron-one-phonon coupling constant $g=$1 and the electron-two-phonon coupling constant $g_{1}=-0.1$. However, as a result of the action-counteraction effect, $\tilde{{E}}_{0} $ is $-2.788t$, but $-\tilde{{A}}_{0} t$ is $-0.735t$. As to the polaron binding energy $(E_{\rm P} )$, for the coherent interaction effect, $E_{\rm P} $ is $-1.38\omega $, but for the action-counteraction effect, $\tilde{{E}}_{\rm P}$ is $-1.88\omega $. In particular, the electron-two-phonon interaction noticeably enlarges the coherent interaction and the coherent squeezed quantum fluctuation correction. By intervening with the quantum entanglement, the evolutions of the squeezed coherent state and the lattice quantum fluctuation begin to take control. At that time, we encounter a new quantum phase coherence phenomenon — the collapse and revival of inversion repeatedly for the coherent state in the entangled evolution.     

Selectivity of anion exchange membrane modified with polyethyleneimine

Previous works have been made on the improvement of selectivity of ion exchange membranes using adsorption of polyelectrolyte on the surface of the materials. The modification of the surface material in the case of an anion exchange membrane concerns the hydrophilic/hydrophobic balance properties and its relationship with the hydration state. Starting from this goal, the AMX membrane has been modified, in this work, by adsorption of polyethyleneimine on its surface. Many conditions of modification of the AMX membrane surface were studied. A factorial experimental design was used for determining the influent parameters on the AMX membrane modification. The results obtained have shown that the initial concentration of polyethyleneimine and the pH of solution were the main influent parameters on the adsorption of polyethyleneimine on the membrane surface. Competitive ion exchange reactions were studied for the modified and the unmodified membrane involving $ {\text{C}}{{\text{l}}^{ - }} $ , $ {\text{NO}}_3^{ - } $ and $ {\text{SO}}_4^{{2 - }} $ ions. All experiments were carried out at constant concentration of 0.3?mol?L^?1 and at 25?°C. Ion exchange isotherms for the binary systems $ \left( {{\text{C}}{{\text{l}}^{ - }}/{\text{NO}}_3^{ - }} \right) $ , $ \left( {{\text{C}}{{\text{l}}^{ - }}/{\text{SO}}_4^{{2 - }}} \right) $ and $ \left( {{\text{NO}}_3^{ - }/{\text{SO}}_4^{{2 - }}} \right) $ were studied. The obtained results show that chloride was the most sorbed and the selectivity order both for the modified membrane and the unmodified one is: $ {\text{Cl}} > {\text{NO}}_3^{ - } > {\text{SO}}_4^{{2 - }} $ , under the experimental conditions. Selectivity coefficients $ {\text{K}}_{{{\text{C}}{{\text{l}}^{ - }}}}^{{{\text{NO}}_3^{ - }}} $ , $ {\text{K}}_{{2{\text{C}}{{\text{l}}^{ - }}}}^{{{\text{SO}}_4^{{2 - }}}} $ and $ {\text{K}}_{{2{\text{NO}}_3^{ - }}}^{{{\text{SO}}_4^{{2 - }}}} $ for the three binary systems and for the two membranes were determined. It was also observed that for the modified membrane the selectivity towards sulfate ion decrease and the modified membrane became more selective towards monovalent anions.     

Einfluß des Randes auf das effektive Verhalten heterogener Körper - Anwendung auf Rayleighwellen

