Kinetics and energetic analysis of the slow dispersive electron transfer from nano-TiO2 to O2 by in situ diffusion reflectance and Laplace transform

2021 ◽  
Author(s):  
Zhizhou Wu ◽  
Liuyang Li ◽  
Xuedong Zhou ◽  
Xiujian Zhao ◽  
Baoshun Liu
Keyword(s):  
Electron Transfer ◽  
Laplace Transform ◽  
Energy Distribution ◽  
Nano Tio2 ◽  
Barrier Energy ◽  
Energetic Analysis ◽  
In Situ Diffusion

In situ diffusion reflectances reveal the trapping-filling effect in the electron transfer from TiO2 to O2 and Laplace transform was developed to derive the broadened apparent barrier energy distribution.

The electron-transfer intermediates of the oxygen evolution reaction (OER) as polarons by in situ spectroscopy

2021 ◽  
Author(s):  
Hanna Lyle ◽  
Suryansh Singh ◽  
Michael Paolino ◽  
Ilya Vinogradov ◽  
Tanja Cuk
Keyword(s):  
Electron Transfer ◽  
Oxygen Evolution ◽  
Oxygen Evolution Reaction ◽  
Catalytic Reactions ◽  
In Situ Spectroscopy ◽  
Chemical Bonds

The conversion of diffusive forms of energy (electrical and light) into short, compact chemical bonds by catalytic reactions regularly involves moving a carrier from an environment that favors delocalization to one that favors localization.

In situ fabrication of PHEMA–BSA core–corona biohybrid particles

2016 ◽  
Vol 4 (25) ◽  
pp. 4430-4438 ◽  
Author(s):  
Jin-Tao Wang ◽  
Yanhang Hong ◽  
Xiaotian Ji ◽  
Mingming Zhang ◽  
Li Liu ◽  
...  
Keyword(s):  
Electron Transfer ◽  
Bovine Serum Albumin ◽  
Serum Albumin ◽  
Bovine Serum ◽  
Atom Transfer ◽  
Hydroxyethyl Methacrylate ◽  
In Situ Fabrication ◽  
Radical Polymerizations

Poly(2-hydroxyethyl methacrylate)–bovine serum albumin core–corona particles were prepared using in situ activators generated by electron transfer for atom transfer radical polymerizations of HEMA initiated by a BSA macroinitiator.

Preparation of nano-TiO2/polyurethane emulsions via in situ RAFT polymerization

2010 ◽  
Vol 69 (4) ◽  
pp. 534-538 ◽  
Author(s):  
Xiang-Chen Che ◽  
Yu-Zi Jin ◽  
Youn-Sik Lee
Keyword(s):  
Raft Polymerization ◽  
Nano Tio2

Modeling of an in-situ diffusion experiment in granite at the Grimsel Test Site

2014 ◽  
Vol 1665 ◽  
pp. 85-91 ◽  
Author(s):  
Josep M. Soler ◽  
Jiri Landa ◽  
Vaclava Havlova ◽  
Yukio Tachi ◽  
Takanori Ebina ◽  
...  
Keyword(s):  
Effective Diffusion ◽  
Test Site ◽  
Diffusion Experiment ◽  
Bulk Rock ◽  
Disturbed Zone ◽  
Mean Grain Size ◽  
Grimsel Test Site ◽  
In Situ Diffusion

ABSTRACTMatrix diffusion is a key process for radionuclide retention in crystalline rocks. Within the LTD project (Long-Term Diffusion), an in-situ diffusion experiment in unaltered non-fractured granite was performed at the Grimsel Test Site (www.grimsel.com, Switzerland). The tracers included 3H as HTO, 22Na+, 134Cs+ and 131I- with stable I- as carrier.The dataset (except for 131I- because of complete decay) was analyzed with different diffusion-sorption models by different teams (NAGRA / IDAEA-CSIC, UJV-Rez, JAEA, Univ. Poitiers) using different codes, with the goal of obtaining effective diffusion coefficients (De) and porosity (ϕ) or rock capacity (α) values. A Borehole Disturbed Zone (BDZ), which was observed in the rock profile data for 22Na+ and 134Cs+, had to be taken into account to fit the experimental observations. The extension of the BDZ (1-2 mm) was about the same magnitude as the mean grain size of the quartz and feldspar grains.De and α values for the different tracers in the BDZ are larger than the respective values in the bulk rock. Capacity factors in the bulk rock are largest for Cs+ (strong sorption) and smallest for 3H (no sorption). However, 3H seems to display large α values in the BDZ. This phenomenon will be investigated in more detail in a second test starting in 2013.

TiCp2Cl-Catalyzed Living Radical and Ring Opening Polymerizations Initiated from Epoxides and Aldehydes in the Synthesis of Linear, Graft and Branched Polymers

2004 ◽  
Vol 856 ◽  
Author(s):  
Alexandru D. Asandei ◽  
Isaac W. Moran ◽  
Gobinda Saha ◽  
Yanhui Chen
Keyword(s):  
Electron Transfer ◽  
Ring Opening ◽  
Glycidyl Methacrylate ◽  
Ring Opening Polymerization ◽  
Branched Polymers ◽  
Single Electron Transfer ◽  
Radical Ring ◽  
Polymer Architectures ◽  
Complex Polymer

ABSTRACTTi(III)Cp2Cl-catalyzed radical ring opening (RRO) of epoxides or single electron transfer (SET) reduction of aldehydes generates Ti alkoxides and carbon centered radicals which add to styrene, initiating a radical polymerization. This polymerization is mediate in a living fashion by the reversible termination of growing chains with the TiCp2Cl metalloradical. In addition, polymers or monomers containing pendant epoxide groups (glycidyl methacrylate) can be used as substrates for radical grafting or branching reactions by self condensing vinyl polymerization. In addition, Ti alkoxides generated in situ by both epoxide RRO and aldehyde SET initiate the living ring opening polymerization of ε-caprolactone. Thus, new initiators and catalysts are introduced for the synthesis of complex polymer architectures.

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