Site Occupancy Research Articles

Atomic-Scale Characterization of Dilute Dopants in Topological Insulators via STEM-EDS Using Registration and Cell Averaging Techniques.

Magnetic dopants in three-dimensional topological insulators (TIs) offer a promising avenue for realizing the quantum anomalous Hall effect (QAHE) without the necessity for an external magnetic field. Understanding the relationship between site occupancy of magnetic dopant elements and their effect on macroscopic property is crucial for controlling the QAHE. By combining atomic-scale energy-dispersive X-ray spectroscopy (EDS) maps obtained by aberration-corrected scanning transmission electron microscopy (AC-STEM) and novel data processing methodologies, including semi-automatic lattice averaging and frame registration, we have determined the substitutional sites of Mn atoms within the 1.2% Mn-doped Sb2Te3 crystal. More importantly, the methodology developed in this study extends beyond Mn-doped Sb2Te3 to other quantum materials, traditional semiconductors, and even electron irradiation sensitive materials.

Enhanced structural stability of P2-Na0.75Ni0.25Mn0.75-xTixO2 cathodes with high-voltage non-phase transitions property by Mn-sites manipulation strategy

Ni/Mn-based cathode is regarded as a competitive candidate for sodium-ion batteries (SIBs) owing to its high theoretical capacity and low cost. Nevertheless, the issue of its poor cycling stability continues to be a significant obstacle. In this work, P2-Na0.75Ni0.25Mn0.75-xTixO2 (NaNMT-x) cathode materials with high-voltage non-phase transitions property were successfully synthesized. Interestingly, Ti-doping strategy could induce a beneficial reinforcement in the occupancy of stabler Nae sites. Especially, the Nae/Naf ratio of NaNMT-0.15 reached the maximum, which was beneficial for stability. Besides, NaNMT-0.15 with the lowest thermodynamic formation energy and narrower band gap could clearly elaborate excellent structural stability and conductivity via the calculation. The results demonstrated the underlying mechanisms. From the capacity-diffusing factor numerical model and GITT, NaNMT-0.15 have best Na+ diffusion ability. Moreover, ex-situ XRD further demonstrated that NaNMT-0.15 cathode did not undergo obvious P2-O2 phase transition phenomenon in high voltage section. The “no phase transitions” effect enabled NaNMT-0.15 cathode to present distinguished initial capacity (126.0 mAh g−1 at 0.1 C) and stability (85.0 % over 100 cycles). These findings might offer a fresh perspective for designing novel Ni/Mn-based cathode materials with no P2-O2 phase transitions property.

Disorder-Dependent Li Diffusion in Li6PS5Cl Investigated by Machine-Learning Potential.

Solid-state electrolytes with argyrodite structures, such as Li6PS5Cl, have attracted considerable attention due to their superior safety compared to liquid electrolytes and higher ionic conductivity than other solid electrolytes. Although experimental efforts have been made to enhance conductivity by controlling the degree of disorder, the underlying diffusion mechanism is not yet fully understood. Moreover, existing theoretical analyses based on ab initio molecular dynamics (MD) simulations have limitations in addressing various types of disorder at room temperature. In this study, we directly investigate Li-ion diffusion in Li6PS5Cl at 300 K using large-scale, long-term MD simulations empowered by machine-learning potentials (MLPs). To ensure the convergence of conductivity values within an error range of 10%, we employ a 25 ns simulation using a 5 × 5 × 5 supercell containing 6500 atoms. The computed Li-ion conductivity, activation energies, and equilibrium site occupancies align well with experimental observations. Notably, Li-ion conductivity peaks when Cl ions occupy 25% of the 4c sites rather than at 50% where the disorder is maximized. In addition, Li-ion diffusion shows non-Arrhenius behavior, leading to different activation energies at high temperatures (>400 K). These phenomena are explained by the interplay between inter- and intracage jumps. By elucidation of the key factors affecting Li-ion diffusion in Li6PS5Cl, this work paves the way for optimizing ionic conductivity in the argyrodite family.

