Fast and spontaneous reduction of gold ions over oxygen-vacancy-rich TiO2: A novel strategy to design defect-based composite photocatalyst

2013 ◽  
Vol 459 ◽  
pp. 34-40 ◽  
Author(s):  
Xiaoyang Pan ◽  
Yi-Jun Xu
2020 ◽  
Vol 276 ◽  
pp. 119167 ◽  
Author(s):  
Chengyang Feng ◽  
Lin Tang ◽  
Yaocheng Deng ◽  
Jiajia Wang ◽  
Yani Liu ◽  
...  

2018 ◽  
Vol 8 (5) ◽  
pp. 1366-1374 ◽  
Author(s):  
Luyue Wang ◽  
Xinxin Xu ◽  
Shijie Wu ◽  
Feng Cao

An oxygen vacancy rich WO3−x based composite material with 3D nitrogen doped carbon as a matrix is synthesized and it exhibits photocatalytic VOC removal and H2 production activities.


Fuel ◽  
2022 ◽  
Vol 312 ◽  
pp. 122975
Author(s):  
Wei Liu ◽  
Wenjie Xiang ◽  
Xi Chen ◽  
Zhongxian Song ◽  
Chunxiang Gao ◽  
...  

RSC Advances ◽  
2016 ◽  
Vol 6 (13) ◽  
pp. 10887-10894 ◽  
Author(s):  
Xiuqi Qin ◽  
Fang He ◽  
Lixia Chen ◽  
Yuhuan Meng ◽  
Jing Liu ◽  
...  

In this work, an effective composite photocatalyst (TC800) was prepared which exhibits higher photocatalytic activity under visible light than previously reported TiO2/non-graphene carbon compounds.


2021 ◽  
Author(s):  
Yuxuan Lu ◽  
Tianyang Liu ◽  
Chunming Yang ◽  
Chung-Li Dong ◽  
Yucheng Huang ◽  
...  

Abstract The electrooxidation of 5-hydroxymethylfurfural (HMF) offers a promising green route to attain high-value chemicals from biomass. The HMF electrooxidation reaction (HMFOR) is a complicated process involving the combined adsorption and coupling of organic molecules and OH- on the electrode surface. An in-depth understanding of these cooperative adsorption behaviors and reaction processes is fundamentally essential. Herein, the adsorption behavior of HMF and OH-, and the role of oxygen vacancy on Co3O4 are initially unraveled. Correspondingly, instead of the competitive adsorption of OH- and HMF on the metal sites, it is observed that the OH- could fill into oxygen vacancy (Vo) before couple with organic molecules through the lattice oxygen oxidation reaction process, which could accelerate the rate-determining step of the dehydrogenation of 5-hydroxymethyl-2-furancarboxylic acid (HMFCA) and enhance the overall conversion of HMF on Vo-Co3O4. This work sheds a depth insight on the catalytic mechanism of oxygen vacancy, which benefits designing a novel strategy to modulate the multi-molecules combined adsorption behaviors.


2019 ◽  
Vol 3 (1) ◽  
pp. 97-105
Author(s):  
Mary Zuccato ◽  
Dustin Shilling ◽  
David C. Fajgenbaum

Abstract There are ∼7000 rare diseases affecting 30 000 000 individuals in the U.S.A. 95% of these rare diseases do not have a single Food and Drug Administration-approved therapy. Relatively, limited progress has been made to develop new or repurpose existing therapies for these disorders, in part because traditional funding models are not as effective when applied to rare diseases. Due to the suboptimal research infrastructure and treatment options for Castleman disease, the Castleman Disease Collaborative Network (CDCN), founded in 2012, spearheaded a novel strategy for advancing biomedical research, the ‘Collaborative Network Approach’. At its heart, the Collaborative Network Approach leverages and integrates the entire community of stakeholders — patients, physicians and researchers — to identify and prioritize high-impact research questions. It then recruits the most qualified researchers to conduct these studies. In parallel, patients are empowered to fight back by supporting research through fundraising and providing their biospecimens and clinical data. This approach democratizes research, allowing the entire community to identify the most clinically relevant and pressing questions; any idea can be translated into a study rather than limiting research to the ideas proposed by researchers in grant applications. Preliminary results from the CDCN and other organizations that have followed its Collaborative Network Approach suggest that this model is generalizable across rare diseases.


Author(s):  
Taddese Mekonnen Ambay ◽  
Philipp Schick ◽  
Michael Grimm ◽  
Maximilian Sager ◽  
Felix Schneider ◽  
...  

2020 ◽  
Author(s):  
Ana Beloqui ◽  
Francesco Suriano ◽  
Matthias Hul ◽  
Yining Xu ◽  
Véronique Préat ◽  
...  

2020 ◽  
Vol 3 (1) ◽  
pp. 58-76 ◽  
Author(s):  
Bohan Rong ◽  
Qiong Wu ◽  
Chao Sun

Melatonin is a well-known molecule for its involvement in circadian rhythm regulation and its contribution to protection against oxidative stress in organisms including unicellular alga, animals and plants. Currently, the bio-regulatory effects of melatonin on the physiology of various peripheral tissues have drawn a great attention of scientists. Although melatonin was previously defined as a neurohormone secreted from pineal gland, recently it has been identified that virtually, every cell has the capacity to synthesize melatonin and the locally generated melatonin has multiple pathophysiological functions, including regulations of obesity and metabolic syndromes. Herein, we focus on the effects of melatonin on fat deposition in various peripheral organs/tissues. The two important regulatory mechanisms related to the topic, i.e., the improvements of circadian rhythms and antioxidative capacity will be thoroughly discussed since they are linked to several biomarkers involved in obesity and energy imbalance, including metabolism and immunity. Furthermore, several other functions of melatonin which may serve to prevent or promote obesity and energy dysmetabolism-induced pathological states are also addressed. The organs of special interest include liver, pancreas, skeletal muscle, adipose tissue and the gut microbiota.


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