2017
DOI: 10.1038/nmat4871
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Pushing the knowledge of interfaces

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Cited by 7 publications
(5 citation statements)
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“… 1 An unresolved scientific challenge for this technology is understanding–and controlling–the mechanism of photoinduced electron–hole (e–h) separation. Specifically, the extent to which Coulombic interactions between the electron and hole directly after exciton dissociation at a donor:acceptor (D:A) interface limit photocurrent generation has remained controversial, 2 because of inconclusive evidence from experimental and theoretical studies producing contradictory e–h separation models. 3 8 There is extensive evidence from transient absorption and photoluminescence (PL) spectroscopic studies for the existence of photogenerated e–h pairs that are spatially localized and subject to stronger Coulombic binding interaction which, once formed, can limit photocurrent generation.…”
Section: Introductionmentioning
confidence: 99%
See 1 more Smart Citation
“… 1 An unresolved scientific challenge for this technology is understanding–and controlling–the mechanism of photoinduced electron–hole (e–h) separation. Specifically, the extent to which Coulombic interactions between the electron and hole directly after exciton dissociation at a donor:acceptor (D:A) interface limit photocurrent generation has remained controversial, 2 because of inconclusive evidence from experimental and theoretical studies producing contradictory e–h separation models. 3 8 There is extensive evidence from transient absorption and photoluminescence (PL) spectroscopic studies for the existence of photogenerated e–h pairs that are spatially localized and subject to stronger Coulombic binding interaction which, once formed, can limit photocurrent generation.…”
Section: Introductionmentioning
confidence: 99%
“…An unresolved scientific challenge for this technology is understanding–and controlling–the mechanism of photoinduced electron–hole (e–h) separation. Specifically, the extent to which Coulombic interactions between the electron and hole directly after exciton dissociation at a donor:acceptor (D:A) interface limit photocurrent generation has remained controversial, because of inconclusive evidence from experimental and theoretical studies producing contradictory e–h separation models. There is extensive evidence from transient absorption and photoluminescence (PL) spectroscopic studies for the existence of photogenerated e–h pairs that are spatially localized and subject to stronger Coulombic binding interaction which, once formed, can limit photocurrent generation. , We refer herein to such states as bound interfacial charge-transfer (CT) states. The presence of such CT states is evidenced by electric-field-dependent studies and pump–push transient studies indicating extra energy can assist in dissociating these intermediate CT states into separated e–h pairs. Some, but not all, transient studies have shown that the yield of separated e–h pairs increases with an increasing enthalpic offset between the photoexcited donor (or acceptor) singlet state and the nominal D:A charge separated state in series of chemically similar blends, suggesting that an increased offset may help photogenerated e–h pairs avoid prompt recombination at the D:A interface by overcoming their Coulombic binding energy. Furthermore, photoluminescence studies probing sub-band-gap CT transitions have demonstrated the existence of CT states with different degrees of an e–h pair separation radius, and hence, binding energy .…”
Section: Introductionmentioning
confidence: 99%
“…Some flavonoids have a selective DNMTs inhibitory activity, for example kaempferol inhibits DNMT1 and DNMT3B but not DNMT3A 0 enzymatic activity in bladder and CRC cancer (Banerji 2017;Lu et al 2018).…”
Section: Phytochemicals Modulating the Epigenetic Alterations Of Dna mentioning
confidence: 99%
“…Organic photovoltaic (OPV) devices have been leading the research into energy science and technology. [1][2][3] In recent years, much attention has been devoted to the perovskite materials and their applications in solar energy conversion because of their high absorbance, low carrier recombination rate, outstanding ferroelectric properties and easier synthesis. [4][5][6] Among them, perovskite solar cells (PSC) with CH 3 NH 3 PbX 3 perovskites (X ¼ Cl, Pb, and I) as absorber layers show great potential in fabricating low-cost and large-scale commercial solar cells, whose efficiency has increased from 3.8% to over 22% in the past ve years.…”
Section: Introductionmentioning
confidence: 99%