Microstructure and mechanical properties of a severely cold-rolled and annealed dual-phase compositionally complex alloy (CCA) with an exceptionally deformable Laves phase

A novel CCA was designed by substituting Nb in (FCC + C14 Laves) CoCrFeNi2.1(Nb)0.2 CCA by (Hf + Nb + Ta). The (HfNbTa)0.2 CCA was homogenized, heavily cold-rolled, and isothermally annealed at 800 °C and 1000 °C for different time intervals. The (HfNbTa)0.2 alloy revealed the presence of a Hf and Ni enriched cubic C15 Laves phase. The considerations of site occupancy behavior, formation energy, and highly off-stoichiometric composition stabilized the (Hf, Ni) rich cubic C15 Laves phase. In contrast to the brittle hexagonal C14 Laves phase in (Nb)0.2 CCA, the C15 Laves phase in (HfNbTa)0.2 CCA showed exceptional deformability owing to the high propensity for nano-twin formation. Meanwhile, the FCC matrix developed a deformation-induced nano-lamellar structure with a spacing of ∼45 nm. Annealing resulted in ultrafine recrystallized FCC matrix and precipitation of DO19 structured ε nano-precipitates. The isothermal grain growth kinetics revealed a high grain growth exponent (n) ∼7, which confirmed a Zener-drag mediated process due to the ε nano-precipitates. The Hall-Petch analysis of the hardness data showed relatively high friction stress originating from the dissolution of Hf, Nb, and Ta in the FCC matrix. A high Hall-Petch coefficient indicated increased shear stress for plastic flow across the boundaries, resulting from the elongated Laves phase at the boundaries. The highly deformable Laves phase, ultrafine grain size, and ε nano-precipitates resulted in high yield strength (∼975 MPa) and superior ductility (∼16 %) in the (HfNbTa)0.2 CCA, even surpassing the (Nb)0.2 CCA. It was envisaged that strong yet deformable Laves phases could pave the pathway for developing Laves phase-based CCAs for advanced structural applications.

Crystal Chemistry of Synthetic Mg(Si1−xGex)O3 Pyroxenes: A Single-Crystal X-ray Diffraction Study

Germanate-pyroxenes often are used as model systems to study the stability and phase relationships of analog silicate systems. Based on such analyses, it is assumed that silicates and germanates behave ideally in terms of mixing. A systematic study was performed to monitor in detail the changes introduced by a Si4+ through Ge4+ replacement in the important rock-forming pyroxene enstatite MgSiO3. Well-shaped, idiomorphic singe crystals of a MgSi1−xGexO3 pyroxene solid solution were grown at ambient pressure from a high-temperature flux-assisted synthesis. Structural analysis using single-crystal X-ray diffraction methods revealed orthorhombic symmetry, Pbca, Z = 8, for the complete solid-solution series. Long-term storage over a period of 8 years at ambient conditions or annealing at 525 °C over a period of 10 weeks did not change the symmetry of the proposed thermodynamically stable monoclinic polymorph. Within the solid-solution series, lattice parameters increased almost linearly with increasing Si4+ by Ge4+ substitution. The main changes occurred on the tetrahedral sites, which showed an almost linear increase in individual and average bond lengths but also in distortion parameters. The refined site occupancy of Si4+ and Ge4+ showed a distinct preference of Ge4+ for the TB site. The altered topology and kinking state in the tetrahedral chains also imposed significant changes to the bonding topology and geometry of the neighboring M1 and M2 sites.

A new perspective on microRNA-guided gene regulation specificity, and its potential generalization to transcription factors and RNA-binding proteins.

