[1] Jewell LL, Davis BH. Review of absorption and adsorption in the hydrogen–palladium system. Applied Catalysis A: General. 2006;310:1–15.
[2] Fovanna T, Nachtegaal M, Clark AH, Krocher O, Ferri D. Preparation, quantification, and reaction of Pd hydrides on Pd/Al2O3 in liquid environment. Acs Catalysis. 2023;13(5):3323–3332.
[3] Wang X, Monta˜na-Mora G, Han X, Yu J, Qi X, Arbiol J, et al. Palladium Hydride on C2N to Boost Formate Oxidation. ACS Sustainable Chemistry & Engineering. 2023;11(31):11399–11405.
[4] Abdellah AM, Ismail F, Siig OW, Yang J, Andrei CM, DiCecco LA, et al. Impact of palladium/palladium hydride conversion on electrochemical CO2 reduction via in-situ transmission electron microscopy and diffraction. Nature Communications. 2024;15(1):938.
[5] Yun S, Oyama ST. Correlations in palladium membranes for hydrogen separation: A review. Journal of membrane science. 2011;375(1-2):28–45.
[6] Yang X, Li H, Ahuja R, Kang T, Luo W. Formation and electronic properties of palladium hydrides and palladium-rhodium dihydride alloys under pressure. Scientific Reports. 2017;7(1):3520.
[7] Chang J, Ding M, Mao JX, Zhang J, Chen X. Reactions and catalytic applications of a PNCNP pincer palladium hydride complex. Dalton Transactions. 2022;51(46):17602–17608.
[8] Xu M, Zhou Y, Ren C, Liang X, Li N. Palladium Hydride Nanopocket Cubes and Their H2-Therapy Function in Amplifying Inhibition of Foam Cells to Attenuate Atherosclerosis. Advanced Functional Materials. 2021;31(46):2104892.
[9] Guo X, Hu Z, Lv J, Qu J, Hu S. Palladium hydride with high-index facets for enhanced methanol oxidation. Dalton Transactions. 2021;50(30):10359–10364.
[10] Zhang Z, Gevorgyan V. Palladium hydrideenabled hydroalkenylation of strained molecules. Journal of the American Chemical Society. 2022;144(45):20875–20883.
[11] Liu Q, Du H, Li Z, Wang C, Zeng X, Wang R, et al. Cyanogel-Induced Facile Synthesis of Palladium Hydride for Electrocatalytic Oxygen Reduction. ChemSusChem. 2024;p. e202400680.
[12] Adams BD, Chen A. The role of palladium in a hydrogen economy. Materials today. 2011;14(6):282–289.
[13] Zhao Y, Truhlar DG. A density functional that accounts for medium-range correlation energies in organic chemistry. Organic Letters. 2006;8(25):5753–5755.
[14] Das P, Lee YS, Lee SC, Bhattacharjee S. Computational design of a new palladium alloy with efficient hydrogen storage capacity and hydrogenation-dehydrogenation kinetics. International Journal of Hydrogen Energy.
2023;48(49):18795–18803.
[15] Cort´es-Guzm´an F, Bader RF. Complementarity of QTAIM and MO theory in the study of bonding in donor–acceptor complexes. Coordination Chemistry Reviews. 2005;249(5-6):633–662.
[16] Farrugia LJ, Evans C, Lentz D, Roemer M. The QTAIM Approach to Chemical Bonding Between Transition Metals and Carbocyclic Rings: A Combined Experimental and Theoretical Study of (η5−C5H5)Mn(CO)3, (η6−C6H6)Cr(CO)3, and (E)−{(η5−C5H4)CF−−CF(η5−C5H4)}(η5−C5H5)2Fe2. Journal of the American Chemical Society. 2009;131(3):1251–1268. PMID: 19102692.
[17] Frisch MJ, Trucks GW, Schlegel HB, Scuseria GE, Robb MA, Cheeseman JR, et al.. Gaussian˜16 Revision C.01; 2016. Gaussian Inc. Wallingford CT.
[18] Andrews L, Wang X, Alikhani ME, Manceron L. Observed and calculated infrared spectra of Pd(H2) 1, 2, 3 complexes and palladium hydrides in solid argon and neon. The Journal of Physical Chemistry A. 2001;105(13):3052–3063.