4.7 Article

Cadmium-Containing Quantum Dots Used in Electronic Displays: Implications for Toxicity and Environmental Transformations

期刊

ACS APPLIED NANO MATERIALS
卷 4, 期 8, 页码 8417-8428

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acsanm.1c01659

关键词

quantum dots; display; environmental fate; ion release; liver cells; toxicity

资金

  1. Natural Science and Engineering Research Council of Canada (NSERC)
  2. Canada Foundation for Innovation (CFI)
  3. McGill Sustainability Systems Initiative (MSSI)
  4. Fonds de Recherche du Quebec-Nature et Technologies (FRQNT) Graduate Scholarship program
  5. Centre for Green Chemistry and Catalysis (CGCC)
  6. Canada Research Chair Program
  7. McGill University

向作者/读者索取更多资源

Cadmium-containing quantum dot nanoparticles are integrated into electronic displays for color conversion, with conflicting accounts on their environmental hazard. This study synthesized QDs with core-shell structure and thick polymer coating to investigate their dissolution under different environmental conditions. Results showed that low pH led to rapid QD dissolution, but the presence of a shell structure decreased Cd dissolution and toxicity. Liver cell experiments supported the lower toxicity of low-pH-exposed QDs compared to pristine QDs.
Cadmium-containing quantum dot (QD) nanoparticles are integrated into electronic displays because of their ability to efficiently convert colors. There are conflicting accounts as to whether these particles present a hazard to the environment, as they have been studied either as (1) embedded QDs in display screen films or (2) as model QDs with small, hydrophilic ligands. Both approaches have limitations that we addressed by synthesizing QDs featuring the core-shell structure and the thick polymer coating present in commercial devices to probe the dissolution of QDs in response to two environmental factors (pH and dissolved oxygen) over 1 day and 6 months. Results show that QDs were chemically stable at circumneutral pH (0% Cd dissolution after 6 months), but low pH initiated rapid dissolution under both aerobic and anaerobic conditions (up to 100% Cd dissolution after 6 months). In addition to the presence of a capping polymer, the QD shell structure led to more chemically stable nanoparticles compared to nonshelled QDs, as the presence of ZnS shells decreased Cd dissolution by 75%. The dense aggregation of QDs into structures of similar to 100 nm diameter over time was observed as well, which could lead to decreased bioavailability. To test this, we used liver cells to compare the toxicity of pristine QDs to those subjected to acid dissolution. Our results reveal that low-pH-exposed QDs separated from dissolved ions are less toxic than pristine QDs (half maximal inhibitory concentration, IC50, of 290 and 150 mg/L, respectively) and suggest a key role of dissolved ions and capping polymers for QD toxicity. These findings highlight the use of a commercially relevant nanoparticle structure to demonstrate fate and toxicity.

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