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Tunable optical activities in chiral transition metal oxide nanoparticles
Chiral transition metal oxides (TMOs) are widely used in various optoelectronic devices. However, the currently poor understanding of how the optical activities of TMOs can be regulated considerably hinders their applications. We have synthesized a series of chiral TMO nanoparticles (NPs), i.e. , Mo...
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Published in: | Nanoscale 2022-10, Vol.14 (41), p.15414-15421 |
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description | Chiral transition metal oxides (TMOs) are widely used in various optoelectronic devices. However, the currently poor understanding of how the optical activities of TMOs can be regulated considerably hinders their applications. We have synthesized a series of chiral TMO nanoparticles (NPs),
i.e.
, MoO
x
(
x
= 2, 2.4 and 2.5) and Co
3
O
4
. Compared with TMO NPs with
l
-/
d
-cysteine molecules as the capping ligand,
l
-/
d
-histidine-capped TMO NPs possess larger anisotropic factors (
g
abs
), which are as high as ∼0.01 and ∼0.02 for
l
-/
d
-histidine-capped MoO
2.5
and Co
3
O
4
NPs, respectively. A nondegenerate coupled oscillator (NDCO) theoretical calculation confirms that
l
-/
d
-histidine molecules can generate a smaller electric dipole moment and thus induce higher optical activity than
l
-/
d
-cysteine molecules. Impressively, the chiral NPs exhibit broadband second harmonic generation. This work indicates that chiral TMO NPs have potential for application in nonlinear optical devices.
The optical activities of chiral transition metal oxide nanoparticles are regulated, achieving a maximum anisotropic factor of approximately 0.02. Impressively, the chiral nanoparticles demonstrate broadband second harmonic generation. |
doi_str_mv | 10.1039/d2nr02555h |
format | article |
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i.e.
, MoO
x
(
x
= 2, 2.4 and 2.5) and Co
3
O
4
. Compared with TMO NPs with
l
-/
d
-cysteine molecules as the capping ligand,
l
-/
d
-histidine-capped TMO NPs possess larger anisotropic factors (
g
abs
), which are as high as ∼0.01 and ∼0.02 for
l
-/
d
-histidine-capped MoO
2.5
and Co
3
O
4
NPs, respectively. A nondegenerate coupled oscillator (NDCO) theoretical calculation confirms that
l
-/
d
-histidine molecules can generate a smaller electric dipole moment and thus induce higher optical activity than
l
-/
d
-cysteine molecules. Impressively, the chiral NPs exhibit broadband second harmonic generation. This work indicates that chiral TMO NPs have potential for application in nonlinear optical devices.
The optical activities of chiral transition metal oxide nanoparticles are regulated, achieving a maximum anisotropic factor of approximately 0.02. Impressively, the chiral nanoparticles demonstrate broadband second harmonic generation.</description><identifier>ISSN: 2040-3364</identifier><identifier>EISSN: 2040-3372</identifier><identifier>DOI: 10.1039/d2nr02555h</identifier><language>eng</language><publisher>Cambridge: Royal Society of Chemistry</publisher><subject>Broadband ; Capping ; Cobalt oxides ; Cysteine ; Dipole moments ; Electric dipoles ; Histidine ; Nanoparticles ; Nonlinear optics ; Optical activity ; Optoelectronic devices ; Second harmonic generation ; Transition metal oxides</subject><ispartof>Nanoscale, 2022-10, Vol.14 (41), p.15414-15421</ispartof><rights>Copyright Royal Society of Chemistry 2022</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c314t-7dc2afb673619da8a58fcf5706cf141e930da9451b3b00f92d839d454ca4387d3</citedby><cites>FETCH-LOGICAL-c314t-7dc2afb673619da8a58fcf5706cf141e930da9451b3b00f92d839d454ca4387d3</cites><orcidid>0000-0002-2663-7881 ; 0000-0003-1040-0596 ; 0000-0002-2496-4053</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,777,781,27905,27906</link.rule.ids></links><search><creatorcontrib>Xiao, Shuyu</creatorcontrib><creatorcontrib>Liang, Jiechun</creatorcontrib><creatorcontrib>Li, Junzi</creatorcontrib><creatorcontrib>Cheng, Jiaji</creatorcontrib><creatorcontrib>Zhu, Xi</creatorcontrib><creatorcontrib>He, Tingchao</creatorcontrib><title>Tunable optical activities in chiral transition metal oxide nanoparticles</title><title>Nanoscale</title><description>Chiral transition metal oxides (TMOs) are widely used in various optoelectronic devices. However, the currently poor understanding of how the optical activities of TMOs can be regulated considerably hinders their applications. We have synthesized a series of chiral TMO nanoparticles (NPs),
i.e.
