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At least 343 records · Page 19

Synthesis and photoluminescence properties of Dy{sup 3+} doped white light emitting CdTa{sub 2}O{sub 6} phosphors

The undoped and CdTa{sub 2}O{sub 6}:Dy{sup 3+} (0.2≤x≤2.0 mol%) phosphors were synthesized at 1100 °C for 12 h by the conventional solid state reaction method. The synthesized CdTa{sub 2}O{sub 6}:Dy{sup 3+} phosphors were characterized by X-ray diffraction (XRD), Scanning electron microscopy (SEM), Energy dispersive spectroscopy (EDS) and Photoluminescence (PL) analyses. The PL spectra showed the presence of excitation peaks between 310 and 440 nm due to the 4f–4f transitions of Dy{sup 3+}. The emission of Dy{sup 3+} ions at 353.0 nm excitation was observed at 487.1 nm (blue) and 577.8 nm (yellow) due to the {sup 4}F{sub 9/2}→{sup 6}H{sub 15/2} transitions and {sup 4}F{sub 9/2}→{sup 6}H{sub 13/2} transitions, respectively. The PL analysis results also showed that the emissions increase with the increasing Dy{sup 3+} ion content. The emissions increased with the doping concentration of up to 1 mol%, and above this level decreased due to concentration quenching effect. The CIE chromaticity color coordinates (x,y) of the CdTa{sub 2}O{sub 6}:Dy{sup 3+} phosphors were found to be in the white light region of the chromaticity diagram. - Graphical abstract: Emission spectra at λ{sub ex}=353.0 nm and CIE chromaticity coordinate diagram of CdTa{sub 2}O{sub 6}:Dy{sup 3+} phosphors. - Highlights: • Pure and CdTa{sub 2}O{sub 6}:Dy{sup 3+} was produced by solid state reaction method. • CdTa{sub 2}O{sub 6}:Dy{sup 3+} phosphor exhibited blue and yellow emissions due to the {sup 4}F{sub 9/2}→{sup 6}H{sub 15/2} and {sup 4}F{sub 9/2}→{sup 6}H{sub 13/2} transitions. • The CCT value for 1.0 mol% CdTa{sub 2}O{sub 6}:Dy{sup 3+} was 5133 K which was located in the cool white daylight region. • Dy{sup 3+} doped CdTa{sub 2}O{sub 6} phosphor has potential in the production of white LEDs.

37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CH↗

White light generation via sequential stepwise absorption and energy-transfer frequency upconversion in Tm{sup 3+}/Er{sup 3+}-codoped glass

White light emission with CIE-1931 coordinates close to the standard equal-energy white light illuminant, and color temperature in the 4000–6500 K range was produced in Tm{sup 3+}/Er{sup 3+}-codoped glasses through frequency upconversion. Multi-Stokes Raman emissions generated in an optical fiber pumped at 1.064 µm were used, seeking out the {sup 3}H{sub 5} thulium absorption band around 1.2 µm as the departure point. The new and efficient excitation approach allowed the generation of near infrared (800 nm), red (650 nm), and blue (480 nm) emission due to frequency upconversion excited via ground-state absorption and excited-state absorption in Tm{sup 3+} ions. Energy-transfer followed by excited-state absorption in Er{sup 3+} ions, provided the generation of the green (530, 550 nm) and red (660 nm) components to compose white light. The excitation mechanism for the Tm{sup 3+} ions is assigned to stepwise multi-wavelength excitation using Stokes Raman emission in an optical fiber, followed by stepwise excited-state absorption of the pump photons. Energy-transfer Tm{sup 3+}[{sup 3}F{sub 4}] + Er{sup 3+}[{sup 4}I{sub 15/2}] →Tm{sup 3+}[{sup 3}H{sub 6}] + Er{sup 3+}[{sup 4}I{sub 9/2}] followed by excited-state absorption of multi-Stokes Raman emissions populate erbium visible emitting level. Excitation power color tuneability of the overall light emission was also achieved. - Graphical abstract: Recorded emission spectrua of visible radiation emanating from the single-doped (Er3+, Tm3+) and codoped (Er3+/Tm3+) samples excited 160 mW average power from the fiber output. Simplified energy-level diagram of the excitation and upconversion emission processes for the Tm3+/Er3+-codoped sample excited using multi-Stokes emissions. Display Omitted.