Our conception of gene regulation specificity has undergone profound changes over the last 20years. Previously, regulators were considered to control few genes, recognized with exquisite specificity by a 'lock and key' mechanism. However, recentlygenome-wide exploration of regulator binding site occupancy (whether on DNA or RNA targets) revealed extensive lists of molecular targets for every studied regulator. Such poor biochemical specificity suggested that each regulator controls many genes, collectively contributing to biological phenotypes. Here, I propose a third model, whereby regulators' biological specificity is only partially due to 'lock and key' biochemistry. Rather, regulators affect many genes at the microscopic scale, but biological consequences for most interactions are attenuated at the mesoscopic scale: only a few regulatory events propagate from microscopic to macroscopic scale;others are made inconsequential by homeostatic mechanisms. This model is well supported by the microRNA literature, and data suggest that it extends to other regulators. It reconciles contradicting observations from biochemistry and comparative genomics on one hand and in vivo genetics on the other hand, but this conceptual unification is obscured by common misconceptions and counter-intuitive modes of graphical display. Profound understanding of gene regulation requires conceptual clarification, and better suited statistical analyses and graphical representation.

Dopant site occupancies and iron valence states in SrZnxFe18−xO27 W-type hexaferrites using site-selective X-ray/electron spectroscopy

Zn-doped W-type Sr hexaferrite (SrZnxFe18−xO27; SrZnx-WHF) is an anticipated rare-earth-free hard magnetic material with strong magnetocrystalline anisotropy and saturation magnetization. To examine the origin of its high magnetic performance, the site distribution of Zn over seven crystallographically inequivalent Fe sites and the site-dependent valence states of Fe were investigated using site-selective elemental/chemical analysis techniques. The dominant occupation of Zn2+ at the 4etet(S) and 4ftet(S) tetrahedral sites was determined quantitatively using high-angular-resolution electron-channeling X-ray spectroscopy and statistical data analysis. The combined application of high-angular-resolution electron channeling electron spectroscopy and atomic-column resolution scanning transmission electron microscopy–electron energy-loss spectroscopy helped unambiguously clarify that most of the Fe2+ ions existed at the 6goct(S-S) octahedral site. Density functional theory calculations have shown that Zn doping leads to a redistribution of the charges toward Fe ions at this site. This redistribution preserves the local charge balance and amplifies the total number of parallel spins. Hence, the enhanced magnetocrystalline anisotropy and saturation magnetization in SrZnx-WHF can be inferred to originate from the charge redistribution at the 6goct(S-S) site, which is influenced by the presence of nonmagnetic Zn.

Revisiting Duvensee 13: Additional Analyses of Lithic Artefacts and Site Contexts of a Small Dwelling at the Ancient Lake Duvensee, Germany

ABSTRACT The paper re-examines the Duvensee 13 site at Lake Duvensee, Germany, dating from 9900 to 8600 calBP, the latest in a series of well-known hazelnut roasting sites of a larger Mesolithic site complex. While the site has previously been studied, its lithic assemblage has not been fully analysed and published. This study presents this previously unstudied material, offering a comprehensive overview of its composition, metric information, and its spatial distribution. Lithic analysis revealed specialised production of pointed and triangular microliths. Additional elements of the assemblage (narrow blades, small cores) suggest microlith production as the primary goal. High-resolution spatial data revealed concentrations of microliths and microburins, pointing towards focussed areas of production. However, the overall assemblage is affected by a redistribution of artefacts through the reworking of the layers surrounding the hearth and repeated overlapping site occupations. Additional archaeological features suggest that in addition to hazelnut roasting, the site likely also accommodated dwelling, tool crafting, and game surveillance during off-harvest times.

