Chiral Molecule Heterostructure for Electric Field Magnetization

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Solution Overview

Problem

Current magnetic memory devices and spintronic applications rely on ferromagnetic layers and struggle to induce local magnetization without magnetic components, limiting their functionality and efficiency.

Innovation Solution

A semiconductor heterostructure with a two-dimensional electron gas layer and a chiral or biological macromolecule assembly, where the chiral/biological layer is bound to the semiconductor layers, enabling electric-field induced ferro- or superparamagnetism without magnetic components, allowing for robust and reversible magnetization control.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Reliability

If ferromagnetic layers are used in magnetic memory devices, then magnetization control is achieved, but device complexity and inability to induce local magnetization without magnetic components worsen

Engineering Contradiction:
Improvemagnetization controlVSAvoidcomplex layered structures
Core Design Contradiction:
ReliabilityVSDevice complexity

Solution Approach 1:

The patent removes ferromagnetic layers from the device structure entirely, extracting the magnetic functionality from traditional magnetic components and replacing it with a non-magnetic semiconductor heterostructure that can be controlled by electric fields and chiral molecules

Inventive Principle:
Principle #2Taking out (Extraction)

Solution Approach 2:

The patent introduces chiral or biological macromolecule assemblies as intermediaries that mediate between the electric field and the two-dimensional electron gas, enabling magnetization control without direct magnetic component contact

Inventive Principle:
Principle #24Intermediary (Mediator)

2Productivity

If electric fields are used to induce local magnetization, then switching speed improves, but the ability to create localized magnetic fields without magnetic components worsens

Engineering Contradiction:
Improveswitching rateVSAvoidstructure simplicity
Core Design Contradiction:
ProductivityVSDevice complexity

Solution Approach 1:

The patent replaces mechanical/magnetic field-based magnetization control with electric field control through chiral molecules, substituting one physical mechanism for another to achieve faster switching speeds while maintaining structural simplicity

Inventive Principle:
Principle #28Mechanics substitution (Replace mechanical system)

Applied Scientific Principles

This section explains which scientific principles are used to turn an abstract innovation direction into a practical engineering solution.

Function Achieved in This Case

This approach enables efficient, electric-field controlled magnetization at room temperature with fast switching rates and the ability to create localized magnetic fields, eliminating the need for complex layered structures and allowing for high-frequency operation in memory devices and spintronic applications.

Implementation Method 1

The observation of chiral-induced spin-selectivity (CISS), a large spin-polarization that arises when electrons transfer through chiral organic molecules, suggests the use of chiral molecules in place of magnetic elements

Methodology Applied
Scientific EffectChiral-induced spin selectivity (CISS):

Implementation Method 2

a semiconductor heterostructure with a two-dimensional electron gas layer and a chiral or biological macromolecule assembly

Methodology Applied
Scientific EffectTwo-dimensional electron gas formation:

Data Source

PatentUS11437501B2Device for electric field induced local magnetization
Publication Date: 2022.09.06 YEDA RES & DEV CO LTD
  • US11437501B2 patent drawing
  • US11437501B2 patent drawing
  • US11437501B2 patent drawing

AI summary

In a technique for inducing local electric field controlled magnetization, despite the absence of magnetic components, there is provided a novel heterostructure, a semiconductor device thereof, or an array of semiconductor devices. The heterostructure includes a semiconductor substrate carrying a plurality of layers forming at least one heterojunction and hosting a two-dimensional electron gas layer when one of the layer of the plurality of layers is bounded to an interacting layer being a chiral or a biological macromolecule assembly.