Zhou, Ping

Liu, Jung-Ching; Li, Chao; Hess, Richard; Chen, Hongyan; Drechsel, Carl; Zhou, Ping; Häner, Robert; Aschauer, Ulrich; Glatzel, Thilo; Decurtins, Silvio; Loss, Daniel; Klinovaja, Jelena; Liu, Shi-Xia; Wulfhekel, Wulf; Meyer, Ernst; Pawlak, Rémy (27 October 2023). Gate-tunable topological superconductivity in a supramolecular electron spin lattice (Cornell University). arXiv 10.48550/arxiv.2310.18134

Liu, Jung-Ching; Pawlak, Rémy; Wang, Xing; Chen, Hongyan; D’Astolfo, Philipp; Drechsel, Carl; Zhou, Ping; Häner, Robert; Decurtins, Silvio; Aschauer, Ulrich; Liu, Shi-Xia; Wulfhekel, Wulf; Meyer, Ernst (2023). Proximity-Induced Superconductivity in Atomically Precise Nanographene on Ag/Nb(110). ACS materials letters, 5(4), pp. 1083-1090. ACS Publications 10.1021/acsmaterialslett.2c00955

Hong, Wenjing; Zhang, Hewei; Zhou, Ping; Daaoub, Abdul; Sangtarash, Sara; Zhao, Shiqiang; Yang, Zixian; Zhou, Yu; Zou, Yuling; Decurtins, Silvio; Häner, Robert; Yang, Yang; Sadeghi, Hatef; Liu, Shi-Xia (2023). Atomically Well-defined Nitrogen Doping in the Cross-plane Transport through Graphene Heterojunctions. Chemical Science, 14(22), pp. 6079-6086. The Royal Society of Chemistry 10.1039/D3SC00075C

Zhou, Ping; Aschauer, Ulrich; Decurtins, Silvio; Feurer, Thomas; Häner, Robert; Liu, Shi-Xia (2023). Merging of Azulene and Perylene Diimide for Optical pH Sensors. Molecules, 28(18), p. 6694. MDPI 10.3390/molecules28186694

Li, Chao; Kaspar, Christoph; Zhou, Ping; Liu, Jung-Ching; Chahib, Outhmane; Glatzel, Thilo; Häner, Robert; Aschauer, Ulrich; Decurtins, Silvio; Liu, Shi-Xia; Thoss, Michael; Meyer, Ernst; Pawlak, Rémy (2023). Strong signature of electron-vibration coupling in molecules on Ag(111) triggered by tip-gated discharging. Nature Communications, 14(1), p. 5956. Springer Nature 10.1038/s41467-023-41601-2

Liu, Shi-Xia; Zhou, Ping; Nazari Haghighi Pashaki, Maryam; Frey, Hans-Martin; Hauser, Andreas; Decurtins, Silvio; Cannizzo, Andrea; Feurer, Thomas; Häner, Robert; Aschauer, Ulrich (2023). Photoinduced Asymmetric Charge Trapping in a Symmetric Tetraazapyrene-Fused Bis(tetrathiafulvalene) Conjugate. Chemical Science, 14(44), pp. 12715-12722. The Royal Society of Chemistry 10.1039/D3SC03184E

Zhou, Ping; Aschauer, Ulrich; Decurtins, Silvio; Feurer, Thomas; Häner, Robert; Liu, Shi-Xia (2021). Effect of tert-butyl groups on electronic communication between redox units in tetrathiafulvalene-tetraazapyrene triads. Chemical communications, 57(96), pp. 12972-12975. Royal Society of Chemistry 10.1039/D1CC05671A

Zhou, Ping; Aschauer, Ulrich; Feurer, Thomas; Häner, Robert; Liu, Shi-Xia (13 September 2021). Photo-induced Charge Transfer in Azapyrene-Tetrathiafulvalene Triads (Unpublished). In: NCCR MUST 2021.

Zhou, Ping; Aschauer, Ulrich; Feurer, Thomas; Häner, Robert; Liu, Shi-Xia (10 September 2021). Photo-induced Charge Transfer in Azapyrene-Tetrathiafulvalene Triads (Unpublished). In: SCS Fall Meeting 2021.

Zhou, Ping; Michel, Volland; Leonie, Wibmer; Feurer, Thomas; Häner, Robert; Decurtins, Silvio; Liu, Shi-Xia; Guldi, Dirk M. (2 June 2020). Nanographene favors electronic interactions with an electron acceptor rather than an electron donor in a planar fused push–pull conjugate (Unpublished). In: NCCR MUST 2020.

Zhou, Ping; Aschauer, Ulrich; Decurtins, Silvio; Feurer, Thomas; Häner, Robert; Liu, Shi-Xia (2020). Chemical control of photoinduced charge-transfer direction in a tetrathiafulvalene-fused dipyrrolylquinoxaline difluoroborate dyad. Chemical communications, 56(87), pp. 13421-13424. Royal Society of Chemistry 10.1039/D0CC05736C

Zhou, Ping; Michel, Volland; Leonie, Wibmer; Häner, Robert; Decurtins, Silvio; Liu, Shi-Xia; Guldi, Dirk M. (6 September 2019). Nanographene Favors Interactions with the Electron Acceptor Rather Than the Electron Donor in a Planar Fused Push-Pull Conjugate (Unpublished). In: Swiss Chemical Society Fall Meeting 2019. September 6, 2019.

Zhou, Ping; Volland, Michel; Leonie, Wibmer; Häner, Robert; Decurtins, Silvio; Liu, Shi-Xia; Guldi, Dirk M. (14 January 2019). Nanographene Favors Interactions with the Electron Acceptor Rather Than the Electron Donor in a Planar Fused Push-Pull Conjugate (Unpublished). In: NCCR MUST. Grindelwald. January 14-16, 2019.

Volland, Michel; Zhou, Ping; Wibmer, Leonie; Häner, Robert; Decurtins, Silvio; Liu, Shi-Xia; Guldi, Dirk M. (2019). Nanographene favors electronic interactions with an electron acceptor rather than an electron donor in a planar fused push–pull conjugate. Nanoscale, 11(3), pp. 1437-1441. Royal Society of Chemistry 10.1039/c8nr06961a