Broadband spectral cyan emission phosphor for full-spectrum LED caused by interstitial site occupation

The phosphor with a highly condensed, rigid framework structure and a single crystallographic site often exhibit symmetrical narrow-band emission. It is challenging to achieve broadband emission by doping Eu2+ ions in similar structures. Here, we propose to control the occupation and quenching concentration of Eu2+ ions in a single-site matrix Sc2Si2O7 to increase efficiency and precise regulation of luminescence spectra substantially. The analysis of photoluminescence spectroscopy through steady-state, transient-state, and Gaussian fitting techniques has discovered two emission centers despite the presence of a single rare-earth substitution site. The theoretical calculations and bond valence sum subsequently prove that Eu2+ ions prefer substituting the Sc3+ and interval sites to emit intense cyan light. Under 340 nm excitation, broad cyan-emission (FWHM = 115 nm) is exhibited with a high quantum yield of 60.67 %. The present phosphor exhibits pronounced thermal stability, and the emission intensity can still keep 68.3 % at 170 °C compared to that at atmospheric temperature. The Sc2Si2O7: Eu2+ phosphor boasts exceptional potential as a highly efficient cyan component in full-spectrum WLEDs. By replacing the blue light component commonly found in WLEDs, the intelligent and healthy alternative Sc2Si2O7: Eu2+ phosphor can effectively decrease the harmful blue light. This work also highlights the critical need to analyze local phosphor distortions upon rare-earth substitution, especially in single crystallographic site structures.

Double Perovskites: Promising Positive Electrode Materials for Potassium Ion Batteries

The popularity of electric vehicles over the last decade has led to a boom in lithium-ion battery production. Large amounts of lithium resources have been consumed resulting in a lithium shortage.[1] To overcome the challenge of excessive consumption of lithium resources, alternative battery technologies to Li-ion batteries must be considered. Potassium-ion batteries (KIBs) have been proposed as an alternative battery technology to Li-ion batteries and are at the early stage of development.This study focuses on investigating the viability of employing the novel double-perovskites as positive electrodes for KIBs. Double perovskites have some structural similarities to the well-developed KIB positive electrode materials, Prussian White or Prussian Blue Analogues. The 3D open framework is favorable for supporting the insertion/deinsertion of K-ions and K-ion diffusion. In this research, new double-perovskites have been successfully synthesized using the solid-state methods, under both inert and reducing atmospheres. The utilization of choice of transition elements on the B-site in the perovskite structure is beneficial for increasing energy density, enhancing electronic conductivity, and improving the structure stability of the material. Preliminary characterization, including powder X-ray diffraction (PXRD), scanning electron microscopy (SEM), and energy dispersive X-ray spectroscopy (EDS), were conducted to verify the phase purity, crystal structure, and atomic ratio of different elements in the synthesized material.At the same time, electrochemistry tests were conducted by cycling the perovskite in half-cells, revealing an irreversible capacity decay in the first cycle. To further investigate structural changes of the perovskite during cycling, operando X-ray absorption spectroscopy (XAS) was employed. This method enabled the study of the oxidation states of the transition metals in the perovskites, providing advanced insights into the redox reactions occurring within cells with positive electrodes.Obtaining a detailed understanding of the structure of these perovskites is crucial. Thus, powder neutron diffraction (PND) and variable temperature neutron diffraction (VT-PND) have been gathered to study the structural evolution, site occupancy and octahedral tilting with upon heating in both inert and reducing atmospheres.Reference:[1] AP News, https://apnews.com/article/china-ev-lithium-united-states-battery-87eb9382a0181bb7ee64e835efe7b170, (accessed December 2023).

A lactate-dependent shift of glycolysis mediates synaptic and cognitive processes in male mice

Astrocytes control brain activity via both metabolic processes and gliotransmission, but the physiological links between these functions are scantly known. Here we show that endogenous activation of astrocyte type-1 cannabinoid (CB1) receptors determines a shift of glycolysis towards the lactate-dependent production of d-serine, thereby gating synaptic and cognitive functions in male mice. Mutant mice lacking the CB1 receptor gene in astrocytes (GFAP-CB1-KO) are impaired in novel object recognition (NOR) memory. This phenotype is rescued by the gliotransmitter d-serine, by its precursor l-serine, and also by lactate and 3,5-DHBA, an agonist of the lactate receptor HCAR1. Such lactate-dependent effect is abolished when the astrocyte-specific phosphorylated-pathway (PP), which diverts glycolysis towards l-serine synthesis, is blocked. Consistently, lactate and 3,5-DHBA promoted the co-agonist binding site occupancy of CA1 post-synaptic NMDA receptors in hippocampal slices in a PP-dependent manner. Thus, a tight cross-talk between astrocytic energy metabolism and gliotransmission determines synaptic and cognitive processes.

