Absolute Electron Spin Quantification via RF Resonator Sensitivity Calibration

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Solution Overview

Problem

Current methods for determining the absolute number of electron spins in samples using electron spin resonance (ESR) spectroscopy require preparing and measuring a reference sample for each unknown sample, which is cumbersome and limited to liquid samples, and relative quantification methods do not provide absolute spin numbers.

Innovation Solution

A method involving the determination of the spatial sensitivity profile of the RF resonator and a resonator sensitivity constant using a calibration sample, allowing for the absolute quantification of electron spins in samples without the need for a reference sample, by weighing the magnetic resonance signal with the integral of the sensitivity profile.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Measurement precision

If a reference sample is prepared and measured for each unknown sample using a double resonator, then absolute quantification of electron spins is achieved, but the device complexity and measurement time increase significantly

Engineering Contradiction:
Improveabsolute quantification of electron spinsVSAvoiddouble resonator construction
Core Design Contradiction:
Measurement precisionVSDevice complexity

Solution Approach 1:

The patent extracts the reference sample measurement from the simultaneous dual-sample measurement approach. Instead of measuring unknown and reference samples together in a double resonator, the method measures the unknown sample first, then separately measures a calibration sample to determine resonator sensitivity. This separates the measurement processes while maintaining absolute quantification capability.

Inventive Principle:
Principle #2Taking out (Extraction)

Solution Approach 2:

The patent performs preliminary calibration by measuring a calibration sample with known spin concentration before measuring unknown samples. The resonator sensitivity constant is determined in advance and stored for subsequent measurements. This preliminary action eliminates the need for simultaneous reference sample measurement during unknown sample analysis.

Inventive Principle:
Principle #10Preliminary action

2Measurement precision

If a reference sample is prepared and measured for each unknown sample, then absolute quantification is achieved, but the loss of time increases due to repeated preparation and measurement

Engineering Contradiction:
Improveabsolute quantification of electron spinsVSAvoidtime for sample preparation and measurement
Core Design Contradiction:
Measurement precisionVSLoss of time

Solution Approach 1:

The resonator sensitivity constant is determined through preliminary calibration using a calibration sample and stored for reuse. This preliminary action eliminates the need to prepare and measure reference samples for each unknown sample, significantly reducing measurement time while maintaining absolute quantification accuracy.

Inventive Principle:
Principle #10Preliminary action

Solution Approach 2:

The method uses a stored sensitivity constant (a form of data copy) from calibration measurements to quantify unknown samples. Instead of physically copying the reference sample for each measurement, the sensitivity information is copied and reused, eliminating repeated preparation time.

Inventive Principle:
Principle #26Copying

3Productivity

If a marker probe sample is measured simultaneously with each sample, then relative quantification is achieved, but the measurement precision for absolute spin numbers is not obtained

Engineering Contradiction:
Improvesimultaneous measurement capabilityVSAvoidabsolute number of electron spins
Core Design Contradiction:
ProductivityVSMeasurement precision

Solution Approach 1:

The patent replaces the physical marker probe sample approach with a computational method. Instead of using a physical marker to normalize signals, the method uses a calculated sensitivity profile and sensitivity constant to directly determine absolute spin numbers from the unknown sample signal, eliminating the need for marker samples.

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

4Measurement precision

If equivalent reference samples are prepared for each unknown sample, then measurement precision is improved, but the ease of operation decreases due to cumbersome preparation requirements

Engineering Contradiction:
Improveabsolute quantification accuracyVSAvoidsample preparation simplicity
Core Design Contradiction:
Measurement precisionVSEase of operation

Solution Approach 1:

The resonator sensitivity constant determined from a single calibration sample serves as a universal parameter for quantifying all unknown samples measured with that resonator. This universal calibration approach eliminates the need to prepare equivalent reference samples for each unknown sample type, greatly simplifying operation while maintaining accuracy.

Inventive Principle:
Principle #6Universality (Multi-functionality)

Solution Approach 2:

The method changes from requiring sample-specific reference preparations to using a general sensitivity constant that accounts for resonator characteristics. By separating the resonator sensitivity parameter from the sample-specific measurements, the system achieves universal applicability across different sample types without cumbersome preparation requirements.

Inventive Principle:
Principle #35Parameter changes

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 method simplifies and accelerates the absolute determination of electron spins, enabling measurement of various sample types, including solids and liquids, without the need for a reference sample, and provides precise quantification using the resonator's known properties.

Implementation Method 1

electron spin resonance (ESR) spectroscopy is a method of analytic instrumentation for the investigation of a sample. The sample must thereby have unpaired electrons. Microwave (generally with constant frequency), are irradiated into the sample which is located in a strong magnetic field B0

Methodology Applied
Scientific EffectElectron spin resonance: Electron Paramagnetic Resonance

Implementation Method 2

measuring the magnetic resonance signal RS of the extended sample in the apparatus with known spatial distribution of the extended sample within the measuring volume

Methodology Applied
Scientific EffectMagnetic resonance detection: Electromagnetic Induction

Data Source

PatentUS7586305B2Method for determining the absolute number of electron spins in a sample of extended size
Publication Date: 2009.09.08 BRUKER BIOSPIN MRI GMBH
  • US7586305B2 patent drawing
  • US7586305B2 patent drawing
  • US7586305B2 patent drawing

AI summary

In a method for determining an absolute number of electron spins in an extended sample (3) with the assistance of an apparatus for measuring magnetic resonance, the extended sample (3) is disposed within a measurement volume (2) of a radiofrequency RF resonator (1) of the apparatus during an electron spin resonance measurement (ESR). The method has the following steps: determining a spatial sensitivity profile f of the RF resonator (1) over the measurement volume (2); determining a resonator sensitivity constant c by means of a comparison to the measurement volume (2) of small calibration sample having a known number of electron spins at a particular position within the measurement volume (2); measuring a magnetic resonance signal RS of the extended sample (3) in the apparatus with a known spatial distribution of extended sample (3) within the measurement volume (2); weighting the magnetic resonance signal RS with the integral of the spatial sensitivity profile f of the RF resonator over the partial volume of the measurement volume (2) occupied by the extended sample (3); and determining the number of electron spins NS in extended sample (3) as a quotient between the weighted resonance signal and the resonator sensitivity constant c. The method facilitates a simpler determination of the absolute number of electron spins in the sample.