Please use this identifier to cite or link to this item: http://hdl.handle.net/10397/100048
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dc.contributorDepartment of Applied Biology and Chemical Technologyen_US
dc.creatorYang, Cen_US
dc.creatorBai, Sen_US
dc.creatorYu, Zen_US
dc.creatorFeng, Yen_US
dc.creatorHuang, Ben_US
dc.creatorLu, Qen_US
dc.creatorWu, Ten_US
dc.creatorSun, Men_US
dc.creatorZhu, Ten_US
dc.creatorCheng, Cen_US
dc.creatorZhang, Len_US
dc.creatorShao, Qen_US
dc.creatorHuang, Xen_US
dc.date.accessioned2023-08-08T01:51:40Z-
dc.date.available2023-08-08T01:51:40Z-
dc.identifier.issn2211-2855en_US
dc.identifier.urihttp://hdl.handle.net/10397/100048-
dc.language.isoenen_US
dc.publisherElsevieren_US
dc.rights© 2021 The Author(s). Published by Elsevier Ltd. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).en_US
dc.rightsThe following publication Yang, C., Bai, S., Yu, Z., Feng, Y., Huang, B., Lu, Q., ... & Huang, X. (2021). A newly-explored Pd-based nanocrystal for the pH-universal electrosynthesis of H2O2. Nano Energy, 89, 106480 is available at https://doi.org/10.1016/j.nanoen.2021.106480.en_US
dc.subjectH2O2 electrosynthesisen_US
dc.subjectHigh selectivityen_US
dc.subjectP-d couplingen_US
dc.subjectPH-universalen_US
dc.subjectSePd alloyen_US
dc.titleA newly-explored Pd-based nanocrystal for the pH-universal electrosynthesis of H2O2en_US
dc.typeJournal/Magazine Articleen_US
dc.identifier.volume89en_US
dc.identifier.issuePart Ben_US
dc.identifier.doi10.1016/j.nanoen.2021.106480en_US
dcterms.abstractFor the generation of hydrogen peroxide (H2O2), a robust electrocatalyst with high activity, selectivity and stability under pH-universal conditions is a formidable challenge. Herein, Pd4Se nanoparticles (NPs) have been proposed as a highly active, selective and durable electrocatalyst for H2O2 production over a wide pH range for the first time. In particular, the Pd4Se NPs show superior H2O2 production selectivities of 93.5%, 89.7%, and 86.7% in 0.1 M HClO4, 0.1 M KCl and 0.1 M KOH electrolytes, respectively. Density functional theory (DFT) calculations reveal that Se incorporation prevents the O=O early-cleavage issue by suppressing the excessive electronegativity of the Pd sites. In addition, a strong p-d repulsive correlation shifts the Pd-4d band towards the electron-depleting centre, allowing near-barrier-free electron transfer and facilitating [OOH-] stabilization. Owing to a high energy barrier of the dissociation of [OOH-], the four-electrons oxygen reduction pathway is significantly suppressed for high H2O2 selectivity. The Pd4Se NPs are also highly stable, with only a 2.4%, 9.6% and 3.4% decrease for H2O2 selectivity in 0.1 M HClO4, 0.1 M KCl and 0.1 M KOH electrolytes, respectively, after 5000 cycles, which shows that these NPs are a unique and robust Pd-based electrocatalyst for H2O2 generation under pH-universal conditions.en_US
dcterms.accessRightsopen accessen_US
dcterms.bibliographicCitationNano energy, Nov. 2021, v. 89, pt. B, 106480en_US
dcterms.isPartOfNano energyen_US
dcterms.issued2021-11-
dc.identifier.scopus2-s2.0-85114141173-
dc.identifier.eissn2211-3282en_US
dc.identifier.artn106480en_US
dc.description.validate202308 bckwen_US
dc.description.oaVersion of Recorden_US
dc.identifier.FolderNumberABCT-0024-
dc.description.fundingSourceOthersen_US
dc.description.fundingTextNatural Science Foundation of Chinaen_US
dc.description.pubStatusPublisheden_US
dc.identifier.OPUS55722498-
dc.description.oaCategoryCCen_US
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