37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CH↗

White upconversion emission in Y{sub 2}O{sub 3}:Er{sup 3+}–Tm{sup 3+}–Yb{sup 3+}phosphor

Graphical abstract: Schematic energy level diagram of Er{sup 3+}–Yb{sup 3+}–Tm{sup 3+} system upon excitation at 980 nm. Highlights: ► Prepared the Er{sup 3+}–Tm{sup 3+}–Yb{sup 3+} codoped Y{sub 2}O{sub 3} phosphor. ► Excitation of the sample by 980 nm diode laser is studied. ► Explored the possibility of getting white light emission from the synthesized phosphor. ► Colour tunability of the prepared phosphor is studied. ► Temperature sensing behaviour is investigated using FIR studied. - Abstract: Er{sup 3+}–Tm{sup 3+}–Yb{sup 3+} codoped Y{sub 2}O{sub 3} phosphor has been synthesized by optimized combustion synthesis process and its white light upconversion emission property is investigated using cheap 980 nm diode laser excitation. Efficient red, green and blue light emission bands, necessary for attaining white light emission, are observed in the codoped sample. The concentration of each rare earth ion is adjusted to get the required emission. In this phosphor, interestingly, emission colour coordinates are found to almost independent on the excitation power density. The temperature sensing behaviour of the prepared samples has also been studied using fluorescence intensity ratio (FIR) technique.

36 MATERIALS SCIENCE↗

Synthesis and luminescent properties of a white light phosphor KBa{sub 2}Nb{sub 5}O{sub 15}:Na{sup +}, Dy{sup 3+} for light-emitting-devices

Graphical abstract: - Highlights: • A novel red phosphor KBa{sub 2}Nb{sub 5}O{sub 15}:Dy{sup 3+} was synthesized and investigated firstly. • Crystal structure and characteristic luminescence properties are discussed. • The charge compensation mechanism is also investigated. • It has low color tolerance and better CIE chromaticity coordinates. - Abstract: The white light emission phosphor KBa{sub 2}Nb{sub 5}O{sub 15}:Dy{sup 3+} was synthesized by solid-state method. X-ray diffraction (XRD) study reveals that all the Dy{sup 3+} doped phosphors are single phase. Strong excitation peaks of KBa{sub 2}Nb{sub 5}O{sub 15}:Dy{sup 3+} were found around 380–400 nm, matched well with the NUV LED chip. Under 388 nm excitation, the phosphor exhibited intense white emission by combining the two emission peaks at 477 nm and 572 nm, attributed to the characteristic {sup 4}F{sub 9/2}–{sup 6}H{sub 15/2} and {sup 4}F{sub 9/2}–{sup 6}H{sub 13/2} transition of Dy{sup 3+}. The optimum doping concentration of Dy{sup 3+} is found to be 3%, whose Commission International de l’ Eclairage (CIE) chromaticity coordinates and correlated color temperature are (0.395, 0.422) and 3925 K, respectively. The results indicate that the KBa{sub 2}Nb{sub 5}O{sub 15}:Dy{sup 3+} phosphor could be considered as a potential candidate for white-LEDs.

36 MATERIALS SCIENCE↗

White light emission and energy transfer in Dy{sup 3+}/Eu{sup 3+} co-doped BaLa{sub 2}WO{sub 7} phosphors

Highlights: • BaLa{sub 2}WO{sub 7}:Dy{sup 3+}, Eu{sup 3+} phosphors were synthesized by solid-state reaction. • Eu{sup 3+} compensated the red emission component of the BaLa{sub 2}WO{sub 7}:Dy{sup 3+} phosphor. • The observed emission lifetimes indicates the energy transfer from Dy{sup 3+} to Eu{sup 3+}. • BaLa{sub 2}WO{sub 7}:Dy{sup 3+}, Eu{sup 3+} are potential phosphors used in n-UV pumped white LEDs. - Abstract: Tunable full color emissive BaLa{sub 1.75−x}WO{sub 7}:0.25Dy{sup 3+}, xEu{sup 3+} phosphors which peaked at 484 nm (blue), 572 nm (yellow), 593 nm (orange), and 617 nm (red) were synthesized by the traditional solid-state reaction method. The as-synthesized phosphors were characterized by X-ray power diffraction, diffused reflectance spectra, photoluminescence decay curves, photoluminescence excitation and emission spectra. The photoluminescence excitation spectra range from 200 to 500 nm, including an O{sup 2−}⟶W{sup 6+} charge transfer band and several 4f–4f transition peaks of Dy{sup 3+} and Eu{sup 3+}. Co-doping with Eu{sup 3+} compensated the red emission component of the BaLa{sub 2}WO{sub 7}:Dy{sup 3+} phosphor. Furthermore, the energy transfer from Dy{sup 3+} to Eu{sup 3+} was confirmed based on the luminescence spectra and decay curves. The intense white light emissions are suggestive exploration for the potential phosphor for optical materials applications used in the ultraviolet excited white light emitting diodes.