Effective Elastic Properties of Finite Heterogeneous Media - Application to Rayleigh-waves Rayleigh waves in a heterogeneous material (multiphase mixtures, composite materials, polycrystals) are governed by integrodifferential equations derived by the aid of known methods for infinite heterogeneous media. According to this wave equation the velocity depends on the frequency, and the waves are damped. After some simplifications (isotropy, nonrandom elastic constants) the following is obtained: if the fluctuations of the mass density are restricted to the vicinity of the boundary, the frequency dependent part of the velocity behaves like \documentclass{article}\pagestyle{empty}\begin{document}$ \frac{{l^3 \omega ^3}}{{{\mathop c\limits^\circ} _t^3}} $\end{document} and the damping is proportional to \documentclass{article}\pagestyle{empty}\begin{document}$ \frac{{l^4 \omega ^5}}{{{\mathop c\limits^\circ} _t^5}} $\end{document}, whereas \documentclass{article}\pagestyle{empty}\begin{document}$ \frac{{l^2 \omega ^2}}{{{\mathop c\limits^\circ} _t^2}} $\end{document} respectively \documentclass{article}\pagestyle{empty}\begin{document}$ \frac{{l^3 \omega ^4}}{{{\mathop c\limits^\circ} _t^4}} $\end{document} is found if the fluctuations are present in the whole half-space. From this it is seen, what assumptions are necessary to describe the waves by differential equations with frequenc y-dependent mass density.     

Diffusion of proton in alumina-rich nonstoichiometric magnesium aluminate spinel

The phenomenon of the diffusion of proton and deuteron in a single crystal of magnesium aluminate spinel was studied by infrared absorption. The chemical diffusion coefficient of proton was determined by the relaxation time of the absorption intensity upon the substitution of deuteron with proton. The temperature dependence of the chemical diffusion coefficient of proton for was expressed as . The chemical diffusion coefficient of proton was found to be independent of the composition of spinel and of the atmosphere. Paper presented at the 11th Euro Conference on the Science and Technology of Ionics, Batz-sur-Mer, Sept. 9–15 2007.     

Contrast Saturation Resonances in the Absorption Band of Rubidium Molecules

We study Doppler-free saturation resonances in the absorption band $ {{\mathrm{B}}^1}{\Pi_{\mathrm{u}}}-{{\mathrm{X}}^1}\Sigma_{{^{\mathrm{g}}}}^{+} $ of rubidium diatomic molecules in the frequency range near the D₂ line of lithium atoms (671 nm). We observe contrast saturation resonances and record a variation in the laser light transmission of 4% due to optical saturation. The large optical nonlinearities in the molecular diatomic gas can be used for investigating the four-wave mixing and other nonlinear effects.     

Stability of {\text{SrCe}}_{{0.9}} {\text{Eu}}_{{0.1}} {\text{O}}_{{3 - \delta }} and {\text{SrZr}}_{{0.2}} {\text{Ce}}_{{0.7}} {\text{Eu}}_{{0.1}} {\text{O}}_{{3 - \delta }} under H2 atmospheres

Previous H₂ permeation tests showed a degradation of H₂ permeation flux with time. To understand the cause of degradation and develop a solution, the stability of $ {\text{SrCe}}_{{0.9}} {\text{Eu}}_{{0.1}} {\text{O}}_{{3 - \delta }} $ and $ {\text{SrZr}}_{{0.2}} {\text{Ce}}_{{0.7}} {\text{Eu}}_{{0.1}} {\text{O}}_{{3 - \delta }} $ samples were studied under dry and wet H₂ atmospheres. Total conductivity of $ {\text{SrCe}}_{{0.9}} {\text{Eu}}_{{0.1}} {\text{O}}_{{3 - \delta }} $ increased with time in dry H₂. The X-ray diffraction pattern of $ {\text{SrCe}}_{{0.9}} {\text{Eu}}_{{0.1}} {\text{O}}_{{3 - \delta }} $ after dry hydrogen atmosphere heat treatments show CeO₂ peaks indicating that $ {\text{SrCe}}_{{0.9}} {\text{Eu}}_{{0.1}} {\text{O}}_{{3 - \delta }} $ decomposes under dry H₂ atmospheres; scanning electron microscopy and energy dispersive X-ray spectroscopy analyses prove that decomposition proceeded along the grain boundaries. $ {\text{SrZr}}_{{0.2}} {\text{Ce}}_{{0.7}} {\text{Eu}}_{{0.1}} {\text{O}}_{{3 - \delta }} $ was investigated and demonstrated greater stability under dry hydrogen atmospheres. However, Zr substitution results in a tradeoff with electrical properties.