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Institution

Suffolk University

EducationBoston, Massachusetts, United States
About: Suffolk University is a education organization based out in Boston, Massachusetts, United States. It is known for research contribution in the topics: Population & Sugar beet. The organization has 6462 authors who have published 9321 publications receiving 235328 citations.


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TL;DR: In this paper, the authors apply a neo-institutional perspective to IAS and find that the structural dimensions of the types of standards themselves can increase the likelihood of organizations adopting IAS standards in form but not in function.
Abstract: A common complaint by academics and practitioners is that the application of international accountability standards (IAS) does not lead to significant improvements in an organization's social responsibility. When organizations espouse their commitment to IAS but do not put forth the effort necessary to operationally enact that commitment, a "credibility cover" is created that perpetuates business as usual. In other words, the legitimacy that organizations gain by formally adopting the standards may shield the organization from closer scrutiny, thus enabling rather than constraining the types of activities the standards were designed to discourage.There is a lack of research on why certain types of IAS are more prone than others to being decoupled from organizational practices. Applying a neo-institutional perspective to IAS, we theorize that the structural dimensions of the types of standards themselves can increase the likelihood of organizations adopting IAS standards in form but not in function.

142 citations

Journal ArticleDOI
TL;DR: In this paper, the authors reported the wet chemical synthesis of colloidal HgTe nanocrystals in aqueous solution at room temperature, and used 1-thioglycerol as the size-regulating capping agent.
Abstract: We have recently reported the wet chemical synthesis of colloidal HgTe nanocrystals in aqueous solution at room temperature. This novel material exhibits very strong and broad photoluminescence (PL) in the near infrared, with the exact wavelength depending on the synthetic conditions. The preparation was an extension to the previously published work on cadmium chalcogenide nanocrystals, i.e., CdS, CdSe, and CdTe, and used 1-thioglycerol as the size-regulating capping agent. Particles with a large distribution of sizes in the 3±6 nm diameter range were produced. Luminescence quantum efficiencies (QEs) of around 50 %, which are among the highest ever reported for a colloidal system, and stability towards oxidation indicate that the surface of the HgTe nanocrystals is extremely well-passivated. Typically, the PL from the freshly prepared material is around 1050 nm, but this moves to longer wavelengths with time, accompanied by an apparent drop in QE, until after two weeks the luminescence has shifted out to around 1200 nm. This aagingo process continues indefinitely, albeit at a slower rate, and presents real cause for concern for the long-term stability of such materials in device applications. In addition, if the colloidal nanocrystal solutions are heated, then a similar but more rapid process occurs with the PL shifting to beyond 1500 nm and the QE dropping to < 1 % with just a few minutes refluxing at 100 C. Again, this lack of stability to heating could be problematic in certain applications if high optical pump powers are used in laser or amplifier devices. A similar, although less-pronounced, effect is also observed in 1-thioglycerol-stabilized CdTe nanoparticles, which undergo a red shift of the PL under prolonged reflux. Whether this shift is caused by a gradual aripeningo of the nanocrystals with heat and/or time, or actually represents a compositional change will be discussed at a later date. Needless to say, the effect is undesirable and for HgTe to be a useful material, operating at the strategic near-infrared telecommunications wavelengths, the problem has to be eliminated. A possible way of achieving this is to cap the surface of the nanocrystals with a higher bandgap inorganic layer. These acore/shello composite materials can increase the luminescence quantum yield due to improved passivation of the surface, and also tend to be more physically robust than the abareo organically passivated clusters. This should therefore produce a much more stable material where not only the aagingo process is suppressed, but which is more tolerant to the processing conditions necessary for incorporation into useful devices. Examples of such core/shell structures include CdSe/ZnS, CdS/ZnS, CdSe/CdS, CdSe/ZnSe, and CdS/HgS with reports of roomtemperature QEs of up to 50 % for the CdSe/ZnS material. It was therefore decided to attempt to overcoat our HgTe nanocrystals with a layer of CdS in order to produce a physically stable core/shell heterostructure. The abareo 1-thioglycerol-stabilized HgTe colloidal nanocrystals were prepared in aqueous solution at room temperature using the method described previously. In order to coat these abareo organically capped nanocrystals with a layer of CdS, H2S gas buffered in N2 was passed through a vigorously stirred, dilute aqueous solution of HgTe nanocrystals and cadmium(II) perchlorate at a pH of around 10 in the presence of extra 1-thioglycerol stabilizer. The mixture was initially slightly turbid, but this cleared upon injection of the H2S, resulting in a clear, goldenbrown solution. This solution was then refluxed for about 30 min as a check of the robustness of the HgTe/CdS system. In order to fully characterize the material, optical absorption and photoluminescence spectra were recorded at all stages of the synthesis, as well as X-ray diffraction (XRD) patterns and high-resolution transmission electron microscopy (HRTEM) images to confirm the presence of HgTe/CdS core/shell particles in the final solution. The optical absorption data is shown in Figure 1, comparing the freshly prepared abareo HgTe prior to capping, and the subsequent HgTe/CdS material. A clear aexcitonico peak is visible for the bare HgTe sample at 850 nm, which clearly shifts to the red when the CdS capping is introduced. The increased optical density at shorter wavelengths could be indicative of some discrete CdS or HgCdTeS alloyed nanoparticles being formed in addition to the core/shell material. The effect of aging and/or heating the samples, both capped and uncapped, is to red-shift and broaden the absorption edges into the region where water absorption caused by a slight cell-mismatch prevents the recording of good-quality spectra. These are, therefore,

142 citations

Journal ArticleDOI
TL;DR: In this paper, the authors contribute to abusive supervision literature by testing supervisors' self-regulation impairment as a key mediator of the relationship between subordinate managers and their supervisors, and demonstrate that this impairment is a predictor of abusive supervision.
Abstract: Drawing on self-regulation theory, we contribute to the abusive supervision literature by testing supervisors’ self-regulation impairment as a key mediator of the relationship between subordinate d...

141 citations

Journal ArticleDOI
TL;DR: This study highlights the experience of stammering on the individual, discusses the variety of strategies used to manage dysfluency and indicates the complexities of day-to-day communication.

141 citations

Journal ArticleDOI
TL;DR: The data suggests that exposure of salmon smolts to atrazine in fresh water may compromise their physiological capabilities to survive in saline conditions.

140 citations


Authors

Showing all 6484 results

NameH-indexPapersCitations
Peter Hall132164085019
Michael R. Hamblin11789959533
Miao Liu11199359811
Rosalind W. Picard10046144750
Simon Jennings9424029030
John A. Clark9444062221
Christopher Hawkes9342341658
Melanie J. Davies8981436939
Andrew Smith87102534127
Andrew Jones8369528290
Catherine E. Costello8241124811
Paul O'Brien7980828228
Rhys E. Green7828530428
Nicholas K. Dulvy7219322962
David L.H. Bennett6932217388
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Performance
Metrics
No. of papers from the Institution in previous years
YearPapers
20236
202232
2021451
2020466
2019369
2018325