36 MATERIALS SCIENCE↗

The site occupation and valence of Mn ions in the crystal lattice of Sr{sub 4}Al{sub 14}O{sub 25} and its deep red emission for high color-rendering white light-emitting diodes

Highlights: • Different valences of Mn ions in Sr{sub 4}Al{sub 14}O{sub 25} were identified using XANES and EPR. • Red luminescence was attributed to Mn{sup 4+} occupying the center of AlO{sub 6} octahedron. • The Mn{sup 3+} incorporated in the center of AlO{sub 4} tetrahedron was non-luminescent. • The bond-valence theory was used to analyze the effective valences of cations. • A white LED device with CRI up to Ra 93.23 was packaged by using the red phosphor. - Abstract: The synthesis and component of red phosphor, Sr{sub 4}Al{sub 14}O{sub 25}: Mn, were optimized for application in white light-emitting diodes. The microstructure and morphology were investigated by the X-ray diffraction and scanning electron microscopy. Different valences of Mn ions in Sr{sub 4}Al{sub 14}O{sub 25} were discriminated using the electron paramagnetic resonance and X-ray absorption near-edge structure spectroscopy techniques. The bond-valence theory was used to analyze the effective valences of Sr{sup 2+} and Al{sup 3+} in Sr{sub 4}Al{sub 14}O{sub 25}. As a result, the strong covalence of Al{sup 3+} in the AlO{sub 4} tetrahedron other than in the AlO{sub 6} octahedron is disclosed. The deep red emission is attributed to Mn{sup 4+} occupying the center of AlO{sub 6} octahedron. The mechanism of energy transfer is mainly through dipole–dipole interaction, revealed by the analyses of critical distance and concentration quench. A high color rendering white LED prototype with color-rendering index up to Ra 93.23 packaged by using the red phosphor demonstrates its applicability.

36 MATERIALS SCIENCE↗

A single-phase Ba{sub 9}Lu{sub 2}Si{sub 6}O{sub 24}:Eu{sup 2+}, Ce{sup 3+}, Mn{sup 2+} phosphor with tunable full-color emission for NUV-based white LED applications

Highlights: • A single phase Ba{sub 9}Lu{sub 2}Si{sub 6}O{sub 24}:Eu{sup 2+}, Ce{sup 3+}, Mn{sup 2+} phosphor with full-color emission was obtained by solid-state reactions. • Eu{sup 2+}, Ce{sup 3+}, and Mn{sup 2+} acts as blue, green, and red luminescence centers, respectively. • The BLS:Eu{sup 2+}, Ce{sup 3+}, Mn{sup 2+} phosphor shows a high quantum efficient of ∼62% and a good color stability. • Combining this single phosphor with a 395 nm NUV-chip, an ideal white LED with a high CRI of 85 and a CCT of 6300 K was obtained. - Abstract: We obtained a single phase BLS:Eu{sup 2+}, Ce{sup 3+}, Mn{sup 2+} phosphor by solid-state reactions. Eu{sup 2+}, Ce{sup 3+}, and Mn{sup 2+} gives rise to the blue, green, and red emission, respectively. The Mn{sup 2+} red emission can be effectively enhanced via energy transfers from both Eu{sup 2+} and Ce{sup 3+}. Thus a tunable full color emission from 410 to 750 nm was realized in this single phosphor. The Eu{sup 2+} → Mn{sup 2+} energy transfer mechanism was investigated by the fluorescence decay curves. This single phosphor exhibits an efficient excitation band covering from 390 to 410 nm, which matches well with the emission light of the efficient NUV chips. The optimized BLS:Eu{sup 2+}, Ce{sup 3+}, Mn{sup 2+} phosphor shows a high quantum efficient of ∼62% and a good color stability. When this single phosphor was combined with a 395 nm NUV-chip, an ideal white LED with a high color render index (CRI) of 85 and a correlated color temperature (CCT) of 6300 K was obtained. This demonstrates the promising application of the BLS:Eu{sup 2+}, Ce{sup 3+}, Mn{sup 2+} single phosphor for the NUV-based white LEDs.