, MoO
x
(
x
= 2, 2.4 and 2.5) and Co
3
O
4
. Compared with TMO NPs with
l
-/
d
-cysteine molecules as the capping ligand,
l
-/
d
-histidine-capped TMO NPs possess larger anisotropic factors (
g
abs
), which are as high as ∼0.01 and ∼0.02 for
l
-/
d
-histidine-capped MoO
2.5
and Co
3
O
4
NPs, respectively. A nondegenerate coupled oscillator (NDCO) theoretical calculation confirms that
l
-/
d
-histidine molecules can generate a smaller electric dipole moment and thus induce higher optical activity than
l
-/
d
-cysteine molecules. Impressively, the chiral NPs exhibit broadband second harmonic generation. This work indicates that chiral TMO NPs have potential for application in nonlinear optical devices.
The optical activities of chiral transition metal oxide nanoparticles are regulated, achieving a maximum anisotropic factor of approximately 0.02. Impressively, the chiral nanoparticles demonstrate broadband second harmonic generation.</description><subject>Broadband</subject><subject>Capping</subject><subject>Cobalt oxides</subject><subject>Cysteine</subject><subject>Dipole moments</subject><subject>Electric dipoles</subject><subject>Histidine</subject><subject>Nanoparticles</subject><subject>Nonlinear optics</subject><subject>Optical activity</subject><subject>Optoelectronic devices</subject><subject>Second harmonic generation</subject><subject>Transition metal oxides</subject><issn>2040-3364</issn><issn>2040-3372</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><recordid>eNpd0M1LwzAYBvAgCs7pxbtQ8CJCNZ9Nc5T5scFQkHkuaZKyjC6pSSv635tZmeApLw-_9yU8AJwjeIMgEbcauwAxY2x9ACYYUpgTwvHhfi7oMTiJcQNhIUhBJmCxGpysW5P5rrdKtplUvf2wvTUxsy5TaxtS2AfpYgq9y7amT4H_tNpkTjrfyZAWWxNPwVEj22jOft8peHt8WM3m-fLlaTG7W-aKINrnXCssm7rgpEBCy1KyslEN47BQDaLICAK1FJShmtQQNgLrkghNGVWSkpJrMgVX490u-PfBxL7a2qhM20pn_BArzDEpEROcJnr5j278EFz63U4JSMuSs6SuR6WCjzGYpuqC3crwVSFY7Vqt7vHz60-r84QvRhyi2ru_1sk36wBz1w</recordid><startdate>20221027</startdate><enddate>20221027</enddate><creator>Xiao, Shuyu</creator><creator>Liang, Jiechun</creator><creator>Li, Junzi</creator><creator>Cheng, Jiaji</creator><creator>Zhu, Xi</creator><creator>He, Tingchao</creator><general>Royal Society of Chemistry</general><scope>AAYXX</scope><scope>CITATION</scope><scope>7SR</scope><scope>7U5</scope><scope>8BQ</scope><scope>8FD</scope><scope>F28</scope><scope>FR3</scope><scope>JG9</scope><scope>L7M</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-2663-7881</orcidid><orcidid>https://orcid.org/0000-0003-1040-0596</orcidid><orcidid>https://orcid.org/0000-0002-2496-4053</orcidid></search><sort><creationdate>20221027</creationdate><title>Tunable optical activities in chiral transition metal oxide nanoparticles</title><author>Xiao, Shuyu ; Liang, Jiechun ; Li, Junzi ; Cheng, Jiaji ; Zhu, Xi ; He, Tingchao</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c314t-7dc2afb673619da8a58fcf5706cf141e930da9451b3b00f92d839d454ca4387d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Broadband</topic><topic>Capping</topic><topic>Cobalt oxides</topic><topic>Cysteine</topic><topic>Dipole moments</topic><topic>Electric dipoles</topic><topic>Histidine</topic><topic>Nanoparticles</topic><topic>Nonlinear optics</topic><topic>Optical activity</topic><topic>Optoelectronic devices</topic><topic>Second harmonic generation</topic><topic>Transition metal