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Organic Long‐Persistent Luminescence from a Thermally Activated Delayed Fluorescence Compound.
Adv. Mater. 32, 2003911 (2020). DOI:10.1002/adma.202003911

[26] Nishimura, N., Lin, Z., Jinnai, K., Kabe, R.*, Adachi, C.*
Many Exciplex Systems Exhibit Organic Long‐Persistent Luminescence.
Adv. Funct. Mater. 30, 2000795 (2020). DOI:10.1002/adfm.202000795
[Inside front cover]

[25] Lin, Z., Kabe, R.*, Adachi, C.*
Orange Organic Long-persistent Luminescence from an Electron Donor/Acceptor Binary System.
Chem. Lett. 49, 203–206 (2020). DOI:10.1246/cl.190823

[24] Lin, Z., Kabe, R.*, Wang, K., Adachi, C.*
Influence of energy gap between charge-transfer and locally excited states on organic long persistence luminescence.
Nat. Commun. 11, 191 (2020). DOI:10.1038/s41467-019-14035-y

[23] Jinnai, K., Nishimura, N., Kabe, R.*, Adachi, C.*
Fabrication-method independence of organic long-persistent luminescence performance.
Chem. Lett. 48, 270–273 (2019). DOI:10.1246/cl.180949

[22] Mieno, H., Kabe, R.*, Allendorf, M.D., Adachi, C.*
Thermally activated delayed fluorescence of a Zr-based metal–organic framework.
Chem. Commun. 54, 631–634 (2018). DOI:10.1039/C7CC08595H

[21] Xia, Z.*, Kabe, R., Liscio, A., Kovtun, A., Treossi, E., Feng, X., Palermo, V.*
Graphene-pyrene nanocomposites obtained using azide chemistry.
J. Nanosci. Nanotechnol. 18, 1290–1295 (2018). DOI:10.1166/jnn.2018.15254

[20] Mieno, H., Kabe, R.*, Adachi, C.*
Reversible control of triplet dynamics in metal-organic framework-entrapped organic emitters via external gases.
Commun. Chem. 1, 27 (2018). DOI:10.1038/s42004-018-0027-x

[19] Lin, Z., Kabe, R.*, Nishimura, N., Jinnai, K., Adachi, C.*
Organic long-persistent luminescence from a flexible and transparent doped polymer.
Adv. Mater. 30, 1803713 (2018). DOI:10.1002/adma.201803713

[18] Jinnai, K., Kabe, R.*, Adachi, C.*
Wide-range tuning and enhancement of organic long-persistent luminescence using emitter dopants.
Adv. Mater. 30, 1800365 (2018). DOI:10.1002/adma.201800365

[17] Jinnai, K., Kabe, R.*, Adachi, C.*
A near-infrared organic light-emitting diode based on an Yb(III) complex synthesized by vacuum co-deposition.
Chem. Commun. 53, 5457–5460 (2017). DOI:10.1039/C7CC01580A

[16] Kabe, R.*, Adachi, C.*
Organic long persistent luminescence.
Nature 550, 384–387 (2017). DOI:10.1038/nature24010

[15] Notsuka, N., Kabe, R.*, Goushi, K., Adachi, C.*
Confinement of long-lived triplet excitons in organic semiconducting host-guest systems.
Adv. Funct. Mater. 27, 1703902 (2017). DOI:10.1002/adfm.201703902

[14] Noda, H., Kabe, R., Adachi, C.*
Blue thermally activated delayed fluorescence molecule having acridane and cyanobenzene units.
Chem. Lett. 45, 1463–1466 (2016). DOI:10.1246/cl.160814

[13] Yanai, N.*, Kozue, M., Amemori, S., Kabe, R., Adachi, C., Kimizuka, N.*
Increased vis-to-UV upconversion performance by energy level matching between a TADF donor and high triplet energy acceptors.
J. Mater. Chem. C. 4, 6447–6451 (2016). DOI:10.1039/C6TC01816E

