4.2 Article

Bioinspired Noncyclic Transfer Pathway Electron Donors for Unprecedented Hydrogen Production

期刊

CCS CHEMISTRY
卷 5, 期 6, 页码 1470-1482

出版社

CHINESE CHEMICAL SOC
DOI: 10.31635/ccschem.022.202202071

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noncyclic electron transfer; Na2S-NaH2PO2; Na2S-NaNO2; electron donor pairs; photocatalytic H-2 production

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This paper reports on a novel and bioinspired electron donor pair that offers a noncyclic electron transfer pathway, providing more electrons without consuming the photogenerated electrons. Compared to the traditional Na2S-Na2SO3 electron donor pair, these new Na2S-NaH2PO2 and Na2S-NaNO2 electron donor pairs enable an unprecedented enhancement of up to 370% and 140% for average photocatalytic H2 production over commercial CdS nanoparticles, and they are versatile for a large series of photocatalysts for visible-light water splitting. The discovery of these novel electron donor pairs can revolutionize photocatalysis and has great significance for industrial visible-light-driven H2 production.
Electron donors are widely exploited in visible-light photocatalytic hydrogen production. As a typical electron donor pair and often the first choice for hydrogen production, the sodium sulfide-sodium sulfite pair has been extensively used. However, the resultant thiosulfate ions consume the photogenerated electrons to form an undesirable pseudocyclic electron transfer pathway during the photocatalytic process, strongly limiting the solar energy conversion efficiency. Here, we report novel and bioinspired electron donor pairs offering a noncyclic electron transfer pathway that provides more electrons without the consumption of the photogenerated electrons. Compared to the state-of-the-art electron donor pair Na2S-Na2SO3, these novel Na2S-NaH2PO2 and Na2S-NaNO2 electron donor pairs enable an unprecedented enhancement of up to 370% and 140% for average photocatalytic H-2 production over commercial CdS nanoparticles, and they are versatile for a large series of photocatalysts for visible-light water splitting. The discovery of these novel electron donor pairs can lead to a revolution in photocatalysis and is of great significance for industrial visible-light-driven H-2 production. [GRAPHICS] .

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