36 MATERIALS SCIENCE↗

Warm white light emission of apatite-type compound Ca4Y6O(SiO4)6 doped with Dy3+

Highlights: • Single-phase phosphor Ca{sub 4}Y{sub 6}O(SiO{sub 4}){sub 6}: Dy{sup 3+} for WLEDs were synthesized. • The CIE coordinates are (0.330, 0.339) for the optimal doping sample. • The CCT (5600 K) is close to that of the midday sunlight. • The emission intensity at 400 K keeps 82% with respect to that at RT. • The CIE coordinates maintain in the white light area in the range of RT-300 °C. - Abstract: A series of Ca{sub 4}Y{sub 6}O(SiO{sub 4}){sub 6}: x%Dy{sup 3+} (x = 1, 3, 5, 7, 9) phosphors were synthesized successfully via a conventional solid-state method at high temperature. The X-ray diffraction results show that all obtained samples are the pure hexagonal crystal structure of the space group P6{sub 3}/m (No.176). The blue ({sup 4}F{sub 9/2} → {sup 6}H{sub 15/2}) and yellow ({sup 4}F{sub 9/2} → {sup 6}H{sub 13/2}) emissions of Ca{sub 4}Y{sub 6}O(SiO{sub 4}){sub 6}:7% Dy{sup 3+} phosphors are of such a ratio to produce almost perfect white light with CIE coordinates of (0.330, 0.339). The correlated color temperature is about 5600 K, close to that of the midday sunlight (5500 K). In addition, both the emission intensity and the CIE coordinates exhibit an excellent thermal stability in the temperature range of RT ∼ 300 °C. Our study illustrates that Ca{sub 4}Y{sub 6}O(SiO{sub 4}){sub 6}:7%Dy{sup 3+} may serve as potential warm white lighting phosphors in NUV-based solid state lighting and optical display applications.

36 MATERIALS SCIENCE↗

Small Cyclic Diammonium Cation Templated (110)-Oriented 2D Halide (X = I, Br, Cl) Perovskites with White-Light Emission

Two-dimensional (2D) halide perovskites exhibit excellent potential for optoelectronics because of their outstanding physical properties and structural diversity. White-light emission is one property of 2D perovskites that originates from self-trapped excitons (STE) in the highly distorted structures. The so-called (110)-oriented 2D perovskites are generally distorted and believed to be good candidates for white-light emitting devices. Here, we report (110)-oriented 2D perovskites, C 4 N 2 H 12 PbX 4 (X = I, Br, Cl), templated by the small cyclic diammonium cation, 3-aminopyrrolidinium (3APr). Structural characterization by single-crystal X-ray diffraction reveals that the distortion of the inorganic part of the structures is influenced by the stereochemical conformation of the cation between the perovskite layers. The experimental bandgaps follow the trend I < Br < Cl (2.56 eV, 3.29 eV, 3.85 eV, respectively). Density functional theory calculations reveal a weak but significant electronic band dispersion along the stacking axis, suggesting a non-negligible interlayer electronic coupling caused by the short proximity of adjacent inorganic layers. The high level of distortion results in the emergence of white-light emission, rarely seen in iodide perovskites, as well as the bromide and chloride isostructural analogues, which provides perfect platform to compare the broad emission mechanism for all three halides. The bromide and chloride perovskites show longer lifetimes and higher color rendering index (CRI) (83 and 85), relevant to solid-state lighting. Lastly, temperature-dependent PL measurements confirm that the broad emission comes from different STE mechanism for different halides, with the peak broadening persisting even at low temperature for the chloride compound.