[12] Mieno, H., Kabe, R.*, Notsuka, N., Allendorf, M.D., Adachi, C.*
Long-lived room-temperature phosphorescence of coronene in zeolitic imidazolate framework ZIF-8.
Adv. Opt. Mater. 4, 1015–1021 (2016). DOI:10.1002/adom.201600103

[11] Kabe, R., Notsuka, N., Yoshida, K., Adachi, C.*
Afterglow organic light-emitting diode.
Adv. Mater. 28, 655–660 (2016). DOI:10.1002/adma.201504321

[10] Nguyen, N.T., Mori, Y., Matsumoto, T., Yatabe, T., Kabe, R., Nakai, H., Yoon, K.-S., Ogo, S.*
A [NiFe]hydrogenase model that catalyses the release of hydrogen from formic acid.
Chem. Commun. 50, 13385–13387 (2014). DOI:10.1039/C4CC05911E

[09] Kabe, R., Feng, X.*, Adachi, C.*, Müllen, K.*
Exfoliation of graphite into graphene in polar solvents mediated by amphiphilic hexa- peri -hexabenzocoronene.
Chem. - An Asian J. 9, 3125–3129 (2014). DOI:10.1002/asia.201402535

[08] Lee, J.-H., Kim, H.-M., Kim, K.-B., Kabe, R., Anzenbacher, P., Kim, J.-J.*
Homogeneous dispersion of organic p-dopants in an organic semiconductor as an origin of high charge generation efficiency.
Appl. Phys. Lett. 98, 173303 (2011). DOI:10.1063/1.3569144

[07] Matsumoto, T., Kabe, R., Nonaka, K., Ando, T., Yoon, K.-S., Nakai, H., Ogo, S.*
Model study of CO inhibition of [NiFe]hydrogenase.
Inorg. Chem. 50, 8902–8906 (2011). DOI:10.1021/ic200965t

[06] Kabe, R., Lynch, V.M., Anzenbacher Jr., P.*
Enhanced phosphorescence in dibenzophosphole chalcogenide mixed crystal.
CrystEngComm. 13, 5423 (2011). DOI:10.1039/c1ce05388d

[05] Kabe, R., Nakanotani, H., Sakanoue, T., Yahiro, M., Adachi, C.*
Effect of molecular morphology on amplified spontaneous emission of bis-styrylbenzene derivatives.
Adv. Mater. 21, 4034–4038 (2009). DOI:10.1002/adma.200803588

[04] Nakanotani, H., Kabe, R., Yahiro, M., Takenobu, T., Iwasa, Y., Adachi, C.*
Blue-light-emitting ambipolar field-effect transistors using an organic single crystal of 1,4-bis(4-methylstyryl)benzene.
Appl. Phys. Express. 1, 091801 (2008). DOI:10.1143/APEX.1.091801

[03] Shimazaki, Y.*, Kabe, R., Huth, S., Tani, F., Naruta, Y., Yamauchi, O.*
Formation and characterization of Co(III)−semiquinonate phenoxyl radical species.
Inorg. Chem. 46, 6083–6090 (2007). DOI:10.1021/ic700596g

[02] Ogo, S.*, Kabe, R., Uehara, K., Kure, B., Nishimura, T., Menon, S.C., Harada, R., Fukuzumi, S., Higuchi, Y., Ohhara, T., Tamada, T., Kuroki, R.
A Dinuclear Ni(µ-H)Ru Complex Derived from H2.
Science 316, 585–587 (2007). DOI:10.1126/science.1138751

[01] Ogo, S.*, Kabe, R., Hayashi, H., Harada, R., Fukuzumi, S.*
Mechanistic investigation of CO2 hydrogenation by Ru(II) and Ir(III) aqua complexes under acidic conditions: two catalytic systems differing in the nature of the rate determining step.
Dalton Trans. 4657 (2006). DOI:10.1039/b607993h