2020
DOI: 10.1007/s12274-020-3061-9
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Light-responsive color switching of self-doped TiO2−x/WO3·0.33H2O hetero-nanoparticles for highly efficient rewritable paper

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Cited by 39 publications
(19 citation statements)
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“…25,26 The formation of oxygen vacancies is generally induced by Ti 3+ substitution of Ti 4+ in the TiO 2−x nanoparticles to compensate the charge imbalance. 27 In the C 1s region, the peaks located at 288.2, 285.4, and 284.6 eV are due to C−O−Ti, C−O, and C−C in the TiO 2−x nanoparticles, respectively (SI Figure S5b). 28,29 The N 1s peak at 400.1 eV is assigned to the molecular N 2 absorbed on the surface or interstitial nitrogen dopant while the peak at 398.8 eV is ascribed to the adsorbed ammonia (Figure 2c).…”
Section: ■ Results and Discussionmentioning
confidence: 99%
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“…25,26 The formation of oxygen vacancies is generally induced by Ti 3+ substitution of Ti 4+ in the TiO 2−x nanoparticles to compensate the charge imbalance. 27 In the C 1s region, the peaks located at 288.2, 285.4, and 284.6 eV are due to C−O−Ti, C−O, and C−C in the TiO 2−x nanoparticles, respectively (SI Figure S5b). 28,29 The N 1s peak at 400.1 eV is assigned to the molecular N 2 absorbed on the surface or interstitial nitrogen dopant while the peak at 398.8 eV is ascribed to the adsorbed ammonia (Figure 2c).…”
Section: ■ Results and Discussionmentioning
confidence: 99%
“…The Ti signal can be deconvoluted by using the multi-Gaussian function into Ti 3+ (at 457.4 and 462.9 eV) and Ti 4+ (at 458.0 and 463.8 eV), respectively, demonstrating the existence of Ti 3+ species in the typical nanoparticles . The XPS spectrum of O 1s shows four peaks at 529.1, 530.5, 531.5, and 532.1 eV, which are assigned to the Ti–O bond, C–O–Ti, the oxygen of surface hydroxyl groups and oxygen vacancies, respectively (Figure b). , The formation of oxygen vacancies is generally induced by Ti 3+ substitution of Ti 4+ in the TiO 2– x nanoparticles to compensate the charge imbalance . In the C 1s region, the peaks located at 288.2, 285.4, and 284.6 eV are due to C–O–Ti, C–O, and C–C in the TiO 2– x nanoparticles, respectively (SI Figure S5b).…”
Section: Resultsmentioning
confidence: 99%
“…We have recently reported photoreductive titania/hydrated tungsten oxide (THTO) heteronanoparticles, which exhibit a super outstanding photoreversible color-switching property under UV irradiation. 34 Since both titania and hydrated tungsten oxide are wide-band-gap semiconductors perfectly corresponding to solar UV radiation, we conjecture that the THTO heteronanoparticles are an alternative for designing solar UV radiation monitors with excellent sensitivity and selectivity to solar UV radiation. Herein, we report on the design and development of a new solar UV radiation monitor by integrating sunlight-responsive color-switchable THTO heteronanoparticles with the sticker paper substrate.…”
Section: ■ Introductionmentioning
confidence: 98%
“…Many research efforts have focused on the production of electrochromic materials (ECMs), such as transition metal oxides [7], polymers [8,9], and small organic molecules [10]. Tungsten oxide (WO 3 ) is a widely studied inorganic ECM because its superior optical memory and cyclic as well as environmental stability can meet commercial requirements [11,12]. Polythiophenes and their derivatives with low-power consumption, facile color tunability through molecular design, and high processability of highly flexible are among the most promising conjugated polymers for the manufacture of electrochromic (EC) devices [13][14][15][16].…”
Section: Introductionmentioning
confidence: 99%