37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CH↗

Efficient and bright white light-emitting diodes based on single-layer heterophase halide perovskites

At present, electric lighting accounts for ~15% of global power consumption and thus the adoption of efficient, low-cost lighting technologies is important. Here, halide perovskites have been shown to be good emitters of pure red, green and blue light, but an efficient source of broadband white electroluminescence suitable for lighting applications is desirable. Here, we report a white light-emitting diode (LED) strategy based on solution-processed heterophase halide perovskites that, unlike GaN white LEDs, feature only one broadband emissive layer and no phosphor. Our LEDs operate with a peak luminance of 12,200 cd m –2 at a bias of 6.6 V and a maximum external quantum efficiency of 6.5% at a current density of 8.3 mA cm –2 . Systematic in situ and ex situ characterizations reveal that the mechanism of efficient electroluminescence is charge injection into the α phase of CsPbI 3 , α to δ charge transfer and α–δ balanced radiative recombination. Future advances in fabrication technology and mechanistic understanding should lead to further improvements in device efficiency and luminance.

36 MATERIALS SCIENCE↗

High performance flexible top-emitting warm-white organic light-emitting devices and chromaticity shift mechanism

Flexible warm-white top-emitting organic light-emitting devices (TEOLEDs) are fabricated onto PET substrates with a simple semi-transparent cathode Sm/Ag and two-color phosphors respectively doped into a single host material TCTA. By adjusting the relative position of the orange-red EML sandwiched between the blue emitting layers, the optimized device exhibits the highest power/current efficiency of 8.07 lm/W and near 13 cd/A, with a correlated color temperature (CCT) of 4105 K and a color rendering index (CRI) of 70. In addition, a moderate chromaticity variation of (-0.025, +0.008) around warm white illumination coordinates (0.45, 0.44) is obtained over a large luminance range of 1000 to 10000 cd/m{sup 2}. The emission mechanism is discussed via delta-doping method and single-carrier device, which is summarized that the carrier trapping, the exciton quenching, the mobility change and the recombination zone alteration are negative to color stability while the energy transfer process and the blue/red/blue sandwiched structure are contributed to the color stability in our flexible white TEOLEDs.

36 MATERIALS SCIENCE↗

Using interlayer step-wise triplet transfer to achieve an efficient white organic light-emitting diode with high color-stability

An efficient phosphorescent white organic light emitting-diode with a red-green-blue tri-emitting-layer structure is reported. The host of the red dopant possesses a lower triplet-energy than the green dye. An interlayer step-wise triplet transfer via blue dye → green dye → red host → red dye is achieved. This mechanism allows an efficient triplet harvesting by the three dopants, thus maintaining a balanced white light and reducing energy loss. Moreover, the color stability of the device is improved significantly. The white device not only achieves a peak external quantum efficiency of 21.1 ± 0.8% and power efficiency of 37.5 ± 1.4 lm/W but shows no color shift over a wide range of voltages.

36 MATERIALS SCIENCE↗

Temperature of broadband anti-Stokes white emission in LiYbP{sub 4}O{sub 12}: Er nanocrystals

The up-conversion emission of LiYb{sub 0.99}Er{sub 0.01}P{sub 4}O{sub 12} nanocrystals was investigated in vacuum upon the focused beam of infrared laser excitation. The intense white broad band emission was observed above the threshold power of 800 mW. An increase of excitation power results in enhancement of temperature of emitting nanocrystals. The temperature of nanocrystals was determined following the thermally equilibrated f-f emission transitions of Er{sup 3+} ions. The highest measured temperature of white emission was determined to be about 900 K. It is concluded that the black body radiation is not responsible for the white broad band emission.

75 CONDENSED MATTER PHYSICS, SUPERCONDUCTIVITY AND↗

Response analysis of a class of quasi-linear systems with fractional derivative excited by Poisson white noise

The Poisson white noise, as a typical non-Gaussian excitation, has attracted much attention recently. However, little work was referred to the study of stochastic systems with fractional derivative under Poisson white noise excitation. This paper investigates the stationary response of a class of quasi-linear systems with fractional derivative excited by Poisson white noise. The equivalent stochastic system of the original stochastic system is obtained. Then, approximate stationary solutions are obtained with the help of the perturbation method. Finally, two typical examples are discussed in detail to demonstrate the effectiveness of the proposed method. The analysis also shows that the fractional order and the fractional coefficient significantly affect the responses of the stochastic systems with fractional derivative.