Novel interplay between agonist and calcium binding sites modulates drug potentiation of α7 acetylcholine receptor.

Drug modulation of the α7 acetylcholine receptor has emerged as a therapeutic strategy for neurological, neurodegenerative, and inflammatory disorders. α7 is a homo-pentamer containing topographically distinct sites for agonists, calcium, and drug modulators with each type of site present in five copies. However, functional relationships between agonist, calcium, and drugmodulator sites remain poorly understood. To investigate these relationships, we manipulated the number of agonist binding sites, and monitored potentiation of ACh-elicited single-channel currents through α7 receptors by PNU-120596 (PNU) both in the presence and absence of calcium. When ACh is present alone, it elicits brief, sub-millisecond channel openings, however when ACh is present with PNU it elicits long clusters of potentiated openings. In receptors harboring five agonist binding sites, PNU potentiates regardless of the presence or absence of calcium, whereas in receptors harboring one agonist binding site, PNU potentiates in the presence but not the absence of calcium. By varying the numbers of agonist and calcium binding sites we show that PNU potentiation of α7 depends on a balance between agonist occupancy of the orthosteric sites and calcium occupancy of the allosteric sites. The findings suggest that in the local cellular environment, fluctuations in the concentrations of neurotransmitter and calcium mayalter this balance and modulate the ability of PNU to potentiate α7.

Insights into enhanced thermoelectric performance of the n-type Mg3Sb2-based materials by amphoteric Al doping

Doping has the potential to alter the levels of anharmonicity in compounds by attenuating bonding strength. In this study, we explore the efficacy of amphoteric Al doping for stimulating anharmonicity in n-type Mg3.25AlxSb1.48Bi0.48Te0.04 to attain enhanced phonon scattering and thermoelectric performance. First-principles calculations and experimental data reveal the occupation of both Sb and Mg2 sites by amphoteric Al atoms in the anionic framework of Mg3.25AlxSb1.48Bi0.48Te0.04. A marginal variation in both carrier concentration and mobility sustains the high power factor without affecting the Seebeck coefficient, implying amphoteric doping induced charge compensation. While phonon velocity, Grüneisen parameter, and crystal orbital Hamilton population calculations results indicate that phonon softening and bond weakening are realized via Al doping, leading to an enhanced lattice anharmonicity and a reduced lattice thermal conductivity. A remarkable enhancement ∼16% in the peak figure of merit ZTpeak and the average ZTavg, was attained for the x = 0.015 sample, when compared with the un-doped sample. Hence, the amphoteric doping can serve as an effective means to optimize ZT values by decoupling the intertwined thermoelectric transport properties.

Diisobutyl-ammonium tri-phenyl(2-thiolato-acetato-κ2 O,S)stannate(IV).

Crystals of the title salt, (C8H20N)[Sn(C6H5)3(C2H2O2S)], comprise diisobutyl-ammonium cations and mercapto-acetato-tri-phenyl-stannate(IV) anions. The bidentate binding mode of the mercapto-acetate ligand gives rise to a five-coordinated, ionic tri-phenyl-tin complex with a distorted cis-trigonal-bipyramidal geometry around the tin atom. In the crystal, charge-assisted ammonium-N-H⋯O(carboxyl-ate) hydrogen-bonding connects two cations and two anions into a four-ion aggregate. Two positions were resolved for one of the phenyl rings with the major component having a site occupancy factor of 0.60 (3).

Survival Probability, Particle Imbalance, and Their Relationship in Quadratic Models.

