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@ARTICLE{Ma:585960,
      author       = {Ma, Xiaoxin and Zheng, Daniel J. and Hou, Shujin and
                      Mukherjee, Soumya and Khare, Rachit and Gao, Guanhui and Ai,
                      Qing and Garlyyev, Batyr and Li, Weijin and Koch, Max and
                      Mink, János and Shao-Horn, Yang and Warnan, Julien and
                      Bandarenka, Aliaksandr S. and Fischer, Roland A.},
      title        = {{S}tructure–{A}ctivity {R}elationships in {N}i-
                      {C}arboxylate-{T}ype {M}etal–{O}rganic {F}rameworks’
                      {M}etamorphosis for the {O}xygen {E}volution {R}eaction},
      journal      = {ACS catalysis},
      volume       = {13},
      number       = {11},
      issn         = {2155-5435},
      address      = {Washington, DC},
      publisher    = {ACS},
      reportid     = {PUBDB-2023-03699},
      pages        = {7587 - 7596},
      year         = {2023},
      note         = {Waiting for fulltext},
      abstract     = {Metal–organic frameworks (MOFs) have been reported to
                      catalyze the oxygen evolution reaction (OER). Despite the
                      established links between the pristine MOFs and their
                      derived metal hydroxide electrocatalysts, several
                      limitations still preclude understanding of the critical
                      factors determining the OER performance. Of prime importance
                      appears the choice of MOF and how its compositions relate to
                      the catalyst stability and in turn to the reconstruction or
                      metamorphosis mechanisms into the active species under OER
                      conditions. An isoreticular series of Ni-carboxylate-type
                      MOFs [Ni$_2$(OH)$_2$L] was chosen to elucidate the effects
                      of the carboxylate linker length expansion and modulation of
                      the linker–linker $π–π$ interactions (L =
                      1,4-benzodicarboxylate, 2,6-napthalenedicarboxylate,
                      biphenyl-4,4′-dicarboxylate, and
                      p-terphenyl-4,4″-dicarboxylate). Degradation and
                      reconstruction of MOFs were systematically investigated. The
                      linker controls the transformation of Ni-MOF into distinct
                      nickel hydroxide phases, and the conversion from
                      $α$-Ni(OH)$_2$ to $β$-Ni(OH)$_2$, thus correlating the
                      Ni-MOF composition with the OER activity of the
                      Ni-MOF-derived metastable nickel hydroxide phase mixture.},
      cin          = {DOOR ; HAS-User / TUM},
      ddc          = {540},
      cid          = {I:(DE-H253)HAS-User-20120731 / I:(DE-588b)36241-4},
      pnm          = {6G3 - PETRA III (DESY) (POF4-6G3)},
      pid          = {G:(DE-HGF)POF4-6G3},
      experiment   = {EXP:(DE-H253)P-P64-20150101},
      typ          = {PUB:(DE-HGF)16},
      UT           = {WOS:001006503200001},
      doi          = {10.1021/acscatal.3c00625},
      url          = {https://bib-pubdb1.desy.de/record/585960},
}