71 CLASSICAL AND QUANTUM MECHANICS, GENERAL PHYSIC↗

Modulation of recombination zone position for white perovskite/organic emitter hybrid light-emitting devices

We report metal halide perovskites present specific challenges as emitters in large area, surface emission lighting devices. Among these challenges is the vast difference in carrier mobilities between the perovskite and many organic buffer layers typically used in such device fabrication as transport and blocking layers. This can make it difficult to engineer recombination to achieve white emitting devices generally. However, in this work, we introduce unique modulation of excitonic confinement within the perovskite layer of the device stack to control overall placement of the recombination zone. This results in a white light emitter that is bright and highly tunable, providing a path to realize white perovskite related light-emitting devices.

42 ENGINEERING↗

White dwarf and subdwarf stars in the Sloan Digital Sky Survey Data Release 16

ABSTRACT White dwarfs are the end state of the evolution of more than 97 per cent of all stars, and therefore carry information on the structure and evolution of the Galaxy through their luminosity function and initial-to-final mass relation. Examining the new spectra of all white or blue stars in the Sloan Digital Sky Survey Data Release 16, we report the spectral classification of 2410 stars, down to our identification cut-off of signal-to-noise ratio equal to three. We newly identify 1404 DAs, 189 DZs, 103 DCs, 12 DBs, and nine CVs. The remaining objects are a mix of carbon or L stars (dC/L), narrow-lined hydrogen-dominated stars (sdA), dwarf F stars, and P Cyg objects. As white dwarf stars were not targeted by SDSS DR16, the number of new discoveries is much smaller than in previous releases. We also report atmospheric parameters and masses for a subset consisting of 555 new DAs, 10 new DBs, and 85 DZs for spectra with signal-to-noise ratio larger than 10.

Kepler, S. O. (ORCID:0000000274705703)↗

Exotic compact objects: The dark white dwarf

Several dark matter models allow for the intriguing possibility of exotic compact object formation. These objects might have unique characteristics that set them apart from their baryonic counterparts. Furthermore, gravitational wave observations of their mergers may provide the only direct window on a potentially entirely hidden sector. Here, we discuss dark white dwarfs, starting with an overview of the microphysical model and analytic scaling relations of macroscopic properties derived from the nonrelativistic limit. We use the full relativistic formalism to confirm these scaling relations and demonstrate that dark white dwarfs, if they exist, would have masses and tidal deformabilities that are very different from those of baryonic compact objects. Further, and most importantly, we demonstrate that dark white dwarf mergers would be detectable by current or planned gravitational observatories across several orders of magnitude in the particle-mass parameter space. Lastly, we find universal relations analogous to the compactness-Love and binary Love relations in neutron star literature. Using these results, we show that gravitational wave observations would constrain the properties of the dark matter particles constituting these objects.

79 ASTRONOMY AND ASTROPHYSICS↗

Coupling Secretomics with Enzyme Activities To Compare the Temporal Processes of Wood Metabolism among White and Brown Rot Fungi

Wood-degrading fungi use a sequence of oxidative and hydrolytic mechanisms to loosen lignocellulose and then release and metabolize embedded sugars. These temporal sequences have recently been mapped at high resolution using directional growth on wood wafers, revealing previously obscured dynamics as fungi progressively colonize wood. Here, we applied secretomics in the same wafer design to track temporal trends on aspen decayed by fungi with distinct nutritional modes: two brown rot-type (BR) fungi (Postia placenta, Gloeophyllum trabeum) and two white rot (WR) (Stereum hirsutum, Trametes versicolor). We matched secretomic data from three zones of decay (early, middle, late) with enzyme activities in these zones, and we included measures of total protein and ergosterol as benchmarks. In line with previous transcriptomics data, all of fungi tested showed an initial investment in pectinases and a delayed investment in other glycoside hydrolases (GHs). Brown rot fungi also staggered abundance of some oxidoreductases ahead of GHs to produce a familiar two-step mechanism. White rot fungi, however, showed late-stage investment in pectinases as well, unlike brown rot fungi. Lignolytic enzyme activities and abundances were also different between the two white rot fungi. Specifically, S. hirsutum lignolytic activity was delayed, explained almost entirely by the activity and abundance of five ‘atypical’ type manganese peroxidases, unlike more varied peroxidases and laccases in T. versicolor. These secretomic analyses support brown rot patterns generated via transcriptomics, they reveal distinct patterns among and within rot types, and they link spectral counts with activities to help functionalize these multi-strain secretomic data.

fungi, secretome, Proteomics, Lignin↗