We argue that the dynamics of particle imbalance in quadratic fermionic models is, for the majority of initial many-body product states in the site occupation basis, virtually indistinguishable from the dynamics of survival probabilities of single-particle states. We then generalize our statement to a similar relationship between the non-equal time and space density correlation functions in many-body states, and the transition probabilities of single-particle states at nonzero distances. Finally, we study the equal-time connected density-density correlation functions in many-body states, which exhibit certain qualitative analogies with the survival and transition probabilities of single-particle states. Our results are numerically tested for two paradigmatic models of single-particle localization: the 3D Anderson model and the 1D Aubry-André model. This work gives an affirmative answer to the question of whether it is possible to measure features of single-particle survival and transition probabilities by the dynamics of observables in many-body states.

Beyond Cation Disorder: Site Symmetry‐Tuned Optoelectronic Properties of the Ternary Nitride Photoabsorber ZrTaN3

AbstractTernary nitrides are rapidly emerging as promising compounds for optoelectronic and energy conversion applications, yet comparatively little of this vast composition space has been explored. Furthermore, the crystal structures of these compounds can exhibit a significant amount of disorder, the consequences of which are not yet well understood. Here, the deposition of bixbyite‐type ZrTaN3 thin films is demonstrated by reactive magnetron co‐sputtering and observed semiconducting character, with a strong optical absorption onset at 1.8 eV and significant photoactivity, with prospective application as functional photoanodes. It is found that Wyckoff‐site occupancy of cations is a critical factor in determining these beneficial optoelectronic properties. First‐principles calculations show that cation disorder leads to minor deviations in the total energy but modulates the bandgap by 0.5 eV, changing orbital hybridization of valence and conduction band states. In addition to demonstrating that ZrTaN3 is a promising visible light‐absorbing semiconductor and active photoanode material, the findings provide important insights regarding the role of cation ordering on the electronic structure of ternary semiconductors. In particular, it is shown that not only cation order, but also the cationic Wyckoff site occupancy has a substantial impact on key optoelectronic properties, which can guide future design and synthesis of advanced semiconductors.

Archaeological landscapes and long-term settlements in the Perputxent valley (eastern Iberia): Exploring land use strategies and sustainability in a Mediterranean mountain area

In this paper, we present the long-term occupation of the Perputxent Valley with the purpose of exploring the factors that could explain the long-lasting and trans-cultural occupation of resilient sites and landscapes for nearly two millennia. The first part describes the archaeological research carried out based on remote sensing and intensive coverage survey methods and geoarchaeological analysis. The characterisation of the intensive agricultural uses has been studied from the geochemical analysis of the soil and sedimentary record. The objective is to reconstruct the palaeoenvironmental processes and the possible evidence of the agricultural practices. This research has identified the residential spaces, the sites and the agrarian land-uses, especially intensive farmlands. The second part analyses the evidence of this long-term settlements in the context of the archaeological, ethnographic and historical record of the region. Understanding these practices of agriculture and land-use can contribute to understandings of what makes societies sustainable.

LacdiNAc to LacNAc: remodelling of bovine α-lactalbumin N-glycosylation during the transition from colostrum to mature milk.

α -Lactalbumin, an abundant protein present in the milk of most mammals, is associated with biological, nutritional and technological functionality. Its sequence presents N-glycosylation motifs, the occupancy of which is species-specific, ranging from no to full occupancy. Here, we investigated the N-glycosylation of bovine α-lactalbumin in colostrum and milk sampled from four individual cows, each at 9 time points starting from the day of calving up to 28.0 d post-partum. Using a glycopeptide-centric mass spectrometry-based glycoproteomics approach, we identified N-glycosylation at both Asn residues found in the canonical Asn-Xxx-Ser/Thr motif, i.e. Asn45 and Asn74 of the secreted protein. We found similar glycan profiles in all four cows, with partial site occupancies, averaging at 35% and 4% for Asn45 and Asn74, respectively. No substantial changes in occupancy occurred over lactation at either site. Fucosylation, sialylation, primarily with N-acetylneuraminic acid (Neu5Ac), and a high ratio of N,N'-diacetyllactosamine (LacdiNAc)/N-acetyllactosamine (LacNAc) motifs were characteristic features of the identified N-glycans. While no substantial changes occurred in site occupancy at either site during lactation, the glycoproteoform (i.e. glycosylated form of the protein) profile revealed dynamic changes; the maturation of the α-lactalbumin glycoproteoform repertoire from colostrum to mature milk was marked by substantial increases in neutral glycans and the number of LacNAc motifs per glycan, at the expense of LacdiNAc motifs. While the implications of α-lactalbumin N-glycosylation on functionality are still unclear, we speculate that N-glycosylation at Asn74 results in a structurally and functionally different protein, due to competition with the formation of its two intra-molecular disulphide bridges.