oxides</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Xiao, Shuyu</creatorcontrib><creatorcontrib>Liang, Jiechun</creatorcontrib><creatorcontrib>Li, Junzi</creatorcontrib><creatorcontrib>Cheng, Jiaji</creatorcontrib><creatorcontrib>Zhu, Xi</creatorcontrib><creatorcontrib>He, Tingchao</creatorcontrib><collection>CrossRef</collection><collection>Engineered Materials Abstracts</collection><collection>Solid State and Superconductivity Abstracts</collection><collection>METADEX</collection><collection>Technology Research Database</collection><collection>ANTE: Abstracts in New Technology & Engineering</collection><collection>Engineering Research Database</collection><collection>Materials Research Database</collection><collection>Advanced Technologies Database with Aerospace</collection><collection>MEDLINE - Academic</collection><jtitle>Nanoscale</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Xiao, Shuyu</au><au>Liang, Jiechun</au><au>Li, Junzi</au><au>Cheng, Jiaji</au><au>Zhu, Xi</au><au>He, Tingchao</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Tunable optical activities in chiral transition metal oxide nanoparticles</atitle><jtitle>Nanoscale</jtitle><date>2022-10-27</date><risdate>2022</risdate><volume>14</volume><issue>41</issue><spage>15414</spage><epage>15421</epage><pages>15414-15421</pages><issn>2040-3364</issn><eissn>2040-3372</eissn><abstract>Chiral transition metal oxides (TMOs) are widely used in various optoelectronic devices. However, the currently poor understanding of how the optical activities of TMOs can be regulated considerably hinders their applications. We have synthesized a series of chiral TMO nanoparticles (NPs),
i.e.
, MoO
x
(
x
= 2, 2.4 and 2.5) and Co
3
O
4
. Compared with TMO NPs with
l
-/
d
-cysteine molecules as the capping ligand,
l
-/
d
-histidine-capped TMO NPs possess larger anisotropic factors (
g
abs
), which are as high as ∼0.01 and ∼0.02 for
l
-/
d
-histidine-capped MoO
2.5
and Co
3
O
4
NPs, respectively. A nondegenerate coupled oscillator (NDCO) theoretical calculation confirms that
l
-/
d
-histidine molecules can generate a smaller electric dipole moment and thus induce higher optical activity than
l
-/
d
-cysteine molecules. Impressively, the chiral NPs exhibit broadband second harmonic generation. This work indicates that chiral TMO NPs have potential for application in nonlinear optical devices.
The optical activities of chiral transition metal oxide nanoparticles are regulated, achieving a maximum anisotropic factor of approximately 0.02. Impressively, the chiral nanoparticles demonstrate broadband second harmonic generation.</abstract><cop>Cambridge</cop><pub>Royal Society of Chemistry</pub><doi>10.1039/d2nr02555h</doi><tpages>8</tpages><orcidid>https://orcid.org/0000-0002-2663-7881</orcidid><orcidid>https://orcid.org/0000-0003-1040-0596</orcidid><orcidid>https://orcid.org/0000-0002-2496-4053</orcidid></addata></record> |
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language | eng |
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source | Royal Society of Chemistry |
subjects | Broadband Capping Cobalt oxides Cysteine Dipole moments Electric dipoles Histidine Nanoparticles Nonlinear optics Optical activity Optoelectronic devices Second harmonic generation Transition metal oxides |
title | Tunable optical activities in chiral transition metal oxide nanoparticles |
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