2018 New's Items

Design Principles for Trap-Free CsPbX3 Nanocrystals: Enumerating and Eliminating Surface Halide Vacancies with Softer Lewis Bases

David P. Nenon
Kimo Pressler
Jun Kang
Brent A. Koscher
Jacob H. Olshansky
Wojciech T. Osowiecki
Matthew A. Koc
Lin-Wang Wang
A. Paul Alivisatos
2018

We introduce a general surface passivation mechanism for cesium lead halide perovskite materials (CsPbX3, X = Cl, Br, I) that is supported by a combined experimental and theoretical study of the nanocrystal surface chemistry. A variety of spectroscopic methods are employed together with ab initio calculations to identify surface halide vacancies as the predominant source of charge trapping. The number of surface traps per nanocrystal is quantified by 1H NMR spectroscopy, and that number is consistent with a simple...

Local Electronic Structure of Molecular Heterojunctions in a Single‐Layer 2D Covalent Organic Framework

T. Joshi
C. Chen
H. Li
C. S. Diercks
G. Wang
P. J. Waller
H. Li
J. Bredas
O. M. Yaghi
M. F. Crommie
2018

The synthesis of a single‐layer covalent organic framework (COF) with spatially modulated internal potentials provides new opportunities for manipulating the electronic structure of molecularly defined materials. Here, the fabrication and electronic characterization of COF‐420: a single‐layer porphyrin‐based square‐lattice COF containing a periodic array of oriented, type II electronic heterojunctions is reported. In contrast to previous donor–acceptor COFs, COF‐420 is constructed from building blocks that yield identical cores upon reticulation, but that are bridged by electrically...

Molecular Weaving of Covalent Organic Frameworks for Adaptive Guest Inclusion

Y. Liu
Y. Ma
J. Yang
C. S. Diercks
N. Tamura
F. Jin
O. M. Yaghi
2018

The synthesis of new isoreticular non-interpenetrated woven covalent organic frameworks (COFs) was achieved by linking aldehyde-functionalized copper(I) bisphenanthroline complexes with benzidine linkers in the presence of a bulky anion, diphenylphosphinate (PO2Ph2-) to give metalated COF-506-Cu and, upon removal of copper(I), the demetalated COF-506. The structures of these COFs were determined by a combination of powder X-ray diffraction and electron microscopy techniques. Guest-accessibility to the pores of the two...

Molecular Mechanics Simulations and Improved Tight-Binding Hamiltonians for Artificial Light Harvesting Systems: Predicting Geometric Distributions, Disorder, and Spectroscopy of Chromophores in a Protein Environment

Lee J
Lee D
Kocherzhenko AA
Greenman L
Finley DT
Francis MB
Whaley KB
2018

We present molecular mechanics and spectroscopic calculations on prototype artificial light harvesting systems consisting of chromophores attached to a tobacco mosaic virus (TMV) protein scaffold. These systems have been synthesized and characterized spectroscopically, but information about the microscopic configurations and geometry of these TMV-templated chromophore assemblies is largely unknown. We use a Monte Carlo conformational search algorithm to determine the preferred positions and orientations of two chromophores, Coumarin 343 together with its linker and Oregon Green 488,...

Identification of the Strong Brønsted Acid Site in a Metal–Organic Framework Solid Acid Catalyst

C. A. Trickett
T. M. Osborn Popp
J. Su
C. Yan
J. Weisberg
A. Huq
P. Urban
J. Jiang
M. J. Kalmutzki
Q. Liu
J. Baek
M. P. Head-Gordon
G. A. Somorjai
J. A. Reimer
O. M. Yaghi
2018

It remains difficult to understand the surface of solid acid catalysts at the molecular level, despite their importance for industrial catalytic applications. A sulfated zirconium-based metal–organic framework, MOF-808-SO4, was previously shown to be a strong solid Brønsted acid material. In this report, we probe the origin of its acidity through an array of spectroscopic, crystallographic and computational characterization techniques. The strongest Brønsted acid site is shown to consist of a specific arrangement of adsorbed water and sulfate moieties on the...

Incarceration of Iodine in a Pyrene-Based Metal-Organic Framework

A.Gładysiak
T. N. Nguyen
M. Spodaryk
J.-H. Lee
J. B. Neaton
A. Züttel
K. C. Stylianou
2018

A pyrene‐based metal‐organic framework (MOF) SION‐8 captured iodine (I2) vapor with a capacity of 460 and 250 mg g−1MOF at room temperature and 75 °C, respectively. Single‐crystal X‐ray diffraction analysis and van‐der‐Waals‐corrected density functional theory calculations confirmed the presence of I2 molecules within the pores of SION‐8 and their interaction with the pyrene‐based ligands. The I2–pyrene interactions...

Leveraging Continuous Material Averaging for Inverse Electromagnetic Design

A. Michaels
E. Yablonovitch
2018

Inverse electromagnetic design has emerged as a way of efficiently designing active and passive electromagnetic devices. This maturing strategy involves optimizing the shape or topology of a device in order to improve a figure of merit–a process which typically requires that we compute the gradient of a figure of merit which describes device performance, potentially with respect to many design variables. In this paper, we introduce a new strategy based on smoothing abrupt material interfaces which enables us to efficiently compute these gradients with high accuracy irrespective of...

Fundamental limitations on photoisomerization from thermodynamic resource theories

N. Yunger Halpern
D.T. Limmer
2018

Small, out-of-equilibrium, and quantum systems defy simple thermodynamic expressions. Such systems are exemplified by molecular switches, which exchange heat with a bath. These molecules can photoisomerize, or change conformation, or switch, upon absorbing light. The photoisomerization probability depends on kinetic details that couple the molecule's energetics to its dissipation. Therefore, a simple, general, thermodynamic-style bound on the photoisomerization probability seems out of reach. We derive such a bound using a resource theory. The resource-theory framework is a set of...

Urea-Linked Covalent Organic Frameworks

C. Zhao
C. S. Diercks
C. Zhu
N. Hanikel
X. Pei
O. M. Yaghi
2018

2D covalent organic frameworks (COFs) with flexible urea linkages have been synthesized by condensation of 1,3,5-triformylphloroglucinol (TFP) with 1,4-phenylenediurea (BDU) or 1,1′-(3,3′-dimethyl-[1,1′-biphenyl]-4,4′-diyl)diurea (DMBDU). The resulting COF-117 and COF-118 undergo reversible structural dynamics within their layers, in response to inclusion and removal of guest molecules, emanating from urea C—N bond rotation and interlayer hydrogen-bonding interactions. These compounds are the first urea-linked COFs, serving to expand the scope of reticular chemistry.

Building a Global Culture of Science —The Vietnam Experience

K. E. Cordova
O. M. Yaghi
2018

We detail the lessons learned, challenges, achievements, and outlook in building a chemistry research center in Vietnam. Through the principles of “global science”, we provide specific insight into the process behind establishing an internationally‐competitive research program—a model that is scalable and adaptable to countries beyond Vietnam. Furthermore, we highlight the prospects for success in advancing global science education, research capacity building, and mentorship.