Solder scavenging from hole-and-cap food cans in the Western Australian goldfields: Identifying site modification processes

Site modification via large and dense can dumps dating from the gold rushes of the 1880s and later in the Western Australian goldfields may profoundly affect the archaeological interpretation of these sites. A can dump has been examined in the abandoned campground of Muslim cameleers that dated from the 1892 gold rush to after the First World War. Here, can dumps comprising hundreds of cans, stacked up and in mutual contact and without other artefacts such as bottles, were not all the unmodified remains of meals and camps of transient people. This work presents a geochemical technique applied to soil samples around these dumps, showing high levels of tin and lead contamination, inconsistent with the underlying geology and similar to the composition of the solder used to seal the cans. This is consistent with the written reminiscences of a family supplementing its income by scavenging solder from hole-and-cap food cans over the period 1894–1909. This process of site modification by solder scavenging must be considered before food-can distribution patterns can be interpreted in terms of primary site occupation.

A single phased full color emitting pyrochlore type phosphor La2Y0.66Sn0.66Sb0.66O7: Bi3+, Eu3+ for white light emitting diode applications (WLEDs)

The phosphor converted white light emitting diodes (pc-WLEDs) are advancing rapidly in replacing the conventional fluorescent and incandescent light sources. However, the current technology of pc-WLEDs limits their large scale indoor lighting applications due to their high correlated color temperature (CCT) and poor color rendering index (CRI). In this work, a single phased full color emitting phosphor in the pyrochlore oxide system, La2Y0.66Sn0.66Sb0.66O7: Bi3+, Eu3+ has been developed by the high temperature ceramic route. The developed phosphors are characterized by powder X-ray diffraction, luminescence and lifetime measurements. Upon near UV excitation wavelength, the singly doped phosphor, La2Y0.66Sn0.66Sb0.66O7: Bi3+ show intense blue green light in the wavelength region 400–600 nm due to the characteristic transitions (3P1 → 1S0) of Bi3+. The emission spectral analysis suggests that there exist two luminescence centers of Bi3+ due to occupation of different crystallographic sites in the pyrochlore lattice of La2Y0.66Sn0.66Sb0.66O7. The deficit of red component in the emission spectra is overcome by the Eu3+ co-doping in the system, La2Y0.66Sn0.66Sb0.66O7: Bi3+, Eu3+ which results in the full color emission covering the visible spectral range up to 700 nm with broad peaks along with sharp narrow characteristic peaks of Eu3+. The full color emission of the La2Y0.66Sn0.66Sb0.66O7: 0.04Bi3+, yEu3+ phosphors can be tuned by adjusting the suitable Eu3+ dopant concentration and using appropriate energy transfer from Bi3+ to Eu3+. The full color emitting phosphor, La2Y0.66Sn0.66Sb0.66O7:0.04Bi3+, 0.06Eu3+ can be realized with the color coordinates (0.30, 0.36), and correlated color temperature (4383K). All these results demonstrate that La2Y0.66Sn0.66Sb0.66O7:xBi3+, yEu3+ are potential single phased full color emitting phosphors for the development of pc-WLEDs.